Wang Bo, Wang Zhixiu, de Avila Jeanene M, Zhu Mei-Jun, Zhang Faya, Gomez Noe Alberto, Zhao Liang, Tian Qiyu, Zhao Junxing, Maricelli Joseph, Zhang Hui, Rodgers Buel D, Du Min
Beijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, Beijing, China.
Department of Animal Sciences, Washington State University, Pullman, Washington, USA.
FASEB J. 2017 Oct;31(10):4612-4622. doi: 10.1096/fj.201700396R. Epub 2017 Jul 5.
Clinically, low and moderate alcohol intake improves human health with protection against metabolic syndromes, including type 2 diabetes; however, mechanisms that are associated with these effects remain to be elucidated. The aims of this study were to investigate the effects of moderate alcohol intake on thermogenic brown/beige adipocyte formation and glucose and lipid homeostasis, as well as the involvement of retinoic acid (RA) signaling in the entire process. C57BL6 male mice were supplemented with 8% (w/v) alcohol in water for 1 or 4 mo. Alcohol intake prevented body weight gain, induced the formation of uncoupling protein 1-positive beige adipocytes in white adipose tissue, and increased thermogenesis in mice, which is associated with decreased serum glucose and triacylglycerol levels. Mechanistically, alcohol intake increased RA levels in serum and adipose tissue, which was associated with increased expression of aldehyde dehydrogenase family 1 subfamily A1 (). When RA receptor-α signaling was conditionally blocked in platelet-derived growth factor receptor-α-positive adipose progenitors, the effects of alcohol on beige adipogenesis were largely abolished. Finally, moderate alcohol prevented high-fat diet-induced obesity and metabolic dysfunction. In conclusion, moderate alcohol intake induces thermogenic brown/beige adipocyte formation and promotes glucose and lipid oxidation elevation of RA signaling.-Wang, B., Wang, Z., de Avila, J. M., Zhu, M.-J., Zhang, F., Gomez, N. A., Zhao, L., Tian, Q., Zhao, J., Maricelli, J., Zhang, H., Rodgers, B. D., Du, M. Moderate alcohol intake induces thermogenic brown/beige adipocyte formation elevating retinoic acid signaling.
临床上,低至中度饮酒可改善人体健康,预防包括2型糖尿病在内的代谢综合征;然而,与这些作用相关的机制仍有待阐明。本研究的目的是探讨中度饮酒对产热棕色/米色脂肪细胞形成以及葡萄糖和脂质稳态的影响,以及视黄酸(RA)信号在整个过程中的作用。给C57BL6雄性小鼠在水中补充8%(w/v)的酒精,持续1或4个月。饮酒可防止体重增加,诱导白色脂肪组织中解偶联蛋白1阳性米色脂肪细胞的形成,并增加小鼠的产热,这与血清葡萄糖和三酰甘油水平降低有关。机制上,饮酒会增加血清和脂肪组织中的RA水平,这与醛脱氢酶家族1亚家族A1()表达增加有关。当在血小板衍生生长因子受体-α阳性脂肪祖细胞中条件性阻断RA受体-α信号时,酒精对米色脂肪生成的作用基本被消除。最后,中度饮酒可预防高脂饮食诱导的肥胖和代谢功能障碍。总之,中度饮酒可诱导产热棕色/米色脂肪细胞形成,并通过提高RA信号促进葡萄糖和脂质氧化。-王,B.;王,Z.;德阿维拉,J.M.;朱,M.-J.;张,F.;戈麦斯,N.A.;赵,L.;田,Q.;赵,J.;马里塞利,J.;张,H.;罗杰斯,B.D.;杜,M. 中度饮酒通过提高视黄酸信号诱导产热棕色/米色脂肪细胞形成