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低氧预处理与高氧预处理在脊髓损伤后神经保护作用的相关研究进展

  • 张雯秀 ,
  • 张妍 ,
  • 张衍军 ,
  • 吴启超 ,
  • 刘亚东 ,
  • 刘宗建 ,
  • 关云 ,
  • 陈学明
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  • 1.首都医科大学附属北京潞河医院,a.中心实验室,b.脊柱外科,北京市101149
张雯秀(1989-),女,汉族,四川乐山市人,实习研究员,主要研究方向:药物及物理方法治疗大鼠脊髓损伤的应用研究。

收稿日期: 2017-09-05

  修回日期: 2017-12-04

  网络出版日期: 2018-01-31

Research Related to Neural Protection of Hypoxic and Hyperoxic Preconditioning after Spinal Cord Injury (review)

  • ZHANG Wen-xiu ,
  • ZHANG Yan ,
  • ZHANG Yan-jun ,
  • WU Qi-chao ,
  • LIU Ya-dong ,
  • LIU Zong-jian ,
  • GUAN Yun ,
  • CHEN Xue-ming
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  • 1. a. Central Laboratory, b. Spine Surgery, Beijing Luhe Hospital, Capital Medical University, Beijing 100191, China

Received date: 2017-09-05

  Revised date: 2017-12-04

  Online published: 2018-01-31

摘要

重复急性间歇性低氧能够增加运动神经元中生长因子与营养因子的表达,在突触可塑性和神经保护中改变关键分子的表达。低氧预处理能有效提高干细胞移植后的存活率,并对神经功能具有保护作用。间歇性低氧也是急性脊髓损伤后增强呼吸运动的方法之一。高压氧预处理能增强中枢神经对缺氧及缺血的耐受性,有效保护细胞、组织结构,缩短神经细胞的再生周期,促进神经纤维再生。有必要进一步探讨低氧及高氧预处理在脊髓损伤中的作用机制。

本文引用格式

张雯秀 , 张妍 , 张衍军 , 吴启超 , 刘亚东 , 刘宗建 , 关云 , 陈学明 . 低氧预处理与高氧预处理在脊髓损伤后神经保护作用的相关研究进展[J]. 中国康复理论与实践, 2018 , 24(1) : 90 -92 . DOI: 10.3969/j.issn.1006-9771.2018.01.017

Abstract

Repeated acute intermittent hypoxia promotes the expression of growth factors and neurotrophic factors, as well as the key molecules for neural protection and plasticity. Hypoxic preconditioning may improve the survival rate of transplanted stem cells and protect the neural function. Meanwhile, acute intermittent hypoxia can be an approach to improve respiratory function after spinal cord injury. Hyperbaric oxygen may improve the neural tolerance to hypoxia and ischemia, to protect the structure of cells and tissues, and promote the neuranagenesis. It is important to study the role of hypoxic and hyperoxic preconditioning in spinal cord injury.

