Field F J, Salome R G
Biochim Biophys Acta. 1982 Sep 14;712(3):557-70. doi: 10.1016/0005-2760(82)90284-3.
The regulation of intestinal acyl-CoA: cholesterol acyltransferase was investigated by dietary manipulation. Rabbits were fed the following diets: normal rabbit chow, 10% safflower oil, safflower oil plus 1% cholesterol, coconut oil plus 1% cholesterol, or cholestyramine. Acyl-CoA: cholesterol acyltransferase activity was increased in intestinal microsomes from animals fed safflower oil but not from animals fed coconut oil. Both diets containing cholesterol increased acyl-CoA: cholesterol acyltransferase activity; however, the safflower oil plus cholesterol diet was a more potent stimulator than coconut oil plus cholesterol. Cholestyramine decreased microsomal acyl-CoA: cholesterol acyltransferase activity. The different diets significantly modified microsomal lipid content in these groups. The two cholesterol diets resulted in equal increments in microsomal cholesterol. Microsomal cholesterol was unchanged in animals on the safflower oil diet; however, coconut oil and cholestyramine decreased the cholesterol content. Linoleic acid content increased in microsomes from animals on both the safflower oil-containing diets. Myristic acid accumulated and linoleic acid was decreased in microsomes from animals on both diets containing coconut oil. Subcellular fractionation of the intestine yielded a 4-fold enhancement of acyl-CoA: cholesterol acyltransferase activity in the rough endoplasmic reticulum. The lipid modifications and the subsequent changes in acyl-CoA: cholesterol acyltransferase activity in the rough endoplasmic reticulum from animals on normal, safflower oil, and safflower oil plus cholesterol diets paralleled that observed in the crude microsomal preparations. The changes in acyl-CoA: cholesterol acyltransferase activity observed with the different diets were not due to changes in microsomal fatty acyl-CoA pool size. It is concluded that dietary manipulation can alter microsomal lipid content. Microsomal fat saturation, independent of microsomal cholesterol content, regulates intestinal acyl-CoA: cholesterol acyltransferase and modifies the stimulatory effect of exogenous cholesterol on this enzyme.
通过饮食调控研究了肠道酰基辅酶A:胆固醇酰基转移酶的调节作用。给兔子喂食以下几种饮食:正常兔饲料、10%红花油、红花油加1%胆固醇、椰子油加1%胆固醇或考来烯胺。喂食红花油的动物肠道微粒体中酰基辅酶A:胆固醇酰基转移酶活性增加,但喂食椰子油的动物则未增加。两种含胆固醇的饮食均增加了酰基辅酶A:胆固醇酰基转移酶活性;然而,红花油加胆固醇饮食比椰子油加胆固醇饮食的刺激作用更强。考来烯胺降低了微粒体酰基辅酶A:胆固醇酰基转移酶活性。不同饮食显著改变了这些组的微粒体脂质含量。两种含胆固醇的饮食使微粒体胆固醇增加量相同。喂食红花油饮食的动物微粒体胆固醇未发生变化;然而,椰子油和考来烯胺降低了胆固醇含量。两种含红花油饮食的动物微粒体中亚油酸含量增加。两种含椰子油饮食的动物微粒体中肉豆蔻酸积累且亚油酸减少。对肠道进行亚细胞分级分离后,粗面内质网中酰基辅酶A:胆固醇酰基转移酶活性提高了4倍。正常饮食、红花油饮食和红花油加胆固醇饮食的动物粗面内质网中的脂质修饰以及随后酰基辅酶A:胆固醇酰基转移酶活性的变化与粗微粒体制剂中观察到的情况相似。不同饮食所观察到的酰基辅酶A:胆固醇酰基转移酶活性变化并非由于微粒体脂肪酰基辅酶A池大小的改变。得出的结论是,饮食调控可改变微粒体脂质含量。微粒体脂肪饱和度独立于微粒体胆固醇含量,调节肠道酰基辅酶A:胆固醇酰基转移酶,并改变外源性胆固醇对该酶的刺激作用。