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给高胆固醇血症大鼠喂食米糠油中的不皂化物不会改变肝脏中胆固醇代谢相关蛋白的mRNA丰度。

Feeding unsaponifiable compounds from rice bran oil does not alter hepatic mRNA abundance for cholesterol metabolism-related proteins in hypercholesterolemic rats.

作者信息

Nagao K, Sato M, Takenaka M, Ando M, Iwamoto M, Imaizumi K

机构信息

Division of Bioscience and Biotechnology, Faculty of Agriculture, Graduate School Kyushu University, Fukuoka, Japan.

出版信息

Biosci Biotechnol Biochem. 2001 Feb;65(2):371-7. doi: 10.1271/bbb.65.371.

Abstract

The hypocholesterolemic effect of rice bran oil (RBO) is defined in human and animal experiments which indicate the presence of active component(s) in the unsaponifiable fraction, but the detailed mechanism is not known yet. Exogenously hypercholesterolemic (ExHC) rats were fed for 2 weeks on a 0.5% cholesterol diet supplemented with 10% each of RBO, RBO-simulated oil (RBOSO) in its fatty acid composition, or RBOSO plus 0.25% unsaponifiable compounds (UC) from RBO. Rats fed RBO or the UC resulted in lowing serum and liver cholesterol concentration and preventing reduction of high density lipoproteinic-cholesterol. Dietary RBO or the UC led to an elevation of fecal neutral sterol excretion, but no significant change in fecal bile acid excretion or in hepatic abundance of mRNAs for 3-hydroxy-3-methylglutaryl-CoA reductase, cholesterol-7alpha-hydroxylase, and low density lipoprotein receptor. Besides, serum and liver alpha-tocopherol concentrations were lowered in RBO or the UC-fed rats. These results show that the UC in RBO leads to a decreased serum cholesterol concentration by interrupting the absorption of intestinal hydrophobic compounds rather than by modifying cholesterol metabolism in the liver.

摘要

米糠油(RBO)的降胆固醇作用已在人体和动物实验中得到证实,这些实验表明在其不皂化物部分存在活性成分,但具体机制尚不清楚。给外源性高胆固醇血症(ExHC)大鼠喂食含0.5%胆固醇的饮食2周,该饮食分别添加了10%的RBO、脂肪酸组成与RBO模拟的油(RBOSO)或添加了0.25%来自RBO的不皂化物(UC)的RBOSO。喂食RBO或UC的大鼠血清和肝脏胆固醇浓度降低,高密度脂蛋白胆固醇水平未降低。饮食中的RBO或UC导致粪便中性固醇排泄增加,但粪便胆汁酸排泄或肝脏中3-羟基-3-甲基戊二酰辅酶A还原酶、胆固醇7α-羟化酶和低密度脂蛋白受体的mRNA丰度无显著变化。此外,喂食RBO或UC的大鼠血清和肝脏α-生育酚浓度降低。这些结果表明,RBO中的UC通过阻断肠道疏水性化合物的吸收而非通过改变肝脏中的胆固醇代谢来降低血清胆固醇浓度。

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