Rusnak N, Krisans S K
Department of Biology, San Diego State University, CA 92182.
Biochem Biophys Res Commun. 1987 Oct 29;148(2):890-5. doi: 10.1016/0006-291x(87)90959-4.
The specific activity of hepatic microsomal and peroxisomal 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase) was determined at different times during a 24 hour cycle from cholestyramine treated rats. The microsomal HMG-CoA reductase activity displayed a peak at D-6 (6th hour of the dark cycle) as previously reported, whereas, the peroxisomal HMG-CoA reductase activity was the highest at L-2 (2nd hour of the light cycle). Immunoblots of the peroxisomal HMG-CoA reductase suggest that the increase in enzyme activity at L-2 is due to changes in enzyme mass. The different cyclic variations observed in microsomal and peroxisomal HMG-CoA reductase activity may suggest different mechanisms of regulation.
在24小时周期的不同时间,测定了消胆胺处理大鼠肝脏微粒体和过氧化物酶体3-羟基-3-甲基戊二酰辅酶A还原酶(HMG-CoA还原酶)的比活性。如先前报道,微粒体HMG-CoA还原酶活性在D-6(暗周期第6小时)出现峰值,而过氧化物酶体HMG-CoA还原酶活性在L-2(光周期第2小时)最高。过氧化物酶体HMG-CoA还原酶的免疫印迹表明,L-2时酶活性的增加是由于酶量的变化。微粒体和过氧化物酶体HMG-CoA还原酶活性中观察到的不同循环变化可能表明调节机制不同。