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两种抑制剂对脑胆碱酯酶作用的比较。

A comparison of the effects of two inhibitors on brain cholinesterase.

作者信息

Hallak M, Giacobini E

出版信息

Neuropharmacology. 1987 Jun;26(6):521-30. doi: 10.1016/0028-3908(87)90143-2.

Abstract

In the present paper various routes of administration (i.m., i.v. and i.c.v.) of physostigmine are compared and the effect of two drugs producing inhibition of cholinesterase, physostigmine and metrifonate, on the activity of cholinesterase in the brain of the rat and on levels of acetylcholine (ACh) and choline (Ch). After intramuscular administration of physostigmine (500 micrograms/kg), the activity of cholinesterase in brain was maximally inhibited (76%) at 5 min and recovered to 50% at 40 min. At 5 min, areas of the brain such as the striatum and medulla oblongata showed 49 and 67% inhibition, respectively. Levels of physostigmine in brain peaked at 5 min (1.28 nmol/g). With the exception of the cerebellum, there was a direct correlation between the concentration of physostigmine and inhibition of cholinesterase in a given area. With the intravenous route of administration (100 micrograms/kg), the activity of cholinesterase in brain was maximally inhibited (67%) at 3 min and recovered to 50% at 12 min. At 60 min, the activity of cholinesterase was 90% of control. Levels of physostigmine in brain peaked at 2 min (0.47 nmol/g). At 15 min, with intraventricular administration (4 micrograms), the activity of cholinesterase was 73% and 31% inhibited in the hippocampus and striatum, respectively. Other areas of brain showed intermediate values of inhibition. Levels of acetylcholine were increased 18 and 22% above control in the striatum and hippocampus, respectively and did not change in the medulla. After intramuscular administration of metrifonate (80 mg/kg), the activity of cholinesterase decreased to 26% at 30 min, recovered to 50% at 180 min and returned to 74% at 360 min. Levels of acetylcholine increased by 45% at 45 min, then returned to normal by 120 min. When metrifonate (2.5 mg) was given intraventricularly the activity of cholinesterase decreased in the left side injected at 30 min to 20% in hippocampus; 22% in the medulla; 50% in the cerebellum; 58% in the striatum and 72% in cortex. Levels of acetylcholine increased maximally at 45 min in hippocampus and cortex and peaked in the striatum at 60 min. The greatest increases were seen in the hippocampus and cortex with 60 and 55%, respectively. The results of this study reveal some major differences between the effects of the two substances in brain. Four major conclusions are apparent from this study. First, based on these results, it is concluded that metrifonate is more likely to produce a therapeutic effect in humans.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在本论文中,比较了毒扁豆碱的各种给药途径(肌肉注射、静脉注射和脑室内注射),以及两种抑制胆碱酯酶的药物——毒扁豆碱和敌百虫,对大鼠脑内胆碱酯酶活性、乙酰胆碱(ACh)水平和胆碱(Ch)水平的影响。肌肉注射毒扁豆碱(500微克/千克)后,脑内胆碱酯酶活性在5分钟时被最大程度抑制(76%),40分钟时恢复到50%。在5分钟时,纹状体和延髓等脑区分别显示出49%和67%的抑制率。脑内毒扁豆碱水平在5分钟时达到峰值(1.28纳摩尔/克)。除小脑外,在给定区域毒扁豆碱浓度与胆碱酯酶抑制之间存在直接相关性。静脉给药途径(100微克/千克)时,脑内胆碱酯酶活性在3分钟时被最大程度抑制(67%),12分钟时恢复到50%。在60分钟时,胆碱酯酶活性为对照的90%。脑内毒扁豆碱水平在2分钟时达到峰值(0.47纳摩尔/克)。脑室内给药(4微克)15分钟时,海马体和纹状体中胆碱酯酶活性分别被抑制73%和31%。脑的其他区域显示出中间抑制值。纹状体和海马体中乙酰胆碱水平分别比对照升高18%和22%,延髓中则无变化。肌肉注射敌百虫(80毫克/千克)后,胆碱酯酶活性在30分钟时降至26%,180分钟时恢复到50%,360分钟时回到74%。乙酰胆碱水平在45分钟时升高45%,然后在120分钟时恢复正常。脑室内注射敌百虫(2.5毫克)时,在30分钟时,左侧注射部位海马体中胆碱酯酶活性降至20%;延髓中为22%;小脑中为50%;纹状体中为58%;皮质中为72%。乙酰胆碱水平在海马体和皮质中45分钟时最大程度升高,在纹状体中60分钟时达到峰值。海马体和皮质中升高最为显著,分别为60%和55%。本研究结果揭示了这两种物质在脑内作用的一些主要差异。从本研究中可明显得出四个主要结论。首先,基于这些结果,得出敌百虫更有可能在人类中产生治疗效果的结论。(摘要截断于400字)

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