作者: Choon Young Kim , Yuyan Zhu , Kimberly K. Buhman , Kee-Hong Kim
DOI: 10.1016/J.JFF.2015.05.008
关键词: Type 2 diabetes 、 Sodium selenate 、 Selenate 、 Metabolic syndrome 、 Biology 、 Endocrinology 、 Adipokine 、 PRDM16 、 Insulin resistance 、 Adipose tissue 、 Internal medicine
摘要: Abstract Selenium is an essential micronutrient required for maintaining cellular redox homeostasis. Despite its potential beneficial role in lowering the risk of type 2 diabetes humans with lower selenium status and diabetic mice, preventing development obesity metabolic syndrome unknown. Here, we report that chronic selenate supplementation to high fat (HF) diet-fed mice resulted resistance diet-induced adiposity insulin resistance. The body weight adipose tissue mass gain associated HF was abrogated by at 0.72 mg/kg weight. This accompanied alteration expression genes involved adipokines, inflammation, transforming growth factor-β (TGF-β) signalling, mitochondria function, beige adipocyte differentiation tissue. Selenate also increase faecal calorie content improved glucose tolerance obese mice. Collectively this study elucidated a novel as dietary micromineral prevention related energy dysfunction.