饲喂不同饲粮条件的受精后7 d仔猪的呼吸测量结果。

Paula Saez-Raez, J. Walters
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引用次数: 0

摘要

在阿巴拉契亚地区,超过三分之一的成年人患有肥胖症,这与高脂肪和高胆固醇的饮食以及糖尿病、高血压和心血管疾病等许多疾病的发展有关。这些饮食会导致慢性炎症和自由基(如活性氧(ROS))的产生而导致细胞损伤。我们比较了受精后7天的斑马鱼(Danio rerio)幼虫在不同饮食条件下的呼吸结果。幼虫要么不喂食,要么喂食低脂肪饮食(LFD),要么喂食高脂肪饮食(HFD),要么喂食高脂肪饮食加减轻氧化应激的药物(茴香酚三硫酮和mito-TEMPO)。我们预计,由于脂质氧化磷酸化,HFD会使线粒体承受更大的压力,并且在药物处理的幼虫中会减少。呼吸测量使用XFe24细胞外通量分析仪(Agilent Technologies)和改进的细胞Mito压力测试。我们发现,高脂肪饮食组的基础呼吸量更高,而其他两种饮食组的基础呼吸量更低,这表明高脂肪饮食确实会在线粒体中产生更多的氧化应激,而测试的药物能够成功地缓解这种氧化应激。药物相互作用读数的分析正在进行中。在未来,我们将测试其他可以影响线粒体代谢的药物(即姜黄素,Pitastatin, Mdivi-1和PPPA)。由美国国立卫生研究院资助P20GM103434西弗吉尼亚IDeA生物医学研究卓越网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Respirometry Outcomes in a 7 Days Post-Fertilization Danio Rerio Fed Different Dietary Conditions.
More than a third of the adults in the Appalachia are affected by obesity, which is associated with diets that are high in fats and cholesterol as well as the development of many diseases such as diabetes, hypertension and cardiovascular diseases. These diets lead tochronic inflammation and cellular damage from production of free radicals such as Reactive Oxygen Species (ROS). We compared the respirometry outcomes in a 7 days post- fertilization zebrafish (Danio rerio) larvae after different diet conditions. Larvae were either fed nothing at all, a low fat diet (LFD), a high fat diet (HFD), or a HFD plus a drug that mitigates oxidative stress (Anethole Trithione and mito-TEMPO). We expected that the HFD would cause the mitochondria to be put under more stress due to oxidative phosphorylation of lipids and would decrease in the larvae treated with the drugs. Respirometry was obtained using the XFe24 Extracellular Flux Analyzer (Agilent Technologies) and a modified Cell Mito Stress Test. We found basal respiration is higher in the HFD and lower in the other two treatment diets, indicating that high fat diets do produce more oxidative stress in mitochondria, and the drugs tested are able to successfully mitigate it. The analysis of drug interaction readings is in progress. In the future, we will test other drugs that can affect mitochondrial metabolism (i.e. Curcumin, Pitastatin, Mdivi-1 and PPPA). Supported by NIH Grant P20GM103434 to the West Virginia IDeA Network for Biomedical Research Excellence.
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