Department of Animal Physiology, Faculty of Biotechnology and Food Sciences, Slovak University of Agriculture in Nitra, Nitra, Slovak Republic.
J Environ Sci Health A Tox Hazard Subst Environ Eng. 2020;55(5):585-595. doi: 10.1080/10934529.2020.1717899. Epub 2020 Mar 16.
The objective of present study was to investigate protective potential of resveratrol in TM3 Leydig cells with induced oxidative stress using hydrogen peroxide (HO). Leydig cells experiencing oxidative stress exhibit reduced activities in androgens production, and become hypofunctional with age, which is also related to growing oxidative stress, while resveratrol has received growing attention as a cytoprotective agent. TM3 mouse Leydig cells were cultivated during 24 h in the presence of resveratrol (5, 10, 25, 50 and 100 μM) alone, or in combination with HO (300/600 μM) to induce oxidative stress. Mitochondrial activity was evaluated using MTT test, triple assay was used in order to assess cell viability parameters, intracellular generation of superoxide was determined by the nitroblue-tetrazolium assay, and quantification of steroid hormones was performed by the enzyme- linked immunosorbent assay. Resveratrol alone treatment led to the most significantly improved values of all tested parameters in the cells of experimental group with addition of 10 μM of resveratrol in comparison to the control group. In the case of cells with induced oxidative stress (300 μM HO) resveratrol administration resulted in significantly increased ( < 0.05) metabolic activity, as well as cell membrane integrity at concentration 10 μM. Significantly improved ( < 0.001) lysosomal activity showed cells treated with 5 and 10 μM of resveratrol, and the level of both measured hormones was significantly higher ( < 0.05) in cells supplemented with 10 μM of resveratrol. Significant decline of superoxide radical production was observed in all experimental groups in comparison to the control exposed to HO alone. With respect to cells exposed to higher concentration of HO (600 μM) results showed positive effect of resveratrol only in biosynthesis of both androgens with significant increased values in experimental group treated with 5 μM ( < 0.05) and 10 μM ( < 0.01) of resveratrol, in addition, in the case of testosterone we recorded significant higher ( < 0.05) values in cells with addition of 25 and 50 μM resveratrol when compared to HO control. More specific and systematic research focused especially on androgen biosynthesis is necessary related to the biological activity of resveratrol in male reproductive system due to inconsistent results of studies.
本研究的目的是研究白藜芦醇对过氧化氢(HO)诱导的 TM3 莱迪希细胞氧化应激的保护作用。经历氧化应激的莱迪希细胞雄激素的产生活性降低,并且随着年龄的增长而功能低下,这也与不断增加的氧化应激有关,而白藜芦醇作为一种细胞保护剂受到越来越多的关注。将 TM3 小鼠莱迪希细胞在存在白藜芦醇(5、10、25、50 和 100 μM)的情况下培养 24 小时,单独或与 HO(300/600 μM)一起诱导氧化应激。使用 MTT 试验评估线粒体活性,使用三联测定法评估细胞活力参数,通过硝基蓝四唑试验测定细胞内超氧阴离子的产生,通过酶联免疫吸附试验测定类固醇激素的定量。与对照组相比,单独添加 10 μM 白藜芦醇的实验组细胞的所有测试参数的改善值最为显著。在诱导氧化应激(300 μM HO)的情况下,添加白藜芦醇导致代谢活性和细胞膜完整性显著增加(<0.05),浓度为 10 μM。用 5 和 10 μM 白藜芦醇处理的细胞显示出显著改善的(<0.001)溶酶体活性,并且补充 10 μM 白藜芦醇的细胞中两种测量激素的水平均显著升高(<0.05)。与单独暴露于 HO 的对照组相比,所有实验组的超氧自由基产生均显著下降。对于暴露于更高浓度 HO(600 μM)的细胞,仅在雄激素的生物合成中观察到白藜芦醇的积极作用,用 5 μM(<0.05)和 10 μM(<0.01)白藜芦醇处理的实验组值显著增加,此外,在睾酮的情况下,与 HO 对照组相比,添加 25 和 50 μM 白藜芦醇的细胞记录到显著更高的(<0.05)值。由于研究结果不一致,因此需要针对男性生殖系统中白藜芦醇的生物学活性进行更具体和系统的研究,特别是雄激素生物合成。