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Impaired Lipid and Glucose Homeostasis in Hexabromocyclododecane-Exposed Mice Fed a High-Fat Diet

机译:喂高脂饮食的十六溴环十二烷接触小鼠的脂质和葡萄糖体内稳态受损

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Background: Hexabromocyclododecane (HBCD) is an additive flame retardant used in the textile industry and in polystyrene foam manufacturing. Because of its lipophilicity and persistency, HBCD accumulates in adipose tissue and thus has the potential of causing metabolic disorders through disruption of lipid and glucose homeostasis. However, the association between HBCD and obesity remains unclear.Objectives: We investigated whether exposure to HBCD contributes to initiation and progression of obesity and related metabolic dysfunction in mice fed a normal diet (ND) or a high-fat diet (HFD).Methods: Male C57BL/6J mice were fed a HFD (62.2 kcal% fat) or a ND and treated orally with HBCD (0, 1.75, 35, or 700 μg/kg body weight) weekly from 6 to 20 weeks of age. We examined body weight, liver weight, blood biochemistry, histopathological changes, and gene expression profiles in the liver and adipose tissue.Results: In HFD-fed mice, body and liver weight were markedly increased in mice treated with the high (700 μg/kg) and medium (35 μg/kg) doses of HBCD compared with vehicle. This effect was more prominent in the high-dose group. These increases were paralleled by increases in random blood glucose and insulin levels and enhancement of microvesicular steatosis and macrophage accumulation in adipose tissue. HBCD-treated HFD-fed mice also had increased mRNA levels of Pparg (peroxisome proliferator-activated receptor-γ) in the liver and decreased mRNA levels of Glut4 (glucose transporter 4) in adipose tissue compared with vehicle-treated HFD-fed mice.Conclusions: Our findings suggest that HBCD may contribute to enhancement of diet-induced body weight gain and metabolic dysfunction through disruption of lipid and glucose homeostasis, resulting in accelerated progression of obesity.Citation: Yanagisawa R, Koike E, Win-Shwe TT, Yamamoto M, Takano H. 2014. Impaired lipid and glucose homeostasis in hexabromocyclododecane-exposed mice fed a high-fat diet. Environ Health Perspect 122:277–283; 
机译:背景:六溴环十二烷(HBCD)是一种添加型阻燃剂,用于纺织工业和聚苯乙烯泡沫塑料生产中。由于其亲脂性和持久性,六溴环十二烷会积聚在脂肪组织中,因此有可能通过破坏脂质和葡萄糖的体内稳态而引起代谢紊乱。然而,尚不清楚HBCD与肥​​胖之间的关系。目的:我们调查了暴露于HBCD的小鼠是否在正常饮食(ND)或高脂饮食(HFD)喂养的小鼠中引发肥胖,肥胖和相关的代谢功能障碍。 :从6至20周龄,每周给雄性C57BL / 6J小鼠喂饲HFD(62.2 kcal%脂肪)或ND,并口服HBCD(0、1.75、35或700μg/ kg体重)进行口服治疗。我们检查了体重,肝脏重量,血液生化,组织病理学变化以及肝脏和脂肪组织中的基因表达谱。结果:在以HFD喂养的小鼠中,高剂量(700μg/ g)的小鼠的体重和肝重量显着增加kg)和中等剂量(35μg/ kg)的六溴环十二烷与媒介相比。在大剂量组中这种作用更为明显。这些增加与随机血糖和胰岛素水平的增加以及脂肪组织中微泡脂肪变性和巨噬细胞积累的增加平行。与用HFD喂养的小鼠相比,用HBCD治疗的HFD喂养的小鼠肝脏中Pparg(过氧化物酶体增殖物激活的受体-γ)的mRNA水平升高,而脂肪组织中的Glut4(葡萄糖转运蛋白4)的mRNA水平降低。结论:我们的发现表明六溴环十二烷可能通过破坏脂质和葡萄糖体内稳态来促进饮食引起的体重增加和代谢功能障碍,从而导致肥胖加速发展。引文:柳泽R,小池E,温瑞特TT,山本M,Takano H.,2014年。喂高脂饮食的六溴环十二烷接触小鼠的脂质和葡萄糖体内稳态受损。环境健康展望122:277–283;

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