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Oral exposure to methylmercury modifies the prostatic microenvironment in adult rats

机译:口服甲基汞会改变成年大鼠前列腺的微环境

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摘要

Methylmercury (MeHg) is an environmental pollutant that is highly toxic to the central nervous system. As its effects on male reproductive system are poorly understood, this study was carried out to analyse the effects of MeHg on the rat prostate. To evaluate the MeHg toxicity on ventral prostate, three groups of adult male Wistar rats received oral doses of 0.5, 1.0 and 3.0 mg/kg MeHg, respectively, on a daily basis for 14 days. A fourth group was used as a control. The prostate weight was decreased in rats treated orally with 0.5 mg/kg MeHg compared to controls. Also, Hg concentration increased significantly in the prostate after treatments. There were reductions in serum testosterone levels and androgen receptor immunoreactivity in animals receiving 3.0 mg MeHg/kg. The stereological data showed changes in the prostatic epithelial, stromal and luminal compartments which varied according to the different doses. Histopathological alterations, such as chronic inflammation, stratified epithelial hyperplasia and epithelial inflammatory reactive atypia, were observed in the 0.5 mg/kg MeHg-treated group. Epithelial atrophy was observed in the 3.0 mg/kg MeHg-treated group. In conclusion, the MeHg affects prostatic homoeostasis resulting in histopathological changes that may be relevant in the pathogenesis of prostatic disease.
机译:甲基汞(MeHg)是一种环境污染物,对中枢神经系统有剧毒。由于其对男性生殖系统的作用了解甚少,因此进行了这项研究以分析甲基汞对大鼠前列腺的影响。为了评估MeHg对腹侧前列腺的毒性,三组成年雄性Wistar大鼠每天分别口服0.5、1.0和3.0 mg / kg MeHg,共14天。第四组用作对照。与对照组相比,口服0.5 mg / kg MeHg治疗的大鼠的前列腺重量降低。而且,治疗后前列腺中的汞浓度显着增加。接受3.0 mg MeHg / kg的动物的血清睾丸激素水平和雄激素受体免疫反应性降低。立体数据显示,前列腺上皮,基质和腔腔的变化随剂量的不同而变化。在0.5 mg / kg MeHg治疗组中观察到组织病理学改变,例如慢性炎症,分层的上皮增生和上皮炎性反应性非典型性。在3.0 mg / kg MeHg治疗组中观察到上皮萎缩。总之,MeHg影响前列腺癌的稳态,导致组织病理学改变,这可能与前列腺疾病的发病机理有关。

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