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大鼠肝脏微粒体中胆固醇代谢的年龄相关变化。

Age-related changes in the metabolism of cholesterol in rat liver microsomes.

作者信息

Ståhlberg D, Angelin B, Einarsson K

机构信息

Department of Medicine, Karolinska Institutet, Huddinge University Hospital, Stockholm, Sweden.

出版信息

Lipids. 1991 May;26(5):349-52. doi: 10.1007/BF02537197.

Abstract

The effects of aging on the hepatic metabolism of cholesterol were studied in 1-, 6- and 24-month-old male Sprague-Dawley rats. Microsomal 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase activity, which regulates cholesterol biosynthesis, decreased from 835 +/- 144 (SEM) pmol/min/mg protein in the youngest group to 219 +/- 34 and 205 +/- 53 pmol/min/mg protein (p less than 0.001) in the 6- and 24-month-old groups, respectively. Cholesterol 7 alpha-hydroxylase activity, which governs bile acid synthesis, was gradually reduced from 70 +/- 14 pmol/min/mg protein in the 1-month-old group to 32 +/- 7 and 16 +/- 3 pmol/min/mg protein (p less than 0.05) in the 6- and 24-month-old groups, respectively. Acyl coenzyme A:cholesterol acyltransferase activity, which catalyzes the esterification of cholesterol, averaged 431 +/- 47 and 452 +/- 48 pmol/min/mg protein in the 1- and 6-month-old groups, respectively, and was increased to 585 +/- 55 pmol/min/mg protein (p less than 0.05) in the 24-month-old group. The level of total cholesterol showed an age-related increase from 1.56 +/- 0.16 mg/g liver in the 1-month-old group to 1.70 +/- 0.15 and 2.20 +/- 0.19 mg/g liver (p less than 0.05) in the 6- and 24-month-old groups, respectively. The increase was mainly caused by an accumulation of esterified cholesterol. We conclude that a marked decrease in HMG-CoA reductase occurs between 1 and 6 months of age; thereafter the enzyme activity stays unchanged. The activity of cholesterol 7 alpha-hydroxylase decreases progressively and drastically with age, whereas the capacity for esterifying cholesterol increases slightly.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在1月龄、6月龄和24月龄的雄性斯普拉格-道利大鼠中研究了衰老对肝脏胆固醇代谢的影响。调节胆固醇生物合成的微粒体3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶活性,在最年幼组中为835±144(标准误)pmol/分钟/毫克蛋白质,在6月龄和24月龄组中分别降至219±34和205±53 pmol/分钟/毫克蛋白质(p<0.001)。控制胆汁酸合成的胆固醇7α-羟化酶活性,从1月龄组的70±14 pmol/分钟/毫克蛋白质逐渐降低至6月龄和24月龄组的32±7和16±3 pmol/分钟/毫克蛋白质(p<0.05)。催化胆固醇酯化的酰基辅酶A:胆固醇酰基转移酶活性,在1月龄和6月龄组中分别平均为431±47和452±48 pmol/分钟/毫克蛋白质,在24月龄组中增加至585±55 pmol/分钟/毫克蛋白质(p<0.05)。总胆固醇水平呈现与年龄相关的增加,从1月龄组的1.56±0.16毫克/克肝脏增加至6月龄和24月龄组的1.70±0.15和2.20±0.19毫克/克肝脏(p<0.05)。这种增加主要是由酯化胆固醇的积累引起的。我们得出结论,HMG-CoA还原酶在1至6月龄之间显著降低;此后酶活性保持不变。胆固醇7α-羟化酶的活性随年龄逐渐急剧下降,而胆固醇酯化能力略有增加。(摘要截短至250字)

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