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Serotonin–norepinephrine–dopamine reuptake inhibitor

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Title: Serotonin–norepinephrine–dopamine reuptake inhibitor  
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Subject: 5-APB, JZ-IV-10, 6-APB, RTI-112, Obsessional jealousy
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Serotonin–norepinephrine–dopamine reuptake inhibitor

GABA is inhibitory; Glutamate is excitatory., Possible MOR, σ-receptor, antihistamine, melatonin etc.

A serotonin–norepinephrine–dopamine reuptake inhibitor (SNDRI), more commonly known as a triple reuptake inhibitor (TRI), or sometimes a TUI (DOV), is a drug that concomitantly acts as a reuptake inhibitor for the monoamine neurotransmitters, serotonin (5-HT), norepinephrine (noradrenaline, NA) and dopamine (DA), by blocking the action of the serotonin transporter (SERT), norepinephrine transporter (NET), and dopamine transporter (DAT), respectively. This, in turn, increases extracellular concentrations of these neurotransmitters and, therefore, an increase in serotonergic, noradrenergic or adrenergic, and dopaminergic neurotransmission.

This group of drugs works in a way similar to the monoamine releasers (e.g., PAL-303, PAL-287), albeit through different mechanism (read reviews by R. Rothman et al.).

Nonselective MAOIs, including tranylcypromine and phenelzine also elevate the extracellular concentration of monoaminergic neurotransmitters (i.e. 5-HT, NA and DA) in the CNS. Many of the substituted amphetamines also display MAOI activity, although they are reversible and not 'suicide inhibitors' (alkylating agents that can form a covalent bond/s with their molecular targets). Note: alkylating agents that can penetrate the CNS have been used as antineoplastics (c.f. cyclomustine and procarbazine).

Such compounds are often (somewhat disparagingly) referred to as 'dirty drugs' (not because low chemical purity of the compounds though); because they recruit a plurality of modes of activity. Bryan Roth used the term selectively–nonselective;.[1][2]


  • Depression 1
  • Pharmacotherapy 2
  • Applications other than for treating Depression 3
  • Examples 4
  • Toxicological 5
  • Addiction 6
    • Relation to cocaine 6.1
  • ADME 7
  • Affordability (i.e. cost) 8
  • Legality 9
  • Role of monoamine neurotransmitters 10
    • Monoamine Hypothesis 10.1
    • Dopaminergic 10.2
    • Noradrenergic 10.3
    • Serotonergic 10.4
    • Anxiety 10.5
    • Neurotrophins 10.6
  • Current antidepressants 11
    • SSRIs 11.1
    • NRIs 11.2
    • NDRIs 11.3
    • SNRIs 11.4
    • NaSSAs 11.5
    • Atypical 11.6
    • MAOIs 11.7
    • TCAs 11.8
  • Beyond Monoamines 12
  • See also 13
  • References 14


depression is the leading cause of disability and the 4th leading contributor to the global burden of disease in 2000. By the year 2020, depression is projected to reach 2nd place in the ranking of DALYs.[13]

About 16% of the population is estimated to be affected by major depression, and another 1% is affected by bipolar disorder.In both cases, during one or more times throughout an individual's lifetime. The presence of the common symptoms of these disorders are collectively called 'depressive syndrome' and includes a long-lasting depressed mood, feelings of guilt, anxiety, and recurrent thoughts of death and suicide.[14] Other symptoms including poor concentration, a disturbance of sleep rhythms (insomnia or hypersomnia), and severe fatigue may also occur. Individual patients present differing subsets of symptoms, which may change over the course of the disease highlighting its multifaceted and heterogeneous nature.[8] Depression is often highly comorbid with other diseases, e.g. cardiovascular disease (myocardial infarction,[15] stroke),[16] diabetes,[17] cancer,[18] Depressed subjects are prone to smoking,[19] substance abuse,[20] eating disorders, obesity, high blood pressure, pathological gambling and internet addiction,[21] and on average have a 15 to 30 year shorter lifetime compared with the general population.[16]

Major depression can strike at virtually any time of life as a function of genetic and developmental pre-disposition in interaction with adverse life-events. Although common in the elderly, over the course of the last century, the average age for a first episode has fallen to ~30 years. However, depressive states (with subtly different characteristics) are now frequently identified in adolescents and even children. The differential diagnosis (and management) of depression in young populations requires considerable care and experience; for example, apparent depression in teenagers may later transpire to represent a prodromal phase of schizophrenia.[8]

The ability to work, familial relationships, social integration, and self-care are all severely disrupted.[8]

The genetic contribution has been estimated as 40-50%. However, combinations of multiple genetic factors may be involved because a defect in a single gene usually fails to induce the multifaceted symptoms of depression.[14]


There remains a need for more efficacious antidepressant agents. Although two-thirds of patients will ultimately respond to anti-depressant treatment, one-third of patients respond to placebo,[22] and remission is frequently sub-maximal (residual symptoms). In addition to post-treatment relapse, depressive symptoms can even recur in the course of long-term therapy (tachyphylaxis). Also, currently available antidepressants all elicit undesirable side-effects, and new agents should be divested of the distressing side-effects of both first and second-generation antidepressants.[8]

Another serious drawback of all antidepressants is the requirement for long-term administration prior to maximal therapeutic efficacy. Although some patients show a partial response within 1–2 weeks, in general one must reckon with a delay of 3–6 weeks before full efficacy is attained. In general, this delay to onset of action is attributed to a spectrum of long-term adaptive changes. These include receptor desensitization, alterations in intracellular transduction cascades and gene expression, the induction of neurogenesis, and modifications in synaptic architecture and signaling.[8]

Depression has been associated with impaired neurotransmission of serotonergic, noradrenergic, and dopaminergic pathways, although most pharmacologic treatment strategies directly enhance only 5-HT and NE neurotransmission.[6] In some patients with depression, DA-related disturbances improve upon treatment with antidepressants, it is presumed by acting on serotonergic or noradrenergic circuits, which then affect DA function. However, most antidepressant treatments do not directly enhance DA neurotransmission, which may contribute to residual symptoms, including impaired motivation, concentration, and pleasure.[23]

Preclinical and clinical research indicates that drugs inhibiting the reuptake of all (3?) of these neurotransmitters can produce a more rapid onset of action and greater efficacy than traditional antidepressants.[10]

DA may promote neurotrophic processes in the adult hippocampus, as 5-HT and NA do. It is thus possible that the stimulation of multiple signalling pathways resulting from the elevation of all three monoamines may account, in part, for an accelerated and/or greater antidepressant response.[5]

Dense connections exist between monoaminergic neurons. Dopaminergic neurotransmission regulates the activity of 5-HT and NE in the dorsal raphe nucleus (DR) and locus coeruleus (LC), respectively. In turn, the ventral tegmental area (VTA) is sensitive to 5-HT and NE release.[5]

In the case of SSRIs, the promiscuity among transporters means that there may be more than a single type of neurotransmitter to consider (e.g. 5-HT, DA, NE, etc.) as mediating the therapeutic actions of a given medication. MATs are able to transport monoamines other than their "native" neurotransmitter. It was advised to consider the role of the plasma membrane monoamine transporter (PMAT).[24]

To examine the role of monoamine transporters in models of depression DAT, NET, and SERT knockout (KO) mice and wild-type littermates were studied in the forced swim test (FST), the tail suspension test, and for sucrose consumption. The effects of DAT KO in animal models of depression are larger than those produced by NET or SERT KO, and unlikely to be simply the result of the confounding effects of locomotor hyperactivity; thus, these data support reevaluation of the role that DAT expression could play in depression and the potential antidepressant effects of DAT blockade.[9]

The SSRIs were intended to be highly selective at binding to their molecular targets. However it may be an oversimplification, or at least controversial in thinking that complex psychiatric (and neurological) diseases are easily solved by such a monotherapy. While it may be inferred that dysfunction of 5-HT circuits is likely to be a part of the problem, it is only one of many such neurotransmitters whose signaling can be affected by suitably designed medicines attempting to alter the course of the disease state.

Most common CNS disorders are highly polygenic in nature; that is, they are controlled by complex interactions between numerous gene products. As such, these conditions do not exhibit the single gene defect basis that is so attractive for the development of highly-specific drugs largely free of major undesirable side-effects ("the magic bullet"). Second, the exact nature of the interactions that occur between the numerous gene products typically involved in CNS disorders remain elusive, and the biological mechanisms underlying mental illnesses are poorly understood.[1]

Clozapine and dimebon are examples of drugs used in the treatment of CNS disorders that have a superior efficacy precisely because of their "multifarious" broadspectrum mode of activity. Likewise, in cancer chemotherapeutics, it has been recognized that drugs active at more than one target have a higher probability of being efficacious.[1][2][25][26][27][28][29][30]

In addition, the nonselective MAOIs and the TCA SNRIs are widely believed to have an efficacy that is superior to the SSRIs that are normally picked as the first-line choice of agents for/in the treatment of MDD and related disorders.[31] The reason for this is based on the fact that SSRIs are safer than nonselective MAOIs and TCAs. This is both in terms of there being less mortality in the event of overdose, but also less risk in terms of dietary restrictions (in the case of the nonselective MAOIs), hepatotoxicity (MAOIs) or cardiotoxicity (TCAs).

'AIDS cocktails' is another example of where it is simply more advantageous to target multiple receptors than it is to find a magic bullet for any one single receptor.

In the case of epibatidine, it is clearly this drug's lack of selectivity that separates its analgesic actions from its potential to cause lethality. However, if we look at a different painkiller called Vioxx, despite being a highly selective agent, it was less safe to use than some of the earlier COX-2 inhibitors.

Applications other than for treating Depression


Licensed Pharmaceuticals
PRC200-SS and PRC025-racemic
Currently in clinical trials
  • Amitifadine (DOV 21,947 or EB-1010) (2003).[38][39][40]
  • EB-1020 see here for details 1 to 6 to 14 ratio for NDS
  • Tesofensine (NS-2330) (2001). This is also said to have an acetylcholinergic component to it in addition to behaving as a functional SNDRI.
    • NS 2360 is the principle metabolite (N-demethylation).
  • AN788 (formally NSD-788) see here for details
  • Tedatioxetine (Lu AA24530).[41][42] (TRI and specific 5-HT2C, 5-HT3, 5-HT2A, α1 modulator)
  • RG-7166 was developed by Roche Holding AG. Phase I development began in the 4Q of 2009. In February 2012, the development of RG-7166 was discontinued, and the reason was not disclosed.
  • Lu-AA37096 see here (TRI and specific 5-HT6 modulator)
  • Lu AA34893 see here (TRI and specific 5-HT2A, α1 and 5-HT6 modulator)
Previously subjected to clinical trials
Designer drugs
Research compounds (with no written record of ever having been taken by humans)
Patented material with no link to University Research Publications

Liming Shao released a citation recently (2014) many of the recent developments in the industry.

