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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Behavioral and immunohistological effects of cholinergic damage in immunolesioned rats: alteration of c-Fos and polysialylated neural cell adhesion molecule expression.
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Behavioral and immunohistological effects of cholinergic damage in immunolesioned rats: alteration of c-Fos and polysialylated neural cell adhesion molecule expression.

机译:胆碱能损害在免疫损伤大鼠中的行为和免疫组织学影响:c-Fos和多唾液酸化神经细胞粘附分子表达的改变。

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摘要

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.
机译:这项研究的目的是确定与胆碱能损害的行为影响有关的大脑结构以及可塑性事件。大鼠在Broca复合体和大细胞基底核的中隔/对角带内注射192种IgG-saporin。在损伤后的不同时间评估c-Fos蛋白和PSA-NCAM(多唾液酸化神经细胞粘附分子)的免疫组织化学表达以及在不匹配位置任务中的行为表现。因此,在注射免疫毒素三天后,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。观察到PSA-NCAM阳性细胞的数量及其在齿状回中的树突乔化急剧增加。在损伤后7天,尽管胆碱能神经元急剧丧失,但在免疫损伤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出c-Fos蛋白表达降低。在后者中,PSA-NCAM诱导较高,表明发生了重塑,这反过来可能有助于维持免疫受损大鼠的某些记忆功能。 1个月后,胆碱能神经元完全消失,行为缺陷严重。 c-Fos表达无变化。相比之下,在损伤后短时间内观察到的PSA-NCAM标记增加得以维持,但由于该分子引起的塑性变化无法弥补免疫毒素引起的行为缺陷。因此,随着损伤后时间的增加,应该发生逐渐退化的过程,这可能会导致记忆障碍。这种神经元的丧失导致分子和细胞的改变,从而可能加剧认知缺陷。

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