Growth Hormone Administration Controls Body Composition Associated with Changes of Thermogenesis in Obese KK-Ay Mice~!2009-08-29~!2010-01-12~!2010-03-26~!

Chizuko Hioki, Toshihide Yoshida, A. Kogure, K. Yoshimoto, A. Shimatsu
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引用次数: 12

Abstract

We investigate the effects of continuous human growth hormone (GH) therapy in young obese mice on thermogenesis. Female KK-A y obese mice (n=10) were injected subcutaneously with GH (3.5 mg/kg/day) for 30 days from 42 days old. As a control, physiological saline was administered (n=10). At the terminal point (71 days old), GH administration affected linear growth, and the Lee obesity index (3 square root body weight/nasoanal length  1000) was significantly decreased. Rates of inguinal and perimetric white adipose pads per body weight also decreased. Free fatty acid levels decreased, while plasma insulin concentrations and homeostasis model assessment insulin resistance were increased (P<0.01). Plasma insulin-like growth factor � (IGF-1) levels markedly rose (P<0.00001). Uncoupling protein1 (UCP1) and UCP3 mRNA expressions in brown adipose tissue were inhibited (P<0.05). Continuous GH therapy changed obese body composition toward lean, however, the consequence could be the negative regulation of thermogenesis.
生长激素控制肥胖KK-Ay小鼠体成分与产热变化的关系
我们研究了持续的人类生长激素(GH)治疗对年轻肥胖小鼠产热的影响。雌性KK-A - y肥胖小鼠(n=10)从42日龄开始皮下注射生长激素(3.5 mg/kg/天),持续30天。作为对照,给予生理盐水(n=10)。在终点(71日龄),GH对线性生长有影响,Lee肥胖指数(3平方根体重/鼻鼻长1000)显著降低。每体重的腹股沟和周围白色脂肪垫率也有所下降。游离脂肪酸水平降低,血浆胰岛素浓度和胰岛素抵抗稳态模型升高(P<0.01)。血浆胰岛素样生长因子- (IGF-1)水平显著升高(P<0.00001)。解偶联蛋白1 (UCP1)和UCP3 mRNA在棕色脂肪组织中的表达受到抑制(P<0.05)。持续的生长激素治疗改变了肥胖的身体组成,然而,其后果可能是产热的负调节。
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