Chambon C, Paban V, Manrique C, Alescio-Lautier B
Université d'Aix-Marseille I, Laboratoire de Neurobiologie Intégrative et Adaptative, UMR/CNRS 6149, 3 Place Victor Hugo, 13331 Marseille Cedex 03, France.
Neuroscience. 2007 Jul 29;147(4):893-905. doi: 10.1016/j.neuroscience.2007.05.022. Epub 2007 Jul 2.
The aim of this study was to determine the brain structures as well as the plasticity events associated with the behavioral effects of cholinergic damage. Rats were submitted to injection of 192 IgG-saporin in the medial septum/diagonal band of Broca complex and the nucleus basalis magnocellularis. The immunohistochemical expression of c-Fos protein and PSA-NCAM (polysialylated neural cell adhesion molecule) and the behavioral performances in the nonmatching-to-position task were assessed at various post-lesion times. Thus, 3 days after injection of the immunotoxin, increased c-Fos labeling was observed in the areas of infusion, indicating these cells were undergoing some plastic changes and/or apoptotic processes. A drastic increase was observed in the number of PSA-NCAM positive cells and in their dendritic arborization in the dentate gyrus. At 7 days post-lesion, no behavioral deficit was observed in immunolesioned rats despite the drastic loss of cholinergic neurons. These neurons showed decreased c-Fos protein expression in the piriform and entorhinal cortex and in the dentate gyrus. In the latter, PSA-NCAM induction was high, suggesting that remodeling occurred, which in turn might contribute to sustaining some mnemonic function in immunolesioned rats. At 1 month, cholinergic neurons totally disappeared and behavioral deficits were drastic. c-Fos expression showed no change. In contrast, the increased PSA-NCAM-labeling observed at short post-lesion times was maintained but the plastic changes due to this molecule could not compensate the behavioral deficit caused by the immunotoxin. Thus, as the post-lesion time increases, a gradual degeneration process should occur that may contribute to mnemonic impairments. This neuronal loss leads to molecular and cellular alterations, which in turn may aggravate cognitive deficits.
本研究的目的是确定与胆碱能损伤行为效应相关的脑结构以及可塑性事件。将大鼠内侧隔区/布罗卡复合体斜角带和大细胞基底核注射192IgG-皂草素。在损伤后的不同时间评估c-Fos蛋白和多唾液酸神经细胞粘附分子(PSA-NCAM)的免疫组化表达以及位置辨别任务中的行为表现。因此,在注射免疫毒素3天后,在注射区域观察到c-Fos标记增加,表明这些细胞正在经历一些可塑性变化和/或凋亡过程。在齿状回中,PSA-NCAM阳性细胞的数量及其树突分支显著增加。损伤后7天,免疫损伤大鼠未观察到行为缺陷,尽管胆碱能神经元大量丧失。这些神经元在梨状皮质、内嗅皮质和齿状回中c-Fos蛋白表达降低。在齿状回中,PSA-NCAM的诱导水平较高,表明发生了重塑,这反过来可能有助于维持免疫损伤大鼠的某些记忆功能。在1个月时,胆碱能神经元完全消失,行为缺陷严重。c-Fos表达无变化。相反,在损伤后短时间内观察到的PSA-NCAM标记增加得以维持,但该分子引起的可塑性变化无法弥补免疫毒素导致的行为缺陷。因此,随着损伤后时间的增加,应会发生逐渐的退化过程,这可能导致记忆障碍。这种神经元丢失会导致分子和细胞改变,进而可能加重认知缺陷。