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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >17beta-estradiol enhances cortical cholinergic innervation and preserves synaptic density following excitotoxic lesions to the rat nucleus basalis magnocellularis.
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17beta-estradiol enhances cortical cholinergic innervation and preserves synaptic density following excitotoxic lesions to the rat nucleus basalis magnocellularis.

机译:17β-雌二醇增强兴奋性皮损后对大鼠大核基底细胞核的皮质胆碱能神经支配并保持突触密度。

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摘要

Estradiol exerts beneficial effects on neurodegenerative disorders associated with the decline of cognitive performance. The present study was designed to further investigate the effect of 17beta-estradiol on learning and memory, and to evaluate its neuroprotective action on cholinergic cells of the nucleus basalis magnocellularis, a neural substrate of cognitive performance. Female rats were ovariectomized at an age of 6 months. Three weeks later they received injections of either a mid-physiological dose of 17beta-estradiol or vehicle (oil), every other day for 2 weeks. The effect of estradiol on cognitive performance was tested in two associative learning paradigms. In the two-way active shock avoidance task estradiol-replaced animals learned significantly faster, while in the passive shock avoidance test no differences were observed between the experimental groups. Subsequent unilateral infusion of N-methyl-D-aspartate in the nucleus basalis magnocellularis resulted in a significant loss of cholinergic neurons concomitant with the loss of their fibers invading the somatosensory cortex. Estradiol treatment did not affect the total number of choline-acetyltransferase-immunoreactive neurons and their coexpression of the p75 low-affinity neurotrophin receptor either contralateral or ipsilateral to the lesion. In contrast, cholinergic fiber densities in estradiol-treated animals were greater both in the contralateral and ipsilateral somatosensory cortices as was detected by quantitative choline-acetyltransferase and vesicular acetylcholine transporter immunocytochemistry. However, estradiol treatment did not affect the lesion-induced relative percentage loss of cholinergic fibers. A significant decline of synaptophysin immunoreactivity paralleled the cholinergic damage in the somatosensory cortex of oil-treated animals, whereas an almost complete preservation of synaptic density was determined in estradiol-treated rats.Our results indicate that estradiol treatment enhances the cortical cholinergic innervation but has no rescuing effect on cholinergic nerve cells in the basal forebrain against excitotoxic damage. Nevertheless, estradiol may restore or maintain synaptic density in the cerebral cortex following cholinergic fiber loss. This estradiol effect may outweigh the lack of cellular protection on cholinergic cells at the functional level.
机译:雌二醇对与认知能力下降有关的神经退行性疾病产生有益作用。本研究旨在进一步研究17β-雌二醇对学习和记忆的影响,并评估其对基底神经节的胆碱能细胞(认知功能的神经底物)的神经保护作用。在6个月大时将雌性大鼠切除卵巢。三周后,他们每隔一天接受中等生理剂量的17β-雌二醇或媒介物(油)注射,持续2周。在两种联想学习范式中测试了雌二醇对认知能力的影响。在双向主动避震任务中,雌二醇替代的动物学习起来明显更快,而在被动避震测试中,实验组之间没有发现差异。随后单侧输注N-甲基-D-天冬氨酸到大细胞基底核中,导致胆碱能神经元的大量损失,并伴有其纤维侵犯体感皮层的损失。雌二醇治疗不影响胆碱乙酰转移酶免疫反应性神经元的总数,也不影响病变对侧或同侧的p75低亲和力神经营养蛋白受体的共表达。相反,通过定量胆碱-乙酰转移酶和囊泡乙酰胆碱转运蛋白免疫细胞化学检测,雌二醇治疗动物的对侧和同侧体感皮质中胆碱能纤维密度更高。但是,雌二醇治疗并未影响病灶引起的胆碱能纤维的相对损失百分比。突触素免疫反应性的显着下降与油处理动物的体感皮层中的胆碱能损害相平行,而雌二醇处理的大鼠中突触密度几乎得以完全保留。我们的结果表明,雌二醇处理可增强皮质胆碱能神经支配,但没有抢救对基底前脑胆碱能神经细胞的兴奋性毒性损害。然而,胆碱能纤维丧失后,雌二醇可恢复或维持大脑皮质的突触密度。在功能水平上,这种雌二醇作用可能胜过对胆碱能细胞缺乏细胞保护的作用。

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