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本文引用的文献

1
Melatonin combats molecular terrorism at the mitochondrial level.褪黑素在线粒体水平对抗分子“恐怖袭击”。
Interdiscip Toxicol. 2008 Sep;1(2):137-49. doi: 10.2478/v10102-010-0030-2.
2
Hyperglycemia-related pathophysiologic mechanisms and potential beneficial actions of melatonin.高血糖相关的病理生理机制及褪黑素的潜在有益作用。
Mini Rev Med Chem. 2008 Oct;8(11):1144-53. doi: 10.2174/138955708785909925.
3
Biogenic amines in the reduction of oxidative stress: melatonin and its metabolites.生物胺在减轻氧化应激中的作用:褪黑素及其代谢产物。
Neuro Endocrinol Lett. 2008 Aug;29(4):391-8.
4
Role of melatonin in the epigenetic regulation of breast cancer.褪黑素在乳腺癌表观遗传调控中的作用。
Breast Cancer Res Treat. 2009 May;115(1):13-27. doi: 10.1007/s10549-008-0103-5. Epub 2008 Jul 1.
5
Antioxidative effects of melatonin administration in elderly primary essential hypertension patients.褪黑素对老年原发性高血压患者的抗氧化作用
J Pineal Res. 2008 Oct;45(3):312-7. doi: 10.1111/j.1600-079X.2008.00592.x. Epub 2008 Mar 25.
6
Oxidative stress impairs oocyte quality and melatonin protects oocytes from free radical damage and improves fertilization rate.氧化应激会损害卵母细胞质量,而褪黑素可保护卵母细胞免受自由基损伤并提高受精率。
J Pineal Res. 2008 Apr;44(3):280-7. doi: 10.1111/j.1600-079X.2007.00524.x.
7
Effects of poly(ADP-ribose) polymerase inhibition in bladder damage caused by cyclophosphamide in rats.聚(ADP - 核糖)聚合酶抑制对环磷酰胺所致大鼠膀胱损伤的影响。
Exp Biol Med (Maywood). 2008 Mar;233(3):338-43. doi: 10.3181/0706-RM-151.
8
Medical implications of melatonin: receptor-mediated and receptor-independent actions.褪黑素的医学意义:受体介导和非受体介导的作用
Adv Med Sci. 2007;52:11-28.
9
Epigenetic regulation: a new research area for melatonin?表观遗传调控:褪黑素的一个新研究领域?
J Pineal Res. 2008 Jan;44(1):41-4. doi: 10.1111/j.1600-079X.2007.00509.x.
10
Melatonin alleviates lung damage induced by the chemical warfare agent nitrogen mustard.褪黑素可减轻化学战剂氮芥所致的肺损伤。
Toxicol Lett. 2007 Sep 10;173(2):124-31. doi: 10.1016/j.toxlet.2007.07.005. Epub 2007 Jul 20.

褪黑素:一种值得用于临床试验的成熟抗氧化剂。

Melatonin: an established antioxidant worthy of use in clinical trials.

作者信息

Korkmaz Ahmet, Reiter Russel J, Topal Turgut, Manchester Lucien C, Oter Sukru, Tan Dun-Xian

机构信息

Department of Physiology, School of Medicine, Gulhane Military Medical Academy, Ankara, Turkey.

出版信息

Mol Med. 2009 Jan-Feb;15(1-2):43-50. doi: 10.2119/molmed.2008.00117. Epub 2008 Nov 4.

DOI:10.2119/molmed.2008.00117
PMID:19011689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2582546/
Abstract

Oxidative stress plays a key role in the pathogenesis of aging and many metabolic diseases; therefore, an effective antioxidant therapy would be of great importance in these circumstances. Nutritional, environmental, and chemical factors can induce the overproduction of the superoxide anion radical in both the cytosol and mitochondria. This is the first and key event that leads to the activation of pathways involved in the development of several metabolic diseases that are related to oxidative stress. As oxidation of essential molecules continues, it turns to nitrooxidative stress because of the involvement of nitric oxide in pathogenic processes. Once peroxynitrite forms, it damages via two distinctive mechanisms. First, it has direct toxic effects leading to lipid peroxidation, protein oxidation, and DNA damage. This mechanism involves the induction of several transcription factors leading to cytokine-induced chronic inflammation. Classic antioxidants, including vitamins A, C, and E, have often failed to exhibit beneficial effects in metabolic diseases and aging. Melatonin is a multifunctional indolamine that counteracts virtually all pathophysiologic steps and displays significant beneficial actions against peroxynitrite-induced cellular toxicity. This protection is related to melatonin's antioxidative and antiinflammatory properties. Melatonin has the capability of scavenging both oxygen- and nitrogen-based reactants, including those formed from peroxynitrite, and blocking transcriptional factors, which induce proinflammatory cytokines. Accumulating evidence suggests that this nontoxic indolamine may be useful either as a sole treatment or in conjunction with other treatments for inhibiting the biohazardous actions of nitrooxidative stress.

摘要

氧化应激在衰老及多种代谢性疾病的发病机制中起关键作用;因此,在这些情况下有效的抗氧化治疗至关重要。营养、环境和化学因素可诱导胞质溶胶和线粒体中超氧阴离子自由基的过量产生。这是导致与氧化应激相关的几种代谢性疾病发生发展的相关途径激活的首个关键事件。随着必需分子的氧化持续进行,由于一氧化氮参与致病过程,进而转变为硝基氧化应激。一旦过氧亚硝酸盐形成,它会通过两种独特机制造成损害。首先,它具有直接毒性作用,导致脂质过氧化、蛋白质氧化和DNA损伤。这种机制涉及多种转录因子的诱导,导致细胞因子诱导的慢性炎症。包括维生素A、C和E在内的传统抗氧化剂在代谢性疾病和衰老中往往未能显示出有益效果。褪黑素是一种多功能吲哚胺,几乎可抵消所有病理生理步骤,并对过氧亚硝酸盐诱导的细胞毒性表现出显著的有益作用。这种保护作用与褪黑素的抗氧化和抗炎特性有关。褪黑素能够清除基于氧和氮的反应物,包括由过氧亚硝酸盐形成的反应物,并阻断诱导促炎细胞因子的转录因子。越来越多的证据表明,这种无毒吲哚胺单独使用或与其他治疗联合使用,可能有助于抑制硝基氧化应激的生物危害作用。