WO 2008025777 
Test compound 5-HT-uptake IC50(μM) DA-uptake IC50(μM) NA-uptake IC50(μM)
4-(3,4-Dichloro-benzyl)-4-methoxymethyl-piperidine 0.022 1.6 0.48
4-Benzyl-4-(3,4-dichloro-phenoxymethyl)-piperidine 0.00026 0.0060 0.0048

Diphenylether compound by Pfizer looks very interesting but no codenames etc. just structure:

Original document: WO 2007036781 
Oxa-azaspiro Derivatives: Bettati, M.; Cavanni, P.; Di Fabio, R.; Oliosi, B.; Perini, O.; Scheid, G.; Tedesco, G.; Zonzini, L.; Micheli, F. (2010). "Oxa-azaspiro Derivatives: A Novel Class of Triple Re-uptake Inhibitors". ChemMedChem 5 (3): 361–6.  
  • Bruce Molino et al. Aryl- and heteroaryl-substituted tetrahydrobenzazepines (2011).[93]
  • Beck et al. Aryl and heteroaryl substituted tetrahydroisoquinolines and use thereof (2009).[94]
RG-7166 Liafensine Indatraline RTI-274 (Taxil) JNJ-39,836,966 (eutomer of JNJ-7,925,476)
EXP-561 Lu-AA42202 Sibutramine Derivative Uliginosin B TP1
[95][96][97] Liming Shao of Sunovion
JZAD-IV-22 4-benzhydryl-1,2,3,6-tetrahydropyridine GSK1360707F GSK-372,475
CA 2717367 
Various industrial attempts at the TRIs[98]

The above-listed compounds constitute only a small percentage of the known triple-reuptake inhibitors that are available, and, in general, have been picked for use in research or possible clinical development because of their favourable pharmacodynamic and pharmacokinetic characteristics that made them stand out from the much larger pool of structurally diverse compounds that show similar high-binding affinity for the target monoamine transporter proteins in vitro.


Toxicological screening is important to ensure safety of the drug molecules. In this regard, the p m-dichloro phenyl analog of venlafaxine was dropped from further development after its potential mutagenicity was called into question.[99] The mutagenicity of this compound is still doubtful though. It was dropped for other reasons likely related to speed at which it could be released onto the market relative to the more developed compound venlafaxine. More recently, the carcinogenicity of PRC200-SS was likewise reported.[100]

(+)-CPCA ("nocaine")[101] is the 3R,4S piperidine stereoisomer of (phenyltropane based) RTI-31.[102] It is non addictive but is not a SNDRI (it is a NDRI). The β-naphthyl analog of "Nocaine"[87] is a SNDRI though in the case of both the SS and RR enantiomers. Consider the piperidine analogs of brasofensine[50] and tesofensine.[103] These were prepared by NeuroSearch (In Denmark) by the chemists Peter Moldt (2002),[104] and Frank Wätjen (2004–2009).[105][106] There are four separate isomers to consider (SS, RR, S/R and R/S). This is because there are two chiral carbon sites of asymmetry (means 2 to the power of n isomers to consider where n is the number of chiral carbons). They are therefore a diastereo(iso)meric pair of racemers. With a racemic pair of diastereomers, there is still the question of syn (cis) or anti (trans). In the case of the phenyltropanes, although there are four chiral carbons, there are only eight possible isomers to consider. This is based on the fact that the compound is bicyclic and therefore does not adhere to the equation given above.

Brasofensine, tesofensine and methoxymethyl analog (GSK-372,475)
Brasofensine, tesofensine and methoxymethyl analog (GSK-372,475).

It is complicated to explain which isomers are desired. For example, although Alan P. Kozikowski showed that R/S nocaine is less addictive than SS Nocaine, studies on variously substituted phenyltropanes by F. Ivy Carroll[107] et at. revealed that the ββ isomers were less likely to cause convulsions, tremor and death than the corresponding trans isomers (more specifically, what is meant is the 1R,2R,3S isomers).[108] While it does still have to be conceded that RTI-55 caused death at a dosage of 100 mg/kg, it's therapeutic index of safety is still much better than the corresponding trans isomers because it is more potent compound.

In discussing cocaine and related compounds such as amphetamines, it is clear that these psychostimulants cause increased blood pressure, decreased appetite (and hence weight loss), increased locomotor activity (LMA) etc. In the United States, cocaine overdose is one of the leading causes of ER admissions each year due to drug overdose. People are at increased risk of heart attack and stroke and also present with an array of psychiatric symptoms including anxiety & paranoia etc. Interestingly, on removal of the 2C tropane bridge and on going from RTI-31 to the simpler SS and RS Nocaine it was seen that these compounds still possessed activity as NDRIs but were not powerful psychostimulants. Hence, this might be viewed as a strategy for increasing the safety of the compounds and would also be preferable to use in patients who are not looking to achieve weight loss.

In light of the above paragraph, another way of reducing the psychomotor stimulant and addictive qualities of phenyltropane stimulants is in picking one that is relatively serotonergic. This strategy was employed with success for RTI-112.[79][109][110]

Another thing that is important and should be mentioned is the risk for serotonin syndrome when incorporating the element of 5-HT transporter inhibition into a compound that is already fully active as a NDRI (or vice versa). The reasons for serotonin syndrome are complicated and not fully understood.


Drug addiction may be regarded as a disease of the brain reward system. This system, closely related to the system of emotional arousal, is located predominantly in the limbic structures of the brain. Its existence was proved by demonstration of the "pleasure centers," that were discovered as the location from which electrical self-stimulation is readily evoked. The main neurotransmitter involved in the reward is dopamine, but other monoamines and acetylcholine may also participate. The anatomical core of the reward system are dopaminergic neurons of the ventral tegmentum that project to the nucleus accumbens, amygdala, prefrontal cortex and other forebrain structures.[111]

There are several groups of substances that activate the reward system and they may produce addiction, which in humans is a chronic, recurrent disease, characterized by absolute dominance of drug-seeking behavior.[111][112][113]

According to various studies, the relative likelihood of rodents and non-human primates self-administering various psychostimulants that modulate monoaminergic neurotransmission is lessened as the dopaminergic compounds become more serotonergic.

The above finding has been found for amphetamine and some of its variously substituted analogs including PAL-287 etc.[114][115][116]

RTI-112 is another good example of the compound becoming less likely to be self-administered by the test subject in the case of a dopaminergic compound that also has a marked affinity for the serotonin transporter.[109]

WIN 35428, RTI-31, RTI-51 and RTI-55 were all compared and it was found that there was a negative correlation between the size of the halogen atom and the rate of self-administration (on moving across the series).[102] Rate of onset was held partly accountable for this, although increasing the potency of the compounds for the serotonin transporter also played a role.

Further evidence that 5-HT dampens the reinforcing actions of dopaminergic medications comes from the co-administration of psychostimulants with SSRIs,[117] and the phen/fen combination was also shown to have limited abuse potential relative to administration of phentermine only.[118]

NET blockade is unlikely to play a major role in mediating addictive behavior. This finding is based on the premise that desipramine is not self-administered,[119] and also the fact that the NRI atomoxetine was not reinforcing.[120] However, it was still shown to facilitate dopaminergic neurotransmission in certain brain regions such as in the core of the PFC.

Relation to cocaine

Chemical structure of cocaine.
Chemical structure of RTI-51.

Cocaine is a short-acting SNDRI that also exerts auxiliary pharmacological actions on other receptors. Cocaine is a relatively "balanced" inhibitor, although facilitation of dopaminergic neurotransmission is what has been linked to the reinforcing and addictive effects. In addition, cocaine has some serious limitations in terms of its cardiotoxicity[121] due to its local anesthetic activity. Thousands of cocaine users are admitted to emergency units in the USA every year because of this; thus, development of safer substitute medications for cocaine abuse could potentially have significant benefits for public health.

Many of the SNDRIs currently being developed have varying degrees of similarity to cocaine in terms of their chemical structure. There has been speculation over whether the new SNDRIs will have an abuse potential like cocaine does. However, for pharmacotherapeutical treatment of cocaine addiction it is advantageous if a substitute medication is at least weakly reinforcing because this can serve to retain addicts in treatment programmes:

... limited reinforcing properties in the context of treatment programs may be advantageous, contributing to improved patient compliance and enhanced medication effectiveness.[122]

However, not all SNDRIs are reliably self-administered by animals. Examples include:

  • PRC200-SS was not reliably self-administered.[64]
  • RTI-112 was not self-administered[109] because at low doses the compound preferentially occupies the SERT and not the DAT.[79][110]
  • Tesofensine was also not reliably self-administered by human stimulant addicts.[123]
  • The nocaine analog JZAD-IV-22 only partly substituted for cocaine in animals, but produced none of the psychomotor activation of cocaine, which is a trait marker for stimulant addiction.[62]


The rate of onset of the drug needs to be sufficiently rapid to ensure a hasty therapeutic response. Although the rate of onset might be thought to be intrinsically related to the compounds molecular structure (c.f. the specific case of the phenytropanes) and the rate at which it penetrates the BBB, the route(or method) of administration is clearly also important. There are a number of choices: transdermal, intravenously, intramuscular, eyes, nose, swallow pill. Dissolving drug in mouth on tongue is the preferred choice. Particularly desirable is cases where the drug is so potent that it can be distributed on blotter paper.

The compounds duration(span) must be sufficiently long to prevent it from being repeatedly self-administered, which would tend to indicate a high propensity for abuse (e.g. nicotine). In terms of risk of overdose, a subject is less likely to redose if the effects of having taken the drug are felt immediately (or at least, within a short time afterwards) relative to a situation where there is a slower onset of action.

Compounds that are extremely lipophilic and resistant to metabolic deactivation are not necessarily desirable. Say that the user takes his drug in the morning after he(she) wakes up. They want the effects of the drug to last all day long without needing to re-dose so the effects of the medication should be long lasting. However, by the time they are thinking about going to bed at the end of the day they will want the drug to be in the stages of wearing off so that it doesn't interrupt their sleeping. Also supposing the subject accidentally takes an overdose or starts experiencing a headache then they will want to abort the experience and to start returning to baseline. In the case of slow-onset, long-duration psychoactive the effects might actually intensify by the time that this point is reached and it could take several days before it is cleared from their system.

