Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Mol Nutr Food Res. 2012 Nov;56(11):1636-46. doi: 10.1002/mnfr.201200237. Epub 2012 Sep 11.
One major health problem in westernized countries is dysregulated fatty acid and cholesterol metabolism that causes pathologies such as metabolic syndrome. Previous studies from our group have shown that proanthocyanidins, which are the most abundant polyphenols in the human diet, regulate lipid metabolism and are potent hypolipidemic agents. The noncoding RNAs, miR-33 and miR-122, regulate genes that are involved in lipid metabolism.
Here, we show that grape seed proanthocyanidins rapidly and transiently repressed the expression of miR-33 and miR-122 in rat hepatocytes in vivo and in vitro. Furthermore, the miR-33 target gene ATP-binding cassette A1 and the miR-122 target gene fatty acid synthase were also modulated by proanthocyanidins. Specifically, ATP-binding cassette A1 mRNA and protein levels were increased, and fatty acid synthase mRNA and protein levels were reduced after the miRNA levels were altered.
These results suggest that proanthocyanidin treatment increased hepatic cholesterol efflux to produce new HDL particles by repressing miR-33, and it reduced lipogenesis by repressing miR-122. These results highlight a new mechanism by which grape seed proanthocyanidins produce hypolipidemia through their effects on miRNA modulators of lipid metabolism.
在西化国家,一个主要的健康问题是脂肪酸和胆固醇代谢失调,导致代谢综合征等病理。我们小组的先前研究表明,原花青素是人类饮食中最丰富的多酚之一,可调节脂质代谢,是有效的降脂剂。非编码 RNA,miR-33 和 miR-122,调节参与脂质代谢的基因。
在这里,我们表明,葡萄籽原花青素在体内和体外迅速且短暂地抑制了大鼠肝细胞中 miR-33 和 miR-122 的表达。此外,miR-33 的靶基因 ATP 结合盒 A1 和 miR-122 的靶基因脂肪酸合酶也被原花青素调节。具体而言,miRNA 水平改变后,ATP 结合盒 A1 mRNA 和蛋白水平增加,脂肪酸合酶 mRNA 和蛋白水平降低。
这些结果表明,原花青素处理通过抑制 miR-33 增加肝脏胆固醇外排以产生新的 HDL 颗粒,并通过抑制 miR-122 减少脂肪生成。这些结果突出了葡萄籽原花青素通过其对脂质代谢 miRNA 调节剂的作用产生降脂作用的新机制。