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Retinoic acid inhibits white adipogenesis by disrupting GADD45A-mediated Zfp423 DNA demethylation.视黄酸通过破坏 GADD45A 介导的 Zfp423 DNA 去甲基化来抑制白色脂肪生成。
J Mol Cell Biol. 2017 Aug 1;9(4):338-349. doi: 10.1093/jmcb/mjx026.
2
Maternal Retinoids Increase PDGFRα Progenitor Population and Beige Adipogenesis in Progeny by Stimulating Vascular Development.母体视黄酸通过刺激血管发育增加 PDGFRα 祖细胞群体并促进后代米色脂肪生成。
EBioMedicine. 2017 Apr;18:288-299. doi: 10.1016/j.ebiom.2017.03.041. Epub 2017 Apr 4.
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Chronic alcohol consumption decreases brown adipose tissue mass and disrupts thermoregulation: a possible role for altered retinoid signaling.慢性酒精摄入会导致棕色脂肪组织质量减少并破坏体温调节:视黄醇信号改变可能起作用。
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Fetal development of subcutaneous white adipose tissue is dependent on Zfp423.皮下白色脂肪组织的胎儿发育依赖于 Zfp423。
Mol Metab. 2016 Nov 21;6(1):111-124. doi: 10.1016/j.molmet.2016.11.009. eCollection 2017 Jan.
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Alcohol Increases Liver Progenitor Populations and Induces Disease Phenotypes in Human IPSC-Derived Mature Stage Hepatic Cells.酒精增加人类诱导多能干细胞衍生的成熟阶段肝细胞中的肝祖细胞群体并诱导疾病表型。
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Roles of alcohol drinking pattern in fatty liver in Japanese women.饮酒模式在日本女性脂肪肝中的作用。
Hepatol Int. 2013 Jul;7(3):859-68. doi: 10.1007/s12072-013-9449-9. Epub 2013 Jul 17.
7
High-fat diet enhanced retinal dehydrogenase activity, but suppressed retinol dehydrogenase activity in liver of rats.高脂饮食增强了大鼠视网膜脱氢酶的活性,但抑制了其肝脏中视黄醇脱氢酶的活性。
J Pharmacol Sci. 2015 Apr;127(4):430-8. doi: 10.1016/j.jphs.2015.03.001. Epub 2015 Mar 7.
8
Resveratrol induces brown-like adipocyte formation in white fat through activation of AMP-activated protein kinase (AMPK) α1.白藜芦醇通过激活AMP活化蛋白激酶(AMPK)α1诱导白色脂肪中棕色样脂肪细胞的形成。
Int J Obes (Lond). 2015 Jun;39(6):967-76. doi: 10.1038/ijo.2015.23. Epub 2015 Mar 12.
9
Impact of chronic low to moderate alcohol consumption on blood lipid and heart energy profile in acetaldehyde dehydrogenase 2-deficient mice.长期低至中度饮酒对乙醛脱氢酶2缺陷小鼠血脂和心脏能量谱的影响。
Acta Pharmacol Sin. 2014 Aug;35(8):1015-22. doi: 10.1038/aps.2014.46. Epub 2014 Jul 7.
10
Grape seed extract prevents skeletal muscle wasting in interleukin 10 knockout mice.葡萄籽提取物可预防白细胞介素10基因敲除小鼠的骨骼肌萎缩。
BMC Complement Altern Med. 2014 May 20;14:162. doi: 10.1186/1472-6882-14-162.

适度饮酒会诱导产热的棕色/米色脂肪细胞形成,增强视黄酸信号传导。

Moderate alcohol intake induces thermogenic brown/beige adipocyte formation elevating retinoic acid signaling.

作者信息

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

机构信息

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.

出版信息

FASEB J. 2017 Oct;31(10):4612-4622. doi: 10.1096/fj.201700396R. Epub 2017 Jul 5.

DOI:10.1096/fj.201700396R
PMID:28679528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6207178/
Abstract

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.

摘要

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