Müller W E, Koch S, Scheuer K, Rostock A, Bartsch R
Department of Psychopharmacology, Central Institute of Mental Health, Mannheim, Germany.
Biochem Pharmacol. 1997 Jan 24;53(2):135-40. doi: 10.1016/s0006-2952(96)00463-7.
In vitro preincubation of brain membranes of aged mice with piracetam (0.1-1.0 mmol/L) enhanced membrane fluidity, as indicated by decreased anisotropy of the membrane-bound fluorescence probe 1,6-diphenyl-1,3,5-hexatriene (DPH). Piracetam had similar in vitro effects on brain membranes of aged rats and humans, but it did not alter brain membrane fluidity in young mice. Chronic treatment of young and aged rats with piracetam (300 mg/kg once daily) significantly increased membrane fluidity in some brain regions of the aged animals, but had no measurable effect on membrane fluidity in the young rats. The same treatment significantly improved active avoidance learning in the aged rats only. It is suggested that some of the pharmacological properties of piracetam can be explained by its effects on membrane fluidity.
用吡拉西坦(0.1 - 1.0 mmol/L)对老年小鼠的脑膜进行体外预孵育,可增强膜流动性,这由膜结合荧光探针1,6 - 二苯基 - 1,3,5 - 己三烯(DPH)各向异性的降低所表明。吡拉西坦对老年大鼠和人类的脑膜有类似的体外作用,但对年轻小鼠的脑膜流动性没有影响。用吡拉西坦(300 mg/kg,每日一次)对年轻和老年大鼠进行慢性治疗,可显著增加老年动物某些脑区的膜流动性,但对年轻大鼠的膜流动性没有可测量的影响。相同的治疗仅显著改善了老年大鼠的主动回避学习能力。提示吡拉西坦的某些药理特性可由其对膜流动性的作用来解释。