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红霉素在肠道中的一种并非通过胃动素受体介导的作用。

An action of erythromycin in the intestine that is not mediated via motilin receptors.

作者信息

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

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 Feb;26(2):100-4. doi: 10.1046/j.1440-1681.1999.03002.x.

Abstract
  1. Erythromycin lactobionate caused a concentration-dependent inhibition of nerve-mediated contractions of the longitudinal muscle of the guinea-pig ileum, with a threshold for effect of 10-30 mumol/L. The non-antibiotic derivative of erythromycin ABT-229 had a similar effect, but was approximately 10-fold less potent. At a greater concentration (1 mmol/L), erythromycin also depressed the direct contractile effect of 10 mumol/L carbachol on the muscle. 2. Human/porcine motilin (up to 100 mumol/L) did not reduce the nerve-mediated contractions, although it did contract the muscle (threshold 30 mumol/L). Antagonists of motilin receptors (phe3leu13motilin, up to 1 mumol/L, and GM-109, up to 3 mumol/L) did not reduce responses to erythromycin. 3. Erythromycin contracted the longitudinal muscle of the rabbit duodenum, with a threshold concentration of 0.1 mumol/L and ABT-229 contracted this tissue at a threshold concentration of 0.01 mumol/L. Effects of both agonists were antagonized by the motilin receptor antagonists phe3leu13motilin (0.3 mumol/L) and GM-109 (1 mumol/L). 4. It is concluded that the site(s) at which erythromycin acts in the guinea-pig ileum is not a motilin receptor and that ABT-229 is selective for the motilin receptor in comparison with non-motilin erythromycin sites and is unlikely to act at the latter site in therapeutic doses.
摘要
  1. 乳糖酸红霉素对豚鼠回肠纵肌神经介导的收缩产生浓度依赖性抑制,起效阈值为10 - 30μmol/L。红霉素的非抗生素衍生物ABT - 229有类似作用,但效力约低10倍。在更高浓度(1mmol/L)时,红霉素也会抑制10μmol/L卡巴胆碱对肌肉的直接收缩作用。2. 人/猪胃动素(浓度高达100μmol/L)虽能使肌肉收缩(阈值为30μmol/L),但不降低神经介导的收缩。胃动素受体拮抗剂(苯丙氨酸3 - 亮氨酸13 - 胃动素,浓度高达1μmol/L,以及GM - 109,浓度高达3μmol/L)不降低对红霉素的反应。3. 红霉素使兔十二指肠纵肌收缩,阈值浓度为0.1μmol/L,ABT - 229使该组织收缩的阈值浓度为0.01μmol/L。两种激动剂的作用均被胃动素受体拮抗剂苯丙氨酸3 - 亮氨酸13 - 胃动素(0.3μmol/L)和GM - 109(1μmol/L)拮抗。4. 得出结论:红霉素在豚鼠回肠的作用位点不是胃动素受体,与非胃动素红霉素位点相比,ABT - 229对胃动素受体具有选择性,且在治疗剂量下不太可能作用于后者位点。

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