首页> 美国卫生研究院文献>American Journal of Physiology - Endocrinology and Metabolism >Mitochondria Dysfunction in Aging and Metabolic Diseases: Pentose phosphate pathway activity parallels lipogenesis but not antioxidant processes in rat liver
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Mitochondria Dysfunction in Aging and Metabolic Diseases: Pentose phosphate pathway activity parallels lipogenesis but not antioxidant processes in rat liver

机译:衰老和代谢性疾病中的线粒体功能障碍:磷酸戊糖途径活性与大鼠肝脏中的脂肪生成平行但与抗氧化过程不平行

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摘要

The pentose phosphate pathway (PPP) is widely assumed to play a key role in both reductive biosynthesis and protection from oxidative stress because it is the major source of NADPH. However, little is known about the activity of the PPP in fatty liver, which is characterized by both oxidative stress and lipogenesis. This study was designed to test whether the PPP is active in parallel with lipogenesis and antioxidant processes in the fatty liver of whole animals. Eight- and 16-wk-old obese Zucker diabetic fatty rats and their lean littermates received [U-13C3]glycerol, and 13C labeling patterns of glucose and triglycerides were analyzed for the assessment of hepatic PPP activity and the potentially related processes simultaneously. Oxidative stress, antioxidant activity, and NADPH-producing enzymes in the liver were further examined. Both PPP activity and lipogenesis increased in the fatty liver of young obese Zucker rats but decreased together in older obese Zucker rats. As expected, lipid peroxidation measured by malondialdehyde increased in the fatty liver of obese Zucker rats at both ages. However, evidence for antioxidant processes such as [glutathione] or activities of glutathione reductase, glutathione peroxidase, and catalase was not altered. Hepatic PPP activity paralleled lipogenesis but was dissociated from biomarkers of oxidative stress or antioxidant processes. In summary, NADPH from the PPP was presumably consumed for reductive biosynthesis rather than antioxidant defense in the fatty liver.
机译:广泛认为磷酸戊糖途径(PPP)在还原性生物合成和防止氧化应激中起关键作用,因为它是NADPH的主要来源。然而,关于PPP在脂肪肝中的活性知之甚少,其特征在于氧化应激和脂肪生成。这项研究旨在测试PPP是否在整个动物的脂肪肝中与脂肪生成和抗氧化过程同时起作用。八和16周龄肥胖Zucker糖尿病高脂大鼠及其瘦仔猪接受[U- 13 C3]甘油,葡萄糖和甘油三酯的 13 C标记方式分别为同时评估肝PPP活动和潜在相关过程的分析。进一步检查了肝脏中的氧化应激,抗氧化活性和产生NADPH的酶。在年轻的肥胖Zucker大鼠的脂肪肝中,PPP活性和脂肪生成均增加,但在年长的肥胖Zucker大鼠中,脂肪活性均降低。如预期的那样,在两个年龄的肥胖Zucker大鼠的脂肪肝中,通过丙二醛测得的脂质过氧化作用均增加。但是,有关抗氧化剂过程(如[谷胱甘肽]或谷胱甘肽还原酶,谷胱甘肽过氧化物酶和过氧化氢酶活性)的证据没有改变。肝PPP活性与脂肪生成平行,但与氧化应激或抗氧化过程的生物标志物分离。总而言之,来自PPP的NADPH可能被用于还原性生物合成,而不是脂肪肝中的抗氧化剂防御作用。

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