Department of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, Michigan.
Department of Physiology, University of Tennessee Health Science Center, Memphis, Tennessee.
Endocrinology. 2018 Jun 1;159(6):2275-2287. doi: 10.1210/en.2018-00147.
The purpose of this study was to determine the effects of glucocorticoid-induced metabolic dysfunction in the presence of diet-induced obesity. C57BL/6J adult male lean and diet-induced obese mice were given dexamethasone, and levels of hepatic steatosis, insulin resistance, and lipolysis were determined. Obese mice given dexamethasone had significant, synergistic effects on fasting glucose, insulin resistance, and markers of lipolysis, as well as hepatic steatosis. This was associated with synergistic transactivation of the lipolytic enzyme adipose triglyceride lipase. The combination of chronically elevated glucocorticoids and obesity leads to exacerbations in metabolic dysfunction. Our findings suggest lipolysis may be a key player in glucocorticoid-induced insulin resistance and fatty liver in individuals with obesity.
本研究旨在确定糖皮质激素诱导的代谢功能障碍在饮食诱导肥胖存在的情况下的影响。给予 C57BL/6J 成年雄性瘦型和饮食诱导肥胖型小鼠地塞米松,并测定肝脂肪变性、胰岛素抵抗和脂肪分解的水平。给予地塞米松的肥胖小鼠的空腹血糖、胰岛素抵抗和脂肪分解标志物以及肝脂肪变性均有显著的协同作用。这与脂肪甘油三酯脂肪酶的协同转录激活有关。慢性升高的糖皮质激素和肥胖的结合导致代谢功能障碍的加重。我们的研究结果表明,脂肪分解可能是肥胖个体中糖皮质激素诱导的胰岛素抵抗和脂肪肝的关键因素。