Harikai Naoki, Hashimoto Ayu, Semma Masanori, Ichikawa Atsushi
School of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Hyogo 663-8179, Japan.
Metabolism. 2007 Jun;56(6):847-55. doi: 10.1016/j.metabol.2007.01.016.
This study shows the characteristics of hormone-dependent lipolysis in white adipose tissues from corpulent spontaneously hypertensive rats (SHR/NDmc-cp(cp/cp)). The glycerol-releasing activity on addition of norepinephrine (NE) and corticotropin (ACTH) was diminished in slices of epididymal, retroperitoneal, and mesenteric adipose tissues from cp/cp rats compared with those from Wistar Kyoto rats and lean spontaneous hypertensive rats (SHR/NDmc-cp(+/+)). 8-Bromo-cyclic adenosine monophosphate had a slight effect on lipolysis in epididymal, retroperitoneal, and mesenteric adipose tissues from cp/cp rats, and addition of NE and ACTH resulted in a slight accumulation of cyclic adenosine monophosphate in epididymal adipose tissue from cp/cp rats. Therefore, the alteration of hormone-dependent lipolysis-related genes was analyzed using quantitative real-time polymerase chain reaction. It was found that the expression of beta(3)-adrenergic receptor, melanocortin 2 receptor, hormone-sensitive lipase, and perilipin messenger RNAs was limited in epididymal, retroperitoneal, mesenteric, and subcutaneous adipose tissues from cp/cp rats compared with +/+ rats. These results indicate that in white adipose tissue from cp/cp rats, the diminished lipolytic response to NE and ACTH may be caused by impaired expression of beta(3)-adrenergic receptor, melanocortin 2 receptor, hormone-sensitive lipase, and perilipin.
本研究显示了肥胖型自发性高血压大鼠(SHR/NDmc-cp(cp/cp))白色脂肪组织中激素依赖性脂肪分解的特征。与Wistar Kyoto大鼠和瘦型自发性高血压大鼠(SHR/NDmc-cp(+/+))相比,cp/cp大鼠附睾、腹膜后和肠系膜脂肪组织切片中,添加去甲肾上腺素(NE)和促肾上腺皮质激素(ACTH)后的甘油释放活性降低。8-溴环磷酸腺苷对cp/cp大鼠附睾、腹膜后和肠系膜脂肪组织的脂肪分解有轻微影响,添加NE和ACTH导致cp/cp大鼠附睾脂肪组织中环状磷酸腺苷略有积累。因此,使用定量实时聚合酶链反应分析了激素依赖性脂肪分解相关基因的变化。结果发现,与+/+大鼠相比,cp/cp大鼠附睾、腹膜后、肠系膜和皮下脂肪组织中β(3)-肾上腺素能受体、促黑素皮质素2受体、激素敏感性脂肪酶和围脂滴蛋白信使核糖核酸的表达受到限制。这些结果表明,在cp/cp大鼠的白色脂肪组织中,对NE和ACTH的脂肪分解反应减弱可能是由于β(3)-肾上腺素能受体、促黑素皮质素2受体、激素敏感性脂肪酶和围脂滴蛋白的表达受损所致。