Ahamed Ibrahim S, Basker L, Balasubramanian K A
Department of Gastrointestinal Sciences, Christian Medical College & Hospital, Vellore, India.
Indian J Biochem Biophys. 1996 Feb;33(1):53-6.
Oxygen-derived free radicals are known to be generated during ischemia/reperfusion injury and biomembranes are the prime target of these active species. In order to study the effect of in vivo generated free radicals on intestinal mucosal membrane, brush border membranes (BBM) were isolated from rat small intestine after subjecting to ischemia (I) and ischemia/reperfusion (I/R) injury and their lipid composition and marker enzyme activity were compared with BBM prepared from control animals. No significant alteration in the lipid composition of BBM was observed after I or I/R as compared to control. Membrane fluidity measurements showed that I/R increased the fluidity of BBM. Activity of alkaline phosphatase, one of the marker enzymes for BBM was reduced by I or I/R whereas activity of another BBM enzyme, sucrase was not altered. The decrease in alkaline phosphatase activity was more after reperfusion. In vitro fluidization of BBM using benzyl alcohol indicated that the inactivation of alkaline phosphatase was not due to change in fluidity. These results suggest that free radicals generated during I/R inactivate BBM alkaline phosphatase partially without altering the membrane lipid composition.
已知在缺血/再灌注损伤期间会产生氧衍生的自由基,生物膜是这些活性物质的主要靶标。为了研究体内产生的自由基对肠黏膜的影响,在大鼠小肠遭受缺血(I)和缺血/再灌注(I/R)损伤后,从小肠分离出刷状缘膜(BBM),并将其脂质组成和标记酶活性与从对照动物制备的BBM进行比较。与对照相比,I或I/R后BBM的脂质组成未观察到明显变化。膜流动性测量表明,I/R增加了BBM的流动性。BBM的标记酶之一碱性磷酸酶的活性在I或I/R后降低,而另一种BBM酶蔗糖酶的活性未改变。再灌注后碱性磷酸酶活性的降低更为明显。使用苯甲醇对BBM进行体外流化表明,碱性磷酸酶的失活不是由于流动性的变化。这些结果表明,I/R期间产生的自由基部分地使BBM碱性磷酸酶失活,而不改变膜脂质组成。