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基底前脑胆碱能系统离散区域选择性免疫损伤的行为、组织化学和生物化学后果。

Behavioural, histochemical and biochemical consequences of selective immunolesions in discrete regions of the basal forebrain cholinergic system.

作者信息

Torres E M, Perry T A, Blockland A, Wilkinson L S, Wiley R G, Lappi D A, Dunnet S B

机构信息

MRC Cambridge Centre for Brain Repair, University of Cambridge, U.K.

出版信息

Neuroscience. 1994 Nov;63(1):95-122. doi: 10.1016/0306-4522(94)90010-8.

Abstract

The effectiveness of a recently developed immunotoxin, 192 IgG-saporin, was evaluated for making selective lesions of subgroups of basal forebrain cholinergic neurons. Following a pilot series of injections into the nucleus basalis magnocellularis to establish the effective dose for intraparenchymal lesions, separate groups of rats received injections of the immunotoxin into the septum, into the diagonal band of Broca or into the nucleus basalis magnocellularis. The lesions produced extensive and effective loss of cholinergic neurons in the discrete areas of the basal forebrain, as identified by loss of cells staining for acetylcholinesterase and p75NGFr, with a parallel loss of acetylcholinesterase staining and choline acetyltransferase activity in the target areas associated with each injection site in the dorsolateral neocortex, cingulate cortex and hippocampus. The selectivity of the lesion for cholinergic neurons was supported by the lack of gliosis and sparing of small to medium-sized cells at the site of injection of the toxin, including the glutamate decarboxylase immunoreactive cells that contribute to the septohippocampal projection. In spite of the extensive disturbance in the cholinergic innervation of the neocortex and hippocampus, immunotoxin lesions produced no detectable deficit in the Morris water maze task in any of the lesion sites within the basal forebrain. By contrast small but significant deficits were seen on tests of nocturnal activity (septal and nucleus basalis magnocellularis lesions), open field activity (septal and diagonal band lesions), passive avoidance (nucleus basalis magnocellularis lesions) and delayed non-matching to position (septal lesions). The results indicate that the 192 IgG-saporin provides a powerful tool for making effective lesions of the basal forebrain cholinergic neurons, and that the behavioural sequelae of such lesions warrant further detailed investigation.

摘要

对最近研制出的免疫毒素192IgG-皂草素进行了评估,以确定其对基底前脑胆碱能神经元亚群造成选择性损伤的效果。在向大细胞基底核进行了一系列预实验性注射以确定实质内损伤的有效剂量后,将几组大鼠分别注射免疫毒素到隔区、布罗卡斜角带或大细胞基底核。通过乙酰胆碱酯酶和p75神经营养因子受体染色细胞的缺失来确定,这些损伤在基底前脑的离散区域导致胆碱能神经元广泛而有效地丧失,同时在背外侧新皮层、扣带回皮层和海马体中与每个注射部位相关的靶区域,乙酰胆碱酯酶染色和胆碱乙酰转移酶活性也出现了相应丧失。毒素注射部位缺乏胶质增生以及中小细胞得以保留,包括对隔海马投射有贡献的谷氨酸脱羧酶免疫反应阳性细胞,这支持了损伤对胆碱能神经元的选择性。尽管新皮层和海马体的胆碱能神经支配受到了广泛干扰,但在基底前脑内的任何损伤部位,免疫毒素损伤在莫里斯水迷宫任务中均未产生可检测到的缺陷。相比之下,在夜间活动测试(隔区和大细胞基底核损伤)、旷场活动测试(隔区和斜角带损伤)、被动回避测试(大细胞基底核损伤)和延迟位置匹配测试(隔区损伤)中出现了小而显著的缺陷。结果表明,192IgG-皂草素为有效损伤基底前脑胆碱能神经元提供了一个有力工具,并且此类损伤的行为后遗症值得进一步详细研究。

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