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Neuropeptidergic characterization of the leptin receptor mutated obese Koletsky rat.

机译:瘦素受体突变的肥胖Koletsky大鼠的神经肽能表征。

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Leptin regulates energy homeostasis and reproduction as evidenced by dysfunctions characterized in several genetic models of leptin pathway deficiency, such as the ob/ob and db/db mice and fa/fa Zucker rat. An additional model, the obese (f/f) Koletsky rat with a nonsense leptin receptor mutation has not been fully characterized. These rats are obese, hyperphagic, diabetic, and infertile; however, little else is known about the effects of the mutation. We have characterized alterations in hypothalamic appetite regulating neuropeptides as well as energy expenditure, metabolic hormones, and the reproductive axis of obese f/f rats. As expected, obese rats of both sexes were hyperinsulinemic, hyperglycemic, and hyperleptinemic. They exhibited reduced uncoupling protein-1 mRNA expression in brown fat, indicating reduced energy expenditure. In addition, hypothalamic expression of orexigenic neuropeptide Y and agouti-related peptide mRNA levels was upregulated while the anorexigenic cocaine and amphetamine regulated transcript and proopiomelanocortin mRNA levels were reduced. We also observed reproductive axis perturbations including reduced hypothalamic luteinizing hormone releasing hormone, serum estradiol and testosterone, and increased serum progesterone levels. In conclusion, obese Koletsky rats are phenotypically similar to other leptin pathway deficiency models with reduced energy expenditure and hypothalamic neuropeptidergic alterations that could account for their obesity and infertility.
机译:瘦素调节能量稳态和繁殖,这是由瘦素途径缺乏的几种遗传模型所表征的功能障碍所证实的,例如ob / ob和db / db小鼠和fa / fa Zucker大鼠。肥胖的(f / f)Koletsky大鼠具有无意义的瘦素受体突变,尚未完全鉴定其模型。这些大鼠肥胖,肥大,糖尿病和不育。但是,关于突变的影响知之甚少。我们已经表征了肥胖f / f大鼠下丘脑食欲调节神经肽以及能量消耗,代谢激素和生殖轴的改变。不出所料,这两种性别的肥胖大鼠都是高胰岛素血症,高血糖症和高脂血症。他们表现出减少的棕色脂肪解偶联蛋白1 mRNA表达,表明减少的能量消耗。此外,下丘脑的食源性神经肽Y和与刺鼠相关肽的mRNA水平被上调,而厌食可卡因和苯丙胺调节的转录本和原黑皮质素mRNA的水平被降低。我们还观察到生殖轴微扰,包括下丘脑促黄体生成激素释放激素,血清雌二醇和睾丸激素水平降低以及血清孕酮水平升高。总之,肥胖的Koletsky大鼠在表型上与其他瘦素途径缺乏模型相似,具有减少的能量消耗和下丘脑神经肽能改变,这可以解释它们的肥胖和不育。

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