新型类固醇抗雄激素TZP-4238和醋酸氯麦地那酮对大鼠垂体、前列腺和肾上腺的影响:组织病理学和免疫细胞化学研究。

M Murakoshi, M Tagawa, R Inada, M Shoji, M Suzuki, K Watanabe
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引用次数: 5

摘要

研究了合成类固醇抗雄激素TZP-4238对大鼠垂体、前列腺和肾上腺的萎缩作用。雄性Sprague-Dawley大鼠分为三个实验组。第一组为对照组。2组和3组分别给予醋酸氯地酮(CMA) 50 mg/kg/d, TZP-4238 10 mg/kg/d,连续3周。CMA组(2组)前列腺明显萎缩。此外,CMA引起肾上腺明显萎缩。组织病理学观察,束状带和网状带肾上腺皮质细胞明显萎缩。最显著的超微结构改变发生在线粒体。此外,有效减少脂质过氧化物的谷胱甘肽过氧化物酶(GSH-PO)在线粒体内的定位也比对照组少。在垂体前叶,CMA诱导ACTH细胞的大小减少。TZP-4238(3组)前列腺明显萎缩。而TZP-4238对肾上腺和垂体前叶ACTH细胞无影响。此外,目前的组织病理学研究表明,TZP-4238或CMA对睾丸和垂体前叶LH细胞没有影响。因此,我们认为,在本实验条件下,TZP-4238导致前列腺萎缩,而肾上腺和垂体前叶ACTH细胞未发生明显的组织病理学改变。我们进一步推测TZP-4238的抗前列腺作用比CMA更强,而TZP-4238对垂体-肾上腺轴的抑制作用比CMA小。
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The effects of new steroidal anti-androgen, TZP-4238, and chlormadinone acetate on the pituitary, prostate and adrenal gland of the rat: histopathological and immunocytochemical studies.

The atrophic effects of a synthetic steroidal anti-androgen, TZP-4238, on the pituitary, prostate and adrenal gland of rats were investigated. Male Sprague-Dawley rats were divided into three experimental groups. Group 1 consisted of controls. Groups 2 and 3 received chlormadinone acetate (CMA) 50 mg/kg/day and TZP-4238 10 mg/kg/day p.o., respectively, for 3 weeks. CMA (Group 2) produced marked atrophy of the prostate. Furthermore, CMA caused marked atrophy of the adrenal gland. Histopathologically, the remarkable atrophy was observed in the adrenal cortical cells of zonae fasciculata and reticularis. The most striking ultrastructural alterations were noted in the mitochondria. In addition, intramitochondrial localization of glutathione-peroxidase (GSH-PO) which effectively reduces the lipid peroxides, was less than that in the controls. In the anterior pituitary gland, CMA induced a reduction in the size of ACTH cells. TZP-4238 (Group 3) produced marked atrophy of the prostate. However, TZP-4238 exerted no effect on the adrenal gland or anterior pituitary ACTH cells. In addition, the present histopathological study showed that TZP-4238 or CMA exerted no effect on the testes or anterior pituitary LH cells. Therefore, it is suggested that TZP-4238 causes atrophy of the prostate without any significant histopathological changes in the adrenal glands or anterior pituitary ACTH cells under the present experimental conditions. We further speculated that TZP-4238 had a more potent anti-prostatic effect than CMA and TZP-4238 had a less inhibitory influence than CMA on the pituitary-adrenal axis.

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