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首页> 外文期刊>Molecular Metabolism >Elevating adipose eosinophils in obese mice to physiologically normal levels does not rescue metabolic impairments
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Elevating adipose eosinophils in obese mice to physiologically normal levels does not rescue metabolic impairments

机译:将肥胖小鼠的嗜酸性粒细胞升高至生理正常水平不能挽救代谢障碍

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Objective Obesity is a metabolic disorder that has reached epidemic proportions worldwide and leads to increased risk for diabetes, cardiovascular disease, asthma, certain cancers, and various other diseases. Obesity and its comorbidities are associated with impaired adipose tissue (AT) function. In the last decade, eosinophils have been identified as regulators of proper AT function. Our study aimed to determine whether normalizing the number of AT eosinophils in obese mice, to those of lean healthy mice, would reduce obesity and/or improve metabolic fitness. Methods C57BL/6J mice fed a high fat diet (HFD) were simultaneously given recombinant interleukin-5 (rIL5) for 8 weeks to increase AT eosinophils. Metabolic fitness was tested by evaluating weight gain, AT inflammation, glucose, lipid, and mixed-meal tolerance, AT insulin signaling, energy substrate utilization, energy expenditure, and white AT beiging capacity. Results Eosinophils were increased ~3-fold in AT of obese HFD-fed mice treated with rIL5, and thus were restored to levels observed in lean healthy mice. However, there were no significant differences in rIL5-treated mice among the above listed comprehensive set of metabolic assays, despite the increased AT eosinophils. Conclusions We have shown that restoring obese AT eosinophils to lean healthy levels is not sufficient to allow for improvement in any of a range of metabolic features otherwise impaired in obesity. Thus, the mechanisms that identified eosinophils as positive regulators of AT function, and therefore systemic health, are more complex than initially understood and will require further study to fully elucidate. Author Video Download video (32MB) Help with mp4 files Author Video . Watch what authors say about their articles.
机译:目的肥胖症是一种代谢性疾病,已在全球范围内达到流行病的程度,并导致罹患糖尿病,心血管疾病,哮喘,某些癌症和各种其他疾病的风险增加。肥胖及其合并症与脂肪组织(AT)功能受损有关。在过去的十年中,嗜酸性粒细胞被确定为正常AT功能的调节剂。我们的研究旨在确定,将肥胖小鼠中的AT嗜酸性粒细胞数量正常化为健康的瘦小鼠,是否可以减少肥胖和/或改善代谢适应性。方法对高脂饮食(HFD)的C57BL / 6J小鼠同时给予重组白介素5(rIL5)8周以增加AT嗜酸性粒细胞。通过评估体重增加,AT炎症,葡萄糖,脂质和混合餐耐受性,AT胰岛素信号传导,能量底物利用率,能量消耗和白色AT补充能力来测试代谢适应性。结果肥胖的HFD喂养rIL5处理的小鼠的嗜酸性粒细胞增加了约3倍,从而恢复到健康瘦小鼠的水平。然而,尽管AT嗜酸性粒细胞增加,但在上述列出的一系列代谢检测中,rIL5处理的小鼠之间没有显着差异。结论我们已经表明,将肥胖的AT嗜酸性粒细胞恢复到瘦弱的健康水平不足以改善肥胖中其他受损的代谢特征。因此,将嗜酸性粒细胞鉴定为AT功能的正向调节剂以及全身健康的机制比最初理解的要复杂得多,需要进一步研究以充分阐明。作者视频下载视频(32MB)mp4文件帮助作者视频。观看作者对文章的评论。

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