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抗氧化剂对体内肠道缺血/再灌注时药物吸收的影响。

Effects of antioxidants on drug absorption in in vivo intestinal ischemia/reperfusion.

作者信息

Takizawa Yusuke, Kitazato Takuya, Kishimoto Hisanao, Tomita Mikio, Hayashi Masahiro

机构信息

Department of Drug Absorption and Pharmacokinetics, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.

出版信息

Eur J Drug Metab Pharmacokinet. 2011 Jan;35(3-4):89-95. doi: 10.1007/s13318-010-0020-y. Epub 2010 Dec 24.

Abstract

Ischemia/reperfusion (I/R) injury must be overcome in order to succeed in small intestinal transplantation. Reactive oxygen species (ROS) are generated by I/R, and they induce lipid peroxidation which is one of the causes of mucosal lesion. We previously reported the protection effects of antioxidants to I/R injury in the in vitro study. In the present study, we examined the inhibitive effect of antioxidants on intestinal I/R injury in the in vivo study. Intestinal ischemia was induced in Wistar/ST rats using the spring scale and the surgical suture for 1 h, followed by reperfusion for 1 h. We used 4,5-dihydroxy-1,3-benzene-disulfonic acid (Tiron), astaxanthin (ATX) and epigallocatechin gallate (EGCG) as antioxidants. The inhibitive effects on mucosal lesion, opening of TJ and decrease in protein expression level of P-gp by in vivo intestinal I/R were admitted by three kinds of antioxidant. Tiron and EGCG inhibited P-gp function but ATX did not. Therefore, for the use of P-gp substrate like immunosuppressants after the intestinal transplantation, ATX, which does not inhibit P-gp is considered to be effective for intestinal I/R injury.

摘要

为了成功进行小肠移植,必须克服缺血/再灌注(I/R)损伤。I/R会产生活性氧(ROS),它们会诱导脂质过氧化,这是粘膜损伤的原因之一。我们之前在体外研究中报道了抗氧化剂对I/R损伤的保护作用。在本研究中,我们在体内研究中检测了抗氧化剂对肠道I/R损伤的抑制作用。使用弹簧秤和手术缝线对Wistar/ST大鼠造成肠道缺血1小时,然后再灌注1小时。我们使用4,5-二羟基-1,3-苯二磺酸(Tiron)、虾青素(ATX)和表没食子儿茶素没食子酸酯(EGCG)作为抗氧化剂。三种抗氧化剂均证实了对体内肠道I/R引起的粘膜损伤、紧密连接开放以及P-糖蛋白表达水平降低具有抑制作用。Tiron和EGCG抑制P-糖蛋白功能,但ATX没有。因此,对于小肠移植后使用免疫抑制剂等P-糖蛋白底物的情况,不抑制P-糖蛋白的ATX被认为对肠道I/R损伤有效。

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