[1]王啸华,何敢声,谢林.氧化应激在椎间盘退变中的作用进展[J].中医正骨,2023,35(05):44-48.
点击复制

氧化应激在椎间盘退变中的作用进展()
分享到:

《中医正骨》[ISSN:1001-6015/CN:41-1162/R]

卷:
第35卷
期数:
2023年05期
页码:
44-48
栏目:
综述
出版日期:
2023-05-20

文章信息/Info

作者:
王啸华何敢声谢林
(江苏省中西医结合医院,江苏 南京 210028)
关键词:
椎间盘退化 氧化性应激 综述
摘要:
椎间盘退变是引起腰痛的主要原因,但其确切的发病机制尚不清楚。目前研究已证实,椎间盘退变的发生与机械载荷异常、免疫异常、代谢紊乱和氧化应激等因素密切相关。近年来,关于氧化应激在椎间盘退变中的作用备受学术界关注。本文对椎间盘的解剖结构以及氧化应激的含义与作用机制进行了概述,对氧化应激在椎间盘退变中的作用进行了综述,并对以抗氧化应激为靶点治疗椎间盘退变的前景进行了展望,以期为椎间盘退变的诊疗提供新思路。

参考文献/References:

[1] GBD 2019 Diseases and Injuries Collaborators.Global burden of 369 diseases and injuries in 204 countries and territories,1990-2019:a systematic analysis for the global burden of disease study 2019[J].Lancet,2020,396(10258):1204-1222.
[2] FRANCISCO V,PINO J,GONZÁLEZ-GAYMÁ,et al.A new immunometabolic perspective of intervertebral disc degeneration[J].Nat Rev Rheumatol,2022,18(1):47-60.
[3] BAO X,WANG Z,JIA Q,et al.HIF-1α-Mediated miR-623 regulates apoptosis and inflammatory responses of nucleus pulposus induced by oxidative stress via targeting TXNIP[J/OL].Oxid Med Cell Longev,2021,2021:6389568[2023-01-20].https://pubmed.ncbi.nlm.nih.gov/34394829/.
[4] MCDONNELL E E,BUCKLEY C T.Consolidating and re-evaluating the human disc nutrient microenvironment[J].J Spine,2022,5(1):e1192.
[5] XIAN D,GUO M,XU J,et al.Current evidence to support the therapeutic potential of flavonoids in oxidative stress-related dermatoses[J].Redox Rep,2021,26(1):134-146.
[6] CHENG Y,YANG H,HAI Y,et al.Scientific literature landscape analysis of researches on oxidative stress in intervertebral disc degeneration in web of science[J].Front Mol Biosci,2022,9:989627.
[7] CHE H,LI J,LI Y,et al.p16 deficiency attenuates intervertebral disc degeneration by adjusting oxidative stress and nucleus pulposus cell cycle[J].Elife,2020,9:e52570.
[8] LU Y,ZHOU L,HE S,et al.Lycopene alleviates disc degeneration under oxidative stress through the Nrf2 signaling pathway[J].Mol Cell Probes,2020,51:101559.
[9] ZEROVNIK E,VENTURA S,KOPITAR-JERALA N.Special issue:“inflammation,oxidative stress and protein aggregation; any links?”[J].Cells,2020,9(11):2461.
[10] WANG L,HE T,LIU J,et al.Revealing the immune infiltration landscape and identifying diagnostic biomarkers for lumbar disc herniation[J].Front Immunol,2021,12:666355.
[11] PARK M S,LEE H M,HAHN S B,et al.The association of the activation-inducible tumor necrosis factor receptor and ligand with lumbar disc herniation[J].Yonsei Med J,2007,48(5):839-846.
[12] XIA C,ZENG Z,FANG B,et al.Mesenchymal stem cell-derived exosomes ameliorate intervertebral disc degeneration via anti-oxidant and anti-inflammatory effects[J].Free Radic Biol Med,2019,143:1-15.
[13] FENG C,YANG M,LAN M,et al.ROS:crucial intermediators in the pathogenesis of intervertebral disc degenera-tion[J/OL].Oxid Med Cell Longev,2017,2017:5601593[2023-01-20].https://pubmed.ncbi.nlm.nih.gov/28392887/.
[14] SUZUKI S,FUJITA N,HOSOGANE N,et al.Excessive reactive oxygen species are therapeutic targets for intervertebral disc degeneration[J].Arthritis Res Ther,2015,17:316.
[15] QUAN M,HONG M W,KO M S,et al.Relationships between disc degeneration and autophagy expression in human nucleus pulposus[J].Orthop Surg,2020,12(1):312-320.
[16] JIANG L,ZHANG X,ZHENG X,et al.Apoptosis,senescence,and autophagy in rat nucleus pulposus cells:implications for diabetic intervertebral disc degeneration[J].J Orthop Res,2013,31(5):692-702.
[17] LIU Z,HUANG Y,JIAO Y,et al.Polystyrene nanoplastic induces ROS production and affects the MAPK-HIF-1/NFkB-mediated antioxidant system in Daphnia pulex[J/OL].Aquat Toxicol,2020,220:105420[2023-01-20].https://pubmed.ncbi.nlm.nih.gov/31986404/.
[18] TANG Z,HU B,ZANG F,et al.Nrf2 drives oxidative stress-induced autophagy in nucleus pulposus cells via a Keap1/Nrf2/p62 feedback loop to protect intervertebral disc from degeneration[J].Cell Death Dis,2019,10(7):510.
[19] HU S,ZHANG C,QIAN T,et al.Promoting Nrf2/Sirt3-dependent mitophagy suppresses apoptosis in nucleus pulposus cells and protects against intervertebral disc degeneration[J/OL].Oxid Med Cell Longev,2021,2021:6694964[2023-01-20].https://pubmed.ncbi.nlm.nih.gov/34211633/.
