Ginseng Nanoparticles Protect Against Methotrexate-Induced Testicular Toxicity in Rats

Madonna E. F. Kamel, H. Mohammad, C. Maurice, Magda M. Hagras
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引用次数: 10

Abstract

Testicular toxicity of methotrexate (MTX) is a clinically important adverse effect. Ginseng has been demonstrated to stimulate spermatogenesis, prevent chemotherapy-induced testicular injury and to possess antiapoptotic and antioxidant actions. Owing to its low bioavailability, ginseng was formulated to nanoform in the current study. As there is no available data about the protective effects of ginseng or ginseng nanoparticles against MTX-induced testicular toxicity, this study was initiated. Seventy-two male rats were enrolled. Rats were given either ginseng (5oo mg/kg/day), or ginseng nanoparticles (125 and 250 mg/kg/day) orally for 28 consecutive days. Rats received a single dose of MTX (20 mg/kg) intraperitoneally on day 25. Ginseng and ginseng nanoparticles pre-treatment in rats significantly alleviated the testicular histopathological effects induced by MTX. Also, they significantly restored the impaired spermatogenesis induced by MTX via significantly increasing the Johnsen's tubular biopsy score (JTBS). Ginseng and ginseng nanoparticles treatment prior to MTX administration in rats significantly ameliorated MTX-induced testicular apoptosis by significantly decreasing the percentage of caspase-3-immunostained testicular area. Ginseng and ginseng nanoparticles pretreatment caused nonsignificant increase in serum testosterone levels that were significantly decreased by MTX. The results indicate that ginseng and ginseng nanoparticles protect against MTX-induced testicular toxicity in rats, which is suggested to be through inhibition of MTX-induced testicular apoptosis. The protective effect of ginseng nanoparticles was supposed to be better than ginseng in the given doses.
人参纳米颗粒对甲氨蝶呤诱导大鼠睾丸毒性的保护作用
甲氨蝶呤(MTX)的睾丸毒性是临床上重要的不良反应。人参已被证明可以刺激精子发生,防止化疗引起的睾丸损伤,并具有抗凋亡和抗氧化作用。由于人参的生物利用度低,本研究将其配制成纳米形式。由于没有关于人参或人参纳米颗粒对MTX诱导的睾丸毒性的保护作用的可用数据,因此启动了这项研究。72只雄性大鼠被纳入研究。大鼠连续28天口服人参(5oo mg/kg/天)或人参纳米颗粒(125和250 mg/kg/天)。大鼠在第25天腹膜内接受单剂量的MTX(20mg/kg)。人参和人参纳米颗粒在大鼠体内的预处理显著减轻了MTX诱导的睾丸组织病理学影响。此外,他们通过显著提高Johnsen氏肾小管活检评分(JTBS),显著恢复了MTX诱导的受损精子发生。在大鼠服用MTX之前,人参和人参纳米颗粒治疗通过显著降低胱天蛋白酶-3免疫染色睾丸面积的百分比,显著改善了MTX诱导的睾丸凋亡。人参和人参纳米颗粒预处理导致血清睾酮水平无显著升高,而MTX显著降低了血清睾酮水平。结果表明,人参和人参纳米粒子对MTX诱导的大鼠睾丸毒性具有保护作用,可能是通过抑制MTX诱导睾丸细胞凋亡。在给定的剂量下,人参纳米粒子的保护作用应该比人参更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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