Hadjiconstantinou M, Neff N H
Department of Psychiatry, Ohio State University College of Medicine and Public Health, Columbus 43210, USA.
Ann N Y Acad Sci. 1998 Jun 19;845:225-31. doi: 10.1111/j.1749-6632.1998.tb09675.x.
Aging is associated with the loss of brain neurotransmitter function, which apparently is the substrate for an adverse constellation of age-associated symptoms. In particular, cholinergic deficits have been associated with cognitive impairment in aging. Systemic administration of GM1 ganglioside, 30 mg/kg, i.p., for 30 days, enhances the cholinergic neurochemical presynaptic markers, choline acetyltransferase, choline uptake, and acetylcholine, in the brain and spinal cord of aged 22-24-month-old Sprague-Dawley rats. In addition to correcting cholinergic neurochemistry, it improves spatial learning and memory impairment, and restores the number and the size of the cholinergic neurons in the basal forebrain and striatum. The induced neuronal recovery by GM1 is long-lasting.
衰老与大脑神经递质功能丧失有关,这显然是一系列与年龄相关的不良症状的基础。特别是,胆碱能缺陷与衰老过程中的认知障碍有关。对22 - 24月龄的Sprague-Dawley大鼠腹腔注射30 mg/kg的GM1神经节苷脂,持续30天,可增强大脑和脊髓中胆碱能神经化学突触前标志物、胆碱乙酰转移酶、胆碱摄取和乙酰胆碱的水平。除了纠正胆碱能神经化学外,它还改善空间学习和记忆障碍,并恢复基底前脑和纹状体中胆碱能神经元的数量和大小。GM1诱导的神经元恢复是持久的。