Hefti F, Weiner W J
Ann Neurol. 1986 Sep;20(3):275-81. doi: 10.1002/ana.410200302.
Alzheimer's disease is associated with a pronounced loss of the cholinergic neurons that form the ascending cholinergic projections of the basal forebrain. Even though the disease is also characterized by changes in other neuronal systems and by a high frequency of neuronal plaques and tangles, the cholinergic deficit seems to be a principal element responsible for the memory loss typical of Alzheimer's disease. This review summarizes findings in experimental animals which indicate that nerve growth factor (NGF), a well-characterized protein, acts as a neurotrophic factor for cholinergic neurons of the basal forebrain. NGF is present in the target areas of these cholinergic neurons and affects their survival, fiber growth, and expression of transmitter-specific enzymes. Furthermore, NGF is able to prevent the degeneration of cholinergic neurons in adult rats with experimental lesions mimicking the cholinergic deficit in Alzheimer's disease. These findings suggest that increasing the availability of NGF to human cholinergic cells might promote their survival in certain disease processes. Additional steps are discussed for establishing the possible involvement of NGF in the pathogenesis of Alzheimer's disease and the development of an effective therapy.
阿尔茨海默病与构成基底前脑胆碱能上行投射的胆碱能神经元的显著丧失有关。尽管该疾病还具有其他神经元系统的变化以及神经元斑块和缠结的高发生率等特征,但胆碱能缺陷似乎是导致阿尔茨海默病典型记忆丧失的主要因素。这篇综述总结了实验动物中的研究结果,这些结果表明神经生长因子(NGF),一种特性明确的蛋白质,作为基底前脑胆碱能神经元的神经营养因子发挥作用。NGF存在于这些胆碱能神经元的靶区域,并影响它们的存活、纤维生长以及递质特异性酶的表达。此外,NGF能够预防成年大鼠实验性损伤中胆碱能神经元的退化,这些损伤模拟了阿尔茨海默病中的胆碱能缺陷。这些发现表明,增加人类胆碱能细胞可获得的NGF量可能会促进它们在某些疾病过程中的存活。文中还讨论了确定NGF可能参与阿尔茨海默病发病机制以及开发有效治疗方法的其他步骤。