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肠道黏膜的解剖学异质性与胆固醇稳态:对正常及遗传性高胆固醇血症(RICO)大鼠研究的综述

Anatomical heterogeneity of the intestinal mucosa and cholesterol homeostasis. A review of studies with normal and genetically hypercholesterolemic (RICO) Rat.

作者信息

Lutton C

机构信息

Laboratoire Physiologie de la Nutrition (Laboratoire associé à l'INRA), Université Paris-Sud, Orsay, France.

出版信息

Digestion. 1996;57(1):1-10. doi: 10.1159/000201305.

DOI:10.1159/000201305
PMID:8626041
Abstract

Quantitative data on cholesterol movements in mucosa cell as a function of its localization in the small intestine have been obtained in normocholesterolemic (SW) or genetically hypercholesterolemic (RICO) rats. Bile cholesterol absorption is greater and more proximal than dietary cholesterol absorption, both taking place mainly in the top cells of the duodenum or the proximal jejunum. Esterification of cholesterol also takes place mainly in the villus cells, while cholesterol synthesis is predominantly carried out in the crypt cells of the proximal duodenum and distal ileum. Cholesterol exchanges, which replace half of the cell cholesterol through the cell life, can be estimated at 3-4%.h-1 between plasma and mucosa cells, according to its location, i.e. 12-25 micrograms.h-1 (per mg cell DNA). In comparison, the cholesterol HDL or LDL uptake appears to be very low (0.02-0.06 and 0.2-0.6 microgram.h-1, respectively). Compartmentalization of cholesterol metabolism in the enterocyte can be suggested by different experimental data. The turnover of newly synthesized cholesterol is about 2-fold lower than that of exogenous (dietary) cholesterol.

摘要

在正常胆固醇水平(SW)或遗传性高胆固醇血症(RICO)大鼠中,已获得小肠黏膜细胞中胆固醇转运的定量数据,该数据是其在小肠中定位的函数。胆汁胆固醇的吸收比膳食胆固醇的吸收更大且更靠近近端,两者主要发生在十二指肠顶部细胞或近端空肠中。胆固醇酯化也主要发生在绒毛细胞中,而胆固醇合成主要在近端十二指肠和远端回肠的隐窝细胞中进行。根据其位置,胆固醇交换在血浆和黏膜细胞之间估计为3 - 4%·h⁻¹,通过细胞寿命可替换细胞胆固醇的一半,即12 - 25微克·h⁻¹(每毫克细胞DNA)。相比之下,胆固醇HDL或LDL的摄取似乎非常低(分别为0.02 - 0.06和0.2 - 0.6微克·h⁻¹)。不同的实验数据表明了肠细胞中胆固醇代谢的区室化。新合成胆固醇的周转比外源性(膳食)胆固醇的周转低约2倍。

相似文献

1
Anatomical heterogeneity of the intestinal mucosa and cholesterol homeostasis. A review of studies with normal and genetically hypercholesterolemic (RICO) Rat.肠道黏膜的解剖学异质性与胆固醇稳态:对正常及遗传性高胆固醇血症(RICO)大鼠研究的综述
Digestion. 1996;57(1):1-10. doi: 10.1159/000201305.
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Cholesterol metabolism in the genetically hypercholesterolemic rat (RICO). I. Measurement of turnover processes.遗传性高胆固醇血症大鼠(RICO)的胆固醇代谢。I. 周转过程的测量。
Biochim Biophys Acta. 1987 Jun 23;919(3):205-12. doi: 10.1016/0005-2760(87)90259-1.
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Regional cholesterol synthesis in the intestinal mucosa of the genetically hypercholesterolaemic RICO rat: kinetic study following whole-body gamma-irradiation.遗传性高胆固醇血症 RICO 大鼠肠黏膜中的局部胆固醇合成:全身γ射线照射后的动力学研究
Int J Radiat Biol. 1999 Feb;75(2):175-81. doi: 10.1080/095530099140627.
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Metabolism of intestinal triglyceride-rich lipoproteins in the genetically hypercholesterolemic rat (RICO).遗传性高胆固醇血症大鼠(RICO)肠道富含甘油三酯脂蛋白的代谢
Atherosclerosis. 1992 Apr;93(3):201-8. doi: 10.1016/0021-9150(92)90256-g.
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Cholesterol synthesis and high density lipoprotein uptake are regulated independently in rat small intestinal epithelium.大鼠小肠上皮细胞中胆固醇合成和高密度脂蛋白摄取是独立调节的。
Gut. 1994 Mar;35(3):343-6. doi: 10.1136/gut.35.3.343.
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Crilvastatin, a new 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitor, inhibits cholesterol absorption in genetically hypercholesterolemic rats.克立伐他汀,一种新型的3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂,可抑制遗传性高胆固醇血症大鼠的胆固醇吸收。
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[Plasma cholesterol distribution in the intestinal villus of the rat].[大鼠肠绒毛中的血浆胆固醇分布]
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Turnover of [14C] sucrose HDL and uptake by organs in the normal or genetically hypercholesterolemic (RICO) rat using a constant infusion method.采用持续输注法研究正常或遗传性高胆固醇血症(RICO)大鼠体内[14C]蔗糖高密度脂蛋白(HDL)的周转率及各器官对其的摄取情况。
Reprod Nutr Dev. 1990;30(1):97-101. doi: 10.1051/rnd:19900110.
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Effect of dietary fat saturation on absorption and intestinal secretion of cholesterol by the hypercholesterolemic rat.膳食脂肪饱和度对高胆固醇血症大鼠胆固醇吸收及肠道分泌的影响。
Lipids. 1973 Aug;8(8):470-2. doi: 10.1007/BF02531766.
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[The RICO rat (genetically hypercholesteremic): a good model for testing a food substance or a drug specific for a key enzyme of cholesterol metabolism].
Reprod Nutr Dev. 1999 Jul-Aug;39(4):481-95.

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