Stephens P H, Tagari P C, Garofalo L, Maysinger D, Piotte M, Cuello A C
Department of Pharmacology and Therapeutics, McGill University, Montreal, Que., Canada.
Neurosci Lett. 1987 Sep 11;80(1):80-4. doi: 10.1016/0304-3940(87)90499-x.
Nucleus basalis magnocellularis (NBM) cholinergic neurons, furnishing the major portion of the extrinsic cholinergic innervation of the rat cortex, undergo specific retrograde changes in cell somata and choline acetyltransferase (ChAT) activity after cortical lesions. These are prevented in young and mature animals, but not in aged rats, by the chronic administration of exogenous ganglioside GM1 after lesioning. However, a delay of 10 days (in young animals) in the commencement of treatment averted the responses to GM1 in lesioned animals. It is suggested that the effects of exogenous gangliosides on retrograde biochemical and morphological alteration of cholinergic neurons may vary with circumstances permissive of plastic changes of central nervous system neurons at the time of administration.
基底大细胞核(NBM)胆碱能神经元为大鼠皮质提供了大部分外在胆碱能神经支配,在皮质损伤后,其细胞体和胆碱乙酰转移酶(ChAT)活性会发生特定的逆行性变化。损伤后对年轻和成年动物长期给予外源性神经节苷脂GM1可防止这些变化,但老年大鼠则不能。然而,(对年轻动物而言)治疗开始延迟10天可避免损伤动物对GM1产生反应。这表明外源性神经节苷脂对胆碱能神经元逆行性生化和形态改变的影响可能会因给药时中枢神经系统神经元可塑性变化的情况而异。