首页> 外文期刊>Growth hormone and IGF research: Official journal of the Growth Hormone Research Society and the International IGF Research Society >CIDE-A gene expression is decreased in white adipose tissue of growth hormone receptor/binding protein gene disrupted mice and with high-fat feeding of normal mice.
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CIDE-A gene expression is decreased in white adipose tissue of growth hormone receptor/binding protein gene disrupted mice and with high-fat feeding of normal mice.

机译:在生长激素受体/结合蛋白基因破坏的小鼠的白色脂肪组织中以及正常小鼠的高脂喂养下,CIDE-A基因表达降低。

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摘要

Growth hormone's (GH) lipolytic activity in white adipose tissue (WAT) results in decreased body fat in giant GH transgenic mice and increased subcutaneous fat in dwarf growth hormone receptor/binding protein gene-disrupted mice (GHR -/-). We therefore hypothesized that GH action would affect expression of CIDE-A (cell-death-inducing DFF45-like effector-A), a protein found in white adipose tissue (WAT) and involved in lipid metabolism. CIDE-A RNA levels were determined in subcutaneous, retroperitoneal and epididymal adipose tissue isolated from wild-type and GHR -/- mice. The adipose tissue was also analyzed for adipocyte size. We determined that the lack of GH action has depot-specific effects on the levels of CIDE-A RNA and affected adipocyte cell size. CIDE-A expression is significantly reduced in GHR -/- subcutaneous fat compared to wild-type but is not altered in retroperitoneal or epididymal fat. Likewise, adipocytes are significantly enlarged in GHR -/- subcutaneous adipose tissue relative wild-type mice. A high-fat diet also influenced the level of CIDE-A RNA in mouse adipose tissue. The high-fat diet significantly reduced CIDE-A expression in wild-type subcutaneous fat but did not alter CIDE-A expression in subcutaneous fat of GHR -/- mice. The diet also reduced CIDE-A expression in wild-type retroperitoneal fat but the levels of CIDE-A in epididymal fat were unchanged. In contrast, the high-fat diet reduced CIDE-A expression in both retroperitoneal and epididymal fat of GHR -/- mice. These data demonstrate that CIDE-A levels are reduced in two different mouse models of obesity and this reduction may contribute to altered lipid metabolism.
机译:在白色脂肪组织(WAT)中生长激素(GH)的脂解活性会导致巨大的GH转基因小鼠体内的脂肪减少,而使矮小的生长激素受体/结合蛋白基因破坏的小鼠(GHR-/-)的皮下脂肪也会增加。因此,我们假设GH作用会影响CIDE-A(诱导细胞死亡的DFF45样效应物-A)的表达,CIDE-A是一种在白色脂肪组织(WAT)中发现并参与脂质代谢的蛋白质。从野生型和GHR-/-小鼠分离的皮下,腹膜后和附睾脂肪组织中测定CIDE-A RNA的水平。还分析了脂肪组织的脂肪细胞大小。我们确定缺乏GH作用对CIDE-A RNA的水平和受影响的脂肪细胞大小具有特定的储库效应。与野生型相比,GHR-/-皮下脂肪中CIDE-A表达显着降低,但腹膜后或附睾脂肪中CIDE-A表达没有改变。同样,相对于野生型小鼠,GHR-/-皮下脂肪组织中的脂肪细胞显着增大。高脂饮食也影响小鼠脂肪组织中CIDE-A RNA的水平。高脂饮食显着降低了野生型皮下脂肪中CIDE-A的表达,但并未改变GHR-/-小鼠皮下脂肪中的CIDE-A的表达。饮食还降低了野生型腹膜后脂肪中CIDE-A的表达,但附睾脂肪中CIDE-A的水平未改变。相反,高脂饮食降低了GHR-/-小鼠腹膜后和附睾脂肪中CIDE-A的表达。这些数据表明,在两种不同的肥胖小鼠模型中CIDE-A水平降低,这种降低可能有助于脂质代谢的改变。

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