首页> 外文期刊>Journal of the Endocrine Society. >Astrocyte-Specific Deletion of Peroxisome-Proliferator Activated Receptor-γ Impairs Glucose Metabolism and Estrous Cycling in Female Mice
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Astrocyte-Specific Deletion of Peroxisome-Proliferator Activated Receptor-γ Impairs Glucose Metabolism and Estrous Cycling in Female Mice

机译:过氧化物酶体增殖物激活受体-γ的星形胶质细胞特异性删除损害了雌性小鼠的葡萄糖代谢和发情循环。

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Mice lacking peroxisome-proliferator activated receptor- γ (PPAR γ ) in neurons do not become leptin resistant when placed on a high-fat diet (HFD). In male mice, this results in decreased food intake and increased energy expenditure, causing reduced body weight, but this difference in body weight is not observed in female mice. In addition, estrous cycles are disturbed and the ovaries present with hemorrhagic follicles. We observed that PPAR γ was more highly expressed in astrocytes than neurons, so we created an inducible, conditional knockout of PPAR γ in astrocytes (AKO). The AKO mice had impaired glucose tolerance and hepatic steatosis that did not worsen with HFD. Expression of gluconeogenic genes was elevated in the mouse livers, as was expression of several genes involved in lipogenesis, lipid transport, and storage. The AKO mice also had a reproductive phenotype with fewer estrous cycles, elevated plasma testosterone levels, reduced corpora lutea formation, and alterations in hypothalamic and ovarian gene expression. Thus, the phenotypes of the AKO mice were very different from those seen in the neuronal knockout mice, suggesting distinct roles for PPAR γ in these two cell types.
机译:接受高脂饮食(HFD)时,神经元中缺乏过氧化物酶体增殖物激活的受体γ(PPARγ)的小鼠不会变得对瘦素具有抵抗力。在雄性小鼠中,这导致食物摄入减少和能量消耗增加,从而导致体重减轻,但是在雌性小鼠中未观察到这种体重差异。此外,动情周期受到干扰,卵巢出现卵泡。我们观察到星形胶质细胞中PPARγ的表达高于神经元,因此我们在星形胶质细胞(AKO)中创建了可诱导的条件性PPARγ敲除。 AKO小鼠的葡萄糖耐量降低和肝脂肪变性均没有因HFD而恶化。糖原异生基因的表达在小鼠肝脏中升高,涉及脂肪生成,脂质转运和贮藏的几种基因的表达也升高。 AKO小鼠还具有生殖表型,发情周期较少,血浆睾丸激素水平升高,黄体形成减少,下丘脑和卵巢基因表达发生改变。因此,AKO小鼠的表型与神经元基因敲除小鼠中的表型非常不同,这表明PPARγ在这两种细胞类型中的作用不同。

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