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首页> 外文期刊>Human and Experimental Toxicology >Protection of cyclophosphamide-induced toxicity in reproductive tract histology, sperm characteristics, and DNA damage by an herbal source; evidence for role of free-radical toxic stress.
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Protection of cyclophosphamide-induced toxicity in reproductive tract histology, sperm characteristics, and DNA damage by an herbal source; evidence for role of free-radical toxic stress.

机译:通过草药来源保护环磷酰胺在生殖道组织学,精子特征和DNA损伤中引起的毒性;自由基毒性应激作用的证据。

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摘要

Cyclophosphamide (CP) as an anticancer alkylating agent has been known as a male reproductive tract toxicant. The aim of this study was to examine whether Satureja khuzestanica essential oil (SKEO) as an established herbal antioxidant, might protect tract rat reproductive system from toxicity of CP. To reach this aim, total antioxidant power (TAP) and lipid peroxidation (LPO) in testis and plasma, blood levels of sex hormones, sperm characteristics, DNA integrity and chromatin quality, and fertility in male rats were tested. Histopathological analysis of testes and epididymides and staining of mast cells were performed for assessment of spermatogenic disorders. CP (6 mg/kg/day) and SKEO (225 mg/kg/day) were administered alone or in combination by gavage for 28 days. In the CP-exposed rats, testicular and plasma LPO increased, TAP decreased, plasma testosterone diminished, and both spermatogenesis and fertility were impaired. In CP-treated rats, a decrease in sperm quality was associated with increased DNA damage and decreased chromatin quality. Coadministration of SKEO significantly improved CP-induced changes in plasma testosterone, sperm quality, spermatogenesis and fertility, toxic stress, and DNA damage. It is concluded that CP-induced toxic effects on androgenesis and spermatogenesis is mediated by free radicals. SKEO protects reproductive system from toxicity of CP through its antioxidant potential and androgenic activity.
机译:环磷酰胺(CP)作为抗癌烷基化剂已被公认为是男性生殖道毒物。这项研究的目的是要检查作为一种已建立的草药抗氧化剂的苦瓜香精油(SKEO)是否可以保护道大鼠生殖系统免受CP的毒性。为了达到这个目的,测试了雄性大鼠睾丸和血浆中的总抗氧化能力(TAP)和脂质过氧化(LPO),性激素的血液水平,精子特征,DNA完整性和染色质质量以及生育能力。进行睾丸和附睾的组织病理学分析以及肥大细胞染色,以评估生精障碍。 CP(6 mg / kg /天)和SKEO(225 mg / kg /天)单独或通过强饲法联合给药28天。在暴露于CP的大鼠中,睾丸和血浆LPO升高,TAP降低,血浆睾丸激素减少,并且精子发生和生育能力均受损。在接受CP治疗的大鼠中,精子质量下降与DNA损伤增加和染色质下降有关。共同施用SKEO可显着改善CP诱导的血浆睾丸激素,精子质量,精子发生和繁殖,毒性应激和DNA损伤的变化。结论是CP诱导的对雄激素生成和精子发生的毒性作用是由自由基介导的。 SKEO通过其抗氧化潜力和雄激素活性保护生殖系统免受CP的毒性。

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