Examples of drugs that are very lipophilic and long-lasting would include such compounds as desoxypipradrol and sibutramine.

Affordability (i.e. cost)

Obviously the more complicated the molecule and the less yielding (more difficult) the chemical reactions that lead to it, then the more expensive a given compound will be. Some chemical reactants and reagents clearly cost more than others. Consider the case where there are sites of asymmetry and more than one isomer that the chemist may need to separate in order to purify the final compound/intermediates.

JZ-IV-10 look like highly sophisticated molecule but it is still questionable how affordable they would be.

Consider the process of epimerization. It may be conceivable that the low energy isomers were chosen because these are cheaper and easier to obtain.

Clearly if a compound is highly potent then less of it has to be consumed for a given dose. This might off-set the increased cost of making a more complicated molecule. As an example for this consider the case of diclofensine versus the Pyrroloisoquinoline derivative of it. The SAR for this is in the JNJ-7925476 document.


Cocaine is a controlled drug (Class A in the UK; Schedule II in the USA); it has not been entirely outlawed in most countries, as despite having some "abuse potential" it is recognized that it does have medical uses.

Brasofensine was made "class A" in the UK under the MDA (misuse of drugs act). BF is an interesting compound in so far as the semi-synthetic procedure for making it actually uses cocaine as the starting material.

Naphyrone first appeared in 2006 as one of quite a large number of analogs of pyrovalerone designed by the well-known medicinal chemist P. Meltzer et al.[55] When the designer drugs mephedrone and methylone became banned in the United Kingdom, vendors of these chemicals needed to find a suitable replacement. Mephedrone and methylone affect the same chemicals in the brain as a SNDRI, although they are thought to act as monoamine releasers and not act through the reuptake inhibitor mechanism of activity.[124] Anyway, a short time after mephedrone and methylone were banned (which had become quite popular by the time they were illegalized), naphyrone appeared under the trade name NRG-1.[56] NRG-1 was promptly illegalized, although it is not known if its use resulted in any hospitalizations or deaths.

Role of monoamine neurotransmitters

Monoamine Hypothesis

The monoamine hypothesis postulates that depression is caused by a deficiency or imbalances in the monoamine neurotransmitters (5-HT, NE, and DA). This has been the central topic of depression research for approximately the last 50 years.[14][125]

When reserpine (an alkaloid with uses in the treatment of hypertension and psychosis) was first introduced to the West from India in 1953, the drug was unexpectedly shown to produce depression-like symptoms. Further testing was able to reveal that reserpine causes a depletion of monoamine concentrations in the brain. Reserpine's effect on monoamine concentrations results from blockade of the vesicular monoamine transporter, leading to their increased catabolism by monoamine oxidase. However, not everyone has been convinced by claims that reserpine is depressogenic, some authors (David Healy in particular) have even claimed that it is antidepressant.[126]

Tetrabenazine, a similar agent to reserpine, which also depletes catecholamine stores, and to a lesser degree 5-HT, was shown to induce depression in many patients.[127][128]

Iproniazid, an inhibitor of MAO, was noted to elevate mood in depressed patients in the early 1950s, and soon thereafter was shown to lead to an increase in NA and 5-HT.[125][128]

Hertting et al. demonstrated that the first TCA, imipramine, inhibited cellular uptake of NA in peripheral tissues. Moreover, both antidepressant agents were demonstrated to prevent reserpine-induced sedation. Likewise, administration of DOPA to laboratory animals was shown to reverse reserpine induced sedation; a finding reproduced in humans. Amphetamine, which releases NA from vesicles and prevents re-uptake was also used in the treatment of depression at the time with varying success.[128]

In 1965 Schildkraut formulated the catecholamine theory of depression.[129] This was subsequently the most widely cited article in the American Journal of Psychiatry.[130] The theory stated that "some, if not all, depressions are associated with an absolute or relative deficiency of catecholamines, in particular noradrenaline (NA), at functionally important adrenergic receptor sites in the brain. However, elation may be associated with an excess of such amines."

Shortly after Schildkraut's catecholamine hypothesis was published, Coppen proposed that 5-HT, rather than NA, was the more important neurotransmitter in depression. This was based on similar evidence to that which produced the NA theory as reserpine, imipramine, and iproniazid affect the 5-HT system, in addition to the noradrenergic system. It was also supported by work demonstrating that if catecholamine levels were depleted by up to 20% but 5-HT neurotransmission remained unaltered there was no sedation in animals. Alongside this, the main observation promoting the 5-HT theory was that administration of a MAOI in conjunction with tryptophan (precursor of 5-HT) elevated mood in control patients and potentiated the antidepressant effect of MAOI. Set against this, combination of an MAOI with DOPA did not produce a therapeutic benefit.[128]

Inserting a chlorine atom into imipramine leads to clomipramine, a drug that is much more SERT selective than the parent compound.[125]

Clomipramine was a predecessor to the development of the more recent SSRIs. There was, in fact, a time prior to the SSRIs when selective NRIs were being considered (c.f. talopram and melitracen). In fact, it is also believed that the selective NRI nisoxetine was discovered prior to the invention of fluoxetine.[131] However, the selective NRIs did not get promoted in the same way as did the SSRIs, possibly due to an increased risk of suicide. This was accounted for on the basis of the energizing effect that these agents have.[132] Moreover, NRIs have the additional adverse safety risk of hypertension that is not seen for SSRIs.[98] Nevertheless NRIs have still found uses.

Further support for the monoamine hypothesis came from monoamine depletion studies:

  • Alpha-methyl-p-tyrosine (AMPT) is a tyrosine hydroxylase enzyme inhibitor that serves to inhibit catecholamine synthesis. AMPT led to a resurgence of depressive symptoms in patients improved by the NE reuptake inhibitor (NRI) desipramine, but not by the SSRI fluoxetine.[133] The mood changes induced by AMPT may be mediated by decreases in norepinephrine, while changes in selective attention and motivation may be mediated by dopamine.
  • Dietary depletion of the DA precursors phenylalanine and tyrosine does not result in the relapse of formerly depressed patients off their medication.[134]
  • Administration of fenclonine (para-chlorophenylalanine) is able able to bring about a depletion of 5-HT. The mechanism of action for this is via tryptophan hydroxylase inhibition. In the 1970s administration of parachlorophenylalanine produced a relapse in depressive symptoms of treated patients,[135][135] but it is considered too toxic for use today.
  • Although depletion of tryptophan — the rate-limiting factor of serotonin synthesis — does not influence the mood of healthy volunteers and untreated patients with depression, it does produce a rapid relapse of depressive symptoms in about 50% of remitted patients who are being, or have recently been treated with serotonin selective antidepressants.[136]


RTI-229 also see for RTI-227
RTI-183 (see RTI-208 also)
Focalin (R,R)

There appears to be a pattern of symptoms that are currently inadequately addressed by serotonergic antidepressants – loss of pleasure (anhedonia), reduced motivation, loss of interest, fatigue and loss of energy, motor retardation, apathy and hypersomnia. Addition of a pro-dopaminergic component into a serotonin based therapy would be expected to address some of these short-comings.[137][138][139]

Several lines of evidence suggest that an attenuated function of the dopaminergic system may play an important role in depression:

  • Mood disorders are highly prevalent in pathologies characterized by a deficit in central DA transmission such as Parkinson's disease (PD). The prevalence of depression can reach up to 50% of individuals suffering from PD.[140]
  • Patients taking strong dopaminergic antagonists such as those used in the treatment of psychosis are more likely than the general population to suffer from symptoms of depression.[141]
  • Data from clinical studies have shown that DA agonists, such as bromocriptine, pramipexole and ropinirole, exhibit antidepressant properties.[12]
  • Amineptine, a TCA-derivative that predominantly inhibits DA re-uptake and has minimal noradrenergic and serotonergic activity has also been shown to possess antidepressant activity. A number of studies have suggested that amineptine has similar efficacy to the TCAs, MAOIs and SSRIs. However, amineptine is no longer available as a treatment for depression due to reports of an abuse potential.
  • The B-subtype selective MAOI selegiline (a drug developed for the treatment of PD) has now been approved for the treatment of depression in the form of a transdermal patch (Emsam). For some reason, there have been numerous reports of users taking this drug in conjunction with β-phenethylamine.
  • Taking psychostimulants for the alleviation of depression is well proven strategy, although in a clinical setting the use of such drugs is usually prohibited because of their strong addiction propensity.[142][143]
  • When users withdraw from psychostimulant drugs of abuse (in particular, amphetamine), they experience symptoms of depression. This is likely because the brain enters into a hypodopaminergic state, although there might be a role for noradrenaline also.

For these drugs to be reinforcing, they must block more than 50% of the DAT within a relatively short time period (<15 minutes from administration) and clear the brain rapidly to enable fast repeated administration.

In addition to mood, they may also improve cognitive performance,[144] although this remains to be demonstrated in humans.

The rate of clearance from the body is faster for ritalin than it is for regular amphetamine.


The decreased levels of NA proposed by Schildkraut, suggested that there would be a compensatory upregulation of β-adrenoceptors. Despite inconsistent findings supporting this, more consistent evidence demonstrates that chronic treatment with antidepressants and electroconvulsive therapy (ECT) decrease β-adrenoceptor density in the rat forebrain. This led to the theory that β-adrenoceptor downregulation was required for clinical antidepressant efficacy. However, some of the newly developed antidepressants do not alter, or even increase β-adrenoceptor density.[128]

Another adrenoceptor implicated in depression is the presynaptic α2-adrenoceptor. Chronic desipramine treatment in rats decreased the sensitivity of α2-adrenoceptors, a finding supported by the fact that clonidine administration caused a significant increase in growth hormone (an indirect measure of α2-adrenoceptor activity) although platelet studies proved inconsistent. This supersensitivity of α2-adrenoceptor was postulated to decrease locus coeruleus (the main projection site of NA in the central nervous system, CNS) NA activity leading to depression.

In addition to enhancing NA release, α2-adrenoceptor antagonism also increases serotonergic neurotransmission due to blockade of α2-adrenoceptors present on 5-HT nerve terminals.



5-Hydroxytryptamine (5-HT or serotonin) is an important cell-to-cell signaling molecule found in all animal phyla. In mammals, substantial concentrations of 5-HT are present in the central and peripheral nervous systems, gastrointestinal tract and cardiovascular system. 5-HT is capable of exerting a wide variety of biological effects by interacting with specific membrane-bound receptors, and at least 13 distinct 5-HT receptor subtypes have been cloned and characterized. With the exception of the 5-HT3 receptor subtype, which is a transmitter-gated ion channel, 5-HT receptors are members of the 7-transmembrane G protein-coupled receptor superfamily. In humans, the serotonergic system is implicated in various physiological processes such as sleep-wake cycles, maintenance of mood, control of food intake and regulation of blood pressure. In accordance with this, drugs that affect 5-HT-containing cells or 5-HT receptors are effective treatments for numerous indications, including depression, anxiety, obesity, nausea, and migraine.

