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Nitric Oxide Ameliorates Zinc Oxide Nanoparticles Phytotoxicity in Wheat Seedlings: Implication of the Ascorbate–Glutathione Cycle

机译:一氧化氮改善小麦幼苗中氧化锌纳米颗粒的植物毒性:抗坏血酸-谷胱甘肽循环的意义

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摘要

The present study investigates ameliorative effects of nitric oxide (NO) against zinc oxide nanoparticles (ZnONPs) phytotoxicity in wheat seedlings. ZnONPs exposure hampered growth of wheat seedlings, which coincided with reduced photosynthetic efficiency (Fv/Fm and qP), due to increased accumulation of zinc (Zn) in xylem and phloem saps. However, SNP supplementation partially mitigated the ZnONPs-mediated toxicity through the modulation of photosynthetic activity and Zn accumulation in xylem and phloem saps. Further, the results reveal that ZnONPs treatments enhanced levels of hydrogen peroxide and lipid peroxidation (as malondialdehyde; MDA) due to severely inhibited activities of the following ascorbate–glutatione cycle (AsA–GSH) enzymes: ascorbate peroxidase, glutathione reductase, monodehydroascorbate reductase and dehydroascorbate reductase, and its associated metabolites ascorbate and glutathione. In contrast to this, the addition of SNP together with ZnONPs maintained the cellular functioning of the AsA–GSH cycle properly, hence lesser damage was noticed in comparison to ZnONPs treatments alone. The protective effect of SNP against ZnONPs toxicity on fresh weight (growth) can be reversed by 2-(4carboxy-2-phenyl)-4,4,5,5-tetramethyl- imidazoline-1-oxyl-3-oxide, a NO scavenger, and thus suggesting that NO released from SNP ameliorates ZnONPs toxicity. Overall, the results of the present study have shown the role of NO in the reducing of ZnONPs toxicity through the regulation of accumulation of Zn as well as the functioning of the AsA–GSH cycle.
机译:本研究调查一氧化氮(NO)对小麦幼苗中氧化锌纳米颗粒(ZnONPs)的植物毒性的改善作用。 ZnONPs暴露阻碍了小麦幼苗的生长,这与降低的光合效率(Fv / Fm和qP)相吻合,这是由于木质部和韧皮部树液中锌(Zn)的积累增加。但是,SNP补充通过调节木质部和韧皮部树液中的光合作用活性和锌积累,部分缓解了ZnONPs介导的毒性。此外,结果显示由于严重抑制了以下抗坏血酸-谷胱甘肽循环(AsA-GSH)酶的活性,ZnONPs处理提高了过氧化氢和脂质过氧化的水平(如丙二醛; MDA):抗坏血酸过氧化物酶,谷胱甘肽还原酶,单脱氢抗坏血酸还原酶和脱氢抗坏血酸还原酶及其相关代谢产物抗坏血酸和谷胱甘肽。与此相反,将SNP与ZnONP一起添加可适当维持AsA–GSH循环的细胞功能,因此与单独使用ZnONP相比,损伤较小。 SNP对ZnONPs毒性对鲜重(生长)的保护作用可以通过2-(4羧基-2-苯基)-4,4,5,5-四甲基咪唑啉-1-氧基-3-氧化物来逆转清除剂,因此表明从SNP释放的NO改善了ZnONPs的毒性。总体而言,本研究的结果表明,NO通过调节Zn的积累以及AsA–GSH循环的功能在减少ZnONPs毒性中发挥作用。

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