Pitombo Cid, Araújo Eliana P, De Souza Cláudio T, Pareja José C, Geloneze Bruno, Velloso Lício A
Department of Internal Medicine, State University of Campinas, UNICAMP, Brazil.
J Endocrinol. 2006 Dec;191(3):699-706. doi: 10.1677/joe.1.07069.
The effect of visceral fat removal upon glucose homeostasis, insulin signal transduction, and serum adipokine levels in an animal model of diet-induced obesity and diabetes mellitus (DIO) was evaluated. Swiss mice were initially divided into two groups fed with regular rodent chow or with chow containing 24 g% saturated fat (DIO). DIO mice became obese and overtly diabetic after 8 weeks. DIO mice were then divided into three groups: control, sham, and visceral (epididymal and perinephric) fat removal. All groups were submitted to evaluation of basal glucose and insulin levels and i.p. insulin tolerance test. Insulin signal transduction in muscle was evaluated by immunoprecipitation and immunoblot, and serum adipokine levels were determined by ELISA. DIO mice became diabetic (228 versus 115 mg/dl), hyperinsulinemic (7.59 versus 3.15 ng/ml) and insulin resistant (K(itt) 2.88 versus 4.97%/min) as compared with control. Visceral fat removal partially reverted all parameters (147 mg/dl glucose; 3.82 ng/ml insulin; and 4.20%/min K(itt)). In addition, visceral fat removal completely reversed the impairment of insulin signal transduction through insulin receptor, insulin receptor substrate (IRS)-1, IRS-2 and Akt in muscle. Finally, serum levels of the pro-inflammatory cytokines tumour necrosis factor-alpha, interleukin (IL)-1beta and IL-6 were significantly increased, while adiponectin levels were significantly reduced in DIO mice. After visceral fat removal the levels of adipokines returned to near control levels. The present study shows that removal of visceral fat improves insulin signal transduction and glucose homeostasis in an animal model of diet-induced obesity and diabetes mellitus and these metabolic and molecular outcomes are accompanied by the restoration of adipokine levels.
在饮食诱导的肥胖和糖尿病(DIO)动物模型中,评估了去除内脏脂肪对葡萄糖稳态、胰岛素信号转导和血清脂肪因子水平的影响。瑞士小鼠最初分为两组,分别喂以常规啮齿动物饲料或含24 g%饱和脂肪的饲料(DIO)。8周后,DIO小鼠变得肥胖并明显患糖尿病。然后将DIO小鼠分为三组:对照组、假手术组和去除内脏(附睾和肾周)脂肪组。所有组均接受基础葡萄糖和胰岛素水平评估以及腹腔注射胰岛素耐量试验。通过免疫沉淀和免疫印迹评估肌肉中的胰岛素信号转导,并通过酶联免疫吸附测定法测定血清脂肪因子水平。与对照组相比,DIO小鼠出现糖尿病(228对115 mg/dl)、高胰岛素血症(7.59对3.15 ng/ml)和胰岛素抵抗(胰岛素敏感指数(K(itt))2.88对4.97%/分钟)。去除内脏脂肪部分逆转了所有参数(血糖147 mg/dl;胰岛素3.82 ng/ml;胰岛素敏感指数4.20%/分钟)。此外,去除内脏脂肪完全逆转了肌肉中胰岛素受体、胰岛素受体底物(IRS)-1、IRS-2和Akt的胰岛素信号转导损伤。最后,DIO小鼠中促炎细胞因子肿瘤坏死因子-α、白细胞介素(IL)-1β和IL-6的血清水平显著升高,而脂联素水平显著降低。去除内脏脂肪后,脂肪因子水平恢复到接近对照水平。本研究表明,在饮食诱导的肥胖和糖尿病动物模型中,去除内脏脂肪可改善胰岛素信号转导和葡萄糖稳态,这些代谢和分子结果伴随着脂肪因子水平的恢复。