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乳糜泻患者空肠黏膜中胆固醇及其前体的合成增强。

Enhanced synthesis of cholesterol and its precursors in jejunal mucosa in coeliac disease.

作者信息

Vuoristo M, Miettinen T A

出版信息

Gut. 1986 Apr;27(4):399-404. doi: 10.1136/gut.27.4.399.

Abstract

Patients with coeliac disease have a greatly enhanced whole body synthesis of cholesterol, but its origin is not known. In this paper the synthesis and concentrations of cholesterol and its precursors, squalene and methyl sterols, were studied in jejunal biopsies from healthy volunteers and adult patients with coeliac disease. The incorporation rates of 14C-acetate and 3H-mevalonate into non-saponifiable lipids (sum of squalene, methyl sterols and cholesterol) were increased 14 and six times in the damaged mucosa, respectively. The cyclisation rate of mucosal squalene and the conversion of squalene to cholesterol were also increased, indicating that cholesterol synthesis was activated before mevalonate, probably at the step of HMG-CoA reductase, and also after mevalonate and squalene. The steps from squalene to cholesterol were apparently not rate limiting because the mucosal concentrations and the percentage distribution of squalene and sterols were similar in the patients and in the controls. A positive correlation of the cholesterol synthesis with the number of crypt cells, suggests that the expanded crypt cell population contributed to the enhanced intestinal cholesterologenesis. Furthermore, the serum cholesterol level was negatively correlated with the 14C- and 3H-counts in the mucosal cholesterol and with the cyclisation rate of squalene probable signs of regulatory role of serum low density lipoprotein cholesterol in intestinal cholesterol synthesis. Consequently, provided that the synthesis of mucosal cholesterol is as high in vivo as in vitro it could contribute to the highly increased overall synthesis of cholesterol in the patients with coeliac disease.

摘要

患有乳糜泻的患者全身胆固醇合成显著增强,但其来源尚不清楚。本文研究了健康志愿者和成年乳糜泻患者空肠活检组织中胆固醇及其前体物质角鲨烯和甲基甾醇的合成及浓度。在受损黏膜中,14C - 乙酸盐和3H - 甲羟戊酸掺入非皂化脂质(角鲨烯、甲基甾醇和胆固醇的总和)的速率分别提高了14倍和6倍。黏膜角鲨烯的环化速率以及角鲨烯向胆固醇的转化也有所增加,这表明胆固醇合成在甲羟戊酸之前被激活,可能是在HMG - CoA还原酶步骤,在甲羟戊酸和角鲨烯之后也被激活。从角鲨烯到胆固醇的步骤显然不是限速步骤,因为患者和对照组中角鲨烯和甾醇的黏膜浓度及百分比分布相似。胆固醇合成与隐窝细胞数量呈正相关,这表明扩大的隐窝细胞群体导致肠道胆固醇生成增强。此外,血清胆固醇水平与黏膜胆固醇中的14C和3H计数以及角鲨烯的环化速率呈负相关,这可能是血清低密度脂蛋白胆固醇在肠道胆固醇合成中起调节作用的迹象。因此,如果黏膜胆固醇的合成在体内与体外一样高,那么它可能导致乳糜泻患者胆固醇总体合成的大幅增加。

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Cholesterol absorption, elimination and synthesis in coeliac disease.乳糜泻中胆固醇的吸收、清除与合成
Eur J Clin Invest. 1982 Aug;12(4):285-91. doi: 10.1111/j.1365-2362.1982.tb02234.x.

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