首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Differences in response to 5-HT4 receptor agonists and antagonists of the 5-HT4-like receptor in human colon circular smooth muscle.
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Differences in response to 5-HT4 receptor agonists and antagonists of the 5-HT4-like receptor in human colon circular smooth muscle.

机译:人结肠环形平滑肌中对5-HT4受体激动剂和5-HT4样受体拮抗剂的反应差异。

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摘要

1. In isolated circular smooth muscle strips of human colon 5-hydroxytryptamine (5-HT) produced a concentration-related inhibition of spontaneous motility. 2. The azabicycloalkyl benzimidazolones, BIMU 8 and BIMU 1, which have 5-HT4 receptor stimulant properties, inhibited motility with EC50 values of 0.76 microM and 3.19 microM respectively and their Emax values were not significantly different from 5-HT (EC50, 0.13 microM). 3. The 5-HT4 receptor antagonist, DAU 6285 (1-10 microM), displaced the 5-HT concentration-response curve to the right in a parallel concentration-dependent manner without depressing the maximum. The Schild plot was linear and the slope did not differ significantly from unity giving a pA2 value of 6.32. 4. The high affinity selective 5-HT4 receptor antagonist, GR 113808, at a concentration of 3 nM displaced the 5-HT concentration-response curve in a parallel manner giving an apparent pKB estimate of 8.9 +/- 0.24. However, higher concentrations of 10-100 nM GR 113808 did not result in a further significant displacement of the 5-HT concentration-response curve and there was no suppression of Emax. 5. GR 113808 (10 nM) also caused a parallel displacement of the concentration-response curve to the 5-HT4 receptor agonist, 5-methoxytryptamine (5-MeOT) giving apparent pKB values ranging from 8.3-9.3. 6. GR 113808 (3-100 nM) failed to displace 5-HT or 5-MeOT concentration-response curves in tissue strips from 3 patients out of a total of 10 patients studied in whom the response to 5-HT and 5-MeOT was normal.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在孤立的人结肠圆形平滑肌条中,5-羟色胺(5-HT)产生了与浓度相关的自发运动抑制作用。 2.具有5-HT4受体刺激特性的氮杂双环烷基苯并咪唑酮,BIMU 8和BIMU 1抑制运动,其EC50值分别为0.76 microM和3.19 microM,并且它们的Emax值与5-HT(EC50,0.13 microM )。 3. 5-HT4受体拮抗剂DAU 6285(1-10 microM)使5-HT浓度-响应曲线以平行的浓度依赖性方式向右移动,而没有降低最大值。 Schild图是线性的,并且斜率与统一性无明显差异,pA2值为6.32。 4.浓度为3 nM的高亲和力选择性5-HT4受体拮抗剂GR 113808以平行方式置换了5-HT浓度-响应曲线,得出pKB的表观估计值为8.9 +/- 0.24。但是,较高浓度的10-100 nM GR 113808不会导致5-HT浓度-响应曲线的进一步显着位移,并且不会抑制Emax。 5. GR 113808(10 nM)还引起浓度响应曲线与5-HT4受体激动剂5-甲氧基色胺(5-MeOT)的平行位移,其pKB值在8.3-9.3范围内。 6. GR 113808(3-100 nM)未能取代10例研究中对5-HT和5-MeOT反应的患者中的3例患者组织条带中的5-HT或5-MeOT浓度-反应曲线正常。(摘要截断为250个字)

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