Laboratorio de Antimutagénesis, Anticarcinogénesis y Antiteratogénesis Ambiental, Facultad de Estudios Superiores-Zaragoza, Universidad Nacional Autónoma de México (UNAM), Mexico City 09230, Mexico.
Posgrado en Ciencias Biológicas, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.
Molecules. 2022 Jun 23;27(13):4028. doi: 10.3390/molecules27134028.
The aim of this study is to examine the ability of resveratrol to counteract hexavalent chromium [Cr(VI)]-induced genetic damage, as well as the possible pathways associated with this protection. Hsd:ICR male mice are divided into groups of the following five individuals each: (a) control 1, distilled water; (b) control 2, ethanol 30%; (c) resveratrol, 50 mg/kg by gavage; (d) CrO, 20 mg/kg intraperitoneally; (e) resveratrol + CrO, resveratrol administered 4 h prior to CrO. The assessment is performed on peripheral blood. Micronuclei (MN) kinetics are measured from 0 to 72 h, while 8-hydroxydeoxyguanosine (8-OHdG) adduct repair levels, endogenous antioxidant system biomarkers, and apoptosis frequency were quantified after 48 h. Resveratrol reduces the frequency of Cr(VI)-induced MN and shows significant effects on the 8-OHdG adduct levels, suggesting that cell repair could be enhanced by this polyphenol. Concomitant administration of resveratrol and Cr(VI) results in a return of the activities of glutathione peroxidase and catalase to control levels, accompanied by modifications of superoxide dismutase activity and glutathione levels. Thus, antioxidant properties might play an important role in resveratrol-mediated inhibition of Cr(VI)-induced oxidant genotoxicity. The increase in apoptotic cells and the decrease in necrosis further confirmed that resveratrol effectively blocks the actions of Cr(VI).
本研究旨在考察白藜芦醇对抗六价铬(Cr(VI))诱导遗传损伤的能力,以及与这种保护相关的可能途径。将 Hsd:ICR 雄性小鼠分为以下五组,每组五个体:(a) 对照组 1,蒸馏水;(b) 对照组 2,30%乙醇;(c) 白藜芦醇,灌胃 50mg/kg;(d) CrO,腹腔内注射 20mg/kg;(e) 白藜芦醇+CrO,CrO 注射前 4 小时给予白藜芦醇。外周血进行评估。微核(MN)动力学从 0 到 72 小时测量,而 8-羟基脱氧鸟苷(8-OHdG)加合物修复水平、内源性抗氧化系统生物标志物和凋亡频率在 48 小时后定量。白藜芦醇降低 Cr(VI)诱导的 MN 频率,并对 8-OHdG 加合物水平表现出显著影响,表明这种多酚可以增强细胞修复。同时给予白藜芦醇和 Cr(VI)可使谷胱甘肽过氧化物酶和过氧化氢酶的活性恢复到对照水平,并伴有超氧化物歧化酶活性和谷胱甘肽水平的改变。因此,抗氧化特性可能在白藜芦醇介导的抑制 Cr(VI)诱导的氧化遗传毒性中发挥重要作用。凋亡细胞的增加和坏死细胞的减少进一步证实了白藜芦醇有效地阻止了 Cr(VI)的作用。