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大鼠肠道中氨基肽酶抗性糖偶联三肽的钠依赖性转运

Na(+)-dependent transport of aminopeptidase-resistant sugar-coupled tripeptides in rat intestine.

作者信息

Mizuma T, Sakai N, Awazu S

机构信息

Department of Biopharmaceutics, Tokyo College of Pharmacy, Japan.

出版信息

Biochem Biophys Res Commun. 1994 Sep 30;203(3):1412-6. doi: 10.1006/bbrc.1994.2342.

Abstract

Aminopeptidase-degradable tripeptide, tyrosylglycylglycine (TGG, a part of aminopeptidase-degradable enkephalines), was coupled with sugars (cellobiose, maltose, lactose, gentiobiose and glucose). These sugar-coupled TGGs were stable enough to be transported from the mucosal to the serosal side in rat everted small intestine, while TGG was not stable enough to be transported. The transport of sugar-coupled TGGs was decreased in the absence of Na+, indicating the Na(+)-dependent transport of sugar-coupled TGG in rat intestine. Cellobiose-coupled TGG and glucose-coupled TGG did not mutually inhibit their transport. It was suggested that the intestinal Na(+)-dependent transporter for disaccharide-coupled tripeptides, which have a pyranose ring, was different from that of monosaccharide-coupled tripeptide, which has no pyranose ring.

摘要

氨肽酶可降解三肽酪氨酰甘氨酰甘氨酸(TGG,氨肽酶可降解脑啡肽的一部分)与糖类(纤维二糖、麦芽糖、乳糖、龙胆二糖和葡萄糖)偶联。这些糖偶联的TGG足够稳定,能够在大鼠外翻小肠中从黏膜侧转运至浆膜侧,而TGG本身稳定性不足,无法实现转运。在无Na⁺的情况下,糖偶联TGG的转运减少,表明大鼠肠道中糖偶联TGG的转运依赖于Na⁺。纤维二糖偶联TGG和葡萄糖偶联TGG之间不存在相互抑制转运的情况。这表明,肠道中负责转运具有吡喃糖环的二糖偶联三肽的Na⁺依赖性转运体,与负责转运无吡喃糖环的单糖偶联三肽的转运体不同。

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