• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

特定近红外光波长对细胞色素 c 氧化酶活性的抑制调节可减轻脑缺血/再灌注损伤。

Inhibitory modulation of cytochrome c oxidase activity with specific near-infrared light wavelengths attenuates brain ischemia/reperfusion injury.

机构信息

Department of Emergency Medicine, Wayne State University School of Medicine, Detroit, MI, 48201, USA.

Department of Emergency Medicine, University of Michigan Medical School, Ann Arbor, MI, 48109, USA.

出版信息

Sci Rep. 2018 Feb 22;8(1):3481. doi: 10.1038/s41598-018-21869-x.

DOI:10.1038/s41598-018-21869-x
PMID:29472564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5823933/
Abstract

The interaction of light with biological tissue has been successfully utilized for multiple therapeutic purposes. Previous studies have suggested that near infrared light (NIR) enhances the activity of mitochondria by increasing cytochrome c oxidase (COX) activity, which we confirmed for 810 nm NIR. In contrast, scanning the NIR spectrum between 700 nm and 1000 nm revealed two NIR wavelengths (750 nm and 950 nm) that reduced the activity of isolated COX. COX-inhibitory wavelengths reduced mitochondrial respiration, reduced the mitochondrial membrane potential (ΔΨ), attenuated mitochondrial superoxide production, and attenuated neuronal death following oxygen glucose deprivation, whereas NIR that activates COX provided no benefit. We evaluated COX-inhibitory NIR as a potential therapy for cerebral reperfusion injury using a rat model of global brain ischemia. Untreated animals demonstrated an 86% loss of neurons in the CA1 hippocampus post-reperfusion whereas inhibitory NIR groups were robustly protected, with neuronal loss ranging from 11% to 35%. Moreover, neurologic function, assessed by radial arm maze performance, was preserved at control levels in rats treated with a combination of both COX-inhibitory NIR wavelengths. Taken together, our data suggest that COX-inhibitory NIR may be a viable non-pharmacologic and noninvasive therapy for the treatment of cerebral reperfusion injury.

摘要

光与生物组织的相互作用已成功地用于多种治疗目的。先前的研究表明,近红外光(NIR)通过增加细胞色素 c 氧化酶(COX)活性来增强线粒体的活性,我们已经证实了 810nm NIR 的这种作用。相比之下,扫描 700nm 至 1000nm 之间的 NIR 光谱发现了两个 NIR 波长(750nm 和 950nm),它们降低了分离的 COX 的活性。COX 抑制波长降低了线粒体呼吸,降低了线粒体膜电位(ΔΨ),减弱了线粒体超氧化物的产生,并减轻了氧葡萄糖剥夺后神经元的死亡,而激活 COX 的 NIR 则没有益处。我们使用全脑缺血大鼠模型评估了 COX 抑制性 NIR 作为脑再灌注损伤的潜在治疗方法。未经治疗的动物在再灌注后 CA1 海马区的神经元损失了 86%,而抑制性 NIR 组则得到了强有力的保护,神经元损失范围为 11%至 35%。此外,通过放射臂迷宫性能评估的神经功能在接受两种 COX 抑制性 NIR 波长联合治疗的大鼠中保持在对照水平。总之,我们的数据表明,COX 抑制性 NIR 可能是治疗脑再灌注损伤的一种可行的非药物和非侵入性治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/6ef9fe5eee8e/41598_2018_21869_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/d9a03f195a02/41598_2018_21869_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/4244e0373012/41598_2018_21869_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/4d54d68dfa62/41598_2018_21869_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/64d54d8f4ac6/41598_2018_21869_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/1f08c88f44ef/41598_2018_21869_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/6ef9fe5eee8e/41598_2018_21869_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/d9a03f195a02/41598_2018_21869_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/4244e0373012/41598_2018_21869_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/4d54d68dfa62/41598_2018_21869_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/64d54d8f4ac6/41598_2018_21869_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/1f08c88f44ef/41598_2018_21869_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea6/5823933/6ef9fe5eee8e/41598_2018_21869_Fig6_HTML.jpg

