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5-羟色胺诱导的离体回肠末端收缩中的种属差异。

Species differences in the 5-hydroxytryptamine-induced contraction in the isolated distal ileum.

作者信息

Yamano M, Ito H, Miyata K

机构信息

Pharmacology Laboratories, Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co., Ltd., Tsukuba, Ibaraki, Japan.

出版信息

Jpn J Pharmacol. 1997 Jul;74(3):267-74. doi: 10.1254/jjp.74.267.

Abstract

We investigated the mechanism of 5-hydroxytryptamine (5-HT)-induced contraction in the longitudinal muscle of isolated distal ileum from ferrets, piglets and rats. 5-HT and 5-methoxytryptamine concentration-dependently contracted the ileum of ferrets, piglets and rats. 2-Methyl-5-HT and m-chlorophenylbiguanide concentration-dependently contracted the ferret ileum, whereas they had no effect in piglets and rats. In ferrets, the 5-HT-induced contraction was inhibited by methysergide and by ramosetron, but not by ketanserin or GR113808. Atropine and tetrodotoxin suppressed contractions elicited by 5-HT, 2-methyl-5-HT and m-chlorophenylbiguanide in ferrets, but not that elicited by 5-methoxytryptamine. In piglets, 5-HT-induced contraction was inhibited by methysergide and by tetrodotoxin, but not by ketanserin, ramosetron, GR113808 or atropine. In rats, 5-HT-induced contraction was inhibited by methysergide and by ketanserin, but not by ramosetron or tetrodotoxin. In contrast, GR113808 enhanced contractions elicited by 5-HT or 5-methoxytryptamine. These results suggest that 5-HT-induced contraction in ferrets is mediated via 5-HT1 receptors on the muscle and by release of acetylcholine via 5-HT3 receptors. In piglets, 5-HT-induced contraction appears to be mediated by release of neurotransmitters other than acetylcholine via 5-HT1 receptors. 5-HT-induced contraction in rats is evoked via 5-HT1 and 5-HT2 receptors on the muscle. Furthermore, 5-HT4 receptors may participate in the relaxation elicited by 5-HT in rats.

摘要

我们研究了5-羟色胺(5-HT)诱导雪貂、仔猪和大鼠离体回肠远端纵行肌收缩的机制。5-HT和5-甲氧基色胺浓度依赖性地使雪貂、仔猪和大鼠的回肠收缩。2-甲基-5-HT和间氯苯双胍浓度依赖性地使雪貂回肠收缩,而对仔猪和大鼠无作用。在雪貂中,5-HT诱导的收缩被麦角新碱和雷莫司琼抑制,但不被酮色林或GR113808抑制。阿托品和河豚毒素抑制雪貂中5-HT、2-甲基-5-HT和间氯苯双胍引起的收缩,但不抑制5-甲氧基色胺引起的收缩。在仔猪中,5-HT诱导的收缩被麦角新碱和河豚毒素抑制,但不被酮色林、雷莫司琼、GR113808或阿托品抑制。在大鼠中,5-HT诱导的收缩被麦角新碱和酮色林抑制,但不被雷莫司琼或河豚毒素抑制。相反,GR113808增强5-HT或5-甲氧基色胺引起的收缩。这些结果表明,雪貂中5-HT诱导的收缩是通过肌肉上的5-HT1受体介导的,并通过5-HT3受体释放乙酰胆碱来实现。在仔猪中,5-HT诱导的收缩似乎是通过5-HT1受体释放除乙酰胆碱以外的神经递质介导的。大鼠中5-HT诱导的收缩是通过肌肉上的5-HT1和5-HT2受体引起的。此外,5-HT4受体可能参与大鼠中5-HT引起的舒张。

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