Because serotonin and the related hormone melatonin are involved in promoting sleep, they counterbalance the wake-promoting action of increased catecholaminergic neurotransmission. This is accounted for by the lethargic feel that some SSRIs can produce, although TCAs and antipsychotics can also cause lethargy albeit through different mechanisms.

5-HT is known to cause hallucinations through activating the 5-HT2A receptor.

In most cases serotonergic activation of receptors can result in a more lucid state. It is dependent upon the exact therapeutic agent under discussion.

Appetite suppression is related to 5-HT2C receptor activation as for example was reported for PAL-287 recently.

Activation of the 5-HT2C receptor has been described as "panicogen" by users of ligands for this receptor (e.g., mCPP). Antagonism of the 5-HT2C receptor is known to augment dopaminergic output. Although SSRIs with 5-HT2C antagonist actions were recommended for the treatment of depression, 5-HT2C receptor agonists were suggested for treating cocaine addiction since this would be anti-addictive. Nevertheless the 5-HT2C is known to be rapidly downregulated upon repeated administration of an agonist agent, and is actually antagonized.

Azapirone-type drugs (e.g., buspirone), which act as 5-HT1A receptor agonists and partial agonists have been developed as novel anxiolytic agents that are not associated with the dependence and side-effect profile of the benzodiazepines. The hippocampal neurogenesis produced by various types of antidepressants, likewise, is thought to be mediated by 5-HT1A receptors. Systemic administration of a 5-HT1A agonist also induces growth hormone and adrenocorticotropic hormone (ACTH) release through actions in the hypothalamus.[146]


The neurocircuitry of fear appears to focus on the amygdala. The amygdala receives noradrenergic innervation from the locus coeruleus and serotonergic projections from the midbrain raphe nuclei. High levels of amygdala activation are associated with an increased prevalence of anxiety symptoms and dispositional negative affect. Electrical stimulation of the amygdala can evoke emotional experiences, especially fear and anxiety, and vivid recall of emotional life events.


A SNDRI may also possibly be considered nootropic. There is evidence linking the use of antidepressants to increased expression of neurotrophins (in particular, BDNF).[147][148][149] These are believed to be neuroprotective.

However, although tranylcypromine and ECS increase BDNF mRNA levels, the more selective antidepressants such as desipramine and fluoxetine have variable effects.[149] Thus, because nonselective SNDRIs recruit a plurality of modes of activity, they are more likely to be effective at elevating BDNF RNA.

The hippocampus is one of several limbic brain structures implicated in the pathophysiology and treatment of mood disorders. Preclinical and clinical studies demonstrate that stress and depression lead to reductions of the total volume of this structure and atrophy and loss of neurons in the adult hippocampus. One of the cellular mechanisms that might account for alterations in hippocampal structure as well as function is the regulation of adult neurogenesis. Stress exerts a profound effect on neurogenesis, leading to a rapid and prolonged decrease in the rate of cell proliferation in the adult hippocampus. In contrast, chronic antidepressant treatment up-regulates hippocampal neurogenesis, and could thereby block or reverse the atrophy and damage caused by stress. Recent studies show that neurogenesis is also requisite for the actions of antidepressants in behavioral models of depression.[150]

Current antidepressants

Most antidepressants on the market today target the monoaminergic system.


The most commonly prescribed class of antidepressants in the USA today are the selective serotonin reuptake inhibitors (SSRIs). These drugs inhibit the uptake of the neurotransmitter 5-HT by blocking the SERT, thus increasing its synaptic concentration, and have shown to be efficacious in the treatment of depression, however sexual dysfunction and weight gain are two very common side-effects that result in discontinuation of treatment.

Although many patients benefit from SSRIs, it is estimated that approximately 50% of depressive individuals do not respond adequately to these agents.[151] Even in remitters, a relapse is often observed following drug discontinuation. The major limitation of SSRIs concerns their delay of action. It appears that the clinical efficacy of SSRIs becomes evident only after a few weeks.[152]

SSRIs can be combined with a host of other drugs including bupropion, α2 adrenergic antagonists (e.g., yohimbine) as well as some of the atypical antipsychotics. The augmentation agents are said to behave synergistically with the SSRI although these are clearly of less value than taking a single compound that contains all of the necessary pharmacophoric elements relative to the consumption of a mixture of different compounds. It is not entirely known what the reason for this is, although ease of dosing is likely to be a considerable factor. In addition, single compounds are more likely to be approved by the FDA than are drugs that contain greater than one pharmaceutical ingredient (polytherapies).

A number of SRIs were under development that had auxiliary interactions with other receptors. Particularly notable were agents behaving as co-joint SSRIs with additional antagonist activity at 5-HT1A receptors. 5-HT1A receptors are located presynaptically as well as post-synaptically. It is the presynaptic receptors that are believed to function as autoreceptors (cf. studies done with pindolol). These agents were shown to elicit a more robust augmentation in the % elevation of extracellular 5-HT relative to baseline than was the case for SSRIs as measured by in vivo microdialysis.[98]


Norepinephrine reuptake inhibitors (NRIs) such as reboxetine prevent the reuptake of norepinephrine, providing a different mechanism of action to treat depression. However reboxetine is no more effective than the SSRIs in treating depression. In addition, atomoxetine has found use in the treatment of ADHD as a non-addictive alternative to Ritalin. The chemical structure of atomoxetine is closely related to that of fluoxetine (an SSRI) and also duloxetine (SNRI).


Bupropion is a commonly prescribed antidepressant that acts as an Norepinephrine-dopamine reuptake inhibitor (NDRI). It prevents the reuptake of NA and DA (weakly) by blocking the corresponding transporters, leading to increased noradrenergic and dopaminergic neurotransmission. This drug does not cause sexual dysfunction or weight gain like the SSRIs but has a higher incidence of nausea. Ritalin is a much more reliable example of an NDRI (the action that it displays on the DAT usually getting preferential treatment). Ritalin is used in the treatment of ADHD, its use in treating depression is not known to have been reported, it is presumed owing to its psychomotor activating effects and it functioning as a positive reinforcer. There are also reports of Ritalin being used in the treatment of psychostimulant addiction, in particular cocaine addiction, since the addictive actions of this drug are believed to be mediated by the dopamine neurotransmitter.


Serotonin–norepinephrine reuptake inhibitors (SNRIs) such as venlafaxine (trade name "Effexor"), its active metabolite desvenlafaxine ("Pristiq"), and duloxetine ("Cymbalta") prevent the reuptake of both serotonin and norepinephrine, however their efficacy appears to be only marginally greater than the SSRIs.[153]

Sibutramine is the name of an SNRI based appetite suppressant with use in the treatment of obesity. This was explored in the treatment of depression, but was shown not to be effective.

Both sibutramine and venlafaxine are phenethylamine based. At high doses, both venlafaxine and sibutramine will start producing dopaminergic effects. The inhibition of DA re-uptake is unlikely to be relevant at clinically approved doses.

These drugs all feel markedly different, although the fact that they are all branded as SNRIs might lead some people into believing that they are similar. One must consider structure-activity-relationships in accounting for this. It is likely that duloxetine is antihistaminergic whereas sibutramine causes hypertension.

A number of analogs of sibutramine are known that behave as SNDRIs, changing the aromatic substituent in venlafaxine can also affect the degree of noradrenergic activation, although it is unclear to what extent the dopaminergic pathways can also be affected.

D Wong was unaware of any analogs of fluoxetine/atomoxetine/nisoxetine/duloxetine based on the same structural motifs that displayed dopaminergic activity.[who?]

Milnacipran is a further example of an SNRI.


The tetracyclic antidepressants (TeCAs), or, to be more specific, the noradrenergic and specific serotonergic antidepressants (NaSSAs), such as mirtazapine, antagonise various serotonergic and noradrenergic receptors leading to a greater outflow of these neurotransmitters. However mirtazapine's strong antagonism of the histamine receptor can result in sedation, and the drug often causes significant weight gain.


Agomelatine also targets the 5-HT2C and the melatonin receptors, (which is a unique action among antidepressants) another monoamine neurotransmitter.

It is interesting to note that tianeptine enhances the reuptake of serotonin (according to earlier studies but disputed later), yet has comparable efficacy to the other antidepressants and an excellent side-effect profile.

Consider also nefazodone and trazodone.

Atypical antipsychotics are also being explored within the context of treating bipolar disorder and related conditions.[154]


Monoamine oxidase inhibitors (MAOIs) were the first antidepressant agents. They were discovered entirely by serendipity.[125] Iproniazide (the first MAOI) was originally developed as an antitubercular agent but was then unexpectedly found to display antidepressant activity.

It is interesting to note that isoniazid also displayed activity as an antidepressant, even though it is not a MAOI.[155] This led some people to question whether it is some property of the hydrazine, which is responsible for mediating the antidepressant effect, even going as far as to state that the MAOI activity could be a secondary side-effect. However, with the discovery of tranylcypromine (the first non-hydrazine MAOI), it was shown that MAOI is thought to underlie the antidepressant bioactivity of these agents. Etryptamine is another example of a non-hydrazine MAOI that was introduced.

The MAOIs work by inhibiting the monoamine oxidase enzymes that, as the name suggests, break down the monoamine neurotransmitters. This leads to increased concentrations of most of the monoamine neurotransmitters in the human brain, serotonin, norepinephrine, dopamine and melatonin. The fact that they are more efficacious than the newer generation antidepressants is what leads scientists to develop newer antidepressants that target a greater range of neurotransmitters. The problem with MAOIs is that they have many potentially dangerous side-effects such as hypotension, and there is a risk of food and drug interactions that can result in potentially fatal serotonin syndrome or a hypertensive crisis. Although selective MAOIs can reduce, if not eliminate these risks, their efficacy tends to be lower.

MAOIs may preferentially treat TCA-resistant depression, especially in patients with features such as fatigue, volition inhibition, motor retardation and hypersomnia. This may be a function of the ability of MAOIs to increase synaptic levels of DA in addition to 5-HT and NE. The MAOIs also seem to be effective in the treatment of fatigue associated with fibromyalgia (FM) or chronic fatigue syndrome (CFS).

