Goetz C G
Rush University/Rush-Presbyterian St. Luke's Medical Center, Chicago, IL 60612, USA.
Neurology. 1998 May;50(5 Suppl 5):S26-30. doi: 10.1212/wnl.50.5_suppl_5.s26.
Catechol O-methyltransferase (COMT) is an important enzyme that is linked directly to therapy with levodopa. Considering the demonstrated mechanism of action and pharmacologic profiles of COMT inhibitors, it is reasonable to hypothesize that these agents would improve the disability associated with Parkinson's disease. Two basic classes of COMT inhibitors are being studied in patients with PD: those that act exclusively extracerebrally or peripherally (e.g., entacapone) and those that cross the blood-brain barrier (e.g., tolcapone). With COMT inhibition, greater peripheral bioavailability of levodopa occurs in humans without an enhancement of peak plasma levels. It is reasonable to suggest that COMT inhibition will be associated with prolonged effects of levodopa in PD, without increased peak dose toxicity in the form of dyskinesias and hallucinations.
儿茶酚-O-甲基转移酶(COMT)是一种与左旋多巴治疗直接相关的重要酶。考虑到已证实的COMT抑制剂的作用机制和药理学特征,推测这些药物会改善帕金森病相关的功能障碍是合理的。两类基本的COMT抑制剂正在帕金森病患者中进行研究:一类仅作用于脑外或外周(如恩他卡朋),另一类可穿过血脑屏障(如托卡朋)。抑制COMT后,左旋多巴在人体的外周生物利用度增加,而血浆峰值水平并未提高。有理由认为,抑制COMT将使左旋多巴在帕金森病中的作用时间延长,且不会增加异动症和幻觉等形式的峰值剂量毒性。