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Preventing High Fat Diet-induced Obesity and Improving Insulin Sensitivity through Neuregulin 4 Gene Transfer

机译:通过神经调节蛋白4基因转移预防高脂饮食引起的肥胖并提高胰岛素敏感性

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摘要

Neuregulin 4 (NRG4), an epidermal growth factor-like signaling molecule, plays an important role in cell-to-cell communication during tissue development. Its function to regulate energy metabolism has recently been reported. This current study was designed to assess the preventive and therapeutic effects of NRG4 overexpression on high fat diet (HFD)-induced obesity. Using the hydrodynamic gene transfer method, we demonstrate that Nrg4 gene transfer in mice suppressed the development of diet-induced obesity, but did not affect pre-existing adiposity and body weight in obese mice. Nrg4 gene transfer curbed HFD-induced hepatic steatosis by inhibiting lipogenesis and PPARγ-mediated lipid storage. Concurrently, overexpression of NRG4 reduced chronic inflammation in both preventive and treatment studies, evidenced by lower mRNA levels of macrophage marker genes including F4/80, Cd68, Cd11b, Cd11c, and macrophage chemokine Mcp1, resulting in improved insulin sensitivity. Collectively, these results demonstrate that overexpression of the Nrg4 gene by hydrodynamic gene delivery prevents HFD-induced weight gain and fatty liver, alleviates obesity-induced chronic inflammation and insulin resistance, and supports the health benefits of NRG4 in managing obesity and obesity-associated metabolic disorders.
机译:神经调节蛋白4(NRG4)是一种表皮生长因子样信号分子,在组织发育过程中在细胞间通讯中起着重要作用。最近已经报道了其调节能量代谢的功能。本研究旨在评估NRG4过表达对高脂饮食(HFD)引起的肥胖的预防和治疗作用。使用流体动力学基因转移方法,我们证明了Nrg4基因转移在小鼠中抑制了饮食诱导的肥胖症的发展,但并未影响肥胖小鼠中先前存在的肥胖和体重。 Nrg4基因转移通过抑制脂肪生成和PPARγ介导的脂质存储来抑制HFD诱导的肝脂肪变性。同时,在预防和治疗研究中,NRG4的过表达减少了慢性炎症,这可通过降低巨噬细胞标记基因(包括F4 / 80,Cd68,Cd11b,Cd11c和巨噬细胞趋化因子Mcp1)的mRNA水平来证明,从而提高了胰岛素敏感性。总的来说,这些结果表明通过流体动力学基因传递来过度表达Nrg4基因可防止HFD诱导的体重增加和脂肪肝,减轻肥胖症引起的慢性炎症和胰岛素抵抗,并支持NRG4在管理肥胖症和与肥胖相关的新陈代谢中的健康益处。疾病。

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