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本文引用的文献

1
Short and long term prognosis in perinatal asphyxia: An update.围产期窒息的短期和长期预后:最新进展
World J Clin Pediatr. 2016 Feb 8;5(1):67-74. doi: 10.5409/wjcp.v5.i1.67.
2
Molecular hydrogen regulates gene expression by modifying the free radical chain reaction-dependent generation of oxidized phospholipid mediators.分子氢通过修饰依赖自由基链反应生成的氧化磷脂介质来调节基因表达。
Sci Rep. 2016 Jan 7;6:18971. doi: 10.1038/srep18971.
3
Neuroprotective potential of molecular hydrogen against perinatal brain injury via suppression of activated microglia.分子氢通过抑制活化小胶质细胞对围产期脑损伤的神经保护潜力。
Free Radic Biol Med. 2016 Feb;91:154-63. doi: 10.1016/j.freeradbiomed.2015.12.015. Epub 2015 Dec 22.
4
Global neurotrauma research challenges and opportunities.全球神经创伤研究的挑战与机遇。
Nature. 2015 Nov 19;527(7578):S193-7. doi: 10.1038/nature16035.
5
Maternal molecular hydrogen administration on lipopolysaccharide-induced mouse fetal brain injury.母体分子氢给药对脂多糖诱导的胎鼠脑损伤的影响。
J Clin Biochem Nutr. 2015 Nov;57(3):178-82. doi: 10.3164/jcbn.15-90. Epub 2015 Oct 21.
6
Molecular hydrogen inhibits lipopolysaccharide-triggered NLRP3 inflammasome activation in macrophages by targeting the mitochondrial reactive oxygen species.分子氢通过靶向线粒体活性氧抑制巨噬细胞中脂多糖触发的NLRP3炎性小体激活。
Biochim Biophys Acta. 2016 Jan;1863(1):50-5. doi: 10.1016/j.bbamcr.2015.10.012. Epub 2015 Oct 18.
7
Beneficial biological effects and the underlying mechanisms of molecular hydrogen - comprehensive review of 321 original articles.分子氢的有益生物学效应及其潜在机制——321篇原创文章的综合综述
Med Gas Res. 2015 Oct 19;5:12. doi: 10.1186/s13618-015-0035-1. eCollection 2015.
8
Oxidative stress and Parkinson's disease.氧化应激与帕金森病
Front Neuroanat. 2015 Jul 8;9:91. doi: 10.3389/fnana.2015.00091. eCollection 2015.
9
Hydrogen-Rich Saline Attenuated Subarachnoid Hemorrhage-Induced Early Brain Injury in Rats by Suppressing Inflammatory Response: Possible Involvement of NF-κB Pathway and NLRP3 Inflammasome.富氢盐水通过抑制炎症反应减轻大鼠蛛网膜下腔出血诱导的早期脑损伤:NF-κB通路和NLRP3炎性小体的可能参与
Mol Neurobiol. 2016 Jul;53(5):3462-3476. doi: 10.1007/s12035-015-9242-y. Epub 2015 Jun 20.
10
Simultaneous oral and inhalational intake of molecular hydrogen additively suppresses signaling pathways in rodents.同时口服和吸入分子氢可累加性抑制啮齿动物的信号通路。
Mol Cell Biochem. 2015 May;403(1-2):231-41. doi: 10.1007/s11010-015-2353-y. Epub 2015 Feb 24.

分子氢作为神经保护剂。

Molecular Hydrogen as a Neuroprotective Agent.

机构信息

Biological Process of Aging, Tokyo Metropolitan Institute of Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo 173-0015, Japan.

出版信息

Curr Neuropharmacol. 2017;15(2):324-331. doi: 10.2174/1570159x14666160607205417.

DOI:10.2174/1570159x14666160607205417
PMID:27281176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5412697/
Abstract

Oxidative stress and neuroinflammation cause many neurological disorders. Recently, it has been reported that molecular hydrogen (H2) functions as an antioxidant and anti-inflammatory agent. The routes of H2 administration in animal model and human clinical studies are roughly classified into three types, inhalation of H2 gas, drinking H2-dissolved water, and injection of H2-dissolved saline. This review discusses some of the remarkable progress that has been made in the research of H2 use for neurological disorders, such as cerebrovascular diseases, neurodegenerative disorders, and neonatal brain disorders. Although most neurological disorders are currently incurable, these studies suggest the clinical potential of H2 administration for their prevention, treatment, and mitigation. Several of the potential effectors of H2 will also be discussed, including cell signaling molecules and hormones that are responsible for preventing oxidative stress and inflammation. Nevertheless, further investigation will be required to determine the direct target molecule of H2.

摘要

氧化应激和神经炎症会导致许多神经紊乱。最近有报道称,氢气(H2)可作为一种抗氧化剂和抗炎剂。在动物模型和人体临床研究中,H2 的给药途径大致可分为三种:吸入 H2 气体、饮用 H2 溶解水和注射 H2 溶解生理盐水。本综述讨论了 H2 在治疗神经紊乱方面的一些显著进展,如脑血管疾病、神经退行性疾病和新生儿脑疾病。尽管目前大多数神经紊乱是无法治愈的,但这些研究表明 H2 给药在预防、治疗和缓解这些疾病方面具有临床潜力。还将讨论 H2 的一些潜在效应因子,包括负责预防氧化应激和炎症的细胞信号分子和激素。然而,仍需要进一步研究以确定 H2 的直接靶分子。