Stanimirovic Julijana, Obradovic Milan, Jovanovic Aleksandra, Sudar-Milovanovic Emina, Zafirovic Sonja, Pitt Samantha J, Stewart Alan J, Isenovic Esma R
Vinca Institute of Nuclear Sciences, University of Belgrade, Laboratory of Radiobiology and Molecular Genetics, Mike Petrovica Alasa 12-14, Belgrade, Serbia.
School of Medicine, University of St Andrews, North Haugh, St Andrews, KY16 9TF, United Kingdom.
Nitric Oxide. 2016 Apr 1;54:51-9. doi: 10.1016/j.niox.2016.02.007. Epub 2016 Feb 26.
Men and women differ substantially with regard to the severity of insulin resistance (IR) but the underlying mechanism(s) of how this occurs is poorly characterized. We investigated whether a high fat (HF) diet resulted in sex-specific differences in nitrite/nitrate production and lipid metabolism and whether these variances may contribute to altered obesity-induced IR. Male and female Wistar rats were fed a standard laboratory diet or a HF diet for 10 weeks. The level of plasma nitrite/nitrate, as well as free fatty acid (FFA), in both plasma and liver lysates were assessed. The levels of inducible nitric oxide (NO) synthase (iNOS), p65 subunit of NFκB, total and phosphorylated forms of Akt, mTOR and PDK-1 in lysates, and the levels of glucose transporter 2 (Glut-2) and fatty acid translocase/cluster of differentiation 36 (FAT/CD36) in plasma membrane fractions of liver were assessed. HF-fed male rats exhibited a significant increase in plasma nitrite/nitrate, and hepatic FFA and FAT/CD36 levels compared with controls. They also displayed a relative decrease in iNOS and Glut-2 levels in the liver. Phosphorylation of Akt (at Ser(473) and Thr(308)), mTOR and PDK-1 was also reduced. HF-fed female rats exhibited increased levels of NFκB-p65 in liver compared with controls, while levels of Glut-2, FAT/CD36 and Akt phosphorylation at Thr(308) and PDK-1 were decreased. Our results reveal that altered lipid and glucose metabolism in obesity, lead to altered iNOS expression and nitrite/nitrate production. It is likely that this mechanism contributes to sex-specific differences in the development of IR.
男性和女性在胰岛素抵抗(IR)的严重程度方面存在显著差异,但这种差异产生的潜在机制仍不清楚。我们研究了高脂(HF)饮食是否会导致亚硝酸盐/硝酸盐生成和脂质代谢的性别特异性差异,以及这些差异是否可能导致肥胖诱导的IR改变。雄性和雌性Wistar大鼠分别喂食标准实验室饮食或HF饮食10周。评估血浆中亚硝酸盐/硝酸盐水平以及血浆和肝脏裂解物中的游离脂肪酸(FFA)水平。评估裂解物中诱导型一氧化氮(NO)合酶(iNOS)、NFκB的p65亚基、Akt、mTOR和PDK-1的总形式和磷酸化形式的水平,以及肝脏质膜部分中葡萄糖转运蛋白2(Glut-2)和脂肪酸转位酶/分化簇36(FAT/CD36)的水平。与对照组相比,喂食HF的雄性大鼠血浆中亚硝酸盐/硝酸盐、肝脏FFA和FAT/CD36水平显著升高。它们肝脏中的iNOS和Glut-2水平也相对降低。Akt(Ser(473)和Thr(308)位点)、mTOR和PDK-1的磷酸化也减少。与对照组相比,喂食HF的雌性大鼠肝脏中NFκB-p65水平升高,而Glut-2、FAT/CD36水平以及Thr(308)位点的Akt磷酸化和PDK-1水平降低。我们的结果表明,肥胖中脂质和葡萄糖代谢的改变导致iNOS表达和亚硝酸盐/硝酸盐生成的改变。这种机制可能导致IR发展中的性别特异性差异。