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介导猪离体近端胃条收缩的平滑肌5-羟色胺2A受体。

Smooth muscle 5-HT2A receptors mediating contraction of porcine isolated proximal stomach strips.

作者信息

Janssen P, Prins N H, Meulemans A L, Lefebvre R A

机构信息

Heymans Institute of Pharmacology, Ghent University, Ghent, Belgium.

出版信息

Br J Pharmacol. 2002 Dec;137(8):1217-24. doi: 10.1038/sj.bjp.0704992.

Abstract
  1. The aim of this study was to characterize the 5-HT receptors involved in the 5-HT-induced contraction of longitudinal muscle (LM) strips of porcine proximal stomach. This was done in a classical organ bath set-up for isotonic measurement. 2. The concentration-contraction curve to 5-HT was not modified by 5-HT(3) and 5-HT(4) receptor antagonism. Methysergide, ketanserin and mesulergine antagonized the curve to 5-HT. Concomitantly, increasing concentrations of ketanserin and mesulergine progressively revealed a biphasic nature of the 5-HT curve. Ketanserin antagonized the low-affinity receptor while it did not modify the high-affinity receptor. 3. Tetrodotoxin did not influence the concentration-contraction curve to 5-HT neither in the absence nor presence of ketanserin, indicating that nerves are not involved. 4. Ketanserin competitively antagonized the monophasic concentration-response curve to alpha-Methyl-5-HT, yielding a Schild slope that was not significantly different from unity. After constraining the Schild slope to unity, a pK(B) estimate of 8.23+/-0.90 was obtained. This affinity estimate of ketanserin closely approximates previously reported affinities at 5-HT(2A) receptors. 5. In the presence of ketanserin (0.1 microM; exposing the high-affinity receptor), a wide range of 5-HT receptor antagonists covering all 5-HT receptors known, was tested. Only methysergide and ritanserin inhibited the response to 5-HT, thus expressing affinity for the high-affinity receptor. This did not reveal the identity of the receptor involved. 6 It can be concluded that 5-HT induces pig proximal stomach (LM) contraction via 5-HT(2A) receptors located on smooth muscle. A ketanserin-insensitive phase of contractions could not be characterized between the actually known classes of 5-HT receptors with the pharmacological tools that were used.
摘要
  1. 本研究的目的是鉴定参与5-羟色胺(5-HT)诱导的猪近端胃纵行肌(LM)条收缩的5-HT受体。这是在用于等张测量的经典器官浴装置中完成的。2. 5-HT(3)和5-HT(4)受体拮抗作用未改变5-HT的浓度-收缩曲线。麦角新碱、酮色林和甲磺麦角林拮抗5-HT曲线。同时,酮色林和甲磺麦角林浓度增加逐渐显示出5-HT曲线的双相性质。酮色林拮抗低亲和力受体,而不改变高亲和力受体。3. 河豚毒素在不存在和存在酮色林时均不影响5-HT的浓度-收缩曲线,表明神经未参与。4. 酮色林竞争性拮抗α-甲基-5-HT的单相浓度-反应曲线,产生的希尔斜率与1无显著差异。将希尔斜率限定为1后,获得的pK(B)估计值为8.23±0.90。酮色林的这种亲和力估计值与先前报道的在5-HT(2A)受体上的亲和力非常接近。5. 在存在酮色林(0.1微摩尔;暴露高亲和力受体)的情况下,测试了涵盖所有已知5-HT受体的多种5-HT受体拮抗剂。只有麦角新碱和利坦色林抑制对5-HT的反应,因此对高亲和力受体表现出亲和力。这并未揭示所涉及受体的身份。6. 可以得出结论,5-HT通过位于平滑肌上的5-HT(2A)受体诱导猪近端胃(LM)收缩。在所使用的药理学工具下,在实际已知的5-HT受体类别之间无法鉴定出对酮色林不敏感的收缩阶段。

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