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氮丙啶乙基胆碱(AF64A)诱导的胆碱能缺陷会短暂影响大鼠脑中生长抑素和神经肽Y的水平。

Cholinergic deficit induced by ethylcholine aziridinium (AF64A) transiently affects somatostatin and neuropeptide Y levels in rat brain.

作者信息

Hörtnagl H, Sperk G, Sobal G, Maas D

机构信息

Institute of Biochemical Pharmacology, University of Vienna, Austria.

出版信息

J Neurochem. 1990 May;54(5):1608-13. doi: 10.1111/j.1471-4159.1990.tb01211.x.

Abstract

The question whether during the process of cholinergic degeneration somatostatin- and/or neuropeptide Y-containing neurons in rat hippocampus and cortex react to the withdrawal of cholinergic function was addressed. After bilateral intracerebroventricular injection of the cholinotoxin ethylcholine aziridinium (AF64A; 1 or 2 nmol/ventricle) in rats, the activity of choline acetyltransferase (ChAT) started to decline in the hippocampus within 24 h. The reduction of ChAT activity reached its maximum within 4 days (34 and 55% after 1 and 2 nmol of AF64A/ventricle, respectively) and persisted during the observation period of 14 days. In the parietal cortex, ChAT activity decreased by 23% 4 days after 2 nmol of AF64A/ventricle. The loss in ChAT activity was accompanied by a transient decline in the levels of somatostatin and a transient increase in the levels of neuropeptide Y in both brain areas. In the hippocampus, the reduction in somatostatin content was most pronounced after 2 days (by 22 and 33% after 1 and 2 nmol of AF64A/ventricle, respectively). Within 14 days, somatostatin levels returned to control values. Neuropeptide Y levels increased slightly by approximately 25% of control values in the hippocampus. The changes described were present in both the dorsal and ventral subfields of the hippocampus. Similar but less pronounced changes in levels of both neuropeptides were observed in the parietal cortex. The present data provide further evidence for a close neuronal interrelationship between cholinergic and somatostatin- and/or neuropeptide Y-containing neurons in rat hippocampus and parietal cortex.

摘要

研究了在胆碱能神经变性过程中,大鼠海马体和皮质中含生长抑素和/或神经肽Y的神经元是否会对胆碱能功能的丧失做出反应。给大鼠双侧脑室内注射胆碱毒素氮丙啶乙基胆碱(AF64A;1或2 nmol/侧脑室)后,海马体中的胆碱乙酰转移酶(ChAT)活性在24小时内开始下降。ChAT活性的降低在4天内达到最大值(分别在注射1和2 nmol AF64A/侧脑室后降低34%和55%),并在14天的观察期内持续存在。在顶叶皮质,注射2 nmol AF64A/侧脑室4天后,ChAT活性下降了23%。两个脑区ChAT活性的丧失都伴随着生长抑素水平的短暂下降和神经肽Y水平的短暂升高。在海马体中,生长抑素含量在2天后下降最为明显(分别在注射1和2 nmol AF64A/侧脑室后下降22%和33%)。在14天内,生长抑素水平恢复到对照值。海马体中神经肽Y水平略有升高,约为对照值的25%。上述变化在海马体的背侧和腹侧亚区均有出现。在顶叶皮质中观察到两种神经肽水平有类似但不太明显的变化。目前的数据为大鼠海马体和顶叶皮质中胆碱能神经元与含生长抑素和/或神经肽Y的神经元之间密切的神经相互关系提供了进一步的证据。

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