外源性性腺类固醇对印度侏儒田鼠生殖功能的影响

S. Arora, P. Singh, P. Basu, C. Haldar
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摘要

不同的促性腺激素阈值对GnRH和促性腺激素的释放有刺激或抑制作用。在生殖活跃期(RAP),内源性性腺激素浓度保持较高,而在生殖非活跃期(RIP),内源性性腺激素浓度保持较低。在RIP期间,HPG轴对性腺类固醇敏感,但循环中的睾酮和雌二醇水平仍然很低。在这一阶段,我们可以方便地观察性腺类固醇对雄性或雌性啮齿动物HPG轴的影响。因此,本研究的目的是发现睾酮和雌二醇对雄性和雌性印度侏儒田鼠(Mus terricolor) RIP期间生殖功能的影响。在RIP期间,雄性小鼠连续15天注射阿卡铁(市售睾酮,1mg/100g体重),雌性小鼠连续15天注射雌二醇-苯甲酸酯(25μg/100g体重)。治疗结束后,两性性腺和附属性器官的重量显著增加。附睾唾液酸、精囊果糖、子宫蛋白等副性器官生化成分含量显著升高,血浆睾酮、雌二醇、黄体酮水平升高。组织学上,性腺和附属性器官表现出细胞活性增加。然而,两性的性腺胆固醇明显下降。总体而言,在RIP期间,雄性和雌性小鼠服用性腺类固醇加速了性腺复发,但没有抑制生殖功能。因此,从本研究可以推断,在RIP过程中,HPG轴对性腺类固醇敏感,因此外源性性腺类固醇诱导性腺活动。
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Effect of Exogenous Gonadal Steroids on Reproductive Functions of the Indian Pygmy Field Mouse Mus terricolor
Different thresholds of gonadal steroids exert stimulatory or inhibitory effects on GnRH and gonadotropin release. During the reproductively active phase (RAP), the concentration of endogenous gonadal steroids remains high while, during reproductively inactive phase (RIP), it remains low. During RIP the HPG axis is sensitive to gonadal steroids but the circulatory levels of testosterone and estradiol remain low. During this phase one can observe conveniently the effects of gonadal steroids on the HPG axis in male or female rodents. Therefore, the aim of the present study was to find the effects of testosterone and estradiol on the reproductive functions of male and female Indian pygmy field mouse, Mus terricolor , during RIP. The male mice were injected aquaviron (commercially available testosterone, 1mg/100g body weight) while the female mice received estradiol-benzoate (25μg/100g body weight) for 15 consecutive days during the RIP. After completion of the treatment, a significant increase in the weights of gonads and accessory sex organs was noted in both the sexes. The biochemical constituents of accessory sex organs such as epididymal sialic acid, seminal vesicular fructose and uterine protein content reflected significant elevation accompanied by increased levels of plasma testosterone, estradiol and progesterone. Histologically, the gonads and accessory sex organs exhibited increased cellular activity. However, the gonadal cholesterol was significantly decreased in both the sexes. Over all, administration of gonadal steroids to both male and female mice accelerated the gonadal recrudescence but did not inhibit the reproductive functions when administered during the RIP. Therefore, it can be inferred from the present study that during the RIP the HPG axis is sensitive to gonadal steroids and, hence, exogenous gonadal steroids induce gonadal activity.
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