[20] LIANG D,HONG D,TANG F,et al.Upregulated lnc HRK 2:1 prompts nucleus pulposus cell senescence in intervertebral disc degeneration[J].Mol Med Rep,2020,22(6):5251-5261.
[21] NOVAIS E J,DIEKMAN B O,SHAPIRO I M,et al.p16Ink4adeletion in cells of the intervertebral disc affects their matrix homeostasis and senescence associated secretory phenotype without altering onset of senescence[J].Matrix Biol,2019,82:54-70.
[22] FENG C,LIU H,YANG M,et al.Disc cell senescence in intervertebral disc degeneration:causes and molecular pathways[J].Cell Cycle,2016,15(13):1674-1684.
[23] CHE H,LI J,LI Y,et al.p16 deficiency attenuates intervertebral disc degeneration by adjusting oxidative stress and nucleus pulposus cell cycle[J].Elife,2020,9:e52570.
[24] PATIL P,FALABELLA M,SAEED A,et al.Oxidative stress-induced senescence markedly increases disc cell bioenergetics[J].Mech Ageing Dev,2019,180:97-106.
[25] 王雁秋.Nrf2抑制氧化应激所致髓核细胞凋亡和衰老的实验研究[D].重庆:陆军军医大学,2020.
[26] CHEN J W,NI B B,LI B,et al.The responses of autophagy and apoptosis to oxidative stress in nucleus pulposus cells:implications for disc degeneration[J].Cell Physiol Biochem,2014,34(4):1175-1189.
[27] 尹思,杜恒,赵为公,等.阻断双侧终板营养途径构建山羊椎间盘退变模型[J].临床骨科杂志,2020,23(1):145-150.
[28] YURUBE T,BUCHSER W J,MOON H J,et al.Serum and nutrient deprivation increase autophagic flux in intervertebral disc annulus fibrosus cells:an in vitro experimental study[J].Eur Spine J,2019,28(5):993-1004.
[29] ZUO R,WANG Y,LI J,et al.Rapamycin induced autophagy inhibits inflammation-mediated endplate degeneration by enhancing Nrf2/Keap1 signaling of cartilage endplate stem cells[J].Stem Cells,2019,37(6):828-840.
[30] KANG L,LIU S,LI J,et al.Parkin and Nrf2 prevent oxidative stress-induced apoptosis in intervertebral endplate chondrocytes via inducing mitophagy and anti-oxidant defensesv[J].Life Sci,2020,243:117244.
[31] WANG H,JIANG Z,PANG Z,et al.Acacetin alleviates inflammation and matrix degradation in nucleus pulposus cells and ameliorates intervertebral disc degeneration in vivo[J].Drug Des Devel Ther,2020,14:4801-4813.
[32] YU C,LI D,WANG C,et al.Injectable kartogenin and apocynin loaded micelle enhances the alleviation of intervertebral disc degeneration by adipose-derived stem cell[J].Bioact Mater,2021,6(10):3568-3579.
[33] 蔡同川,张亮.白藜芦醇与椎间盘退变性疾病[J].国际骨科学杂志,2021,42(1):22-25.
[34] CHEN D,XIA D,PAN Z,et al.Metformin protects against apoptosis and senescence in nucleus pulposus cells and ameliorates disc degeneration in vivo[J].Cell Death Dis,2016,7(10):e2441.
[35] KRUPKOVA O,HANDA J,HLAVNA M,et al.The natural polyphenol epigallocatechin gallate protects intervertebral disc cells from oxidative stressv[J/OL].Oxid Med Cell Longev,2016,2016:7031397[2023-01-20].https://pubmed.ncbi.nlm.nih.gov/27119009/.
[36] LIU Q,WANG X,HUA Y,et al.Estrogen deficiency exacerbates intervertebral disc degeneration induced by spinal instability in rats[J].Spine(Phila Pa 1976),2019,44(9):E510-519.
[37] XIA C,ZENG Z,FANG B,et al.Mesenchymal stem cell-derived exosomes ameliorate intervertebral disc degeneration via anti-oxidant and anti-inflammatory effects[J].Free Radic Biol Med,2019,143:1-15.
[38] HU Y,TAO R,WANG L,et al.Exosomes derived from bone mesenchymal stem cells alleviate compression-induced nucleus pulposus cell apoptosis by inhibiting oxidative stress[J/OL].Oxid Med Cell Longev,2021,2021:2310025[2023-01-20].https://pubmed.ncbi.nlm.nih.gov/34733401/.

相似文献/References:

[1]刘晨,李兴勇,姚兴璋,等.绝经后骨质疏松症的流行病学概况及发病机制研究进展[J].中医正骨,2018,30(03):52.
[2]桑廷瑞,王想福,李晨旭,等.腰椎间盘突出症中医证候与Pfirrmann分级的关系探讨[J].中医正骨,2022,34(02):51.
[3]田增辉,陈云刚,李颖颖,等.干细胞外泌体治疗椎间盘退变作用机制的研究进展[J].中医正骨,2022,34(12):56.
[4]王啸华,谢林.椎间盘退变的生物疗法研究进展[J].中医正骨,2023,35(07):40.
[5]王晨宇,陈双,孙道喜,等.中药延缓终板软骨细胞退变相关信号通路的研究进展[J].中医正骨,2023,35(08):57.
[6]雷尚文,元宝华,刘学睿,等.中医药疗法治疗运动性骨骼肌损伤作用机制的研究进展[J].中医正骨,2024,36(1):57.

备注/Memo

备注/Memo:
基金项目:江苏省中医药科技发展计划项目(ZD202008) 通讯作者:谢林 E-mail:xielin@njucm.edu.cn
更新日期/Last Update: 1900-01-01