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人结肠环形平滑肌对5-HT4受体激动剂和5-HT4样受体拮抗剂反应的差异。

Differences in response to 5-HT4 receptor agonists and antagonists of the 5-HT4-like receptor in human colon circular smooth muscle.

作者信息

Tam F S, Hillier K, Bunce K T, Grossman C

机构信息

Clinical Pharmacology Group, Faculty of Medicine, University of Southampton, UK.

出版信息

Br J Pharmacol. 1995 May;115(1):172-6. doi: 10.1111/j.1476-5381.1995.tb16335.x.

Abstract
  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. 7. The 5-HT4 receptor antagonist, SDZ 205-557 (0.3-10 microM), had no significant effect on 5-HT-induced inhibition of spontaneous motility.8. The present results are discussed in the light of variability of response to GR 113808 and SDZ205-557 in other tissues.9. Overall, our data indicate that human colon circular smooth muscle can be regarded as a site in which 5-HT4-like receptors are present but it is as yet unclear whether these results are also an indication of receptor variation.
摘要
  1. 在人结肠离体环形平滑肌条中,5-羟色胺(5-HT)对自发运动产生浓度相关的抑制作用。2. 具有5-HT4受体激动特性的氮杂双环烷基苯并咪唑酮类化合物BIMU 8和BIMU 1抑制运动,其半数有效浓度(EC50)值分别为0.76微摩尔/升和3.19微摩尔/升,且其最大效应值(Emax)与5-HT(EC50为0.13微摩尔/升)无显著差异。3. 5-HT4受体拮抗剂DAU 6285(1 - 10微摩尔/升)以平行浓度依赖方式使5-HT浓度 - 反应曲线右移,且不降低最大效应。Schild图呈线性,斜率与1无显著差异,pA2值为6.32。4. 高亲和力选择性5-HT4受体拮抗剂GR 113808在3纳摩尔浓度时以平行方式使5-HT浓度 - 反应曲线右移,表观pKB估计值为8.9±0.24。然而,10 - 100纳摩尔的更高浓度GR 113808并未导致5-HT浓度 - 反应曲线进一步显著右移,且最大效应未受抑制。5. GR 113808(10纳摩尔)也使5-HT4受体激动剂5-甲氧基色胺(5-MeOT)的浓度 - 反应曲线平行右移,表观pKB值在8.3 - 9.3之间。6. 在总共研究的10例患者中,有3例患者的组织条中,GR 113808(3 - 100纳摩尔)未能使5-HT或5-MeOT浓度 - 反应曲线右移,这些患者对5-HT和5-MeOT的反应正常。7. 5-HT4受体拮抗剂SDZ 205 - 557(0.3 - 10微摩尔/升)对5-HT诱导的自发运动抑制无显著影响。8. 根据其他组织中对GR 113808和SDZ205 - 557反应的变异性对本研究结果进行了讨论。9. 总体而言,我们的数据表明人结肠环形平滑肌可被视为存在5-HT4样受体的部位,但目前尚不清楚这些结果是否也表明受体存在变异。

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