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红霉素衍生物ABT 229和GM 611作用于兔十二指肠的胃动素受体。

Erythromycin derivatives ABT 229 and GM 611 act on motilin receptors in the rabbit duodenum.

作者信息

Clark M J, Wright T, Bertrand P P, Bornstein J C, Jenkinson K M, Verlinden M, Furness J B

机构信息

Department of Anatomy and Cell Biology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1999 Mar;26(3):242-5. doi: 10.1046/j.1440-1681.1999.03022.x.

Abstract
  1. The present study was undertaken to determine whether the macrolide antibiotic erythromycin, its stable motilide derivatives ABT 229 and GM 611 and motilin act at the same receptors on intestinal muscle 2. Each compound contracted the longitudinal muscle of the rabbit duodenum in a concentration-dependent manner that was unaffected by 1 mumol/L tetrodotoxin. The potency order (pEC50 values in brackets) was motilin (8.4), ABT 229 (7.6), GM 611 (7.5) and erythromycin (6.0). 3. The motilin receptor antagonists GM 109 and [phe3, leu13]-motilin, both shifted the concentration-response curves for each agonist to the right, but did not affect concentration-response relationships for the muscarinic agonist carbachol. Schild regression analysis yielded similar pA2 values for GM 109 (in the range 7.2-7.5) for all agonists. This analysis was not done for [phe3, leu13]motilin, which was a non-competitive antagonist and partial agonist. 4. It is concluded that erythromycin, the motilides and motilin act at the same (motilin) receptor on rabbit duodenal muscle and do not have any detectable actions at other receptors in this preparation.
摘要
  1. 本研究旨在确定大环内酯类抗生素红霉素、其稳定的胃动素衍生物ABT 229和GM 611以及胃动素是否作用于肠肌上的同一受体。2. 每种化合物均以浓度依赖性方式使兔十二指肠纵肌收缩,且不受1 μmol/L河豚毒素的影响。效价顺序(括号内为pEC50值)为胃动素(8.4)、ABT 229(7.6)、GM 611(7.5)和红霉素(6.0)。3. 胃动素受体拮抗剂GM 109和[苯丙氨酸3,亮氨酸13] - 胃动素均使每种激动剂的浓度 - 反应曲线右移,但不影响毒蕈碱激动剂卡巴胆碱的浓度 - 反应关系。对于所有激动剂,Schild回归分析得出GM 109的pA2值相似(范围为7.2 - 7.5)。对于[苯丙氨酸3,亮氨酸13] - 胃动素未进行此分析,其为非竞争性拮抗剂和部分激动剂。4. 得出结论,红霉素、胃动素类似物和胃动素作用于兔十二指肠肌上的同一(胃动素)受体,且在该制剂中对其他受体无任何可检测到的作用。

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