|Dopamine Receptor agonist|
|Use||Parkinson's disease, Attention deficit/hyperactivity disorder(ADHD), restless legs syndrome, clinical depression, etc.|
|Biological target||Dopamine receptors|
A dopamine receptor agonist is a compound that activates dopamine receptors. Dopamine receptor agonists activate signaling pathways through trimeric G-proteins and β-arrestins, ultimately leading to changes in gene transcription.
Some medical drugs act as dopamine agonists and can treat hypodopaminergic (low dopamine) conditions; they are typically used for treating Parkinson's disease, attention deficit/hyperactivity disorder (in the form of stimulants) and certain pituitary tumors (prolactinoma), and may be useful for restless legs syndrome (RLS). Both ropinirole and pramipexole are FDA-approved for the treatment of RLS. There is also an ongoing clinical trial to test the effectiveness of the dopamine agonist ropinirole in reversing the symptoms of SSRI-induced sexual dysfunction. Additionally, a systematic review and meta-analysis concluded that prophylactic treatment with cabergoline reduces the incidence, but not the severity, of ovarian hyperstimulation syndrome (OHSS), without compromising pregnancy outcomes, in females undergoing stimulated cycles of in vitro fertilization (IVF).
- Pericardial effusion
- Fibrous thickening of lining that covers some of the internal organs including the heart or the lungs (fibrotic reaction)
- Causing or worsening psychosis
- Orthostatic hypotension
- Increased orgasmic intensity
- Weight loss
- Anorexia (symptom)
- Nausea and possible vomiting
- Unusual tiredness or weakness
- Possible Narcolepsy manifestations (Sleep attacks)
- Raynaud's phenomenon (common side effect of ergot derivatives)
- Twitching, twisting, or other unusual body movements
- Pathological addiction (gambling, shopping, internet pornography, hyper-sexuality) – specifically D3-preferring agonists
Examples of dopamine agonists include:
- Aripiprazole (Partial agonist of the D2 family receptors - Trade name "Abilify" in the United States; atypical antipsychotic)
- Phencyclidine (a.k.a. PCP; partial agonist. Psychoactivity mainly due to NMDA antagonism)
- Quinpirole (Partial agonist of the D2 and D3 family of receptors)
- Salvinorin A (chief active constituent of the psychedelic herb salvia divinorum, the psychoactivity of which is mainly due to Kappa-opioid receptor agonism; partial agonist at the D2 with an Intrinsic activity of 40-60%, binding affinity of Ki=5-10nM and EC50=50-90nM)
Agonists of full/unknown efficacy
- Apomorphine (Apokyn – used to treat Parkinson's disease/Restless leg syndrome) – G-protein bias at the D1 receptor.
- Bromocriptine (Parlodel – used to treat Parkinson's disease/Restless leg syndrome)
- Cabergoline (Dostinex – used to treat Parkinson's disease/Restless leg syndrome)
- Ciladopa (used to treat Parkinson's disease/Restless leg syndrome)
- Dihydrexidine (used to treat Parkinson's disease/Restless leg syndrome)
- Dinapsoline (used to treat Parkinson's disease/Restless leg syndrome)
- Doxanthrine (used to treat Parkinson's disease/Restless leg syndrome)
- Epicriptine (used to treat Parkinson's disease/Restless leg syndrome)
- Lisuride (used to treat Parkinson's disease/Restless leg syndrome)
- Pergolide (used to treat Parkinson's disease/Restless leg syndrome) – previously available as Permax, but removed from the market in the USA March 29, 2007.
- Piribedil (Pronoran and Trivastal – used to treat Parkinson's disease/Restless leg syndrome)
- Pramipexole (Mirapex and Sifrol – used to treat Parkinson's disease/Restless leg syndrome)
- Propylnorapomorphine (used to treat Parkinson's disease/Restless leg syndrome)
- Quinagolide (Norprolac – used to treat Parkinson's disease/Restless leg syndrome)
- Ropinirole (Requip – used to treat Parkinson's disease/Restless leg syndrome)
- Rotigotine (Neupro – used to treat Parkinson's disease/Restless leg syndrome)
- Roxindole (used to treat Parkinson's disease/Restless leg syndrome)
- Sumanirole (used to treat Parkinson's disease/Restless leg syndrome)
The most commonly prescribed indirect agonists of dopamine receptors include:
- Amphetamine and/or dextroamphetamine (used to treat attention deficit hyperactivity disorder, narcolepsy, and obesity)
- Bupropion (used to facilitate smoking cessation and treat nicotine addiction and clinical depression)
- Lisdexamfetamine (used to treat attention deficit hyperactivity disorder and binge eating disorder)
- Methylphenidate or dexmethylphenidate (used to treat attention deficit hyperactivity disorder and narcolepsy)
Other examples include:
- Cathinone (no medical uses)
- Cocaine (no medical uses as a central nervous system stimulant)
- Methamphetamine (used in rare circumstances to treat attention deficit hyperactivity disorder and obesity)
- Phenethylamine (endogenous trace amine with no medical uses)
- p-Tyramine (endogenous trace amine with no medical uses)
- Dopamine antagonist
- Dopamine reuptake inhibitor
- Receptor agonist
- GABA receptor agonist
- Serotonin agonist
- Adrenergic agonist (Sympathomimetic)
- Parasympathomimetic drug (acetylcholine agonist)
- Histamine agonist
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- Clinical trial number NCT00334048 at ClinicalTrials.gov - "Treating Sexual Dysfunction From SSRI Medication: a Study Comparing Requip CR to Placebo"
- Youssef MA, van Wely M, Hassan MA, et al. (March 2010). "Can dopamine agonists reduce the incidence and severity of OHSS in IVF/ICSI treatment cycles? A systematic review and meta-analysis". Hum Reprod Update. 16 (5): 459–66. PMID 20354100. doi:10.1093/humupd/dmq006.
- "MedlinePlus Drug Information: Pramipexole (Systemic)". United States National Library of Medicine. Archived from the original on 2006-09-26. Retrieved 2006-09-27.
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- Seeman P, Guan HC, Hirbec H (2009). "Dopamine D2High receptors stimulated by phencyclidines, lysergic acid diethylamide, salvinorin A, and modafinil". Synapse 63 (8): 698–704. doi:10.1002/syn.20647. PMID 19391150.
- FDA Announces Voluntary Withdrawal of Pergolide Products
- Matera, Carlo; Quadri, Marta; Pelucchi, Silvia; Amici, Marco De; Dallanoce, Clelia (2014-07-01). "A convenient synthesis of 4-(2-hydroxyethyl)indolin-2-one, a useful intermediate for the preparation of both dopamine receptor agonists and protein kinase inhibitors". Monatshefte für Chemie - Chemical Monthly. 145 (7): 1139–1144. ISSN 0026-9247. doi:10.1007/s00706-014-1211-z.
- Ng SS, Pang CC (March 2000). "In vivo venodilator action of fenoldopam, a dopamine D(1)-receptor agonist". Br. J. Pharmacol. 129 (5): 853–8. PMC . PMID 10696081. doi:10.1038/sj.bjp.0703119.
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- Dopamine Agonists at the US National Library of Medicine Medical Subject Headings (MeSH)