复方降脂3号对高胆固醇日粮新西兰大白兔胆固醇-胆汁酸代谢的影响

Qi-qi Mao, Dong-ni Qiu, Xiao-dong Fu, Yi Liu, Wen-jian Wang, Xue-Jiao Sun
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摘要

研究了复方降脂3号对饲喂高胆固醇日粮的新西兰大白兔胆固醇-胆汁酸代谢的影响。将24只雄性新西兰大白兔随机分为对照组(A组)、高胆固醇血症模型组(B组)和复方降脂3号治疗组(C组)。B组和C组在给药4周期间分别饲喂高胆固醇饲粮(含1%胆固醇)120 g/d建立高胆固醇血症模型,A组饲喂普通兔饲料120 g/d。C组患者在开始高胆固醇饮食暴露的同时,给予复方降脂3号灌胃(0.5袋/20 ml蒸馏水,每天早晨)。实验结束时对24只家兔进行血清CHO、LDL-C和BA的测定。采用酶联免疫吸附法(elisa)检测肝脏中CYP7A1的活性。采用实时聚合酶链反应(RT-PCR)检测肝脏组织中CYP7A1 mRNA、胆管盐输出泵(BSEP) mRNA和小异源二聚体伴侣(SHP) mRNA的表达。B组血清CHO显著高于A组(P<0.05), C组血清CHO显著低于B组(P<0.05)。C组BSEP mRNA和SHP mRNA表达水平显著低于B组(P<0.01)。上述结果提示,复方降脂3号能够上调CYP7A1 mRNA的表达,增强CYP7A1的活性。这可能是其预防高胆固醇饮食引起的新西兰大白兔高胆固醇血症的机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Fufang Jiangzhi No. 3 on cholesterol-bile acid metabolism in New Zealand white rabbit fed with cholesterol-rich diet
The effect of Fufang Jiangzhi No. 3 on cholesterol-bile acid metabolism in New Zealand white rabbit fed with cholesterol-rich diet was studied. 24 male New Zealand white rabbits were randomly assigned into control group (Group A), hypercholesterolemia model group (Group B), and Fufang Jiangzhi No. 3 treatment group (Group C). Groups B and C were fed with cholesterol-rich diet (containing 1% cholesterol) 120 g/day during 4 weeks’ administration in order to establish hypercholesterolemia model while Group A was fed with common rabbit fodder 120 g/day. Group C received Fufang Jiangzhi No. 3 by intragastric administration (0.5 bag/20 ml distilled water, every morning) at the same time as the start of the cholesterol-rich diet exposure. Serum CHO, LDL-C and BA assessment of 24 rabbits was performed at the end of the experiment. The activity of CYP7A1 in the liver was measured by enzymelinked immunosorbent assay (ELISAs). The expressions of CYP7A1 mRNA, bile salt export pump (BSEP) mRNA and small heterodimer partner (SHP) mRNA in the liver were measured by real time polymerase chain reaction (RT-PCR). Serum CHO in Group B was much higher than that in Group A (P<0.05), moreover, the serum CHO in Group C was lower than that in Group B ( P<0.05). The level of BSEP mRNA and SHP mRNA in Group C were much lower than those of Group B ( P<0.01). These results suggested that Fufang Jiangzhi No. 3 can up-regulate the expression of CYP7A1 mRNA and enhance the activity of CYP7A1. It may be one of the mechanisms involved in its preventive effect in cholesterolrich diet-induced hyperchlesterolemia in New Zealand white rabbit.
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