Suppr超能文献

5-羟色胺对豚鼠离体结肠推进活动的抑制作用。

Inhibitory action of 5-hydroxytryptamine on propulsive activity of the guinea-pig isolated colon.

作者信息

Ishizawa M

机构信息

Laboratory of Physiology, School of Health Sciences, Sapporo Medical University, Japan.

出版信息

Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1996 May;114(1):1-6. doi: 10.1016/0742-8413(96)00010-2.

Abstract

The effects of 5-hydroxytryptamine (5-HT) and its receptor subtype agonists on spontaneous propulsive activities of the segment, and on changes in tension of the muscle strips were examined in the guinea-pig isolated distal colon. 5-HT, 5-carboxamidotryptamine (5-CT), alpha-methyl-5-HT and t-methoxytryptamine (5-MeOH), applied to the serosal side of the segment, inhibited spontaneous propulsive activities, but 2-methyl-5-HT did not. On the indomethacin-treated segment, 5-HT and its receptor subtype agonists all stimulated propulsive activity. 5-HT, 5-CT, alpha-methyl-5-HT and 5-MeOH relaxed circular muscle strips, which were inhibited in the presence of tetrodotoxin. However, these agonists showed contractile effects on the indomethacin-treated circular muscle strips. These results suggest that 5-HT may inhibit spontaneous propulsive activities of the colonic segment via release of endogenous PGs (e.g., E and I types) in the circular muscle cells mediated by an inhibitory neurotransmitter, which release was stimulated by 5-HT1-like 5-HT2 and 5-HT4 receptors on the myenteric neurones in the circular muscle layer.

摘要

在豚鼠离体远端结肠中,研究了5-羟色胺(5-HT)及其受体亚型激动剂对肠段自发推进活动以及肌条张力变化的影响。将5-HT、5-羧基色胺(5-CT)、α-甲基-5-HT和对甲氧基色胺(5-MeOH)应用于肠段浆膜侧,可抑制自发推进活动,但2-甲基-5-HT无此作用。在吲哚美辛处理的肠段上,5-HT及其受体亚型激动剂均刺激推进活动。5-HT、5-CT、α-甲基-5-HT和5-MeOH使环行肌条松弛,此作用在河豚毒素存在时受到抑制。然而,这些激动剂对吲哚美辛处理的环行肌条表现出收缩作用。这些结果提示,5-HT可能通过由抑制性神经递质介导的环行肌细胞内源性PGs(如E型和I型)释放来抑制结肠段的自发推进活动,而这种释放受到环行肌层肌间神经元上5-HT1样、5-HT2和5-HT4受体的刺激。

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