相似文献

1
Inhibitory modulation of cytochrome c oxidase activity with specific near-infrared light wavelengths attenuates brain ischemia/reperfusion injury.特定近红外光波长对细胞色素 c 氧化酶活性的抑制调节可减轻脑缺血/再灌注损伤。
Sci Rep. 2018 Feb 22;8(1):3481. doi: 10.1038/s41598-018-21869-x.
2
Non-invasive treatment with near-infrared light: A novel mechanisms-based strategy that evokes sustained reduction in brain injury after stroke.近红外光无创治疗:一种基于新机制的策略,可引发中风后脑损伤的持续减少。
J Cereb Blood Flow Metab. 2020 Apr;40(4):833-844. doi: 10.1177/0271678X19845149. Epub 2019 May 21.
3
Modulation of mitochondrial function with near-infrared light reduces brain injury in a translational model of cardiac arrest.近红外光调节线粒体功能可减轻心脏骤停转化模型中的脑损伤。
Crit Care. 2023 Dec 14;27(1):491. doi: 10.1186/s13054-023-04745-7.
4
Cytochrome c oxidase-modulatory near-infrared light penetration into the human brain: Implications for the noninvasive treatment of ischemia/reperfusion injury.细胞色素 c 氧化酶调节近红外光穿透人脑:对缺血/再灌注损伤的非侵入性治疗的影响。
IUBMB Life. 2021 Mar;73(3):554-567. doi: 10.1002/iub.2405. Epub 2020 Nov 9.
5
Near infrared radiation rescues mitochondrial dysfunction in cortical neurons after oxygen-glucose deprivation.近红外辐射可挽救氧糖剥夺后皮质神经元的线粒体功能障碍。
Metab Brain Dis. 2015 Apr;30(2):491-6. doi: 10.1007/s11011-014-9515-6. Epub 2014 Mar 6.
6
Clinical and experimental applications of NIR-LED photobiomodulation.近红外发光二极管光生物调节的临床与实验应用
Photomed Laser Surg. 2006 Apr;24(2):121-8. doi: 10.1089/pho.2006.24.121.
7
Hydrogen-rich saline attenuates neuronal ischemia--reperfusion injury by protecting mitochondrial function in rats.富氢盐水通过保护大鼠线粒体功能减轻神经元缺血-再灌注损伤。
J Surg Res. 2014 Dec;192(2):564-72. doi: 10.1016/j.jss.2014.05.060. Epub 2014 May 24.
8
Effect of the NADPH oxidase inhibitor apocynin on ischemia-reperfusion hippocampus injury in rat brain.缺血再灌注海马损伤中 NADPH 氧化酶抑制剂夹竹桃麻素的作用。
Biomed Pharmacother. 2018 Jan;97:458-472. doi: 10.1016/j.biopha.2017.10.123. Epub 2017 Nov 6.
9
Postconditioning mitigates cell death following oxygen and glucose deprivation in PC12 cells and forebrain reperfusion injury in rats.后适应减轻PC12细胞氧糖剥夺后的细胞死亡以及大鼠前脑再灌注损伤。
J Neurosci Res. 2015 Jan;93(1):140-8. doi: 10.1002/jnr.23460. Epub 2014 Jul 31.
10
Effect of Red-to-Near Infrared Light on the Reaction of Isolated Cytochrome c Oxidase with Cytochrome c.红光至近红外光对分离的细胞色素c氧化酶与细胞色素c反应的影响。
Photomed Laser Surg. 2016 Dec;34(12):631-637. doi: 10.1089/pho.2015.4042. Epub 2016 Apr 25.

引用本文的文献

1
Accelerated Molecular Transportation in the Brain Extracellular Space with 755-nm Light Attenuates Post-Stroke Cognitive Impairment in Rats.755纳米光加速大鼠脑外间隙分子转运可减轻中风后认知障碍
Cyborg Bionic Syst. 2025 May 6;6:0262. doi: 10.34133/cbsystems.0262. eCollection 2025.
2
Photobiomodulation: shining a light on depression.光生物调节疗法:照亮抑郁症的治疗之路
Theranostics. 2025 Jan 1;15(2):362-383. doi: 10.7150/thno.104502. eCollection 2025.
3
Potential and Challenges of Transcranial Photobiomodulation for the Treatment of Stroke.

