Sofroniew M V, Pearson R C, Cuello A C, Tagari P C, Stephens P H
Brain Res. 1986 Nov 29;398(2):393-6. doi: 10.1016/0006-8993(86)91503-9.
The effect of daily intraperitoneal injections of GM1 ganglioside on retrograde degeneration in the basal forebrain has been examined, using a monoclonal antibody directed against choline acetyltransferase to identify the cholinergic neurones. Rats underwent extensive damage of the cerebral cortex and underlying hippocampus. From the day of operation on, they received daily injections of ganglioside. After a survival of 30 days, the animals were killed and the cholinergic cells of the basal forebrain were examined. These were compared with material treated in the same way from animals who had received the injections of ganglioside but no lesion, animals who had been operated upon but without the ganglioside treatment, and normal animals. Intraperitoneal ganglioside administration markedly reduces the retrograde death of the cholinergic neurones of the medial septal nucleus and abolishes the shrinkage of the remaining neurones following hippocampal damage.
利用一种针对胆碱乙酰转移酶的单克隆抗体来识别胆碱能神经元,研究了每日腹腔注射GM1神经节苷脂对基底前脑逆行性变性的影响。大鼠经历了大脑皮层和下方海马体的广泛损伤。从手术当天起,它们每天接受神经节苷脂注射。存活30天后,处死动物并检查基底前脑的胆碱能细胞。将这些细胞与接受神经节苷脂注射但无损伤的动物、接受手术但未接受神经节苷脂治疗的动物以及正常动物以相同方式处理的材料进行比较。腹腔注射神经节苷脂可显著减少内侧隔核胆碱能神经元的逆行性死亡,并消除海马体损伤后剩余神经元的萎缩。