参考文献

[1] Barnabé-Heider F, Göritz C, Sabelström H, et al. Origin of new glial cells in intact and injured adult spinal cord [J]. Cell Stem Cell, 2010, 7(4): 470-482.
[2] Gonzalez R, Glaser J, Liu MT, et al. Reducing inflammation decreases secondary degeneration and functional deficit after spinal cord injury [J]. Exp Neurol, 2003, 184(1): 456-463.
[3] Hu R, Zhou J, Luo C, et al. Glial scar and neuroregeneration: histological, functional, and magnetic resonance imaging analysis in chronic spinal cord injury [J]. J Neurosurg spine, 2010, 13(2): 169-180.
[4] Satriotomo I, Nichols NL, Dale EA, et al. Repetitive acute intermittent hypoxia increases growth/neurotrophic factor expression in non-respiratory motor neurons [J]. Neuroscience, 2016, 322: 479-488.
[5] Prabhakar NR. Sensory plasticity of the carotid body: role of reactive oxygen species and physiological significance [J]. Respir Physiol Neurobiol, 2011, 178(3): 375-380.
[6] Kline DD. Chronic intermittent hypoxia affects integration of sensory input by neurons in the nucleus tractussolitarii [J]. Respir Physiol Neurobiol, 2010, 174(1-2): 29-36.
[7] Baker-Herman TL, Fuller DD, Bavis RW, et al. BDNF is necessary and sufficient for spinal respiratory plasticity following intermittent hypoxia [J]. Nat Neurosci, 2004, 7(1): 48-55.
[8] Lovett-Barr MR, Satriotomo I, Muir GD, et al. Repetitive intermittent hypoxia induces respiratory and somatic motor recovery after chronic cervical injury [J]. J Neurosci, 2012,32(11): 3591-3600.
[9] Satriotomo I, Dale EA, Dahlberg JM, et al. Repetitive acute intermittent hypoxia increases expression of proteins associated with plasticity in the phrenic motor nucleus [J]. Exp Neurol, 2012, 237(1): 103-115.
[10] Prosser-Loose EJ, Hassan A, Mitchell GS, et al. Delayed intervention with intermittent hypoxia and training task improves forelimb function in a rat model of cervical spinal injury [J]. J Neurotrauma, 2015, 32(18): 1403-1412.
[11] Kafitz KW, Rose CR, Thoenen H, et al. Neurotrophin evoked rapid excitation through TrkB receptors [J]. Nature, 1999, 401(6756): 918-921.
[12] Gomez-Pinilla F, Ying Z, Opazo P, et al. Differential regulation by exercise of BDNF and NT-3 in rat spinal cord and skeletal muscle [J]. Eur J Neurosci, 2001, 13(6): 1078-1084.
[13] Wang Z, Fang B, Tan Z, et al. Hypoxic preconditioning increases the protective effect of bone marrow mesenchymal stem cells on spinal cord ischemia/reperfusion injury [J]. Mol Med Rep, 2016, 13(3): 1953-1960.
[14] Theus MH, Wei L, Cui L, et al. In vitro hypoxic preconditioning of embryonic stem cells as a strategy of promoting cell survival and functional benefits after transplantation into the ischemic rat brain [J]. Exp Neurol, 2008, 210(2): 656-670.
[15] Fang B, Wang H, Sun XJ, et al. Intrathecal transplantation of bone marrow stromal cells attenuates blood spinal cord barrier disruption induced by spinal cord ischemia reperfusion injury in rabbits [J]. J VascSurg, 2013, 58(4): 1043-1052.
[16] Huang X, Su K, Zhou L, et al. Hypoxia preconditioning of mesenchymal stromal cells enhances PC3 cell lymphatic metastasis accompanied by VEGFR 3/CCR7 activation [J]. J Cell Biochem, 2013, 114(12): 2834-2841.
[17] Peterson KM, Aly A, Lerman A, et al. Improved survival of mesenchymal stromal cell after hypoxia preconditioning: role of oxidative stress [J]. Life Sci, 2011, 88(1-2): 65-73.
[18] Liu H, Liu S, Li Y, et al. The role of SDF 1 CXCR4/CXCR7 axis in the therapeutic effects of hypoxia preconditioned mesenchymal stem cells for renal ischemia/reperfusion injury [J]. PLoS One, 2012, 7(4): e34608.
[19] Chang CP, Chio CC, Cheong CU, et al. Hypoxic preconditioning enhances the therapeutic potential of the secretome from cultured human mesenchymal stem cells in experimental traumatic brain injury [J]. Clin Sci (Lond), 2013, 124(3): 165-176.
[20] Wang JA, He A, Hu X, et al. Anoxic preconditioning: A way to enhance the cardioprotection of mesenchymal stem cells [J]. Int J Cardiol, 2009, 133(3): 410-412.
[21] He A, Jiang Y, Gui C, et al. The anti-apoptotic effect of mesenchymal stem cell transplantation on ischemic myocardium is enhanced by anoxic preconditioning [J]. Can J Cardiol, 2009, 25(6): 353-358.
[22] Kim SU. Human neural stem cells genetically modified for brain repair in neurological disorders [J]. Neuropathology, 2004, 24(3): 159-171.
[23] Oh JS, Ha Y, An SS, et al. Hypoxia-preconditioned adipose tissue-derived mesenchymal stem cell increase the survival and gene expression of engineered neural stem cells in a spinal cord injury model [J]. Neurosci Lett, 2010, 472(3): 215-219.
[24] Golder FJ, Mitchell GS. Spinal synaptic enhancement with acute intermittent hypoxia improves respiratory function after chronic cervical spinal cord injury [J]. J Neurosci, 2005, 25(11): 2925-2932.
[25] Blight AR. Just one word: plasticity [J]. Nat Neurosci, 2004, 7(3):206-208.
[26] Tai PA, Chang CK, Niu KC, et al. Attenuating experimental spinal cord injury by hyperbaric oxygen: stimulating production of vasculoendothelial and glial cell line-derived neurotrophic growth factors and interleukin-10 [J]. J Neurotrauma, 2010, 27(6): 1121-1127.
[27] Cristante AF, Damasceno ML, Barros Filho TE, et al. Evaluation of the effects of hyperbaric oxygen therapy for spinal cord lesion in correlation with the moment of intervention [J]. Spinal Cord, 2012, 50(7): 502-506.
[28] Dayan K, Keser A, Konyalioglu S, et al. The effect of hyperbaric oxygen on neuroregeneration following acute thoracic spinal cord injury [J]. Life Sci, 2012, 90(9-10): 360-364.
[29] Topuz K, Colak A, Cemil B, et al. Combined hyperbaric oxygen and hypothermia treatment on oxidative stress parameters after spinal cord injury: an experimental study [J]. Archiv Med Res, 2010, 41(7): 506-512.
[30] Al-Waili NS, Butler GJ, Beale J, et al. Hyperbaric oxygen in the treatment of patients with cerebral stroke, brain trauma, and neurologic disease [J]. Adv Ther, 2005, 22(6): 659-678.
[31] Lu PG, Hu SL, Hu R, et al. Functional recovery in rat spinal cord injury induced by hyperbaric oxygen preconditioning [J]. Neurol Res, 2012,34(10): 944-951.
[32] Chen MH, Ren QX, Yang WF, et al. Influences of HIF-lα on Bax/Bcl-2 and VEGF expressions in rats with spinal cord injury [J]. Int J Clin Exp Pathol, 2013, 6(11): 2312-2322.
[33] Liu H, Xue W, Ge G, et al. Hypoxic preconditioning advances CXCR4 and CXCR7 expression by activating HIF 1alpha in MSCs [J]. Biochem Biophys Res Commun, 2010, 401(4): 509-515.
[34] 卢培刚,冯华,胡荣,等.高压氧预处理对脊髓损伤后轴突再生影响实验研究[J]. 中华神经外科疾病研究杂志, 2011, 10(4): 316-320.
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