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Hypocholesterolaemic effect of whole-grain highland hull-less barley in rats fed a high-fat diet

Xia, Xuejuan, Li, Guannan, Song, Jiaxin, Zheng, Jiong, Kan, Jianquan
The British journal of nutrition 2018 v.119 no.10 pp. 1102-1110
AMP-activated protein kinase, Western blotting, abdominal fat, barley, bile acids, bioactive compounds, cholesteremic effect, cholesterol, cholesterol 7alpha-monooxygenase, coenzyme A, excretion, feces, high fat diet, hydroxymethylglutaryl-CoA reductases, ileum, laboratory animals, liver, low density lipoprotein receptors, males, peroxisome proliferator-activated receptor alpha, quantitative polymerase chain reaction, rats, resorption, whole grain foods
Whole-grain highland hull-less barley (WHLB) contains high amounts of bioactive compounds that potentially exhibit cholesterol-lowering effects. This study investigated the hypocholesterolaemic effect of WHLB. A total of seventy-two male Sprague–Dawley rats were divided into four groups and were fed with the normal control diet, high-fat diet (HFD) and HFD containing low or high dose (10 or 48·95 %) of WHLB. High dose of WHLB significantly decreased the organ indexes of liver and abdominal fat and lipid levels of plasma and liver in HFD rats. The lipid regulation effect of WHLB, which was reconfirmed through hepatocyte morphologic observation, was accompanied by a large excretion of bile acids in the small intestinal contents and the faeces. Real-time PCR analyses, which were further reconfirmed through Western blot analyses, revealed that a high dose of WHLB significantly enhanced the hepatic expressions of AMP-activated protein kinase α, cholesterol 7α-hydroxylase, LDL receptor, liver X receptor, and PPARα and decreased the expression of 3-hydroxy-3-methylglutaryl coenzyme A reductase. It also enhanced the ileal expression of farnesoid X receptor and resulted in the decrease of expression of apical sodium-dependent bile acid transporter. WHLB exhibited hypocholesterolaemic effects mainly by inhibiting cholesterol synthesis, cholesterol accumulation in peripheral tissue, and bile acid reabsorption and by stimulating bile acid synthesis.