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Dopaminergic

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Dopaminergic means "related to dopamine" (literally, "working on dopamine"), dopamine being a common neurotransmitter.^[1] Dopaminergic substances or actions increase dopamine-related activity in the brain. Dopaminergic brain pathways facilitate dopamine-related activity. For example, certain proteins such as the dopamine transporter (DAT), vesicular monoamine transporter 2 (VMAT₂), and dopamine receptors can be classified as dopaminergic, and neurons that synthesize or contain dopamine and synapses with dopamine receptors in them may also be labeled as dopaminergic. Enzymes that regulate the biosynthesisormetabolism of dopamine such as aromatic L-amino acid decarboxylaseorDOPA decarboxylase, monoamine oxidase (MAO), and catechol O-methyl transferase (COMT) may be referred to as dopaminergic as well. Also, any endogenousorexogenous chemical substance that acts to affect dopamine receptors or dopamine release through indirect actions (for example, on neurons that synapse onto neurons that release dopamine or express dopamine receptors) can also be said to have dopaminergic effects, two prominent examples being opioids, which enhance dopamine release indirectly in the reward pathways, and some substituted amphetamines, which enhance dopamine release directly by binding to and inhibiting VMAT₂.

Supplements and drugs[edit]

The following are examples of dopaminergic substances:

Precursors[edit]

• Dopamine precursors including L-phenylalanine and L-tyrosine are used as dietary supplements. L-DOPA (Levodopa), another precursor, is used in the treatment of Parkinson's disease.

Receptor agonists[edit]

• Dopamine receptor agonists such as apomorphine, bromocriptine, cabergoline, dihydrexidine (LS-186,899), dopamine, fenoldopam, piribedil, lisuride, pergolide, pramipexole, ropinirole, and rotigotine, are used in the treatment of Parkinson's disease and to treat depression and anxiety.

Receptor antagonists and blockers[edit]

• Dopamine receptor antagonists including typical antipsychotics such as chlorpromazine (Thorazine), fluphenazine, haloperidol (Haldol), loxapine, molindone, perphenazine, pimozide, thioridazine, thiothixene, and trifluoperazine, the atypical antipsychotics such as amisulpride, clozapine, olanzapine, quetiapine (Seroquel), risperidone (Risperdal), sulpiride, and ziprasidone, and antiemetics like domperidone, metoclopramide, and prochlorperazine, among others, which are used in the treatment of schizophrenia and bipolar disorderasantipsychotics, and nausea and vomiting.

Reuptake inhibitors and transporter blockers[edit]

• Dopamine reuptake inhibitors (DRIs) or dopamine transporter (DAT) inhibitors such as methylphenidate (Ritalin), amineptine, and nomifensine, cocaine, methylenedioxypyrovalerone (MDPV; "Sonic"), ketamine, and phencyclidine (PCP), among others, which are used in the treatment of attention-deficit hyperactivity disorder (ADHD) and narcolepsyaspsychostimulants, obesityasanorectics, depression and anxietyasantidepressants and anxiolytics, respectively, drug addictionasanticraving agents, and sexual dysfunction, as well as illicit street drugs.
• Vesicular monoamine transporter 2 (VMAT₂) inhibitors such as reserpine, tetrabenazine, and deserpidine, which are used as sympatholyticsorantihypertensives, and in the past as antipsychotics.

Releasing agents[edit]

• Dopamine releasing agents (DRAs) such as phenethylamine, amphetamine, lisdexamfetamine (Vyvanse), methamphetamine, methylenedioxymethamphetamine (MDMA), phenmetrazine, pemoline, 4-methylaminorex (4-MAR), and benzylpiperazine, among many others, which, like DRIs, are used in the treatment of attention-deficit hyperactivity disorder (ADHD) and narcolepsyaspsychostimulants, obesityasanorectics, depression and anxietyasantidepressants and anxiolytics respectively, drug addictionasanticraving agents, and sexual dysfunctionasaphrodisiacs. Many of these compounds are also illicit street drugs.

"Activity enhancers"[edit]

• Dopamine "activity enhancers" such as BPAP and PPAP, which are currently only research chemicals, but are being investigated for clinical development in the treatment of a number of medical disorders. To date, only phenylethylamine and tryptamine have been identified as endogenous "activity enhancers".^[2]

Monoamine oxidase inhibitors[edit]

• Monoamine oxidase (MAO) inhibitors (MAOIs) including nonselective agents such as phenelzine, tranylcypromine, and isocarboxazid, MAO_A selective agents like moclobemide, and MAO_B selective agents such as selegiline, rasagiline, and pargyline, as well as the harmala alkaloids like harmine, harmaline, tetrahydroharmine, harmalol, harman, and norharman, which are found to varying degrees in Nicotiana tabacum (tobacco), Banisteriopsis caapi (ayahuasca, yage), Peganum harmala (Harmal, Syrian Rue), Passiflora incarnata (Passion Flower), and Tribulus terrestris, among others, which are used in the treatment of depression and anxietyasantidepressants and anxiolytics, respectively, in the treatment of Parkinson's disease and dementia, and for the recreational purpose of boosting the effects of certain drugs like phenethylamine (PEA) and psychedelics like dimethyltryptamine (DMT) via inhibiting their metabolism.

Dopamine synthesis enhancers[edit]

• Tyrosine hydroxylase (TH) mRNA upregulators such as bromantane and low dose aspirin.^[3][4] Bromantane's upregulation of TH may persist for a time (up to at least one month) after its discontinuation based on data related to its efficacy in treating asthenic disorders in Russia.^[5]

Other enzyme inhibitors[edit]

• Catechol O-methyl transferase (COMT) inhibitors such as entacapone and tolcapone, which are used in the treatment of Parkinson's disease.
• Dopamine β-hydroxylase inhibitors like disulfiram (Antabuse), which can be used in the treatment of addiction to cocaine and similar dopaminergic drugs as a deterrent drug. The excess dopamine resulting from inhibition of the dopamine β-hydroxylase enzyme increases unpleasant symptoms such as anxiety, higher blood pressure, and restlessness. Disulfiram is not an anticraving agent, because it does not decrease craving for drugs. Instead, positive punishment from its unpleasant effects deters drug consumption.^[6]
• Phenylalanine hydroxylase inhibitors like 3,4-dihydroxystyrene), which is currently only a research chemical with no suitable therapeutic indications, likely because such drugs would induce the potentially highly dangerous hyperphenylalaninemiaorphenylketonuria.
• Tyrosine hydroxylase inhibitors like metirosine, which is used in the treatment of pheochromocytoma as a sympatholyticorantihypertensive agent.
• Aromatic L-amino acid decarboxylaseorDOPA decarboxylase inhibitors including benserazide, carbidopa, and methyldopa, which are used in the treatment of Parkinson's diseaseinaugmentationofL-DOPA to block the peripheral conversion of dopamine, thereby inhibiting undesirable side-effects, and as sympatholyticorantihypertensive agents.
• Others such as hyperforin and adhyperforin (both found in Hypericum perforatum St. John's Wort), L-theanine (found in Camellia sinensis, the tea plant), and S-adenosyl-L-methionine (SAMe)

See also[edit]

• Adrenergic
• Cholinergic
• Cocaine and amphetamine regulated transcript (CART)
• GABAergic
• Histaminergic
• Serotonergic

References[edit]