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体内多胺氧化酶的特异性抑制是阐明其生理作用的一种方法。

Specific inhibition of polyamine oxidase in vivo is a method for the elucidation of its physiological role.

作者信息

Bolkenius F N, Bey P, Seiler N

出版信息

Biochim Biophys Acta. 1985 Jan 28;838(1):69-76. doi: 10.1016/0304-4165(85)90251-x.

Abstract

N1-Methyl-N2-(2,3-butadienyl)-1,4-butanediamine (MDL 72521) and N1,N2-bis(2,3-butadienyl)-1,4-butanediamine (MDL 72527) are specific, potent, enzyme-activated, irreversible inhibitors of polyamine oxidase in vitro. These compounds are also capable of completely inhibiting polyamine oxidase in mouse tissues at intraperitoneal doses greater than 20 mg/kg. Enzyme activity reappears in the various organs within 2-3 days to 50% of the control values. Irreversible inhibition of polyamine oxidase in mice led to decreased putrescine (30-40%) and spermidine (10-20%) levels in liver and some other organs. At the same time N1-acetylspermidine and, to a lesser extent, N1-acetylspermine were accumulating at rates which are assumed to be related to the rates of polyamine degradation. Even after treatment with polyamine oxidase inhibitors over a period of 6 weeks at doses which produced complete inhibition of polyamine oxidase in all organs, including the brain, neither toxic effects nor changes in body weight or behaviour were observed.

摘要

N1-甲基-N2-(2,3-丁二烯基)-1,4-丁二胺(MDL 72521)和N1,N2-双(2,3-丁二烯基)-1,4-丁二胺(MDL 72527)在体外是多胺氧化酶特异性、强效、酶激活的不可逆抑制剂。这些化合物在腹腔注射剂量大于20mg/kg时,也能够完全抑制小鼠组织中的多胺氧化酶。酶活性在2-3天至5天内在各个器官中重新出现,达到对照值的50%。对小鼠多胺氧化酶的不可逆抑制导致肝脏和其他一些器官中的腐胺(30-40%)和亚精胺(10-20%)水平降低。与此同时,N1-乙酰亚精胺以及程度较轻的N1-乙酰精胺以假定与多胺降解速率相关的速率积累。即使在以能完全抑制包括脑在内的所有器官中的多胺氧化酶的剂量进行6周的多胺氧化酶抑制剂治疗后,也未观察到毒性作用、体重或行为的变化。

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