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左旋丙炔苯丙胺(司来吉兰)停药后人类大脑单胺氧化酶B恢复缓慢。

Slow recovery of human brain MAO B after L-deprenyl (Selegeline) withdrawal.

作者信息

Fowler J S, Volkow N D, Logan J, Wang G J, MacGregor R R, Schyler D, Wolf A P, Pappas N, Alexoff D, Shea C

机构信息

Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973.

出版信息

Synapse. 1994 Oct;18(2):86-93. doi: 10.1002/syn.890180203.

Abstract

L-Deprenyl (Selegeline) is an enzyme-activated irreversible inhibitor of monoamine oxidase B (MAO B; EC 1.4.3.4). It is used to treat Parkinson's disease at a dose of 5 mg twice a day. Since enzyme inhibition is irreversible, the recovery of functional enzyme activity after withdrawal from L-deprenyl requires the synthesis of new enzyme. We have measured a 40 day half-time for brain MAO B synthesis in Parkinson's disease and in normal subjects after withdrawal from L-deprenyl. This is the first measurement of the synthesis rate of a specific protein in the living human brain. L-Deprenyl is currently used by 50,000 patients with Parkinson's disease in the United States and its use is expected to increase with reports that it may be beneficial in Alzheimer's disease. The slow turnover of brain MAO B suggests that the current clinical dose of L-deprenyl may be excessive and that the clinical efficacy of reduced dosing should be evaluated. Such an evaluation may have mechanistic importance as well as an impact on reducing the side effects and the costs arising from excessive drug use.

摘要

L-司来吉兰(Selegeline)是一种酶激活的单胺氧化酶B(MAO B;EC 1.4.3.4)不可逆抑制剂。它以每日两次、每次5毫克的剂量用于治疗帕金森病。由于酶抑制是不可逆的,停用L-司来吉兰后功能性酶活性的恢复需要新酶的合成。我们已测定帕金森病患者和正常受试者停用L-司来吉兰后脑MAO B合成的半衰期为40天。这是首次对活体人脑中特定蛋白质的合成速率进行测量。目前美国有50000名帕金森病患者使用L-司来吉兰,随着有报道称其可能对阿尔茨海默病有益,其使用量预计会增加。脑MAO B周转缓慢表明目前L-司来吉兰的临床剂量可能过高,应评估降低剂量后的临床疗效。这样的评估可能具有机制重要性,同时对减少过度用药引起的副作用和成本也有影响。

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