Although a substantial number of MAOIs were approved in the 1960s, many of these were taken off the market as rapidly as they were introduced. The reason for this is that they were hepatotoxic and could cause jaundice.


The first Tricyclic antidepressant (TCA), imipramine, was derived from the antipsychotic drug chlorpromazine, which was developed as a useful antihistaminergic agent with possible use as a hypnotic sedative.[125] Imipramine is an iminodibenzyl (dibenzazepine).

The TCAs such as imipramine and amitriptyline typically prevent the reuptake of serotonin or norepinephine.

It is the histaminiergic (H1), muscarinic acetylcholinergic (M1), and alpha adrenergic (α1) blockade that is responsible for the side-effects of TCAs. These include somnolence and lethargy, anticholinergic side-effects, and hypotension. Due to the narrow gap between their ability to block the biogenic amine uptake pumps versus the inhibition of fast sodium channels, even a modest overdose of one of the TCAs could be lethal. TCAs were, for 25 years, the leading cause of death from overdoses in many countries. Patients being treated with antidepressants are prone to attempt suicide and one method they use is to take an overdose of their medications.[156]

Another example of an interesting TCA is amineptine which is the only one believed to function as a DRI. Although this used to be available it is no longer available now and was replaced with tianeptine instead.

Beyond Monoamines

Certain studies have suggested the inclusion of other neurotransmitters and molecular targets than just the monoamines in the treatment of depression.[8][151][157][158]

Cocaine also has auxiliary actions on other receptors: it has muscarinic activity, is a sigma agonist and has sodium channel blocking activity.

Ketamine is antidepressant and behaves as a NMDA antagonist.

Both the glutamate (c.f. ketamine) and GABA neurotransmitters are involved in depression.[159]

Opiates are known to exhibit antidepressant activities.[160] Additionally, the compound JDTic has exhibited significant antidepressant activity and works by antagonising the kappa-opioid receptor.

The neuronal-type nicotinic acetylcholine receptors have been found to have a role in depression as well. Consequently, it's been found that in non-smoking depressed patients nicotine patches alleviates depression.[161] The antidepressant, bupropion has also been found act as a nicotinic acetylcholine receptor antagonist. Additionally, its been found that around 50-60% of depressed patients are smokers compared to around 25% of the general population.[162]

