首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >Endocrine mechanisms of suppressive effect of low dose estrogen-antiandrogen treatment on androgen-dependent organs of male rats.
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Endocrine mechanisms of suppressive effect of low dose estrogen-antiandrogen treatment on androgen-dependent organs of male rats.

机译:低剂量雌激素-抗雄激素治疗对雄性大鼠雄激素依赖性器官抑制作用的内分泌机制。

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摘要

The effects of low doses of hexestrol (Hex) (2-40 micrograms/kg bw) and flutamide (FI) (10 mg/kg bw) on some endocrine mechanisms in mature intact male rats are described in the present paper. It has been shown that each preparation, administered separately for 10 days, induced a moderate decrease in the weight of the ventral prostate (VP), anterior prostate lobe or coagulating gland (CG) and seminal vesicles (SV), in the DNA content and number of cells in the VP. 5 alpha-reductase activity was also decreased; the epithelium secretory activity of the VP was suppressed. After combined FI (10 mg/kg bw) and Hex (40 micrograms/kg bw) the following castration-like effects were observed: an abrupt fall in the weight of the accessory sexual glands, a decrease of DNA level and cell number in the VP as well as a suppression of the production of 5 alpha-reductase metabolites in this structure. Histologically, a marked degenerative changes in the VP secretory epithelium was observed; on the contrary an hyperplasia of connective and smooth muscle cells was evident. When FI alone was administered to rat, the above-mentioned changes were accompanied by a pronounced elevation of plasma bio-LH and testosterone (T) levels, also an increase of testicular delta 5-3 beta-hydroxysteroid dehydrogenase activity was observed. On the contrary, when Hex was administered alone or in combination with FI, bio-LH and T levels and enzyme activity decreased. We conclude that Hex administration in low doses, in combination with FI, could be an alternative method for a complete androgen blockade of the accessory sexual glands.
机译:本文介绍了低剂量己雌醇(Hex)(2-40微克/千克体重)和氟酰胺(FI)(10毫克/千克体重)对成熟完整雄性大鼠某些内分泌机制的影响。已经表明,每种制剂分别施用 10 天,诱导腹侧前列腺 (VP)、前列腺或凝血腺 (CG) 和精囊泡 (SV) 的重量适度降低,在 VP 中的 DNA 含量和细胞数量。5α-还原酶活性也降低;VP的上皮分泌活性受到抑制。在联合FI(10毫克/千克体重)和六角(40微克/千克体重)后,观察到以下去势样效应:辅助性腺重量突然下降,VP中DNA水平和细胞数量降低,以及抑制该结构中5种α-还原酶代谢物的产生。在组织学上,观察到VP分泌上皮细胞的明显退行性变化;相反,结缔肌细胞和平滑肌细胞的增生是显而易见的。当单独给予大鼠FI时,上述变化伴随着血浆生物LH和睾酮(T)水平的显着升高,还观察到睾丸δ 5-3β-羟基类固醇脱氢酶活性的增加。相反,当Hex单独或与FI联合施用时,bio-LH和T水平以及酶活性降低。我们得出结论,低剂量的六角给药与FI相结合,可能是完全雄激素阻断辅助性腺的替代方法。

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