Jagiellonian University Medical College, Faculty of Medicine, Chair of Medical Biochemistry, 7 Kopernika St., 31-034 Krakow, Poland.
Jagiellonian University Medical College, Faculty of Health Sciences, Chair of Medical Biology, 7 Kopernika St., 31-034 Krakow, Poland.
Biomolecules. 2020 Apr 9;10(4):574. doi: 10.3390/biom10040574.
The investigations showed changes of the cystathionine γ-lyase (CTH), 3-mercaptopyruvate sulfurtransferase (MPST) and rhodanese (TST) activity and gene expression in the brain, heart, liver, kidney, skeletal muscles and testes in frogs , and in response to Pb, Hg and Cd stress. The results were analyzed jointly with changes in the expression of selected antioxidant enzymes (cytoplasmic and mitochondrial superoxide dismutase, glutathione peroxidase, catalase and thioredoxin reducatase) and with the level of malondialdehyde (a product of lipid peroxidation). The obtained results allowed for confirming the role of sulfurtransferases in the antioxidant protection of tissues exposed to heavy metal ions. Our results revealed different transcriptional responses of the investigated tissues to each of the examined heavy metals. The CTH, MPST and TST genes might be regarded as heavy metal stress-responsive. The CTH gene expression up-regulation was confirmed in the liver (Pb, Hg, Cd) and skeletal muscle (Hg), MPST in the brain (Pb, Hg), kidney (Pb, Cd), skeletal muscle (Pb, Hg,Cd) and TST in the brain (Pb) and kidney (Pb, Hg, Cd). Lead, mercury and cadmium toxicity was demonstrated to affect the glutathione (GSH) and cysteine levels, the concentration ratio of reduced to oxidized glutathione ([GSH]/[GSSG]) and the level of sulfane sulfur-containing compounds, which in case of enhanced reactive oxygen species generation can reveal their antioxidative properties. The present report is the first to widely describe the role of the sulfane sulfur/HS generating enzymes and the cysteine/glutathione system in Pb, Hg and Cd stress in various frog tissues, and to explore the mechanisms mediating heavy metal-related stress.
研究表明,在受到 Pb、Hg 和 Cd 胁迫时,青蛙的大脑、心脏、肝脏、肾脏、骨骼肌和睾丸中的胱硫醚γ-裂解酶(CTH)、3-巯基丙酮酸硫转移酶(MPST)和硫氧还蛋白还原酶(TST)的活性和基因表达都发生了变化。这些结果与选定抗氧化酶(细胞质和线粒体超氧化物歧化酶、谷胱甘肽过氧化物酶、过氧化氢酶和硫氧还蛋白还原酶)的表达变化以及丙二醛(脂质过氧化产物)水平一起进行了分析。研究结果证实了硫转移酶在组织对抗重金属离子的抗氧化保护中的作用。我们的结果揭示了研究的组织对每种被检测重金属的不同转录反应。CTH、MPST 和 TST 基因可能被视为重金属应激反应基因。在肝脏(Pb、Hg、Cd)和骨骼肌(Hg)中证实了 CTH 基因的表达上调,在大脑(Pb、Hg)、肾脏(Pb、Cd)、骨骼肌(Pb、Hg、Cd)和 TST 中证实了 MPST 基因的表达上调,在大脑(Pb)和肾脏(Pb、Hg、Cd)中证实了 TST 基因的表达上调。Pb、Hg 和 Cd 的毒性被证明会影响谷胱甘肽(GSH)和半胱氨酸水平、还原型谷胱甘肽与氧化型谷胱甘肽的浓度比([GSH]/[GSSG])以及含硫烷的化合物的水平,这些化合物在活性氧生成增加的情况下,可以显示其抗氧化特性。本报告首次广泛描述了含硫烷/HS 生成酶和半胱氨酸/谷胱甘肽系统在各种青蛙组织中在 Pb、Hg 和 Cd 胁迫中的作用,并探讨了介导重金属相关应激的机制。