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.

译文

这项研究的目的是确定与胆碱能损伤的行为效应相关的大脑结构以及可塑性事件。大鼠在Broca复合体的内侧间隔/对角线带和巨大的基底核中注射192 IgG-saporin。在不同的病变后时间评估了c-Fos蛋白和psa-ncam (聚唾液酸化神经细胞粘附分子) 的免疫组织化学表达以及与位置不匹配的行为表现。因此,注射免疫毒素3天后,在输注区域观察到c-Fos标记增加,表明这些细胞正在经历一些塑性变化和/或凋亡过程。在齿状回中观察到psa-ncam阳性细胞的数量及其树突状乔木化急剧增加。病变后7天,尽管胆碱能神经元急剧丧失,但在免疫强化的大鼠中未观察到行为缺陷。这些神经元在梨状和内嗅皮层以及齿状回中显示c-Fos蛋白表达降低。在后者中,psa-ncam诱导很高,表明发生了重塑,这反过来可能有助于维持免疫强化大鼠的某些助记符功能。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,在病变后短时间内观察到的psa-ncam标记增加得以维持,但是由于该分子引起的塑性变化无法补偿由免疫毒素引起的行为缺陷。因此,随着病变后时间的增加,应发生逐渐的变性过程,这可能会导致助记符障碍。这种神经元丢失导致分子和细胞改变,进而可能加剧认知缺陷。

+1
+2
100研值 100研值 ¥99课程
检索文献一次
下载文献一次

去下载>

成功解锁2个技能,为你点赞

《SCI写作十大必备语法》
解决你的SCI语法难题!

技能熟练度+1

视频课《玩转文献检索》
让你成为检索达人!

恭喜完成新手挑战

手机微信扫一扫,添加好友领取

免费领《Endnote文献管理工具+教程》

微信扫码, 免费领取

手机登录

获取验证码
登录