Lovato Fabricio Luís, Teixeira da Rocha João Batista, Dalla Corte Cristiane Lenz
Departamento de Bioquímica e Biologia Molecular, Programa de Pós-graduação em Ciências Biológicas: Bioquímica Toxicológica, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria , Cep 97105-900 Santa Maria, RS, Brazil.
Universidade Federal do Pampa , Campus Caçapava do Sul, Av. Pedro Anunciação, 111, Vila Batista, 96570-000 Caçapava do Sul, RS, Brazil.
Chem Res Toxicol. 2017 May 15;30(5):1134-1144. doi: 10.1021/acs.chemrestox.6b00449. Epub 2017 May 4.
Methylmercury (MeHg) is a ubiquitous and persistent environmental pollutant that induces serious neurotoxic effects. Diphenyl diselenide [(PhSe)], an organoseleno compound, exerts protective effects against MeHg toxicity, although the complete mechanism remains unclear. The aim of this study was to investigate the mechanisms involved in the protective effect of (PhSe) on the toxicity induced by MeHg using wild-type Saccharomyces cerevisiae and mutants with defects in enzymes and proteins of the antioxidant defense system (yap1Δ, ybp1Δ, ctt1Δ, cat1Δ, sod1Δ, sod2Δ, gsh1Δ, gsh2Δ, gtt1Δ, gtt2Δ, gtt3Δ, gpx1Δ, gpx2Δ, trx1Δ, trx2Δ, trx3Δ, and trr2Δ). In the wild-type strain, (PhSe) protected against the growth inhibition, reactive oxygen species production, and decrease in membrane integrity induced by MeHg and restored thiol levels to values indistinguishable from the control. Single deletions of yap1, sod1, sod2, gsh1, gsh2, gpx1, gpx2, trx1, trx2, and trx3 decreased the capacity of (PhSe) to prevent MeHg toxicity in yeast, indicating their involvement in (PhSe) protection. Together, these results suggest a role of (PhSe) in modulating the gene expression of antioxidant enzymes and ABC transporters through the action of the transcription factor YAP1, preventing the oxidative damage caused by MeHg in S. cerevisiae.
甲基汞(MeHg)是一种普遍存在且持久的环境污染物,会引发严重的神经毒性效应。二苯基二硒醚[(PhSe)]是一种有机硒化合物,尽管其完整机制尚不清楚,但它对MeHg毒性具有保护作用。本研究的目的是利用野生型酿酒酵母以及抗氧化防御系统中酶和蛋白质存在缺陷的突变体(yap1Δ、ybp1Δ、ctt1Δ、cat1Δ、sod1Δ、sod2Δ、gsh1Δ、gsh2Δ、gtt1Δ、gtt2Δ、gtt3Δ、gpx1Δ、gpx2Δ、trx1Δ、trx2Δ、trx3Δ和trr2Δ),研究(PhSe)对MeHg诱导的毒性的保护作用机制。在野生型菌株中,(PhSe)可防止MeHg诱导的生长抑制、活性氧生成以及膜完整性降低,并使硫醇水平恢复到与对照无显著差异的值。yap1、sod1、sod2、gsh1、gsh2、gpx1、gpx2、trx1、trx2和trx3的单基因缺失降低了(PhSe)预防酵母中MeHg毒性的能力,表明它们参与了(PhSe)的保护作用。总之,这些结果表明(PhSe)通过转录因子YAP1的作用,在调节抗氧化酶和ABC转运蛋白的基因表达中发挥作用,从而防止酿酒酵母中由MeHg引起的氧化损伤。