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抑制miR-27b-3p可增强高脂饮食诱导的肥胖小鼠附睾脂肪的褐变。

MiR-27b-3p Inhibition Enhances Browning of Epididymal Fat in High-Fat Diet Induced Obese Mice.

作者信息

Yu Jing, Lv Yifan, Wang Fengliang, Kong Xiaocen, Di Wenjuan, Liu Juan, Sheng Yunlu, Lv Shan, Ding Guoxian

机构信息

Division of Geriatric Endocrinology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Breast Surgery, The Affiliated Obstetrics and Gynaecology Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.

出版信息

Front Endocrinol (Lausanne). 2019 Feb 4;10:38. doi: 10.3389/fendo.2019.00038. eCollection 2019.

Abstract

Long-term dysregulation of energy balance is the key component of the obesity epidemic. Given the harm of central obesity and the discovery that beige cells appear within white adipose tissue (WAT), enhancing the energy-expending or "browning" ability of visceral adipose tissue (VAT) has become of therapeutic interest. In this study, we focused on the regulating role of microRNA (miRNA)-27b-3p in mice epididymal white adipose tissue (eWAT) browning. High-fat diet (HFD) induced obese mice model was constructed. Expression of miR-27b-3p and Ucp1 in eWAT was measured during the course of HFD. Through tail vein injection of antimiR-27b-3p, miR-27b-3p expression was inhibited to analyze the potential role of miR-27b-3p in fat browning and metabolism. miR-27b-3p was predominantly expressed in eWAT and browning ability of eWAT in HFD induced obese mice was impaired. Inhibition of miR-27b-3p enhanced browning capacity of eWAT in mice fed an HFD and led to weight loss and insulin sensitivity improvement. High expression of miR-27b-3p in eWAT inhibits browning ability and leads to visceral fat accumulation. It is suggested miR-27b-3p may become a potential therapeutic option for visceral obesity and its associated diseases.

摘要

能量平衡的长期失调是肥胖流行的关键因素。鉴于中心性肥胖的危害以及白色脂肪组织(WAT)中出现米色细胞的发现,增强内脏脂肪组织(VAT)的能量消耗或“褐变”能力已成为治疗研究的热点。在本研究中,我们聚焦于微小RNA(miRNA)-27b-3p在小鼠附睾白色脂肪组织(eWAT)褐变中的调节作用。构建高脂饮食(HFD)诱导的肥胖小鼠模型。在高脂饮食过程中测量eWAT中miR-27b-3p和Ucp1的表达。通过尾静脉注射抗miR-27b-3p抑制miR-27b-3p表达,以分析miR-27b-3p在脂肪褐变和代谢中的潜在作用。miR-27b-3p主要在eWAT中表达,高脂饮食诱导的肥胖小鼠eWAT的褐变能力受损。抑制miR-27b-3p可增强高脂饮食喂养小鼠eWAT的褐变能力,并导致体重减轻和胰岛素敏感性改善。eWAT中miR-27b-3p的高表达抑制褐变能力并导致内脏脂肪堆积。提示miR-27b-3p可能成为内脏肥胖及其相关疾病的潜在治疗选择。

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