Jackson M J, Wagenmakers A J, Edwards R H
Biochem J. 1987 Jan 15;241(2):403-7. doi: 10.1042/bj2410403.
The role of arachidonic acid metabolism in the efflux of intracellular enzymes from damaged skeletal muscle has been examined in vitro using inhibitors of cyclo-oxygenase and lipoxygenase enzymes. Damage to skeletal muscle induced by either calcium ionophore A23187 (25 microM) or dinitrophenol (1 mM) caused an increase in the efflux of prostaglandins E2 and F2 alpha together with a large efflux of intracellular creatine kinase. Use of a cyclo-oxygenase inhibitor completely prevented the efflux of prostaglandins, but had no effect on creatine kinase efflux. However, several agents having the ability to inhibit lipoxygenase enzymes dramatically reduced creatine kinase efflux following damage. These data suggest that a product or products of lipoxygenase enzymes may be mediators of the changes in plasma membrane integrity which permit efflux of intracellular enzymes as a consequence of skeletal muscle damage.
利用环氧化酶和脂氧化酶的抑制剂,在体外研究了花生四烯酸代谢在受损骨骼肌细胞内酶流出中的作用。钙离子载体A23187(25微摩尔)或二硝基苯酚(1毫摩尔)诱导的骨骼肌损伤导致前列腺素E2和F2α流出增加,同时细胞内肌酸激酶大量流出。使用环氧化酶抑制剂可完全阻止前列腺素的流出,但对肌酸激酶流出没有影响。然而,几种能够抑制脂氧化酶的药物在损伤后显著降低了肌酸激酶的流出。这些数据表明,脂氧化酶的一种或多种产物可能是质膜完整性变化的介质,质膜完整性变化会导致骨骼肌损伤后细胞内酶的流出。