首页> 美国卫生研究院文献>Oxidative Medicine and Cellular Longevity >The Impact of High-Fat Diet on Mitochondrial Function Free Radical Production and Nitrosative Stress in the Salivary Glands of Wistar Rats
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The Impact of High-Fat Diet on Mitochondrial Function Free Radical Production and Nitrosative Stress in the Salivary Glands of Wistar Rats

机译:高脂饮食对Wistar大鼠唾液腺线粒体功能自由基产生和亚硝化应激的影响

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摘要

Oxidative stress plays a crucial role in the salivary gland dysfunction in insulin resistance; however, the cause of increased free radical formation in these conditions is still unknown. Therefore, the aim of the study was to investigate the effect of high-fat diet (HFD) on the mitochondrial respiratory system, prooxidant enzymes, ROS production, and nitrosative/oxidative stress in the submandibular and parotid glands of rats. The experiment was performed on male Wistar rats divided into two groups (n = 10): control and HFD. The 8-week feeding of HFD affects glucose metabolism observed as significant increase in plasma glucose and insulin as well as HOMA-IR as compared to the control rats. The activity of mitochondrial Complex I and Complex II+III was significantly decreased in the parotid and submandibular glands of HFD rats. Mitochondrial cytochrome c oxidase (COX) activity and the hydrogen peroxide level were significantly increased in the parotid and submandibular glands of the HFD group as compared to those of the controls. HFD rats also showed significantly lower reduced glutathione (GSH) and reduced : oxidized glutathione (GSH : GSSG) ratio, as well as a higher GSSG level in the parotid glands of HFD rats. The activity of NADPH oxidase, xanthine oxidase, and levels of oxidativeitrosative stress (malonaldehyde, nitric oxide, nitrotyrosine, and peroxynitrite) and inflammation/apoptosis (interleukin-1β and caspase-3) biomarkers were statistically elevated in the HFD group in comparison to the controls. HFD impairs mitochondrial function in both types of salivary glands by enhancing ROS production, as well as stimulating inflammation and apoptosis. However, free radical production, protein nitration, and lipid peroxidation were more pronounced in the parotid glands of HFD rats.
机译:氧化应激在唾液腺胰岛素抵抗中起着至关重要的作用。然而,在这些条件下增加自由基形成的原因仍然未知。因此,本研究的目的是研究高脂饮食(HFD)对大鼠颌下腺和腮腺中线粒体呼吸系统,促氧化酶,ROS的产生以及亚硝化/氧化应激的影响。实验分为两组(n = 10):雄性Wistar大鼠:对照组和HFD。与对照大鼠相比,HFD的8周喂养影响了葡萄糖代谢,这是由于血浆葡萄糖和胰岛素以及HOMA-IR显着增加。在HFD大鼠的腮腺和颌下腺中,线粒体复合物I和复合物II + III的活性显着降低。与对照组相比,HFD组腮腺和下颌下腺的线粒体细胞色素C氧化酶(COX)活性和过氧化氢水平显着增加。 HFD大鼠还显示了HFD大鼠腮腺中还原型谷胱甘肽(GSH)和γ:ion氧化型谷胱甘肽(GSH:GSSG)的比例明显降低,以及GSSG水平较高。与之相比,在HFD组中,NADPH氧化酶,黄嘌呤氧化酶的活性以及氧化/亚硝化应激(丙二醛,一氧化氮,硝化酪氨酸和过氧亚硝酸盐)和炎症/凋亡(白介素-1β和胱天蛋白酶-3)的生物标志物水平显着升高。到控件。 HFD通过增加ROS的产生以及刺激炎症和凋亡来损害两种类型唾液腺的线粒体功能。但是,在HFD大鼠的腮腺中,自由基产生,蛋白质硝化和脂质过氧化作用更为明显。

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