首页> 外文期刊>European Journal of Pharmacology: An International Journal >Epigallocatechin gallate enhances biliary cholesterol secretion in healthy rats and lowers plasma and liver cholesterol in ethinylestradiol-treated rats
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Epigallocatechin gallate enhances biliary cholesterol secretion in healthy rats and lowers plasma and liver cholesterol in ethinylestradiol-treated rats

机译:没食子儿茶素没食子酸酯可增强健康大鼠的胆汁胆固醇分泌,并降低乙炔雌二醇治疗的大鼠的血浆和肝胆固醇

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摘要

The beneficial effect of the major green tea catechin, epigallocatechin gallate (EGCG), on cholesterol homeostasis has been studied mainly in relation to the intestinal absorption of cholesterol; however, how EGCG affects cholesterol metabolism in the liver is not entirely known. The present study investigated the effect of EGCG on liver cholesterol metabolism in healthy and ethinylestradiol-treated rats. EGCG treatment reduced plasma total cholesterol in ethinylestradiol-treated animals and very low density lipoprotein cholesterol in both groups receiving EGCG. In healthy rats, despite the decrease in bile flow, EGCG markedly enhanced biliary secretion of cholesterol and phospholipids. These changes were correlated with increased expression of ATP-binding cassette transporter G5 and G8 and scavenger receptor class B type 1, and decreased expression of acyl-CoA:cholesterol acyltransferase. Ethinylestradiol treatment caused marked hepatic cholesterol accumulation with a concomitant liver weight increase and plasma cholesterol reduction. In ethinylestradiol-treated rats, EGCG co-administration attenuated the increase in liver cholesterol and liver weight. Furthermore, EGCG blunted induction of acyl-CoA:cholesterol acyltransferase and raised reduced levels of ATP-binding cassette transporter G5 and G8 and 3-hydroxy-3-methyl-glutaryl-CoA reductase in ethinylestradiol- treated rats. In conclusion, this study has demonstrated for the first time the ability of EGCG to enhance biliary cholesterol secretion and to attenuate ethinylestradiol-induced liver cholesterol accumulation. Changes in the expression of relevant enzymes and transporters suggest evidence of another mechanism that may contribute to the overall effect of EGCG on cholesterol metabolism and imply new physiological consequences of this widely used compound.
机译:主要研究了绿茶儿茶素表没食子儿茶素没食子酸酯(EGCG)对胆固醇稳态的有益作用,主要与胆固醇的肠道吸收有关。但是,EGCG如何影响肝脏中的胆固醇代谢尚不完全清楚。本研究调查了EGCG对健康和炔雌醇治疗的大鼠肝脏胆固醇代谢的影响。 EGCG治疗降低了接受乙炔雌二醇治疗的动物的血浆总胆固醇,并降低了接受EGCG的两组的低密度脂蛋白胆固醇。在健康大鼠中,尽管胆汁流量减少,但EGCG显着增强了胆汁中胆固醇和磷脂的分泌。这些变化与ATP结合盒转运蛋白G5和G8和清道夫受体B类1型的表达增加以及酰基辅酶A:胆固醇酰基转移酶的表达减少有关。乙炔雌二醇治疗会引起明显的肝胆固醇蓄积,并伴随肝脏重量增加和血浆胆固醇降低。在乙炔雌二醇治疗的大鼠中,EGCG共同给药可减轻肝脏胆固醇和肝脏重量的增加。此外,EGCG在乙炔雌二醇处理的大鼠中减弱了酰基辅酶A:胆固醇酰基转移酶的诱导,并提高了ATP结合盒转运蛋白G5和G8和3-羟基-3-甲基-戊二酰辅酶A还原酶水平的降低。总之,这项研究首次证明了EGCG具有增强胆汁胆固醇分泌和减弱乙炔雌二醇诱导的肝胆固醇积累的能力。相关酶和转运蛋白表达的变化提示了另一种机制的证据,该机制可能有助于EGCG对胆固醇代谢的整体作用,并暗示这种广泛使用的化合物会产生新的生理后果。

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