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首页> 外文期刊>Frontiers in Endocrinology >Lipoprotein Lipase Expression in Hypothalamus Is Involved in the Central Regulation of Thermogenesis and the Response to Cold Exposure
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Lipoprotein Lipase Expression in Hypothalamus Is Involved in the Central Regulation of Thermogenesis and the Response to Cold Exposure

机译:下丘脑中脂蛋白脂肪酶表达参与了热生成的中央调节和对冷暴露的反应

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Lipoprotein lipase (LPL) is expressed in different areas of the brain, including the hypothalamus and plays an important role in neural control of the energy balance, including feeding behavior and metabolic fluxes. This study tested the hypothesis that hypothalamic LPL participates in the control of body temperature. We first showed that cold exposure induces decreased activity and expression of LPL in the mouse hypothalamus. We then selectively deleted LPL in the mediobasal hypothalamus (MBH) through an adeno-associated virus approach in LPL-floxed mice and generated MBHΔ ~(Lpl) mice with 30–35% decrease in hypothalamic LPL activity. Results showed a decrease in body temperature in MBHΔ ~(Lpl) mice when compared with controls at 22°C. Exposure to cold (4°C for 4?h) decreased the body temperature of the control mice while that of the MBHΔ ~(Lpl) mice remained similar to that observed at 22°C. MBHΔ ~(Lpl) mice also showed increased energy expenditure during cold exposure, when compared to controls. Finally, the selective MBH deletion of LPL also increased the expression of the thermogenic PRMD16 and Dio2 in subcutaneous and perigonadal adipose tissues. Thus, the MBH LPL deletion seems to favor thermogenesis. These data demonstrate that for the first time hypothalamic LPL appears to function as a regulator of body temperature and cold-induced thermogenesis.
机译:脂蛋白脂肪酶(LPL)在大脑的不同区域中表达,包括下丘脑,并在能量平衡的神经控制中起重要作用,包括饲养行为和代谢助焊剂。该研究测试了下丘脑LPL参与体温控制的假设。我们首先表明冷曝光诱导小鼠下丘脑中LPL的活性和表达。然后,我们通过LPL-氟化小鼠中的腺相关病毒方法选择性地删除了Mediobasal下丘脑(MBH)中的LPL,并产生了30-35%下丘脑LPL活性的MBHδ〜(LPL)小鼠。结果在与22℃的对照相比时,MbHδ〜(LPL)小鼠体温下降。暴露于冷(4℃4℃)降低对照小鼠的体温,而MBHδ〜(LPL)小鼠的体温保持与在22℃下观察到的。与对照相比,MbHΔ〜(LPL)小鼠在冷暴露过程中也显示出的能量消耗。最后,LPL的选择性MBH缺失还增加了在皮下和Perigonadal脂肪组织中的热生成PRMD16和DIO2的表达。因此,MBH LPL缺失似乎有利于热生成。这些数据表明,对于第一次下丘脑LPL似乎用作体温和冷致热生成的调节器。

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