Basivireddy Jayasree, Jacob Molly, Ramamoorthy Prabhu, Pulimood Anna B, Balasubramanian Kunissery A
The Wellcome Trust Research Laboratory, Department of Gastrointestinal Sciences, Christian Medical College and Hospital, Vellore 632004, India.
Biochem Pharmacol. 2003 Feb 15;65(4):683-95. doi: 10.1016/s0006-2952(02)01616-7.
Nonsteroidal anti-inflammatory drugs (NSAIDs) cause small intestinal damage but the pathogenesis of this toxicity is not well established. Our earlier work has shown that villus enterocytes are most susceptible to the effects of indomethacin, a commonly used NSAID. This study looked at the acute effect of indomethacin on brush border membranes (BBM), which are present mainly in the villus cells and are in immediate contact with the contents of the small intestinal lumen. Evidence of oxidative stress was found in the mucosa of the small intestine of rats dosed with indomethacin, as indicated by increased activity of xanthine oxidase with corresponding decrease in the levels of several free radical scavenging enzymes. These changes were associated with an increase in peroxidation parameters in the BBM and a fall in the level of alpha-tocopherol. These BBM also exhibited impairment in glucose transport. Significant changes were seen in the lipid composition of these membranes, with upregulation of an 85kDa isoform of phospholipase A(2). Pretreatment of animals with allopurinol, arginine or zinc protected against these effects of indomethacin. Thus this study suggests that in an acute model of indomethacin dosing there is impairment in structure and function of the BBM in enterocytes, with the effects possibly mediated by free radicals and phospholipases.
非甾体抗炎药(NSAIDs)会导致小肠损伤,但其毒性的发病机制尚未完全明确。我们早期的研究表明,绒毛肠上皮细胞对常用的非甾体抗炎药吲哚美辛的作用最为敏感。本研究观察了吲哚美辛对刷状缘膜(BBM)的急性影响,刷状缘膜主要存在于绒毛细胞中,并与小肠腔内容物直接接触。在用吲哚美辛给药的大鼠小肠黏膜中发现了氧化应激的证据,表现为黄嘌呤氧化酶活性增加,同时几种自由基清除酶的水平相应降低。这些变化与BBM中过氧化参数的增加以及α-生育酚水平的下降有关。这些BBM还表现出葡萄糖转运受损。这些膜的脂质组成发生了显著变化,磷脂酶A(2)的85kDa同工型上调。用别嘌呤醇、精氨酸或锌对动物进行预处理可预防吲哚美辛的这些作用。因此,本研究表明,在吲哚美辛给药的急性模型中,肠上皮细胞中BBM的结构和功能受损,其作用可能由自由基和磷脂酶介导。