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高盐饮食可降低果糖喂养的胰岛素抵抗大鼠肝脏的抗氧化防御能力。

High dietary salt decreases antioxidant defenses in the liver of fructose-fed insulin-resistant rats.

机构信息

Research in Biological Sciences - NUPEB, Federal University of Ouro Preto, Minas Gerais, Brazil.

出版信息

J Nutr Biochem. 2013 Dec;24(12):2016-22. doi: 10.1016/j.jnutbio.2013.06.006. Epub 2013 Oct 14.

Abstract

In this study we investigated the hypothesis that a high-salt diet to hyperinsulinemic rats might impair antioxidant defense owing to its involvement in the activation of sodium reabsorption to lead to higher oxidative stress. Rats were fed a standard (CON), a high-salt (HS), or a high-fructose (HF) diet for 10 weeks after which, 50% of the animals belonging to the HF group were switched to a regimen of high-fructose and high-salt diet (HFS) for 10 more weeks, while the other groups were fed with their respective diets. Animals were then euthanized and their blood and liver were examined. Fasting plasma glucose was found to be significantly higher (approximately 50%) in fructose-fed rats than in the control and HS rats, whereas fat liver also differed in these animals, producing steatosis. Feeding fructose-fed rats with the high-salt diet triggered hyperinsulinemia and lowered insulin sensitivity, which led to increased levels of serum sodium compared to the HS group. This resulted in membrane perturbation, which in the presence of steatosis potentially enhanced hepatic lipid peroxidation, thereby decreasing the level of antioxidant defenses, as shown by GSH/GSSG ratio (HFS rats, 7.098±2.1 versus CON rats, 13.2±6.1) and superoxide dismutase (HFS rats, 2.1±0.05 versus CON rats, 2.3±0.1%), and catalase (HFS rats, 526.6±88.6 versus CON rats, 745.8±228.7 U/mg ptn) activities. Our results indicate that consumption of a salt-rich diet by insulin-resistant rats may lead to regulation of sodium reabsorption, worsening hepatic lipid peroxidation associated with impaired antioxidant defenses.

摘要

在这项研究中,我们研究了一个假设,即高盐饮食可能会通过激活钠重吸收来损害胰岛素抵抗大鼠的抗氧化防御能力,从而导致更高的氧化应激。大鼠被喂食标准饮食(CON)、高盐饮食(HS)或高果糖饮食(HF)10 周,之后 HF 组的 50%动物切换为高果糖和高盐饮食(HFS)再喂食 10 周,而其他组继续喂食相应的饮食。然后对动物进行安乐死,并检查其血液和肝脏。发现果糖喂养的大鼠空腹血糖显著升高(约 50%),高于对照组和 HS 组,而这些动物的脂肪肝也不同,产生脂肪变性。给果糖喂养的大鼠喂食高盐饮食会引发高胰岛素血症和降低胰岛素敏感性,导致血清钠水平升高,与 HS 组相比。这导致膜扰动,在脂肪变性存在的情况下,可能会增强肝脂质过氧化,从而降低抗氧化防御水平,如 GSH/GSSG 比值(HFS 大鼠,7.098±2.1 与 CON 大鼠,13.2±6.1)和超氧化物歧化酶(HFS 大鼠,2.1±0.05 与 CON 大鼠,2.3±0.1%)和过氧化氢酶(HFS 大鼠,526.6±88.6 与 CON 大鼠,745.8±228.7 U/mg ptn)活性。我们的结果表明,胰岛素抵抗大鼠摄入富含盐的饮食可能会导致钠重吸收的调节,从而加重与抗氧化防御受损相关的肝脂质过氧化。

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