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本文引用的文献

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The relationship between antioxidant enzymes and lipid peroxidation in senescent rat erythrocytes.衰老大鼠红细胞中抗氧化酶与脂质过氧化之间的关系。
Physiol Res. 2015;64(6):891-6. doi: 10.33549/physiolres.932890. Epub 2015 Jun 5.
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Peroxiredoxin 2, glutathione peroxidase, and catalase in the cytosol and membrane of erythrocytes under H2O2-induced oxidative stress.过氧化氢诱导氧化应激下红细胞胞质和膜中的过氧化物酶2、谷胱甘肽过氧化物酶和过氧化氢酶
Free Radic Res. 2015;49(8):990-1003. doi: 10.3109/10715762.2015.1028402. Epub 2015 Apr 24.
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Glutathione transferases and neurodegenerative diseases.谷胱甘肽转移酶与神经退行性疾病
Neurochem Int. 2015 Mar;82:10-8. doi: 10.1016/j.neuint.2015.01.008. Epub 2015 Feb 7.
4
[The correlations between aging of the human body, oxidative stress and reduced efficiency of repair systems].[人体衰老、氧化应激与修复系统效率降低之间的相关性]
Postepy Hig Med Dosw (Online). 2014 Dec 15;68:1483-91. doi: 10.5604/17322693.1132010.
5
Epigallocatechin-3-Gallate Protects Erythrocyte Ca(2+)-ATPase and Na(+)/K(+)-ATPase Against Oxidative Induced Damage During Aging in Humans.表没食子儿茶素-3-没食子酸酯可保护人体衰老过程中红细胞的Ca(2+)-ATP酶和Na(+)/K(+)-ATP酶免受氧化诱导的损伤。
Adv Pharm Bull. 2014 Oct;4(Suppl 1):443-7. doi: 10.5681/apb.2014.065. Epub 2014 Aug 25.
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Additive solution-7 reduces the red blood cell cold storage lesion.添加剂溶液-7可减轻红细胞冷藏损伤。
Transfusion. 2015 Mar;55(3):491-8. doi: 10.1111/trf.12867. Epub 2014 Sep 19.
7
Relative importance of redox buffers GSH and NAD(P)H in age-related neurodegeneration and Alzheimer disease-like mouse neurons.氧化还原缓冲剂谷胱甘肽(GSH)和烟酰胺腺嘌呤二核苷酸(磷酸)(NAD(P)H)在与年龄相关的神经退行性变及阿尔茨海默病样小鼠神经元中的相对重要性。
Aging Cell. 2014 Aug;13(4):631-40. doi: 10.1111/acel.12216. Epub 2014 Mar 21.
8
Naringin mitigates erythrocytes aging induced by paclitaxel: an in vitro study.柚皮苷减轻紫杉醇诱导的红细胞衰老:一项体外研究。
J Biochem Mol Toxicol. 2014 Mar;28(3):129-36. doi: 10.1002/jbt.21544. Epub 2013 Dec 27.
9
Markers of oxidative stress and erythrocyte antioxidant enzyme activity in older men and women with differing physical activity.不同体力活动的老年男性和女性的氧化应激标志物和红细胞抗氧化酶活性。
Exp Gerontol. 2013 Nov;48(11):1141-6. doi: 10.1016/j.exger.2013.07.010. Epub 2013 Jul 30.
10
Membrane peroxidation and methemoglobin formation are both necessary for band 3 clustering: mechanistic insights into human erythrocyte senescence.膜过氧化和高铁血红蛋白形成对于带 3 聚集都是必需的:人类红细胞衰老的机制见解。
Biochemistry. 2013 Aug 27;52(34):5760-9. doi: 10.1021/bi400405p. Epub 2013 Aug 16.

作为人类年龄函数的红细胞氧化应激生物标志物。

Biomarkers of oxidative stress in erythrocytes as a function of human age.

作者信息

Maurya Pawan Kumar, Kumar Prabhanshu, Chandra Pranjal

机构信息

Pawan Kumar Maurya, Interdisciplinary Laboratory of Clinical Neuroscience (LINC), Department of Psychiatry, Federal University of São Paulo, São Paulo 04039-032, Brazil.

出版信息

World J Methodol. 2015 Dec 26;5(4):216-22. doi: 10.5662/wjm.v5.i4.216.

DOI:10.5662/wjm.v5.i4.216
PMID:26713282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4686419/
Abstract

Despite more than 300 theories to explain the aging process, oxidative stress theory offers the best mechanism to explain aging and age related disorders. Several studies has shown the importance of oxidative stress during aging. PubMed, Science Direct and Springer online data bases are taken into consideration to write this mini-review. Human erythrocytes are most abundant and specialized cells in the body. Erythrocytes were extensively studied due to their metabolism and gas transport functions. Recent studies on erythrocytes have provided us detailed information of cell membrane and its structural organization that may help in studying the aging and age associated changes. The susceptibility of an organism is associated with the antioxidant potential of the body. Erythrocytes have potent antioxidant protection consisting of enzymatic and non-enzymatic pathways that counteract with reactive oxygen species, thus maintaining the redox regulation in the body. The non-enzymatic and enzymatic antioxidants and other biomarkers associated with erythrocyte membrane transport functions are the main content of this review. Biomarkers of oxidative stress in erythrocytes and its membrane were taken into the consideration during human aging that will be the main subject of this mini- review.

摘要

尽管有300多种理论来解释衰老过程,但氧化应激理论为解释衰老及与年龄相关的疾病提供了最佳机制。多项研究表明了氧化应激在衰老过程中的重要性。撰写本综述时参考了PubMed、Science Direct和Springer在线数据库。人类红细胞是体内数量最多且特殊的细胞。由于其代谢和气体运输功能,红细胞得到了广泛研究。近期对红细胞的研究为我们提供了关于细胞膜及其结构组织的详细信息,这可能有助于研究衰老及与年龄相关的变化。生物体的易感性与身体的抗氧化潜力有关。红细胞具有强大的抗氧化保护机制,包括酶促和非酶促途径,可与活性氧相互作用,从而维持体内的氧化还原调节。与红细胞膜运输功能相关的非酶促和酶促抗氧化剂及其他生物标志物是本综述的主要内容。人类衰老过程中红细胞及其膜内氧化应激的生物标志物是本综述的主要主题。