首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Perinatal High-Fat Diet Influences Ozone-Induced Responses on Pulmonary Oxidant Status and the Molecular Control of Mitophagy in Female Rat Offspring
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Perinatal High-Fat Diet Influences Ozone-Induced Responses on Pulmonary Oxidant Status and the Molecular Control of Mitophagy in Female Rat Offspring

机译:围产期高脂饮食影响臭氧诱导的肺氧化状态和雌性大鼠后代乳化剂的分子控制

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摘要

Previous research has shown that a perinatal obesogenic, high-fat diet (HFD) is able to exacerbate ozone-induced adverse effects on lung function, injury, and inflammation in offspring, and it has been suggested that mitochondrial dysfunction is implicated herein. The aim of this study was to investigate whether a perinatal obesogenic HFD affects ozone-induced changes in offspring pulmonary oxidant status and the molecular control of mitochondrial function. For this purpose, female Long-Evans rats were fed a control diet or HFD before and during gestation, and during lactation, after which the offspring were acutely exposed to filtered air or ozone at a young-adult age (forty days). Directly following this exposure, the offspring lungs were examined for markers related to oxidative stress; oxidative phosphorylation; and mitochondrial fusion, fission, biogenesis, and mitophagy. Acute ozone exposure significantly increased pulmonary oxidant status and upregulated the molecular machinery that controls receptor-mediated mitophagy. In female offspring, a perinatal HFD exacerbated these responses, whereas in male offspring, responses were similar for both diet groups. The expression of the genes and proteins involved in oxidative phosphorylation and mitochondrial biogenesis, fusion, and fission was not affected by ozone exposure or perinatal HFD. These findings suggest that a perinatal HFD influences ozone-induced responses on pulmonary oxidant status and the molecular control of mitophagy in female rat offspring.
机译:以前的研究表明,围产期嗜菌,高脂饮食(HFD)能够加剧对后代肺功能,损伤和炎症的臭氧诱导的不利影响,并且已经提出了在此涉及线粒体功能障碍。本研究的目的是探讨围产期obesogensicHFD是否会影响臭氧诱导的后代肺氧化状态和线粒体功能的分子控制。为此目的,在妊娠之前和妊娠之前和泌乳期间喂养雌性饲料或HFD,之后将后代暴露于在年轻成人年龄(40天)的过滤空气或臭氧中。在这种暴露之后,检查后代肺部用于与氧化应激相关的标记;氧化磷酸化;和线粒体融合,裂变,生物发生和乳化物。急性臭氧暴露显着增加了肺氧化剂状态,并上调了控制受体介导的乳化剂的分子机械。在女性后代,围产期HFD加剧了这些反应,而在雄性后代,饮食群体的反应相似。参与氧化磷酸化和线粒体生物发生,融合和裂变的基因和蛋白质的表达不受臭氧暴露或围产期HFD的影响。这些发现表明,围产期HFD影响了臭氧诱导的肺氧化状态和雌性大鼠后代水肿的分子控制。

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