From Wikipedia, the free encyclopedia
A COMT inhibitor is a drug that inhibits the action of catechol-O-methyl transferase . This enzyme is involved in degrading neurotransmitters . COMT inhibitors are used in the treatment of Parkinson's disease .
Pharmaceutical examples include entacapone ,[1] tolcapone ,[2] and nitecapone .
References [ edit ]
^ Nissinen E; Nissinen H; Larjonmaa H; et al. (September 2005). "The COMT inhibitor, entacapone, reduces levodopa-induced elevations in plasma homocysteine in healthy adult rats". J Neural Transm . 112 (9): 1213–1221. doi :10.1007/s00702-004-0262-4 . PMID 15614425 .
^ Giakoumaki SG, Roussos P, Bitsios P (June 2008). "Improvement of Prepulse Inhibition and Executive Function by the COMT Inhibitor Tolcapone Depends on COMT Val158Met Polymorphism". Neuropsychopharmacology . 33 (13): 3058–3068. doi :10.1038/npp.2008.82 . PMID 18536698 .
α1
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