Harsing L G, Magyar K, Tekes K, Vizi E S, Knoll J
Pol J Pharmacol Pharm. 1979 Jul-Aug;31(4):297-307.
Optical isomers of deprenyl inhibit the resting and ouabain induced release of acetylcholine (ACh) in isolated striatal slices of the rat and this effect correlates with the capability of deprenyl to inhibit the uptake of 3H-dopamine in striatal homogenate in a concentration of 10(-4)--10(-4) M. The release of ACh is significantly increased in striatal slices taken from rats pretreated with a single dose of 250 micrograms of 6-hydroxydopamine. 5 mg/kg of deprenyl given 30 min prior to 6-hydroxydopamine treatment prevented completely the chemical destruction of the dopaminergic neurons. In contrast to deprenyl, clorgyline potentiated the effect of 6-hydroxydopamine.
司来吉兰的光学异构体可抑制大鼠离体纹状体切片中乙酰胆碱(ACh)的基础释放以及哇巴因诱导的释放,且这种效应与司来吉兰在10⁻⁴ - 10⁻⁴ M浓度下抑制纹状体匀浆中³H-多巴胺摄取的能力相关。在单次给予250微克6-羟基多巴胺预处理的大鼠所取的纹状体切片中,ACh的释放显著增加。在6-羟基多巴胺处理前30分钟给予5毫克/千克的司来吉兰可完全防止多巴胺能神经元的化学性破坏。与司来吉兰相反,氯吉兰增强了6-羟基多巴胺的作用。