维生素A、C和E在氧化锌纳米颗粒暴露后大鼠睾丸中发挥抗凋亡功能。

Nasrin Ziamajidi, Sajedeh Daei, Maryam Khajvand-Abedini, Roghayeh Abbasalipourkabir, Alireza Nourian
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摘要

一些报道强调氧化锌纳米颗粒(ZnO NPs)对动物生殖器官有害。因此,本研究旨在探讨氧化锌NPs对睾丸的凋亡潜力,以及维生素(V) A、C和E对氧化锌NPs诱导的损伤的有益作用。为此,本研究选用54只健康雄性Wistar大鼠,将其分为9组,每组6只,G1:对照组1 (Water);G2:对照2(橄榄油);G3: VA (1000 IU/kg), G4: VC (200 mg/kg), G5: VE (100 IU/kg), G6: ZnO NPs暴露动物(200 mg/kg);G7、8和9:分别用VA、C或e预处理氧化锌nps暴露的动物,通过western blotting和qRT-PCR检测凋亡调节标志物,包括Bcl-2相关X (Bax)和b细胞淋巴瘤蛋白2 (Bcl-2)的水平,估计凋亡率。结果表明,氧化锌NPs使Bax蛋白和基因表达水平升高,而Bcl-2蛋白和基因表达水平降低。此外,暴露于氧化锌NPs后,caspase-3,7的活化发生,而与氧化锌NPs组相比,VA、C或E和氧化锌NPs共处理的大鼠上述变化明显减轻。综上所述,VA、C和E在给药ZnO NPs后对大鼠睾丸具有抗凋亡功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vitamins A, C, and E Exert Anti-apoptotic Function in the Testis of Rats After Exposure to Zinc Oxide Nanoparticles.

Vitamins A, C, and E Exert Anti-apoptotic Function in the Testis of Rats After Exposure to Zinc Oxide Nanoparticles.

Vitamins A, C, and E Exert Anti-apoptotic Function in the Testis of Rats After Exposure to Zinc Oxide Nanoparticles.

Vitamins A, C, and E Exert Anti-apoptotic Function in the Testis of Rats After Exposure to Zinc Oxide Nanoparticles.

Some reports emphasize that zinc oxide nanoparticles (ZnO NPs) are detrimental to the reproductive organs of animals. As such, this research aimed at exploring the apoptotic potential of ZnO NPs on testis along with the beneficial role of Vitamins (V) A, C, and E against ZnO NP-induced damage. To this aim, a population of 54 healthy, male Wistar rats were used in this work and then assigned into nine groups of 6 rats as G1: Control 1 (Water); G2: Control 2 (Olive oil); G3: VA (1000 IU/kg), G4: VC (200 mg/kg), G5: VE (100 IU/kg), G6: ZnO NPs exposed animals (200 mg/kg); and G7, 8 and 9: ZnO NPs-exposed animals that were pre-treated with either VA, C, or E. Apoptosis rates were estimated by measuring the level of apoptotic regulatory markers including Bcl-2-associated X (Bax) and B-cell lymphoma protein 2 (Bcl-2) using western blotting and qRT-PCR assays. The data indicated that ZnO NPs exposure elevates the level of Bax protein and gene expression, whereas the protein and gene expression of Bcl-2 was reduced. Further, the activation of caspase-3,7 occurred after exposure to ZnO NPs, while the above alterations were significantly alleviated in the rats that were co-treated with VA, C, or E and ZnO NPs relative to the rats in the ZnO NPs group. In summary, VA, C, and E exerted anti-apoptotic functions in the testis of rats following administration of ZnO NPs.

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