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Can small non-peptide motilin agonists force a breakthrough as gastroprokinetic drugs?

机译:小型非肽胃动素激动剂能否作为胃肠动力药物取得突破?

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摘要

GSK962040 is a small selective motilin receptor agonist currently under investigation in clinical trials for the treatment of conditions associated with delayed gastric emptying. As reported in this issue of the British Journal of Pharmacology, Broad et al., studied for the first time the region-dependent contractile effects of motilin and GSK962040 in human smooth muscle strips. Both compounds facilitated cholinergically mediated contractions of human gastric antral muscle strips at low concentrations and induced smooth muscle contractions at high concentrations. The effect was less pronounced in the fundus and almost absent in the colon. The long-lasting facilitation of cholinergic responses in the antrum by GSK962040 compared with the fading responses to motilin may be of importance from a clinical point of view. The approach used by Broad et al. with human tissue is a validated model to identify motilin receptor agonists with therapeutic value.LINKED ARTICLEThis article is a commentary on Broad et al., pp. 763–774 of this issue. To view this paper visit
机译:GSK962040是一种小型选择性胃动素受体激动剂,目前正在临床试验中进行研究,用于治疗与胃排空延迟有关的疾病。正如本期《英国药理学杂志》(Broad)等报道的那样,第一次研究了胃动素和GSK962040在人平滑肌条中的区域依赖性收缩作用。两种化合物均在低浓度时促进胆碱介导的人胃窦肌条的收缩,并在高浓度时诱导平滑肌收缩。这种影响在眼底不太明显,而在结肠几乎没有。从临床的角度来看,与对胃动素的褪色反应相比,GSK962040对胃内胆碱能反应的长期促进作用可能是重要的。 Broad等人使用的方法。人体组织模型是鉴定具有治疗价值的胃动素受体激动剂的有效模型。链接的文章本文是对Broad等人,第763-774页的评论。要查看本文,请访问

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