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Effect of scuba diving on the oxidant/antioxidant status, SIRT1 and SIRT3 expression in recreational divers after a winter nondive period

机译:水肺潜水对冬季循环后休闲潜水员氧化/抗氧化状态,SIRT1和SIRT3表达的影响

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The aim of this study was to examine the effects of scuba diving on oxidative damage markers in erythrocytes and plasma, antioxidant system in peripheral blood mononuclear cells (PBMCs), as well as sirtuin 1 (SIRT1) and sirtuin 3 (SIRT3) gene expressions in recreational divers after a winter nondive period (at least 5 months). For that purpose, 17 male recreational divers performed an immersion at a depth of 30 m for 30 min. Blood samples were collected immediately before and after diving, 3 and 6 h after diving. Erythrocyte lipid peroxidation measured by thiobarbituric-reactive substances (TBARS) method was significantly increased immediately after diving, but returned to the baseline 6 h after diving, while no significant change was found for plasma TBARS and protein carbonyl derivates in both plasma and erythrocytes. Diving-induced catalase (CAT), superoxide dismutase 2 (SOD2), and consequently total superoxide dismutase (SOD) activities in the PBMC samples (significantly increased immediately after diving, reached the maximum activities 3 h after diving, while 6 h after diving only CAT activity remained significantly increased). No significant change was observed for SOD1 activity and gene expression, as well as SOD2 expression, while CAT and SIRT1 expressions were slightly decreased immediately after diving and 3 h after diving. Interestingly, SIRT3 expression was significantly increased 6 h after diving. In conclusion, after the first dive to 30 m after a nondive season, activation of antioxidant defence was not sufficient to prevent oxidative damage, while SIRT3 upregulation could be a step towards an adaptive response to the diving. ?2018 Informa UK Limited, trading as Taylor & Francis Group.
机译:本研究的目的是检查水肺潜水对红细胞和血浆中氧化损伤标志物的影响,外周血单核细胞(PBMC)中的抗氧化系统,以及Sirtuin 1(SIRT1)和SIRTUIN 3(SIRT3)基因表达冬季疯狂的时期(至少5个月)后休闲休闲潜水员。为此目的,17名雄性娱乐潜水员在30分钟的深度下进行浸入30分钟。在潜水后3和6小时之前和之后立即收集血样。在潜水后立即测量的红细胞脂质过氧化在潜水后立即显着增加,但在潜水后返回基线6小时,同时对血浆和红细胞中的血浆TBAR和蛋白质羰基衍生物没有显着变化。潜水诱导的过氧化氢酶(猫),超氧化物歧化酶2(SOD2),并因此在PBMC样品中的超氧化物歧化酶(SOD)活性(潜水后明显增加,潜水后3小时达到最大的活性,而潜水后6小时猫活动仍然显着增加)。对于SOD1活性和基因表达没有观察到显着的变化,以及SOD2表达,而潜水后患有猫和SIRT1表达略微降低,潜水后3小时。有趣的是,潜水后SIRT3表达明显增加了6小时。总之,在第一次潜水到30米后,在融合季节后,激活抗氧化剂的防御是不足以防止氧化损伤,而SIRT3上调可能是对潜水的适应性反应的一步。 ?2018年Informa UK Limited,贸易为泰勒和弗朗西斯集团。

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