Tanaka H, Gibb W, Ducharme J R, Collu R
Department of Pediatrics, Hospital Ste-Justine, Montreal, Quebec, Canada.
Steroids. 1988 Jan-Feb;51(1-2):115-22. doi: 10.1016/0039-128x(88)90188-2.
The present study was undertaken to evaluate the state of glucocorticoid cytosol receptor binding in muscle hypertrophied by compensatory overload in normal, testosterone-treated, and castrated male rats. Compensatory hypertrophy in plantaris muscles was induced by myomectomy of the gastrocnemius and the soleus of 100 male Sprague-Dawley rats. The controlateral sham-operated limb was used as control. The rats were divided in 3 groups: control injected with peanut oil, castrated injected with peanut oil, and castrated injected with testosterone propionate (1 mg/rat). Five days later the animals were sacrificed and the muscles obtained for glucocorticoid receptor binding studies using [3H]dexamethasone as ligand. Receptor concentrations (Bmax) were significantly increased in hypertrophied muscle and the increase was not affected either by castration or by androgen treatment. These results tend to suggest that gonadal steroids do not participate in hypertrophy-induced proliferation of glucocorticoid receptors.
本研究旨在评估正常、经睾酮处理及去势雄性大鼠中因代偿性负荷过重而发生肌肉肥大时糖皮质激素胞质受体结合的状态。通过切除100只雄性Sprague-Dawley大鼠的腓肠肌和比目鱼肌来诱导跖肌的代偿性肥大。对侧假手术肢体用作对照。大鼠分为3组:注射花生油的对照组、注射花生油的去势组和注射丙酸睾酮(1mg/只大鼠)的去势组。5天后处死动物,获取肌肉用于以[3H]地塞米松为配体的糖皮质激素受体结合研究。肥大肌肉中的受体浓度(Bmax)显著增加,且这种增加不受去势或雄激素处理的影响。这些结果倾向于表明性腺类固醇不参与肥大诱导的糖皮质激素受体增殖。