Suppr超能文献

在体外,组胺通过H2受体兴奋大鼠小脑浦肯野细胞。

Histamine excites rat cerebellar Purkinje cells via H2 receptors in vitro.

作者信息

Tian L, Wen Y Q, Li H Z, Zuo C C, Wang J J

机构信息

Department of Biological Science and Technology, Nanjing University, China.

出版信息

Neurosci Res. 2000 Jan;36(1):61-6. doi: 10.1016/s0168-0102(99)00109-1.

Abstract

Recent neuroanatomical studies have revealed a direct hypothalamocerebellar histaminergic pathway. However, the functional significance of the histaminergic fibers in the cerebellum is not yet clear. In this study, the effects of histamine on the firing of cerebellar Purkinje cells (PCs) were investigated in vitro. Histamine predominantly produced excitatory (106/111, 95.5%) and in a few cases inhibitory (5/111, 4.5%) responses in PCs. The histamine-induced excitation was not blocked by perfusing the slice with low Ca2+ high/Mg2+ medium (n = 8), supporting a direct postsynaptic action of histamine. The histamine H2 receptor antagonist ranitidine effectively blocked the excitatory response of PCs to histamine (n = 20), but triprolidine, an H1 receptor antagonist, could not significantly block the histamine-induced excitation, or only very slightly decreased the excitatory effect of histamine on the cells (n = 13). On the other hand, the highly selective H2 receptor agonist dimaprit mimicked the excitatory effect of histamine on PCs and this dimaprit-induced excitation was also blocked by ranitidine (n = 20), but not triprolidine (n = 8). However, the H1 receptor agonists betahistine and 2-thiazolylethylamine did not show any effect on the PCs (n = 9 and 14). These results reveal that histamine excites cerebellar PCs via H2 receptors and suggest that the hypothalamocerebellar histaminergic fibers may play an important role in functional activities of the cerebellum.

摘要

近期的神经解剖学研究揭示了一条直接的下丘脑 - 小脑组胺能通路。然而,小脑内组胺能纤维的功能意义尚不清楚。在本研究中,我们在体外研究了组胺对小脑浦肯野细胞(PCs)放电的影响。组胺主要使PCs产生兴奋性反应(106/111,95.5%),少数情况下产生抑制性反应(5/111,4.5%)。用低钙高镁培养基灌注脑片并不能阻断组胺诱导的兴奋(n = 8),这支持了组胺的直接突触后作用。组胺H2受体拮抗剂雷尼替丁能有效阻断PCs对组胺的兴奋性反应(n = 20),但H1受体拮抗剂曲普利啶不能显著阻断组胺诱导的兴奋,或仅非常轻微地降低组胺对细胞的兴奋作用(n = 13)。另一方面,高度选择性的H2受体激动剂二甲双胍模拟了组胺对PCs的兴奋作用,且这种二甲双胍诱导的兴奋也被雷尼替丁阻断(n = 20),但未被曲普利啶阻断(n = 8)。然而,H1受体激动剂倍他司汀和2 - 噻唑乙胺对PCs没有任何作用(n = 9和14)。这些结果表明,组胺通过H2受体兴奋小脑PCs,并提示下丘脑 - 小脑组胺能纤维可能在小脑的功能活动中起重要作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验