See also


  1. ^ a b c Musk, P (2004). "Magic shotgun methods for developing drugs for CNS disorders". Discovery medicine 4 (23): 299–302.  
  2. ^ a b Roth, BL; Sheffler, DJ; Kroeze, WK (2004). "Magic shotguns versus magic bullets: Selectively non-selective drugs for mood disorders and schizophrenia". Nature Reviews Drug Discovery 3 (4): 353–9.  
  3. ^ Millan, MJ (2009). "Dual- and triple-acting agents for treating core and co-morbid symptoms of major depression: Novel concepts, new drugs". Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 6 (1): 53–77.  
  4. ^ Kulkarni, SK; Dhir, A (2009). "Current investigational drugs for major depression". Expert Opinion on Investigational Drugs 18 (6): 767–88.  
  5. ^ a b c Guiard, BP; El Mansari, M; Blier, P (2009). "Prospect of a dopamine contribution in the next generation of antidepressant drugs: The triple reuptake inhibitors". Current drug targets 10 (11): 1069–84.  
  6. ^ a b Marks, DM; Pae, CU; Patkar, AA (2008). "Triple reuptake inhibitors: The next generation of antidepressants". Current neuropharmacology 6 (4): 338–43.  
  7. ^ a b Chen, Z; Skolnick, P (2007). "Triple uptake inhibitors: Therapeutic potential in depression and beyond". Expert Opinion on Investigational Drugs 16 (9): 1365–77.  
  8. ^ a b c d e f g Millan, MJ (2006). "Multi-target strategies for the improved treatment of depressive states: Conceptual foundations and neuronal substrates, drug discovery and therapeutic application". Pharmacology & therapeutics 110 (2): 135–370.  
  9. ^ a b Perona, MT; Waters, S; Hall, FS; Sora, I; Lesch, KP; Murphy, DL; Caron, M; Uhl, GR (2008). "Animal models of depression in dopamine, serotonin, and norepinephrine transporter knockout mice: Prominent effects of dopamine transporter deletions". Behavioural Pharmacology 19 (5–6): 566–74.  
  10. ^ a b Chen, Z; Yang, J; Tobak, A (2008). "Designing new treatments for depression and anxiety". IDrugs : the investigational drugs journal 11 (3): 189–97.  
  11. ^ Perović, B; Jovanović, M; Miljković, B; Vezmar, S (2010). "Getting the balance right: Established and emerging therapies for major depressive disorders". Neuropsychiatric disease and treatment 6: 343–64.  
  12. ^ a b Rakofsky, JJ; Holtzheimer, PE; Nemeroff, CB (2009). "Emerging targets for antidepressant therapies". Current Opinion in Chemical Biology 13 (3): 291–302.  
  13. ^ "Depression".  
  14. ^ a b c Lee, S; Jeong, J; Kwak, Y; Park, SK (2010). "Depression research: Where are we now?". Molecular brain 3: 8.  
  15. ^ Larsen, KK; Vestergaard, M; Søndergaard, J; Christensen, B (2012). "Screening for depression in patients with myocardial infarction by general practitioners". European journal of preventive cardiology 20 (5): 800.  
  16. ^ a b Saravane, D; Feve, B; Frances, Y; Corruble, E; Lancon, C; Chanson, P; Maison, P; Terra, JL et al. (2009). "Drawing up guidelines for the attendance of physical health of patients with severe mental illness". L'Encephale 35 (4): 330–9.  
  17. ^ Rustad, JK; Musselman, DL; Nemeroff, CB (2011). "The relationship of depression and diabetes: Pathophysiological and treatment implications". Psychoneuroendocrinology 36 (9): 1276–86.  
  18. ^ Li, M; Fitzgerald, P; Rodin, G (2012). "Evidence-based treatment of depression in patients with cancer". Journal of clinical oncology : official journal of the American Society of Clinical Oncology 30 (11): 1187–96.  
  19. ^ Tsuang, MT; Francis, T; Minor, K; Thomas, A; Stone, WS (2012). "Genetics of smoking and depression". Human Genetics 131 (6): 905–15.  
  20. ^ Davis, LL; Wisniewski, SR; Howland, RH; Trivedi, MH; Husain, MM; Fava, M; McGrath, PJ; Balasubramani, GK et al. (2010). "Does comorbid substance use disorder impair recovery from major depression with SSRI treatment? An analysis of the STAR*D level one treatment outcomes". Drug and alcohol dependence 107 (2–3): 161–70.  
  21. ^ Barrault, S; Varescon, I (2012). "Psychopathology in online pathological gamblers: A preliminary study". L'Encephale 38 (2): 156–63.  
  22. ^ Belmaker, RH (2008). "The future of depression psychopharmacology". CNS spectrums 13 (8): 682–7.  
  23. ^ Dunlop, BW; Nemeroff, CB (2007). "The role of dopamine in the pathophysiology of depression". Archives of General Psychiatry 64 (3): 327–37.  
  24. ^ Daws, LC (2009). "Unfaithful neurotransmitter transporters: Focus on serotonin uptake and implications for antidepressant efficacy". Pharmacology & therapeutics 121 (1): 89–99.  
  25. ^ Buccafusco, JJ (2009). "Multifunctional receptor-directed drugs for disorders of the central nervous system". Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 6 (1): 4–13.  
  26. ^ Enna, SJ; Williams, M (2009). "Challenges in the search for drugs to treat central nervous system disorders". The Journal of Pharmacology and Experimental Therapeutics 329 (2): 404–11.  
  27. ^ Frantz, S (2005). "Drug discovery: Playing dirty". Nature 437 (7061): 942–3.  
  28. ^ Hopkins, AL (2009). "Drug discovery: Predicting promiscuity". Nature 462 (7270): 167–8.  
  29. ^ Hopkins, AL; Mason, JS; Overington, JP (2006). "Can we rationally design promiscuous drugs?". Current Opinion in Structural Biology 16 (1): 127–36.  
  30. ^ Hopkins, AL (2008). "Network pharmacology: The next paradigm in drug discovery". Nature chemical biology 4 (11): 682–90.  
  31. ^ Jain, R (2004). "Single-action versus dual-action antidepressants". Primary care companion to the Journal of clinical psychiatry 6 (Suppl 1): 7–11.  
  32. ^ a b Yang, AR; Yi, HS; Warnock, KT; Mamczarz, J; June Jr, HL; Mallick, N; Krieter, PA; Tonelli, L et al. (2012). "Effects of the Triple Monoamine Uptake Inhibitor DOV 102,677 on Alcohol-Motivated Responding and Antidepressant Activity in Alcohol-Preferring (P) Rats". Alcoholism, clinical and experimental research 36 (5): 863–73.  
  33. ^ McMillen, BA; Shank, JE; Jordan, KB; Williams, HL; Basile, AS (2007). "Effect of DOV 102,677 on the volitional consumption of ethanol by Myers' high ethanol-preferring rat". Alcoholism, clinical and experimental research 31 (11): 1866–71.  
  34. ^ Gardner, Eliot L.; Liu, Xinhe; Paredes, William; Giordano, Anthony; Spector, Jordan; Lepore, Marino; Wu, Kuo-Ming; Froimowitz, Mark (2006). "A slow-onset, long-duration indanamine monoamine reuptake inhibitor as a potential maintenance pharmacotherapy for psychostimulant abuse: Effects in laboratory rat models relating to addiction". Neuropharmacology 51 (5): 993–1003.  
  35. ^ Tizzano, JP; Stribling, DS; Perez-Tilve, D; Strack, A; Frassetto, A; Chen, RZ; Fong, TM; Shearman, L et al. (2008). "The triple uptake inhibitor (1R,5S)-(+)-1-(3,4-dichlorophenyl)-3-azabicyclo3.1.0 hexane hydrochloride (DOV 21947) reduces body weight and plasma triglycerides in rodent models of diet-induced obesity". The Journal of Pharmacology and Experimental Therapeutics 324 (3): 1111–26.  
  36. ^
  37. ^ Basile, AS; Janowsky, A; Golembiowska, K; Kowalska, M; Tam, E; Benveniste, M; Popik, P; Nikiforuk, A et al. (2007). "Characterization of the antinociceptive actions of bicifadine in models of acute, persistent, and chronic pain". The Journal of Pharmacology and Experimental Therapeutics 321 (3): 1208–25.  
  38. ^ Skolnick, P; Popik, P; Janowsky, A; Beer, B; Lippa, AS (2003). "Antidepressant-like actions of DOV 21,947: A "triple" reuptake inhibitor". European Journal of Pharmacology 461 (2–3): 99–104.  
  39. ^ Golembiowska, K; Kowalska, M; Bymaster, FP (2012). "Effects of the triple reuptake inhibitor amitifadine on extracellular levels of monoamines in rat brain regions and on locomotor activity". Synapse 66 (5): 435–44.  
  40. ^ Tran, P; Skolnick, P; Czobor, P; Huang, NY; Bradshaw, M; McKinney, A; Fava, M (2012). "Efficacy and tolerability of the novel triple reuptake inhibitor amitifadine in the treatment of patients with major depressive disorder: A randomized, double-blind, placebo-controlled trial". Journal of Psychiatric Research 46 (1): 64–71.  
  41. ^ "Development programme - Lundbeck". 
  42. ^ "Search of: Lu AA24530 - List Results -". 
  43. ^ Ahmadi, A; Khalili, M; Marami, S; Ghadiri, A; Nahri-Niknafs, B (2014). "Synthesis and pain perception of new analogues of phencyclidine in NMRI male mice". Mini reviews in medicinal chemistry 14 (1): 64–71.  
  44. ^ Epstein, JW; Brabander, HJ; Fanshawe, WJ; Hofmann, CM; McKenzie, TC; Safir, SR; Osterberg, AC; Cosulich, DB; Lovell, FM (1981). "1-Aryl-3-azabicyclo3.1.0hexanes, a new series of nonnarcotic analgesic agents". Journal of Medical Chemistry 24 (5): 481–90.  
  45. ^ Xu, Feng; Murry, Jerry A.; Simmons, Bryon; Corley, Edward; Fitch, Kenneth; Karady, Sandor; Tschaen, David (2006). "Stereocontrolled Synthesis of Trisubstituted Cyclopropanes:  Expedient, Atom-Economical, Asymmetric Syntheses of (+)-Bicifadine and DOV21947". Organic Letters 8 (17): 3885–8.  
  46. ^ "SEP-225289". Retrieved 7 February 2010. 
  47. ^ Delorenzo, C; Lichenstein, S; Schaefer, K; Dunn, J; Marshall, R; Organisak, L; Kharidia, J; Robertson, B et al. (2011). "SEP-225289 serotonin and dopamine transporter occupancy: A PET study". Journal of nuclear medicine : official publication, Society of Nuclear Medicine 52 (7): 1150–5.  
  48. ^ Beer, B; Stark, J; Krieter, P; Czobor, P; Beer, G; Lippa, A; Skolnick, P (2004). "DOV 216,303, a "triple" reuptake inhibitor: Safety, tolerability, and pharmacokinetic profile". Journal of clinical pharmacology 44 (12): 1360–7.  
  49. ^ Prins, J; Westphal, KG; Korte-Bouws, GA; Quinton, MS; Schreiber, R; Olivier, B; Korte, SM (2011). "The potential and limitations of DOV 216,303 as a triple reuptake inhibitor for the treatment of major depression: A microdialysis study in olfactory bulbectomized rats". Pharmacology, Biochemistry, and Behavior 97 (3): 444–52.  
  50. ^ a b EP 0756596 
  51. ^ Learned, S; Graff, O; Roychowdhury, S; Moate, R; Krishnan, KR; Archer, G; Modell, JG; Alexander, R et al. (2012). "Efficacy, safety, and tolerability of a triple reuptake inhibitor GSK372475 in the treatment of patients with major depressive disorder: Two randomized, placebo- and active-controlled clinical trials". Journal of psychopharmacology (Oxford, England) 26 (5): 653–62.  
  52. ^ Keller, HH; Schaffner, R; Carruba, MO; Burkard, WP; Pieri, M; Bonetti, EP; Scherschlicht, R; Da Prada, M; Haefely, WE (1982). "Diclofensine (Ro 8-4650)--a potent inhibitor of monoamine uptake: Biochemical and behavioural effects in comparison with nomifensine". Advances in biochemical psychopharmacology 31: 249–63.  
  53. ^ Omer, LM (1982). "Pilot trials with diclofensine, a new psychoactive drug in depressed patients". International journal of clinical pharmacology, therapy, and toxicology 20 (7): 320–6.  
  55. ^ a b Meltzer, PC; Butler, D; Deschamps, JR; Madras, BK (2006). "1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: A promising class of monoamine uptake inhibitors". Journal of Medical Chemistry 49 (4): 1420–32.  
  56. ^ a b Alan Travis, home affairs editor (2010-04-01). "NRG-1 may be next legal high to face ban by ministers | Politics". The Guardian. Retrieved 2010-04-03. 
