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瘦型和肥胖型 Zucker 大鼠的血清胆固醇、卵磷脂胆固醇酰基转移酶及肝脏羟甲基戊二酰辅酶 A 还原酶活性

Serum cholesterol, lecithin-cholesterol acyltransferase, and hepatic hydroxymethylglutaryl coenzyme A reductase activities of lean and obese Zucker rats.

作者信息

Lin R C

出版信息

Metabolism. 1985 Jan;34(1):19-24. doi: 10.1016/0026-0495(85)90054-x.

Abstract

Serum cholesterol concentrations, lecithin-cholesterol acyltransferase (LCAT), and hepatic 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase activities of lean and obese Zucker rats were compared. The excess serum cholesterol of the female obese rat is found to be mainly free cholesterol associated with very low-density lipoproteins, whereas that of the male obese rat is carried as cholesterol esters associated with high-density lipoproteins. The high level of serum free cholesterol in the female obese rat is not due to a deficiency in lecithin-cholesterol acyltransferase activity. This enzyme activity is found to be elevated in the male obese rat. Hepatic HMG-CoA reductase activity declines as rats mature; this observation is most apparent in obese male rats. Lean rats exhibit the normal diurnal rhythm, but mature obese rats show little diurnal variation in HMG-CoA reductase activity. Obese female rats maintain high reductase activities, but the activities of obese male rats remain low at all times. Starvation suppresses liver HMG-CoA reductase and serum cholesterol in both lean and obese female rats. Thus, an increase in hepatic cholesterol synthesis may contribute to hypercholesterolemia in the obese female Zucker rat. On the other hand, factors such as nonhepatic synthesis or a decreased cholesterol catabolism may play more important roles in maintaining high serum cholesterol in the obese male Zucker rat.

摘要

对瘦型和肥胖型 Zucker 大鼠的血清胆固醇浓度、卵磷脂胆固醇酰基转移酶(LCAT)以及肝脏 3-羟基-3-甲基戊二酰辅酶 A(HMG-CoA)还原酶活性进行了比较。发现雌性肥胖大鼠血清中过量的胆固醇主要是与极低密度脂蛋白相关的游离胆固醇,而雄性肥胖大鼠的过量胆固醇则以与高密度脂蛋白相关的胆固醇酯形式存在。雌性肥胖大鼠血清中高水平的游离胆固醇并非由于卵磷脂胆固醇酰基转移酶活性不足。发现该酶活性在雄性肥胖大鼠中升高。随着大鼠成熟,肝脏 HMG-CoA 还原酶活性下降;这一现象在肥胖雄性大鼠中最为明显。瘦型大鼠表现出正常的昼夜节律,但成熟的肥胖大鼠 HMG-CoA 还原酶活性几乎没有昼夜变化。肥胖雌性大鼠维持较高的还原酶活性,但肥胖雄性大鼠的活性始终较低。饥饿会抑制瘦型和肥胖雌性大鼠肝脏中的 HMG-CoA 还原酶以及血清胆固醇。因此,肝脏胆固醇合成增加可能导致肥胖雌性 Zucker 大鼠出现高胆固醇血症。另一方面,非肝脏合成或胆固醇分解减少等因素可能在维持肥胖雄性 Zucker 大鼠的高血清胆固醇水平中发挥更重要的作用。

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