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遗传性坏血病大鼠(ODS大鼠)的胆固醇代谢

Cholesterol metabolism in inherently scorbutic rats (ODS rats).

作者信息

Kono K, Hayakawa M, Asai K, Kuzuya F

机构信息

Department of Geriatrics, Nagoya University School of Medicine, Japan.

出版信息

J Nutr Sci Vitaminol (Tokyo). 1988 Feb;34(1):35-45. doi: 10.3177/jnsv.34.35.

Abstract

We observed the cholesterol metabolism of a colony of Wistar rats with a hereditary defect in vitamin C synthesizing ability (the ODS (osteogenic disorder-Shionogi) rats) in six kinds of experiments. Female ODS rats aged 36 days had a low HDL (high-density lipoprotein)-cholesterol level in serum as compared with age-matched control rats in spite of the absence of scorbutic symptoms. Female ODS rats aged 63 days which revealed severe scorbutic symptoms had a very low HDL-cholesterol level (mean value; 17 mg/dl). And male ODS rats, whose lives had been prolonged by supplementing with L-ascorbic acid, also had lower serum HDL-cholesterol and had increased total cholesterol in serum and liver when the acid supplement dose was relatively insufficient. On the other hand, we examined HDL2- and HDL3-cholesterol levels in serum to determine the mechanism of low HDL-cholesterol. As a result, we observed a low HDL2-cholesterol level in ODS rats but normal HDL3-cholesterol level. But the authors observed no decrease of LCAT (lecithin: cholesterol acyltransferase) activity in serum of ODS rats. These results could be due to disturbance of lipid metabolism in a vitamin C-deficient condition, that is to say, there might be abnormalities of the cholesterol excretion pathway of bile acid from liver, and maturity of the HDL-cholesterol particle due to other factors except that of LCAT activity.

摘要

我们通过六种实验观察了一群维生素C合成能力存在遗传性缺陷的Wistar大鼠(ODS(成骨障碍-品系)大鼠)的胆固醇代谢情况。36日龄的雌性ODS大鼠尽管没有坏血病症状,但与年龄匹配的对照大鼠相比,血清中的高密度脂蛋白(HDL)胆固醇水平较低。63日龄出现严重坏血病症状的雌性ODS大鼠HDL胆固醇水平极低(平均值为17mg/dl)。而通过补充L-抗坏血酸延长寿命的雄性ODS大鼠,当酸补充剂量相对不足时,血清HDL胆固醇水平也较低,血清和肝脏中的总胆固醇水平升高。另一方面,我们检测了血清中HDL2和HDL3胆固醇水平,以确定HDL胆固醇水平低的机制。结果,我们观察到ODS大鼠的HDL2胆固醇水平较低,但HDL3胆固醇水平正常。但作者未观察到ODS大鼠血清中卵磷脂胆固醇酰基转移酶(LCAT)活性降低。这些结果可能是由于维生素C缺乏状态下脂质代谢紊乱所致,也就是说,除LCAT活性外,可能存在肝脏胆汁酸胆固醇排泄途径异常以及HDL胆固醇颗粒成熟异常等其他因素。

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