Tóth M
Acta Biochim Biophys Acad Sci Hung. 1978;13(1-2):23-34.
Androgen dependent gross changes in RNA concentration of the androgen responsive cells of rat seminal vesicle were monitored by measuring RNA/DNA ratios. The time course of the changes in the RNA/DNA ratio following castration and after replacement of testosterone obeys the predictions of a kinetic model which permits determination of the rate constants for RNA degradation separately for the state of withdrawal and replacement of testosterone. For both states the apparent rate constant for RNA degradation was found to be 0.4 day-1/t1/2 approximately or equal to 1.8 days). The rate constant was shown to be independent of the testosterone dose applied. The testosterone-induced increase in the RNA/DNA ratio could be prevented by the administration of Actinomycin D. These findings are consistent with the view that testosterone controls the RNA level in vesicular target cells through the regulation of the rate of RNA synthesis. The results indicate that the rate of RNA synthesis in the vesicular cells of castrated rats is a regular hyperbolic function of the dose of testosterone propionate administered to these rats. On the basis of this finding a new approach to the accurate determination of the relative androgenicity of androgenic steroids is suggested.
通过测量RNA/DNA比率,监测了大鼠精囊雄激素反应细胞中雄激素依赖性RNA浓度的总体变化。去势后及补充睾酮后RNA/DNA比率变化的时间进程符合动力学模型的预测,该模型允许分别确定睾酮撤药和补充状态下RNA降解的速率常数。在两种状态下,RNA降解的表观速率常数均为0.4天-1(t1/2约等于1.8天)。已证明该速率常数与所应用的睾酮剂量无关。放线菌素D的给药可阻止睾酮诱导的RNA/DNA比率升高。这些发现与以下观点一致,即睾酮通过调节RNA合成速率来控制精囊靶细胞中的RNA水平。结果表明,去势大鼠精囊细胞中RNA合成速率是给予这些大鼠丙酸睾酮剂量的常规双曲线函数。基于这一发现,提出了一种准确测定雄激素类固醇相对雄激素活性的新方法。