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不同来源丁酸对鸡肠道药物代谢细胞色素P450的营养调控

Nutritional modulation of intestinal drug-metabolizing cytochrome P450 by butyrate of different origin in chicken.

作者信息

Kulcsár Anna, Mátis Gábor, Molnár Andor, Petrilla Janka, Wágner László, Fébel Hedvig, Husvéth Ferenc, Dublecz Károly, Neogrády Zsuzsanna

机构信息

Department of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2, Budapest, Hungary.

Department of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2, Budapest, Hungary.

出版信息

Res Vet Sci. 2017 Aug;113:25-32. doi: 10.1016/j.rvsc.2017.07.033. Epub 2017 Aug 1.

Abstract

Intestinal cytochrome P450 (CYP) enzymes play key role in the first pass metabolism of orally ingested xenobiotics, providing a primary metabolic barrier, being of special importance in maintaining animal health and production. This study was aimed to investigate how intestinal drug-metabolizing CYPs can be modulated by nutritional factors in broiler chicken. We investigated the effects of the natural growth promoter (n-)butyrate of different origin (feed supplementation of protected or non-protected forms and/or inducing caecal microbial production by supporting higher level of dietary non-starch polysaccharides [NSP]) on the activity of duodenal CYPs. To observe the connection between intestinal CYP activity and butyrate concentration, the distribution of differently originated butyrate was also assessed by measuring its concentration in various intestinal segments and different vessels of portal and systemic circulation. Butyrate of different origin showed varying distribution properties as being absorbed from different parts of the gastrointestinal tract. Intestinal CYP1A and CYP2H2 activities were increased by dietary butyrate supplementation and by the increased caecal microbial butyrate production, while CYP3A37 activity was minimally influenced by microbial butyrate only. The present study proved that both dietary and microbial butyrate could alter the activity of CYPs in the duodenal epithelium. Our findings suggest that intestinal CYPs could be induced not only by the intestinal luminal butyrate, but also from basolateral side, by the already absorbed butyrate. Such action of butyrate can be of special importance from food safety and pharmacotherapeutic point of view as it may modify the metabolism and intestinal kinetics of simultaneously applied xenobiotics.

摘要

肠道细胞色素P450(CYP)酶在口服摄入的外源性物质的首过代谢中起关键作用,是维持动物健康和生产的重要初级代谢屏障。本研究旨在探讨营养因素如何调节肉鸡肠道药物代谢CYP。我们研究了不同来源的天然生长促进剂丁酸(补充受保护或未受保护形式的饲料和/或通过支持更高水平的膳食非淀粉多糖[NSP]诱导盲肠微生物产生丁酸)对十二指肠CYP活性的影响。为了观察肠道CYP活性与丁酸浓度之间的联系,还通过测量其在各个肠段以及门静脉和体循环不同血管中的浓度,评估了不同来源丁酸的分布情况。不同来源的丁酸表现出不同的分布特性,因为它们从胃肠道的不同部位吸收。日粮添加丁酸以及盲肠微生物丁酸产生增加可提高肠道CYP1A和CYP2H2活性,而CYP3A37活性仅受微生物丁酸的轻微影响。本研究证明,日粮丁酸和微生物丁酸均可改变十二指肠上皮细胞中CYP的活性。我们的研究结果表明,肠道CYP不仅可被肠腔丁酸诱导,也可被已吸收的丁酸从基底外侧诱导。从食品安全和药物治疗的角度来看,丁酸的这种作用可能特别重要,因为它可能会改变同时应用的外源性物质的代谢和肠道动力学。

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