本文引用的文献

1
Mitochondrial dynamics following global cerebral ischemia.全脑缺血后的线粒体动力学
Mol Cell Neurosci. 2016 Oct;76:68-75. doi: 10.1016/j.mcn.2016.08.010. Epub 2016 Aug 25.
2
Interplay between up-regulation of cytochrome-c-oxidase and hemoglobin oxygenation induced by near-infrared laser.近红外激光诱导的细胞色素 c-氧化酶上调与血红蛋白氧合之间的相互作用。
Sci Rep. 2016 Aug 3;6:30540. doi: 10.1038/srep30540.
3
Neuronal hypoxia disrupts mitochondrial fusion.神经元缺氧会破坏线粒体融合。
经颅光生物调节治疗中风的潜力与挑战
CNS Neurosci Ther. 2024 Dec;30(12):e70142. doi: 10.1111/cns.70142.
4
Regulation of mitochondrial oxidative phosphorylation through tight control of cytochrome c oxidase in health and disease - Implications for ischemia/reperfusion injury, inflammatory diseases, diabetes, and cancer.通过对细胞色素c氧化酶的严格控制来调节线粒体氧化磷酸化在健康与疾病中的作用——对缺血/再灌注损伤、炎症性疾病、糖尿病和癌症的影响
Redox Biol. 2024 Dec;78:103426. doi: 10.1016/j.redox.2024.103426. Epub 2024 Nov 10.
5
Modulation of mitochondrial function with near-infrared light reduces brain injury in a translational model of cardiac arrest.近红外光调节线粒体功能可减轻心脏骤停转化模型中的脑损伤。
Crit Care. 2023 Dec 14;27(1):491. doi: 10.1186/s13054-023-04745-7.
6
Antioxidant effects of LEDT in dystrophic muscle cells: involvement of PGC-1α and UCP-3 pathways.LEDT 在营养不良肌肉细胞中的抗氧化作用:涉及 PGC-1α 和 UCP-3 途径。
Photochem Photobiol Sci. 2024 Jan;23(1):107-118. doi: 10.1007/s43630-023-00506-1. Epub 2023 Dec 6.
7
Mitoquinone Alleviates Donation after Cardiac Death Kidney Injury during Hypothermic Machine Perfusion in Rat Model.甲萘醌减轻低温机器灌注大鼠模型中心脏死亡后供肾损伤。
Int J Mol Sci. 2023 Sep 30;24(19):14772. doi: 10.3390/ijms241914772.
8
Synergistic photobiomodulation with 808-nm and 1064-nm lasers to reduce the β-amyloid neurotoxicity in the Alzheimer's disease models.808纳米和1064纳米激光协同光生物调节以降低阿尔茨海默病模型中的β-淀粉样蛋白神经毒性。
Front Neuroimaging. 2022 Jul 22;1:903531. doi: 10.3389/fnimg.2022.903531. eCollection 2022.
9
Non-invasive treatment of ischemia/reperfusion injury: Effective transmission of therapeutic near-infrared light into the human brain through soft skin-conforming silicone waveguides.缺血/再灌注损伤的无创治疗:通过柔软贴合皮肤的硅胶波导将治疗性近红外光有效传输至人脑。
Bioeng Transl Med. 2023 Feb 7;8(3):e10496. doi: 10.1002/btm2.10496. eCollection 2023 May.
10
Photobiomodulation in Alzheimer's Disease-A Complementary Method to State-of-the-Art Pharmaceutical Formulations and Nanomedicine?阿尔茨海默病中的光生物调节——一种现有药物制剂和纳米医学的补充方法?
Pharmaceutics. 2023 Mar 11;15(3):916. doi: 10.3390/pharmaceutics15030916.
Neuroscience. 2015 Aug 20;301:71-8. doi: 10.1016/j.neuroscience.2015.05.078. Epub 2015 Jun 3.
4
Release of mitochondrial Opa1 following oxidative stress in HT22 cells.氧化应激后HT22细胞中线粒体Opa1的释放。
Mol Cell Neurosci. 2015 Jan;64:116-22. doi: 10.1016/j.mcn.2014.12.007. Epub 2015 Jan 8.
5
Near infrared radiation rescues mitochondrial dysfunction in cortical neurons after oxygen-glucose deprivation.近红外辐射可挽救氧糖剥夺后皮质神经元的线粒体功能障碍。
Metab Brain Dis. 2015 Apr;30(2):491-6. doi: 10.1007/s11011-014-9515-6. Epub 2014 Mar 6.
6
Cytochrome C is tyrosine 97 phosphorylated by neuroprotective insulin treatment.细胞色素 C 是由神经保护作用的胰岛素治疗所磷酸化的酪氨酸 97。
PLoS One. 2013 Nov 5;8(11):e78627. doi: 10.1371/journal.pone.0078627. eCollection 2013.
7
2-vessel occlusion/hypotension: a rat model of global brain ischemia.双血管闭塞/低血压:全脑缺血大鼠模型
J Vis Exp. 2013 Jun 22(76):50173. doi: 10.3791/50173.
8
Molecular mechanisms of ischemia-reperfusion injury in brain: pivotal role of the mitochondrial membrane potential in reactive oxygen species generation.脑缺血再灌注损伤的分子机制:线粒体膜电位在活性氧生成中的关键作用。
Mol Neurobiol. 2013 Feb;47(1):9-23. doi: 10.1007/s12035-012-8344-z. Epub 2012 Sep 26.
9
PKR-like endoplasmic reticulum kinase (PERK) activation following brain ischemia is independent of unfolded nascent proteins.脑缺血后蛋白激酶 R 样内质网激酶 (PERK) 的激活不依赖于未折叠新生蛋白。
Neuroscience. 2010 Sep 1;169(3):1307-14. doi: 10.1016/j.neuroscience.2010.05.076. Epub 2010 Jun 9.
10
Hyperoxic reperfusion after global cerebral ischemia promotes inflammation and long-term hippocampal neuronal death.全脑缺血后再氧化再灌注促进炎症和长期海马神经元死亡。
J Neurotrauma. 2010 Apr;27(4):753-62. doi: 10.1089/neu.2009.1186.