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胆碱能和谷氨酸能激活通过阻断大鼠海马组胺H1受体逆转工作记忆障碍。

Cholinergic and glutamatergic activation reverses working memory failure by hippocampal histamine H1 receptor blockade in rats.

作者信息

Nakazato E, Yamamoto T, Ohno M, Watanabe S

机构信息

Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Life Sci. 2000;67(10):1139-47. doi: 10.1016/s0024-3205(00)00713-x.

Abstract

Intrahippocampal administration of the histamine H1 receptor antagonist pyrilamine (3.2-32 ug/ side) but not the histamine H2 receptor antagonist cimetidine (1.0-10 microg/side) increased the number of errors in the working memory task with a three-panel runway setup. The increase in working memory errors induced by intrahippocampal 32 microg/side pyrilamine was significantly reduced by concurrent infusion of the histamine H1 receptor agonist 2-pyridylethylamine (3.2 and 10 microg/side). The cholinesterase inhibitor physostigmine ( 1.0 and 3.2 microg/side) and D-cycloserine (0.32 and 1.0 microg/side), the partial agonist at the glycine binding site on the NMDA receptor/channel complex, reduced the increase in working memory errors induced by intrahippocampal 32 microg/side pyrilamine. These results suggest that the hippocampal histaminergic activity via histamine H1 receptor is necessary for normal working memory processes and that the septohippocampal cholinergic activation and positive modulation of the NMDA receptor/channel through activation of the glycine site can alleviate dysfunction of hippocampal histamine H1 receptor-mediated neurotransmission involved in working memory function.

摘要

在三室式跑道装置的工作记忆任务中,海马内注射组胺H1受体拮抗剂吡苄明(每侧3.2 - 32微克)而非组胺H2受体拮抗剂西咪替丁(每侧1.0 - 10微克)会增加错误数量。同时注射组胺H1受体激动剂2 - 吡啶乙胺(每侧3.2和10微克)可显著减少海马内每侧32微克吡苄明诱导的工作记忆错误增加。胆碱酯酶抑制剂毒扁豆碱(每侧1.0和3.2微克)以及NMDA受体/通道复合物甘氨酸结合位点的部分激动剂D - 环丝氨酸(每侧0.32和1.0微克)可减少海马内每侧32微克吡苄明诱导的工作记忆错误增加。这些结果表明,通过组胺H1受体的海马组胺能活性对于正常工作记忆过程是必要的,并且通过激活甘氨酸位点对NMDA受体/通道进行隔海马胆碱能激活和正向调节可以减轻参与工作记忆功能的海马组胺H1受体介导的神经传递功能障碍。

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