Hoffler Undi, Hobbie Kristen, Wilson Ralph, Bai Re, Rahman Akef, Malarkey David, Travlos Greg, Ghanayem Burhan I
Laboratory of Pharmacology, National Institutes of Health, National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
Endocrine. 2009 Oct;36(2):311-25. doi: 10.1007/s12020-009-9224-9. Epub 2009 Aug 11.
Obesity and obesity-related illnesses are global epidemics impacting the health of adults and children. The purpose of the present work is to evaluate a genetically intact obese mouse model that more accurately reflects the impact of aging on diet-induced obesity and type 2 diabetes in humans. Male C57Bl/6J mice consumed either a control diet or one in which 60% kcal were due to lard beginning at 5-6 weeks of age. Body weight and fat measurements were obtained and necropsy performed at 15, 20, 30, and 40 weeks of age. Serum chemistry, histopathology, gene expression of the liver, and renal and hepatic function were also evaluated. In concert with significant increases in percent body fat and weight, mice fed the high-fat versus control diet had significantly increased levels of serum cholesterol. At ages 20 and 30 weeks, serum glucose was significantly higher in obese versus controls, while serum insulin levels were >/=4-fold higher in obese mice at ages 30 and 40 weeks. The effect of age exacerbated the effects of consuming a high-fat diet. In addition to being hyperinsulinemic and leptin resistant, older obese mice exhibited elevated hepatic PAI-1 and downregulation of GLUT4, G6PC, IGFBP-1, and leptin receptor mRNA in the liver, steatosis with subsequent inflammation, glomerular mesangial proliferation, elevated serum ALT, AST, and BUN, and increased numbers of pancreatic islets.
肥胖及与肥胖相关的疾病是影响成人和儿童健康的全球性流行病。本研究的目的是评估一种基因完整的肥胖小鼠模型,该模型能更准确地反映衰老对人类饮食诱导的肥胖和2型糖尿病的影响。雄性C57Bl/6J小鼠从5 - 6周龄开始,要么食用对照饮食,要么食用一种其中60%千卡热量来自猪油的饮食。在15、20、30和40周龄时测量体重和脂肪,并进行尸检。还评估了血清化学指标、组织病理学、肝脏基因表达以及肾脏和肝脏功能。与体脂百分比和体重的显著增加相一致,喂食高脂饮食的小鼠与对照小鼠相比,血清胆固醇水平显著升高。在20和30周龄时,肥胖小鼠的血清葡萄糖显著高于对照小鼠,而在30和40周龄时,肥胖小鼠的血清胰岛素水平高出对照小鼠≥4倍。年龄的影响加剧了食用高脂饮食的影响。除了高胰岛素血症和瘦素抵抗外,老年肥胖小鼠还表现出肝脏PAI - 1升高,肝脏中GLUT4、G6PC、IGFBP - 1和瘦素受体mRNA下调,脂肪变性并随后出现炎症,肾小球系膜增生,血清ALT、AST和BUN升高,以及胰岛数量增加。