一种新型抗胆碱酯酶THB013:生化和行为研究。

A Adem, A H Mohammed, B Winblad, B E Henriksson
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引用次数: 3

摘要

他克林(THA)的临床试验已导致阿尔茨海默病患者肝酶升高,表现出改善。为了尽量减少这些副作用,合成了几种THA类似物。这些类似物在生化和行为研究中与THA进行了比较。本研究考察了THA及其类似物thb013对成年大鼠血浆胆碱酯酶活性、胆碱能受体的生化影响以及对空间学习的影响。较低浓度的THB 013在东莨菪碱注射前10 min给予时,对血浆胆碱酯酶的抑制作用和对东莨菪碱引起的空间学习障碍的阻断作用更有效。THB 013具有比THA更强的胆碱能作用,可能有助于治疗阿尔茨海默病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel anticholinesterase THB013: biochemical and behavioural studies.

Clinical trials with tacrine (THA) have resulted in elevations of liver enzymes in Alzheimer patients that showed improvement. In an effort to minimize these side effects several THA analogues were synthesized. These analogues were compared to THA in biochemical as well as behavioural studies. In this study, the biochemical effects of THA and one of these analogs, THB 013, on plasma cholinesterase activity, cholinergic receptors as well as the effect of these drugs on spatial learning in adult rats were examined. THB 013 was, at lower concentration, more efficacious in inhibiting plasma cholinesterase as well as blocking the scopolamine induced disruption of spatial learning when administered 10 min before the scopolamine injection. It is possible that THB 013 with more potent cholinergic effects than THA might be useful in the treatment of Alzheimer's disease.

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