Shen Minqian, Shi Haifei
Cell, Molecular, and Structural Biology, Department of Biology, Miami University, 700 E. High Street, Oxford, OH 45056, USA.
Int J Endocrinol. 2015;2015:294278. doi: 10.1155/2015/294278. Epub 2015 Sep 27.
The liver is one of the most essential organs involved in the regulation of energy homeostasis. Hepatic steatosis, a major manifestation of metabolic syndrome, is associated with imbalance between lipid formation and breakdown, glucose production and catabolism, and cholesterol synthesis and secretion. Epidemiological studies show sex difference in the prevalence in fatty liver disease and suggest that sex hormones may play vital roles in regulating hepatic steatosis. In this review, we summarize current literature and discuss the role of estrogens and androgens and the mechanisms through which estrogen receptors and androgen receptors regulate lipid and glucose metabolism in the liver. In females, estradiol regulates liver metabolism via estrogen receptors by decreasing lipogenesis, gluconeogenesis, and fatty acid uptake, while enhancing lipolysis, cholesterol secretion, and glucose catabolism. In males, testosterone works via androgen receptors to increase insulin receptor expression and glycogen synthesis, decrease glucose uptake and lipogenesis, and promote cholesterol storage in the liver. These recent integrated concepts suggest that sex hormone receptors could be potential promising targets for the prevention of hepatic steatosis.
肝脏是参与能量稳态调节的最重要器官之一。肝脂肪变性是代谢综合征的主要表现,与脂质生成与分解、葡萄糖生成与分解代谢以及胆固醇合成与分泌之间的失衡有关。流行病学研究表明,脂肪肝疾病的患病率存在性别差异,并提示性激素可能在调节肝脂肪变性中发挥重要作用。在本综述中,我们总结了当前的文献,并讨论了雌激素和雄激素的作用以及雌激素受体和雄激素受体调节肝脏脂质和葡萄糖代谢的机制。在女性中,雌二醇通过雌激素受体调节肝脏代谢,减少脂肪生成、糖异生和脂肪酸摄取,同时增强脂肪分解、胆固醇分泌和葡萄糖分解代谢。在男性中,睾酮通过雄激素受体发挥作用,增加胰岛素受体表达和糖原合成,减少葡萄糖摄取和脂肪生成,并促进肝脏中的胆固醇储存。这些最新的综合概念表明,性激素受体可能是预防肝脂肪变性的潜在有前景的靶点。