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本文引用的文献

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Preliminary evidence of reductive stress in human cytotoxic T cells following exercise.运动后人类细胞毒性 T 细胞中还原性应激的初步证据。
J Appl Physiol (1985). 2018 Aug 1;125(2):586-595. doi: 10.1152/japplphysiol.01137.2017. Epub 2018 Apr 12.
2
Cell Signaling with Extracellular Thioredoxin and Thioredoxin-Like Proteins: Insight into Their Mechanisms of Action.细胞外硫氧还蛋白和硫氧还蛋白样蛋白的信号转导:对其作用机制的深入了解。
Oxid Med Cell Longev. 2017;2017:8475125. doi: 10.1155/2017/8475125. Epub 2017 Sep 12.
3
Exercise redox biochemistry: Conceptual, methodological and technical recommendations.运动氧化还原生物化学:概念、方法和技术建议。
Redox Biol. 2017 Aug;12:540-548. doi: 10.1016/j.redox.2017.03.022. Epub 2017 Mar 27.
4
Disruption of Membranes of Extracellular Vesicles Is Necessary for ELISA Determination of Urine AQP2: Proof of Disruption and Epitopes of AQP2 Antibodies.细胞外囊泡膜的破坏是尿液AQP2酶联免疫吸附测定所必需的:AQP2抗体的破坏及表位验证
Int J Mol Sci. 2016 Sep 26;17(10):1634. doi: 10.3390/ijms17101634.
5
Extracellular superoxide dismutase is present in secretory vesicles of human neutrophils and released upon stimulation.细胞外超氧化物歧化酶存在于人类中性粒细胞的分泌小泡中,并在受到刺激时释放出来。
Free Radic Biol Med. 2016 Aug;97:478-488. doi: 10.1016/j.freeradbiomed.2016.07.004. Epub 2016 Jul 6.
6
Peroxiredoxin 1 induces inflammatory cytokine response and predicts outcome of cardiogenic shock patients necessitating extracorporeal membrane oxygenation: an observational cohort study and translational approach.过氧化物酶1诱导炎性细胞因子反应并预测需要体外膜肺氧合的心源性休克患者的预后:一项观察性队列研究及转化医学方法
J Transl Med. 2016 May 4;14(1):114. doi: 10.1186/s12967-016-0869-x.
7
Multiple Roles of Peroxiredoxins in Inflammation.过氧化物还原酶在炎症中的多重作用
Mol Cells. 2016 Jan;39(1):60-4. doi: 10.14348/molcells.2016.2341. Epub 2016 Jan 25.
8
Low volume-high intensity interval exercise elicits antioxidant and anti-inflammatory effects in humans.小运动量高强度间歇运动对人体具有抗氧化和抗炎作用。
J Sports Sci. 2016;34(1):1-9. doi: 10.1080/02640414.2015.1035666. Epub 2015 Apr 27.
9
Monitoring changes in thioredoxin and over-oxidised peroxiredoxin in response to exercise in humans.监测人体运动后硫氧还蛋白和过度氧化的过氧化物酶体增殖物激活受体的变化。
Free Radic Res. 2015 Mar;49(3):290-8. doi: 10.3109/10715762.2014.1000890. Epub 2015 Feb 4.
10
Peroxiredoxin 3 has a crucial role in the contractile function of skeletal muscle by regulating mitochondrial homeostasis.过氧化物酶 3 通过调节线粒体稳态在骨骼肌的收缩功能中起着至关重要的作用。
Free Radic Biol Med. 2014 Dec;77:298-306. doi: 10.1016/j.freeradbiomed.2014.09.010. Epub 2014 Sep 16.

运动对人体细胞外氧化还原酶浓度的影响特征。

Characterization of extracellular redox enzyme concentrations in response to exercise in humans.

机构信息

National Centre for Sport and Exercise Medicine, School of Sport, Exercise, and Health Sciences, Loughborough University, Loughborough, United Kingdom.

University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

出版信息

J Appl Physiol (1985). 2019 Sep 1;127(3):858-866. doi: 10.1152/japplphysiol.00340.2019. Epub 2019 Jun 27.

