Kawashima Y, Uy-Yu N, Kozuka H
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Japan.
Biochem J. 1989 Nov 1;263(3):897-904. doi: 10.1042/bj2630897.
The effects of the peroxisome proliferators clofibric acid (p-chlorophenoxyisobutyric acid), tiadenol [2,2'-(decamethylenedithio)diethanol] and perfluoro-octanoic acid (PFOA) on hepatic stearoyl-CoA desaturation in male and female rats were compared. Treatment of male rats with the three peroxisome proliferators increased markedly the activity of stearoyl-CoA desaturase. Administration of clofibric acid or tiadenol to female rats increased greatly the hepatic activity of stearoyl-CoA desaturase, the extent of the increases being slightly less pronounced than those of male rats. In contrast with the other two peroxisome proliferators, however, PFOA did not change the activity of stearoyl-CoA desaturase in female rats. Hormonal manipulations revealed that this sex-related difference in the effect of PFOA on stearoyl-CoA desaturase activity is strongly dependent on testosterone. The increase in stearoyl-CoA desaturase activity by peroxisome proliferators was not accompanied by any notable increases in the microsomal content of cytochrome b5 or the activity of NADH: cytochrome b5 reductase. The administration of the peroxisome proliferators greatly altered the acyl composition of hepatic phosphatidylcholine and phosphatidylethanolamine (namely the proportions of C18:1 and C20:3,n-9 fatty acids increased in both phospholipids), and the alterations were partially associated with the increase in stearoyl-CoA desaturase activity.
比较了过氧化物酶体增殖剂氯贝酸(对氯苯氧基异丁酸)、替阿地诺[2,2'-(十亚甲基二硫代)二乙醇]和全氟辛酸(PFOA)对雄性和雌性大鼠肝脏硬脂酰辅酶A去饱和作用的影响。用这三种过氧化物酶体增殖剂处理雄性大鼠,显著提高了硬脂酰辅酶A去饱和酶的活性。给雌性大鼠施用氯贝酸或替阿地诺,大大提高了肝脏硬脂酰辅酶A去饱和酶的活性,其增加程度略低于雄性大鼠。然而,与其他两种过氧化物酶体增殖剂不同,PFOA并未改变雌性大鼠硬脂酰辅酶A去饱和酶的活性。激素处理表明,PFOA对硬脂酰辅酶A去饱和酶活性的这种性别相关差异强烈依赖于睾酮。过氧化物酶体增殖剂使硬脂酰辅酶A去饱和酶活性增加,但细胞色素b5的微粒体含量或NADH:细胞色素b5还原酶的活性并未显著增加。施用这些过氧化物酶体增殖剂极大地改变了肝脏磷脂酰胆碱和磷脂酰乙醇胺的酰基组成(即两种磷脂中C18:1和C20:3,n-9脂肪酸的比例增加),这些改变部分与硬脂酰辅酶A去饱和酶活性的增加有关。