Gregg R G, Sabine J R, Wilce P A
Biochem J. 1982 May 15;204(2):457-62. doi: 10.1042/bj2040457.
Characteristics of 3-hydroxy-3-methylglutaryl-CoA reductase from normal liver, Morris hepatomas 5123C, 5123t.c. and 9618A, and host liver were studied. Animals were fed on control and 5%-cholesterol diets. Microsomal membranes from all tissues were found to accumulate cholesterol after 3 days on the 5%-cholesterol diet. The enzyme of the tumours showed no feedback inhibition by dietary cholesterol, and that of host liver gave a variable response, whereas that of control liver was constantly inhibited by 90% or more. Arrhenius-plot analysis was conducted on the microsomal enzyme isolated from the various tissues. Control animals showed that the phase transition present at 27 degrees C was removed when animals were fed on 5%-cholesterol diet for 12 h. The hepatomas failed to show this change even after 3 days of 5%-cholesterol diet and a significant increase in microsomal cholesterol. This failure to remove the break in Arrhenius plots also occurred in host liver, even though enzyme inhibition occurred. The reason why hepatomas fail to regulate 3-hydroxy-3-methylglutaryl-CoA reductase activity in response to dietary cholesterol may be a decreased membrane-enzyme interaction.
对正常肝脏、莫里斯肝癌5123C、5123t.c.和9618A以及宿主肝脏中的3-羟基-3-甲基戊二酰辅酶A还原酶的特性进行了研究。给动物喂食对照饮食和5%胆固醇饮食。在5%胆固醇饮食喂养3天后,发现所有组织的微粒体膜都积累了胆固醇。肿瘤的酶不受饮食胆固醇的反馈抑制,宿主肝脏的酶反应不一,而对照肝脏的酶则持续受到90%或更高程度的抑制。对从不同组织分离出的微粒体酶进行了阿累尼乌斯曲线分析。对照动物显示,当动物喂食5%胆固醇饮食12小时后,27摄氏度时出现的相变消失。即使在5%胆固醇饮食喂养3天且微粒体胆固醇显著增加后,肝癌仍未出现这种变化。宿主肝脏也出现了阿累尼乌斯曲线断点未消除的情况,尽管酶受到了抑制。肝癌未能根据饮食胆固醇调节3-羟基-3-甲基戊二酰辅酶A还原酶活性的原因可能是膜与酶的相互作用减弱。