Suppr超能文献

[多巴胺能药物对不同脑区中前列腺素E2和前列腺素F2α浓度的影响]

[Effects of dopaminergic drugs on the concentrations of PGE2 and PGF2alpha in various brain regions].

作者信息

Grasso A A, Millia C C, Rampello L, Reggio A, De Simone D, Bousquet E, Rapisarda E

出版信息

Boll Soc Ital Biol Sper. 1983 Jan 31;59(1):58-64.

PMID:6573881
Abstract

It has long been shown by Biggio and Guidotti that multisynaptic nigro-cerebellar pathway of dopaminergic origin can control cerebellar cyclic guanosinmonophosphate (cGMP) content, a good index of the activity of Purkinje cells. In this line, it has been reported that haloperidol and sulpiride, significantly decrease cerebellar cGMP content while opposite changes are observed with apomorphine. In an attempt to establish whether other cerebellar cGMP-related parameters may be influenced by dopamine drugs. Authors have investigated the effects of haloperidol, sulpiride and apomorphine on cerebellar PGE2 and PGF2alpha. Results obtained indicate that haloperidol and sulpiride significantly reduce cerebellar PGE2 and PGF2alpha content while opposite changes are induced by apomorphine. Similar results have been observed in substantia nigra but not in other brain regions, such as corpus striatum and medial basal hypothalamus. The possibility that the observed changes in cerebellar PG-content may result from the modulation of striatal dopamine receptors is discussed.

摘要

比焦和吉多蒂早就指出,多巴胺能起源的多突触黑质 - 小脑通路可以控制小脑环磷酸鸟苷(cGMP)含量,这是浦肯野细胞活性的一个良好指标。按照这一思路,有报道称氟哌啶醇和舒必利会显著降低小脑cGMP含量,而阿扑吗啡则会产生相反的变化。为了确定其他与小脑cGMP相关的参数是否会受到多巴胺药物的影响,作者研究了氟哌啶醇、舒必利和阿扑吗啡对小脑前列腺素E2(PGE2)和前列腺素F2α(PGF2α)的影响。所得结果表明,氟哌啶醇和舒必利会显著降低小脑PGE2和PGF2α含量,而阿扑吗啡则会引发相反的变化。在黑质中观察到了类似结果,但在纹状体和内侧基底下丘脑等其他脑区未观察到。文中讨论了小脑PG含量的观察变化可能是由纹状体多巴胺受体调节引起的可能性。

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