  57. ^ Carroll, FI; Lewin, AH; Mascarella, SW; Seltzman, HH; Reddy, PA (2012). "Designer drugs: A medicinal chemistry perspective". Annals of the New York Academy of Sciences 1248: 18–38.  
  58. ^ Iversen, L.; Gibbons, S.; Treble, R.; Setola, V.; Huang, X. P.; Roth, B. L. (2012). "Neurochemical profiles of some novel psychoactive substances". European Journal of Pharmacology.  
  59. ^ Bøgesø, KP; Christensen, AV; Hyttel, J; Liljefors, T (1985). "3-Phenyl-1-indanamines. Potential antidepressant activity and potent inhibition of dopamine, norepinephrine, and serotonin uptake". Journal of Medical Chemistry 28 (12): 1817–28.  
  60. ^ U.S. Patent 4,556,676
  61. ^ WO 2005041875 
  62. ^ a b Caldarone, BJ; Paterson, NE; Zhou, J; Brunner, D; Kozikowski, AP; Westphal, KG; Korte-Bouws, GA; Prins, J et al. (2010). "The novel triple reuptake inhibitor JZAD-IV-22 exhibits an antidepressant pharmacological profile without locomotor stimulant or sensitization properties". The Journal of Pharmacology and Experimental Therapeutics 335 (3): 762–70.  
  63. ^ Lile, JA; Wang, Z; Woolverton, WL; France, JE; Gregg, TC; Davies, HM; Nader, MA (2003). "The reinforcing efficacy of psychostimulants in rhesus monkeys: The role of pharmacokinetics and pharmacodynamics". The Journal of Pharmacology and Experimental Therapeutics 307 (1): 356–66.  
  64. ^ a b Liang, Y; Shaw, AM; Boules, M; Briody, S; Robinson, J; Oliveros, A; Blazar, E; Williams, K et al. (2008). "Antidepressant-like pharmacological profile of a novel triple reuptake inhibitor, (1S,2S)-3-(methylamino)-2-(naphthalen-2-yl)-1-phenylpropan-1-ol (PRC200-SS)". The Journal of Pharmacology and Experimental Therapeutics 327 (2): 573–83.  
  65. ^ Carnmalm, B; Rämsby, S; Renyi, AL; Ross, SB; Ogren, SO; Stjernstrom, Nils E. (1978). "Antidepressant agents. 9. 3,3-Diphenylcyclobutylamines, a new class of central stimulants". Journal of Medical Chemistry 21 (1): 78–82.  
  66. ^ Houlihan, WJ; Ahmad, UF; Koletar, J; Kelly, L; Brand, L; Kopajtic, TA (2002). "Benzo- and cyclohexanomazindol analogues as potential inhibitors of the cocaine binding site at the dopamine transporter". Journal of Medical Chemistry 45 (19): 4110–8.  
  67. ^ Houlihan, WJ; Kelly, L; Pankuch, J; Koletar, J; Brand, L; Janowsky, A; Kopajtic, TA (2002). "Mazindol analogues as potential inhibitors of the cocaine binding site at the dopamine transporter". Journal of Medical Chemistry 45 (19): 4097–109.  
  68. ^ Aluisio, L; Lord, B; Barbier, AJ; Fraser, IC; Wilson, SJ; Boggs, J; Dvorak, LK; Letavic, MA et al. (2008). "In-vitro and in-vivo characterization of JNJ-7925476, a novel triple monoamine uptake inhibitor". European Journal of Pharmacology 587 (1–3): 141–6.  
  69. ^ Deschamps, NM; Elitzin, VI; Liu, B; Mitchell, MB; Sharp, MJ; Tabet, EA (2011). "An enyne cycloisomerization approach to the triple reuptake inhibitor GSK1360707F". The Journal of Organic Chemistry 76 (2): 712–5.  
  70. ^ Micheli, F; Cavanni, P; Andreotti, D; Arban, R; Benedetti, R; Bertani, B; Bettati, M; Bettelini, L et al. (2010). "6-(3,4-dichlorophenyl)-1-(methyloxy)methyl-3-azabicyclo4.1.0heptane: A new potent and selective triple reuptake inhibitor". Journal of Medical Chemistry 53 (13): 4989–5001.  
  71. ^ Enyedy, IJ; Zaman, WA; Sakamuri, S; Kozikowski, AP; Johnson, KM; Wang, S (2001). "Pharmacophore-based discovery of 3,4-disubstituted pyrrolidines as a novel class of monoamine transporter inhibitors". Bioorganic & Medicinal Chemistry Letters 11 (9): 1113–8.  
  72. ^ Bannwart, LM; Carter, DS; Cai, HY; Choy, JC; Greenhouse, R; Jaime-Figueroa, S; Iyer, PS; Lin, CJ et al. (2008). "Novel 3,3-disubstituted pyrrolidines as selective triple serotonin/norepinephrine/dopamine reuptake inhibitors". Bioorganic & Medicinal Chemistry Letters 18 (23): 6062–6.  
  73. ^ a b Lucas, MC; Weikert, RJ; Carter, DS; Cai, HY; Greenhouse, R; Iyer, PS; Lin, CJ; Lee, EK et al. (2010). "Design, synthesis, and biological evaluation of new monoamine reuptake inhibitors with potential therapeutic utility in depression and pain". Bioorganic & Medicinal Chemistry Letters 20 (18): 5559–66.  
  74. ^ Dutta, AK; Ghosh, B; Biswas, S; Reith, ME (2008). "D-161, a novel pyran-based triple monoamine transporter blocker: Behavioral pharmacological evidence for antidepressant-like action". European Journal of Pharmacology 589 (1–3): 73–9.  
  75. ^ Roggen, H; Kehler, J; Stensbøl, TB; Hansen, T (2007). "Synthesis of enantiomerically pure milnacipran analogs and inhibition of dopamine, serotonin, and norepinephrine transporters". Bioorganic & Medicinal Chemistry Letters 17 (10): 2834–7.  
  76. ^ Wong, DT; Bymaster, FP (1978). "An inhibitor of dopamine uptake, LR5182, cis-3-(3,4-dichlorophenyl)-2-n,n-dimethylaminomethyl-bicyclo-2,2,2-octane, hydrochloride". Life Sciences 23 (10): 1041–7.  
  77. ^ Fuller, RW; Perry, KW; Snoddy, HD (1979). "In vivo effects of LR5182, cis-3-(3,4-dichlorophenyl)-2-n,n-dimethylaminomethyl- bicyclo-2,2,2-octane hydrochloride, an inhibitor of uptake into dopamine and norepinephrine neurons". Neuropharmacology 18 (5): 497–501.  
  78. ^ Wong, DT; Bymaster, FP; Reid, LR (1980). "Competitive inhibition of catecholamine uptake in synaptosomes of rat brain by rigid bicyclo-octanes". Journal of Neurochemistry 34 (6): 1453–8.  
  79. ^ a b c Carroll, FI (2003). "2002 Medicinal Chemistry Division Award address: Monoamine transporters and opioid receptors. Targets for addiction therapy". Journal of Medical Chemistry 46 (10): 1775–94.  
  80. ^ Lee, KH; Park, CE; Min, KH; Shin, YJ; Chung, CM; Kim, HH; Yoon, HJ; Won-Kim et al. (2010). "Synthesis and pharmacological evaluation of 3-aryl-3-azolylpropan-1-amines as selective triple serotonin/norepinephrine/dopamine reuptake inhibitors". Bioorganic & Medicinal Chemistry Letters 20 (18): 5567–71.  
  81. ^ Tian, JW; Jiang, WL; Zhong, Y; Meng, Q; Gai, Y; Zhu, HB; Hou, J; Xing, Y; Li, YX (2011). "Preclinical pharmacology of TP1, a novel potent triple reuptake inhibitor with antidepressant properties". Neuroscience 196: 124–30.  
  82. ^ Zhang, R.; Li, X.; Shi, Y.; Shao, Y.; Sun, K.; Wang, A.; Sun, F.; Liu, W.; Wang, D.; Jin, J.; Li, Y. (2014). "The Effects of LPM570065, a Novel Triple Reuptake Inhibitor, on Extracellular Serotonin, Dopamine and Norepinephrine Levels in Rats". PLoS ONE 9 (3): e91775.  
  83. ^ Micheli, F; Cavanni, P; Bettati, M; Bonanomi, G; Di Fabio, R; Fazzolari, E; Marchioro, C; Roscic, M et al. (2011). "1-Heteroaryl-6-(3,4-dichlorophenyl)-3-azabicyclo4.1.0heptane: Further insights into a class of triple re-uptake inhibitors". Bioorganic & Medicinal Chemistry 19 (11): 3451–61.  
  84. ^ Gopishetty, B; Hazeldine, S; Santra, S; Johnson, M; Modi, G; Ali, S; Zhen, J; Reith, M; Dutta, A (2011). "Further structure-activity relationship studies on 4-((((3S,6S)-6-benzhydryltetrahydro-2H-pyran-3-yl)amino)methyl)phenol: Identification of compounds with triple uptake inhibitory activity as potential antidepressant agents". Journal of Medical Chemistry 54 (8): 2924–32.  
  85. ^ Shao, L; Wang, F; Malcolm, SC; Ma, J; Hewitt, MC; Campbell, UC; Bush, LR; Spicer, NA et al. (2011). "Synthesis and pharmacological evaluation of 4-(3,4-dichlorophenyl)-N-methyl-1,2,3,4-tetrahydronaphthalenyl amines as triple reuptake inhibitors". Bioorganic & Medicinal Chemistry 19 (1): 663–76.  
  86. ^ Shao L, Hewitt MC, Malcolm SC, et al. (2011). "Synthesis and pharmacological characterization of bicyclic triple reuptake inhibitor 3-aryl octahydrocyclopenta[c]pyrrole analogues". Journal of Medicinal Chemistry 54 (15): 5283–95.  
  87. ^ a b Tamiz, AP; Zhang, J; Flippen-Anderson, JL; Zhang, M; Johnson, KM; Deschaux, O; Tella, S; Kozikowski, AP (2000). "Further SAR studies of piperidine-based analogues of cocaine. 2. Potent dopamine and serotonin reuptake inhibitors". Journal of Medical Chemistry 43 (6): 1215–22.  
  88. ^ Criado, Elisa (2 May 2014). "A fast-acting antidepressant could be on the horizon".  
  89. ^
  90. ^ Fang, X.; Guo, L.; Jia, J.; Jin, G. Z.; Zhao, B.; Zheng, Y. Y.; Li, J. Q.; Zhang, A.; Zhen, X. C. (2013). "SKF83959 is a novel triple reuptake inhibitor that elicits anti-depressant activity". Acta Pharmacologica Sinica 34 (9): 1149–55.  
  91. ^ Stein, A. C.; Viana, A. F.; Müller, L. G.; Nunes, J. M.; Stolz, E. D.; Do Rego, J. C.; Costentin, J; von Poser, G. L.; Rates, S. M. (2012). "Uliginosin B, a phloroglucinol derivative from Hypericum polyanthemum: A promising new molecular pattern for the development of antidepressant drugs". Behavioural Brain Research 228 (1): 66–73.  
  92. ^ Fehske, C. J.; Leuner, K.; Müller, W. E. (2009). "Ginkgo biloba extract (EGb761®) influences monoaminergic neurotransmission via inhibition of NE uptake, but not MAO activity after chronic treatment". Pharmacological Research 60 (1): 68–73.  
  93. ^ U.S. Patent 7,956,050
  94. ^ U.S. Patent 7,612,090
  95. ^
  96. ^ Shao, L.; Hewitt, M. C.; Wang, F.; Malcolm, S. C.; Ma, J.; Campbell, J. E.; Campbell, U. C.; Engel, S. R.; Spicer, N. A.; Hardy, L. W.; Schreiber, R.; Spear, K. L.; Varney, M. A. (2011). "Discovery of N-methyl-1-(1-phenylcyclohexyl)methanamine, a novel triple serotonin, norepinephrine, and dopamine reuptake inhibitor". Bioorganic & Medicinal Chemistry Letters 21 (5): 1438–1441.  
  97. ^ Shao, L.; Hewitt, M. C.; Wang, F.; Malcolm, S. C.; Ma, J.; Campbell, J. E.; Campbell, U. C.; Engel, S. R.; Spicer, N. A.; Hardy, L. W.; Schreiber, R.; Spear, K. L.; Varney, M. A. (2011). "Discovery of N-methyl-1-(1-phenylcyclohexyl)ethanamine, a novel triple serotonin, norepinephrine and dopamine reuptake inhibitor". Bioorganic & Medicinal Chemistry Letters 21 (5): 1434–1437.  
  98. ^ a b c Moltzen, EK; Bang-Andersen, B (2006). "Serotonin reuptake inhibitors: The corner stone in treatment of depression for half a century--a medicinal chemistry survey". Current topics in medicinal chemistry 6 (17): 1801–23.  
  99. ^ Yardley, John P.; Husbands, G. E. Morris; Stack, Gary; Butch, Jacqueline; Bicksler, James; Moyer, John A.; Muth, Eric A.; Andree, Terrance et al. (1990). "2-Phenyl-2-(1-hydroxycycloalkyl)ethylamine derivatives: Synthesis and antidepressant activity". Journal of Medicinal Chemistry 33 (10): 2899–905.  
  100. ^ Guha, M; Heier, A; Price, S; Bielenstein, M; Caccese, RG; Heathcote, DI; Simpson, TR; Stong, DB; Bodes, E (2011). "Assessment of biomarkers of drug-induced kidney injury in cynomolgus monkeys treated with a triple reuptake inhibitor".  
  101. ^ Kozikowski, AP; Araldi, GL; Boja, J; Meil, WM; Johnson, KM; Flippen-Anderson, JL; George, C; Saiah, E (1998). "Chemistry and pharmacology of the piperidine-based analogues of cocaine. Identification of potent DAT inhibitors lacking the tropane skeleton". Journal of Medical Chemistry 41 (11): 1962–9.  
  102. ^ a b Wee, S; Carroll, FI; Woolverton, WL (2006). "A reduced rate of in vivo dopamine transporter binding is associated with lower relative reinforcing efficacy of stimulants". Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 31 (2): 351–62.  
  103. ^ U.S. Patent 6,395,748
