Mondadori C, Ducret T, Häusler A
Ciba-Geigy Ltd., Pharmaceutical Research Department, Basle, Switzerland.
Psychopharmacology (Berl). 1992;108(1-2):11-5. doi: 10.1007/BF02245278.
Oral pretreatment of mice with aldosterone or corticosterone blocked the memory-enhancing effects of piracetam, pramiracetam, aniracetam and oxiracetam in a dose-related manner, without, however, impairing the animals' learning performance. The improvement of memory induced by physostigmine, arecoline, and tacrine (THA) was similarly inhibited. The fact that elevated steroid levels suppress the memory-enhancing effects of entirely different substances could indicate that these substances have a common site of action. In the light of new observations showing increased cortisol concentrations in Alzheimer patients, this steroid dependency of the effects of memory enhancers might explain why only a limited number of these patients respond to therapy with nootropics or cholinomimetics.
用醛固酮或皮质酮对小鼠进行口服预处理,会以剂量相关的方式阻断吡拉西坦、普拉西坦、阿尼西坦和奥拉西坦的记忆增强作用,不过,这并不会损害动物的学习表现。毒扁豆碱、槟榔碱和他克林(THA)诱导的记忆改善也同样受到抑制。类固醇水平升高会抑制完全不同物质的记忆增强作用,这一事实可能表明这些物质具有共同的作用位点。鉴于新的观察结果显示阿尔茨海默病患者的皮质醇浓度升高,记忆增强剂作用的这种类固醇依赖性可能解释了为什么只有有限数量的此类患者对促智药或拟胆碱药治疗有反应。