DOI:10.1152/japplphysiol.00340.2019
PMID:31246554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6766710/
Abstract

Redox enzymes modulate intracellular redox balance and are secreted in response to cellular oxidative stress, potentially modulating systemic inflammation. Both aerobic and resistance exercise are known to cause acute systemic oxidative stress and inflammation; however, how redox enzyme concentrations alter in extracellular fluids following bouts of either type of exercise is unknown. Recreationally active men ( = 26, mean ± SD: age 28 ± 8 yr) took part in either: 1) two separate energy-matched cycling bouts: one of moderate intensity (MOD) and a bout of high intensity interval exercise (HIIE) or 2) an eccentric-based resistance exercise protocol (RES). Alterations in plasma (study 1) and serum (study 2) peroxiredoxin (PRDX)-2, PRDX-4, superoxide dismutase-3 (SOD3), thioredoxin (TRX-1), TRX-reductase and interleukin (IL)-6 were assessed before and at various timepoints after exercise. There was a significant increase in SOD3 (+1.5 ng/mL) and PRDX-4 (+5.9 ng/mL) concentration following HIIE only, peaking at 30- and 60-min post-exercise respectively. TRX-R decreased immediately and 60 min following HIIE (-7.3 ng/mL) and MOD (-8.6 ng/mL), respectively. In non-resistance trained men, no significant changes in redox enzyme concentrations were observed up to 48 h following RES, despite significant muscle damage. IL-6 concentration increased in response to all trials, however there was no significant relationship between absolute or exercise-induced changes in redox enzyme concentrations. These results collectively suggest that HIIE, but not MOD or RES increase the extracellular concentration of PRDX-4 and SOD3. Exercise-induced changes in redox enzyme concentrations do not appear to directly relate to systemic changes in IL-6 concentration. Two studies were conducted to characterize changes in redox enzyme concentrations after single bouts of exercise to investigate the emerging association between extracellular redox enzymes and inflammation. We provide evidence that SOD3 and PRDX-4 concentration increased following high-intensity aerobic but not eccentric-based resistance exercise. Changes were not associated with IL-6. The results provide a platform to investigate the utility of SOD3 and PRDX-4 as biomarkers of oxidative stress following exercise.

摘要

氧化还原酶调节细胞内氧化还原平衡,并在细胞氧化应激时分泌,可能调节全身炎症。有氧运动和抗阻运动均已知会引起急性全身氧化应激和炎症;然而,单次运动后氧化还原酶浓度在细胞外液中如何变化尚不清楚。有规律运动的男性(n=26,平均±标准差:年龄 28±8 岁)参与以下两种运动之一:1)两次单独的能量匹配的骑行运动,一次为中等强度(MOD),一次为高强度间歇运动(HIIE),或 2)离心抗阻运动方案(RES)。在运动前和运动后不同时间点评估血浆(研究 1)和血清(研究 2)中过氧化物酶(PRDX)-2、PRDX-4、超氧化物歧化酶-3(SOD3)、硫氧还蛋白(TRX-1)、TRX-还原酶和白细胞介素(IL)-6 的变化。只有 HIIE 后 SOD3(增加 1.5ng/mL)和 PRDX-4(增加 5.9ng/mL)浓度显著增加,分别在运动后 30 和 60 分钟达到峰值。TRX-R 在 HIIE 后立即和 60 分钟(-7.3ng/mL)和 MOD(-8.6ng/mL)时降低。在非抗阻训练的男性中,尽管肌肉损伤明显,但在 RES 后 48 小时内,氧化还原酶浓度没有明显变化。IL-6 浓度随着所有试验而增加,但氧化还原酶浓度的绝对值或运动诱导变化与 IL-6 浓度之间没有显著关系。这些结果表明,高强度有氧运动而非中等强度有氧运动或抗阻运动可增加细胞外 PRDX-4 和 SOD3 的浓度。氧化还原酶浓度的运动诱导变化似乎与 IL-6 浓度的全身变化没有直接关系。进行了两项研究以描述单次运动后氧化还原酶浓度的变化,以研究细胞外氧化还原酶与炎症之间新出现的关联。我们提供的证据表明,高强度有氧运动后 SOD3 和 PRDX-4 浓度增加,但基于离心的抗阻运动后则没有增加。变化与 IL-6 无关。这些结果为研究 SOD3 和 PRDX-4 作为运动后氧化应激的生物标志物的效用提供了一个平台。