  104. ^ U.S. Patent 6,376,673
  105. ^ WO 2004039778 
  106. ^ U.S. Patent 7,560,562
  107. ^
  108. ^ Carroll, FI; Runyon, SP; Abraham, P; Navarro, H; Kuhar, MJ; Pollard, GT; Howard, JL (2004). "Monoamine transporter binding, locomotor activity, and drug discrimination properties of 3-(4-substituted-phenyl)tropane-2-carboxylic acid methyl ester isomers". Journal of Medical Chemistry 47 (25): 6401–9.  
  109. ^ a b c Kimmel, HL; O'Connor, JA; Carroll, FI; Howell, LL (2007). "Faster onset and dopamine transporter selectivity predict stimulant and reinforcing effects of cocaine analogs in squirrel monkeys". Pharmacology, Biochemistry, and Behavior 86 (1): 45–54.  
  110. ^ a b Lindsey, KP; Wilcox, KM; Votaw, JR; Goodman, MM; Plisson, C; Carroll, FI; Rice, KC; Howell, LL (2004). "Effects of dopamine transporter inhibitors on cocaine self-administration in rhesus monkeys: Relationship to transporter occupancy determined by positron emission tomography neuroimaging". The Journal of Pharmacology and Experimental Therapeutics 309 (3): 959–69.  
  111. ^ a b  
  112. ^ Howell, LL; Kimmel, HL (2008). "Monoamine transporters and psychostimulant addiction".  
  113. ^ Koob, GF; Volkow, ND (2010). "Neurocircuitry of addiction". Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 35 (1): 217–38.  
  114. ^ Baumann, MH; Clark, RD; Woolverton, WL; Wee, S; Blough, BE; Rothman, RB (2011). "In vivo effects of amphetamine analogs reveal evidence for serotonergic inhibition of mesolimbic dopamine transmission in the rat". The Journal of Pharmacology and Experimental Therapeutics 337 (1): 218–25.  
  115. ^ Rothman, RB; Blough, BE; Baumann, MH (2008). "Dual dopamine/serotonin releasers: Potential treatment agents for stimulant addiction". Experimental and clinical psychopharmacology 16 (6): 458–74.  
  116. ^ Kimmel, HL; Manvich, DF; Blough, BE; Negus, SS; Howell, LL (2009). "Behavioral and neurochemical effects of amphetamine analogs that release monoamines in the squirrel monkey". Pharmacology, Biochemistry, and Behavior 94 (2): 278–84.  
  117. ^ Howell, LL; Carroll, FI; Votaw, JR; Goodman, MM; Kimmel, HL (2007). "Effects of combined dopamine and serotonin transporter inhibitors on cocaine self-administration in rhesus monkeys". The Journal of Pharmacology and Experimental Therapeutics 320 (2): 757–65.  
  118. ^ Rothman, RB; Elmer, GI; Shippenberg, TS; Rea, W; Baumann, MH (1998). "Phentermine and fenfluramine. Preclinical studies in animal models of cocaine addiction". Annals of the New York Academy of Sciences 844: 59–74.  
  119. ^ Wee, S; Wang, Z; He, R; Zhou, J; Kozikowski, AP; Woolverton, WL (2006). "Role of the increased noradrenergic neurotransmission in drug self-administration". Drug and alcohol dependence 82 (2): 151–7.  
  120. ^ Wee, S; Woolverton, WL (2004). "Evaluation of the reinforcing effects of atomoxetine in monkeys: Comparison to methylphenidate and desipramine". Drug and alcohol dependence 75 (3): 271–6.  
  121. ^ Phillips, K; Luk, A; Soor, GS; Abraham, JR; Leong, S; Butany, J (2009). "Cocaine cardiotoxicity: A review of the pathophysiology, pathology, and treatment options". American journal of cardiovascular drugs : drugs, devices, and other interventions 9 (3): 177–96.  
  122. ^ Howell, LL; Wilcox, KM (2001). "The dopamine transporter and cocaine medication development: Drug self-administration in nonhuman primates". The Journal of Pharmacology and Experimental Therapeutics 298 (1): 1–6.  
  123. ^ Schoedel, KA; Meier, D; Chakraborty, B; Manniche, PM; Sellers, EM (2010). "Subjective and objective effects of the novel triple reuptake inhibitor tesofensine in recreational stimulant users". Clinical pharmacology and therapeutics 88 (1): 69–78.  
  124. ^ Baumann, MH; Ayestas Jr, MA; Partilla, JS; Sink, JR; Shulgin, AT; Daley, PF; Brandt, SD; Rothman, RB et al. (2012). "The designer methcathinone analogs, mephedrone and methylone, are substrates for monoamine transporters in brain tissue". Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 37 (5): 1192–203.  
  125. ^ a b c d e López-Muñoz, F; Alamo, C (2009). "Monoaminergic neurotransmission: The history of the discovery of antidepressants from 1950s until today". Current pharmaceutical design 15 (14): 1563–86.  
  126. ^ Baumeister, AA; Hawkins, MF; Uzelac, SM (2003). "The myth of reserpine-induced depression: Role in the historical development of the monoamine hypothesis". Journal of the history of the neurosciences 12 (2): 207–20.  
  127. ^ Lingjaerde, O (1963). "Tetrabenazine (Nitoman) in the Treatment of Psychoses. With a Discussion on the Central Mode of Action of Tetrabenazine and Reserpine". Acta Psychiatrica Scandinavica 39: SUPPL170:1–109.  
  128. ^ a b c d e Slattery, DA; Hudson, AL; Nutt, DJ (2004). "Invited review: The evolution of antidepressant mechanisms". Fundamental & clinical pharmacology 18 (1): 1–21.  
  129. ^ Schildkraut, JJ (1965). "The catecholamine hypothesis of affective disorders: A review of supporting evidence". The American Journal of Psychiatry 122 (5): 509–22.  
  130. ^
  131. ^ Wong, DT; Perry, KW; Bymaster, FP (2005). "Case history: The discovery of fluoxetine hydrochloride (Prozac)". Nature Reviews Drug Discovery 4 (9): 764–74.  
  132. ^
  133. ^ Miller, HL; Delgado, PL; Salomon, RM; Berman, R; Krystal, JH; Heninger, GR; Charney, DS (1996). "Clinical and biochemical effects of catecholamine depletion on antidepressant-induced remission of depression". Archives of General Psychiatry 53 (2): 117–28.  
  134. ^ Roiser, JP; McLean, A; Ogilvie, AD; Blackwell, AD; Bamber, DJ; Goodyer, I; Jones, PB; Sahakian, BJ (2005). "The subjective and cognitive effects of acute phenylalanine and tyrosine depletion in patients recovered from depression". Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 30 (4): 775–85.  
  135. ^ a b Shopsin, B; Gershon, S; Goldstein, M; Friedman, E; Wilk, S (1975). "Use of synthesis inhibitors in defining a role for biogenic amines during imipramine treatment in depressed patients". Psychopharmacology communications 1 (2): 239–49.  
  136. ^ Castrén, E (2005). "Is mood chemistry?". Nature Reviews Neuroscience 6 (3): 241–6.  
  137. ^ Nutt, D; Demyttenaere, K; Janka, Z; Aarre, T; Bourin, M; Canonico, PL; Carrasco, JL; Stahl, S (2007). "The other face of depression, reduced positive affect: The role of catecholamines in causation and cure". Journal of psychopharmacology (Oxford, England) 21 (5): 461–71.  
  138. ^ Nestler, EJ; Carlezon Jr, WA (2006). "The mesolimbic dopamine reward circuit in depression". Biological Psychiatry 59 (12): 1151–9.  
  139. ^ Papakostas, GI; Nutt, DJ; Hallett, LA; Tucker, VL; Krishen, A; Fava, M (2006). "Resolution of sleepiness and fatigue in major depressive disorder: A comparison of bupropion and the selective serotonin reuptake inhibitors". Biological Psychiatry 60 (12): 1350–5.  
  140. ^ McDonald, WM; Richard, IH; Delong, MR (2003). "Prevalence, etiology, and treatment of depression in Parkinson's disease". Biological Psychiatry 54 (3): 363–75.  
  141. ^ Cohen, BM; Carlezon Jr, WA (2007). "Can't get enough of that dopamine". The American Journal of Psychiatry 164 (4): 543–6.  
  142. ^ Orr, K; Taylor, D (2007). "Psychostimulants in the treatment of depression : A review of the evidence". CNS Drugs 21 (3): 239–57.  
  143. ^ Candy, M; Jones, L; Williams, R; Tookman, A; King, M (2008). Candy, Bridget, ed. "Psychostimulants for depression". Cochrane Database of Systematic Reviews (2): CD006722.  
  144. ^ Nieoullon, A (2002). "Dopamine and the regulation of cognition and attention". Progress in neurobiology 67 (1): 53–83.  
  145. ^ Dell'Osso, B; Palazzo, MC; Oldani, L; Altamura, AC (2011). "The noradrenergic action in antidepressant treatments: Pharmacological and clinical aspects". CNS neuroscience & therapeutics 17 (6): 723–32.  
  146. ^ Nichols, DE; Nichols, CD (2008). "Serotonin receptors". Chemical reviews 108 (5): 1614–41.  
  147. ^ Sen, S; Duman, R; Sanacora, G (2008). "Serum brain-derived neurotrophic factor, depression, and antidepressant medications: Meta-analyses and implications". Biological Psychiatry 64 (6): 527–32.  
  148. ^ Gur, TL; Conti, AC; Holden, J; Bechtholt, AJ; Hill, TE; Lucki, I; Malberg, JE; Blendy, JA (2007). "CAMP response element-binding protein deficiency allows for increased neurogenesis and a rapid onset of antidepressant response". The Journal of neuroscience : the official journal of the Society for Neuroscience 27 (29): 7860–8.  
  149. ^ a b Malberg, JE; Blendy, JA (2005). "Antidepressant action: To the nucleus and beyond". Trends in pharmacological sciences 26 (12): 631–8.  
  150. ^ Warner-Schmidt, JL; Duman, RS (2006). "Hippocampal neurogenesis: Opposing effects of stress and antidepressant treatment". Hippocampus 16 (3): 239–49.  
  151. ^ a b Berton, O; Nestler, EJ (2006). "New approaches to antidepressant drug discovery: Beyond monoamines". Nature Reviews Neuroscience 7 (2): 137–51.  
  152. ^ Blier, P (2003). "The pharmacology of putative early-onset antidepressant strategies". European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 13 (2): 57–66.  
  153. ^ Papakostas, GI; Thase, ME; Fava, M; Nelson, JC; Shelton, RC (2007). "Are antidepressant drugs that combine serotonergic and noradrenergic mechanisms of action more effective than the selective serotonin reuptake inhibitors in treating major depressive disorder? A meta-analysis of studies of newer agents". Biological Psychiatry 62 (11): 1217–27.  
  154. ^ Quintin, P; Thomas, P (2004). "Efficacy of atypical antipsychotics in depressive syndromes". L'Encephale 30 (6): 583–9.  
  155. ^ Ban, TA (2001). "Pharmacotherapy of depression: A historical analysis". Journal of neural transmission (Vienna, Austria : 1996) 108 (6): 707–16.  
  156. ^ Preskorn, SH (2010). "CNS drug development: Part II: Advances from the 1960s to the 1990s". Journal of Psychiatric Practice 16 (6): 413–5.  
  157. ^ Alamo, C; López-Muñoz, F (2009). "New antidepressant drugs: Beyond monoaminergic mechanisms". Current pharmaceutical design 15 (14): 1559–62.  
  158. ^ Bosker, FJ; Westerink, BH; Cremers, TI; Gerrits, M; Van Der Hart, MG; Kuipers, SD; Van Der Pompe, G; Ter Horst, GJ et al. (2004). "Future antidepressants: What is in the pipeline and what is missing?". CNS Drugs 18 (11): 705–32.  
  159. ^ Kugaya, A; Sanacora, G (2005). "Beyond monoamines: Glutamatergic function in mood disorders". CNS spectrums 10 (10): 808–19.  
  160. ^ Tenore, PL (2008). "Psychotherapeutic benefits of opioid agonist therapy". Journal of addictive diseases 27 (3): 49–65.  
  161. ^ Salín-Pascual, RJ; Rosas, M; Jimenez-Genchi, A; Rivera-Meza, BL; Delgado-Parra, V (1996). "Antidepressant effect of transdermal nicotine patches in nonsmoking patients with major depression". The Journal of clinical psychiatry 57 (9): 387–9.  
  162. ^ Glassman, AH; Helzer, JE; Covey, LS; Cottler, LB; Stetner, F; Tipp, JE; Johnson, J (1990). "Smoking, smoking cessation, and major depression". JAMA 264 (12): 1546–9.  

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