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首页> 外文期刊>Nature Metabolism >Small extracellular vesicle-mediated targeting of hypothalamic AMPK alpha 1 corrects obesity through BAT activation
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Small extracellular vesicle-mediated targeting of hypothalamic AMPK alpha 1 corrects obesity through BAT activation

机译:小细胞外vesicle-mediated瞄准的下丘脑AMPKα1纠正肥胖通过蝙蝠激活

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Current pharmacological therapies for treating obesity are of limited efficacy. Genetic ablation or loss of function of AMP-activated protein kinase alpha 1 (AMPK alpha 1) in steroidogenic factor 1 (SF1) neurons of the ventromedial nucleus of the hypothalamus (VMH) induces feeding-independent resistance to obesity due to sympathetic activation of brown adipose tissue (BAT) thermogenesis. Here, we show that body weight of obese mice can be reduced by intravenous injection of small extracellular vesicles (sEVs) delivering a plasmid encoding an AMPK alpha 1 dominant negative mutant (AMPK alpha 1-DN) targeted to VMH-SF1 neurons. The beneficial effect of SF1-AMPK alpha 1-DN-loaded sEVs is feeding-independent and involves sympathetic nerve activation and increased UCP1-dependent thermogenesis in BAT. Our results underscore the potential of sEVs to specifically target AMPK in hypothalamic neurons and introduce a broader strategy to manipulate body weight and reduce obesity.
机译:目前的药物疗法治疗肥胖是有限的功效。或损失的活化蛋白的功能激酶在steroidogenicα1 (AMPKα1)因子1 (SF1)神经元的腹内侧下丘脑核(VMH)诱发feeding-independent抵抗肥胖原因交感神经激活棕色脂肪组织(蝙蝠)生热作用。可以减少肥胖老鼠的重量小细胞外的静脉注射囊泡(股票)提供一个质粒编码AMPKα1显性负突变(AMPKα1-DN)针对VMH-SF1神经元。影响SF1-AMPKα1-DN-loaded签订feeding-independent和包括同情神经激活和UCP1-dependent增加生热作用的蝙蝠。潜在的专门针对AMPK的股票下丘脑神经元和更广泛的介绍战略控制体重和减少肥胖。

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