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硬脊膜完整性可影响脑脊液中细胞因子的水平

Dura mater spinalis integrity may influence cytokine levels in the cerebrospinal fluid
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摘要 背景:脊髓损伤后的病理生理机制非常复杂,人们对此认识还很不全面、深入。目的:观察脊髓损伤动物模型中硬脊膜完整性对脑脊液内细胞因子水平的影响。方法:采用钳夹压迫法建立新西兰大白兔脊髓损伤模型,随机分为无硬脊膜缺损组、硬脊膜缺损组、硬脊膜缺损复合膜修复组、硬脊膜缺损自体筋膜修复组。术后 30 min、1 h、3 h、6 h、12 h、36 h 采用酶联免疫吸附实验方法检测各组脑脊液中细胞因子白细胞介素 6、白细胞介素 10、肿瘤坏死因子α的变化。结果与结论:无硬脊膜缺损组、硬脊膜缺损复合膜修复组和硬脊膜缺损自体筋膜修复组术后 6 h 脑脊液中白细胞介素 6、白细胞介素 10、肿瘤坏死因子α水平均显著低于硬脊膜缺损组(P < 0.05)。其余时间点 4 组间各因子水平差异无显著性意义(P > 0.05)。说明维护脊髓损伤模型中硬脊膜的完整性可影响脑脊液中白细胞介素6、白细胞介素 10、肿瘤坏死因子α水平,抑制炎症反应。 BACKGROUND: Pathophysioiogical mechanisms after spinal cord injury are very complex, so there is no compressive and in-depth understanding on it. OBJECTIVE: To study the effect of dura mater spinalis integrity on cytokine levels in the cerebrospinal fluid of animal models of spinal cord injury. METHODS: The white rabbit models of spinal cord injury were established using clamp compression method, and then the models were randomly divided into four groups: no dura mater spinalis defect group, dura mater spinalis defect group, dura mater spinalis defect composite with membrane repaidng group and dura mater spinalis defect composite with autologous fascia repair group. Enzyme-linked immunosorbent assay was performed to detect the changes of levels of cytokines (interleukin-6, interleukin-10 and tumor necrosis factor a) in the cerebrospinal fluid at 30 minutes, 1, 3, 6, 12 and 36 hours after surgery. RESULTS AND CONCLUSION: The levels of interleukin-6, interleukin-10 and tumor necrosis factor a in the cerebrospina! fluid of the dura mater spinalis defect group, dura mater spinalis defect composite with membrane repairing group and dura mater spinalis defect composite with autologous fascia repair group were significantly lower than those of the no dura mater spinalis defect group at 6 hours after surgery (P 〈 0.05). There were no significant differences in the levels of interleukin-6, interleukin-10 and tumor necrosis factor a at other time points between groups (P 〉 0.05). The results indicate that maintaining the integrity of dura mater spinalis of the spinal cord injury model can affect the leve^s of intedeukin-6, intefleukin-10 and tumor necrosis factor a in the cerebrospinal fluid, thus inhibiting the inflammatory response.
出处 《中国组织工程研究》 CAS CSCD 2013年第33期6001-6004,共4页 Chinese Journal of Tissue Engineering Research
关键词 组织构建 组织构建与生物活性因子 脊髓损伤 白细胞介素 6 白细胞介素 10 肿瘤坏死因子 α 硬脊膜 tissue construction tissue construction and bioactive factors spinal cord injury interleukin-6 interleukin-10 tumor necrosis factor a dura mater spinalis
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参考文献14

  • 1Garbossa D,Fontanel a M,Fronda C. New strategies for repairing the injured spinal cord:the role of stem cel s[J].{H}Neurological Research,2006,(05):500-504.
  • 2Streit WJ,Semple-Rowland SL,Hurley SD. Cytokine mRNA profiles in contused spinal cord and axotomiazed facial mucleus suggest a beneficial role for inflammation and gliosis[J].{H}EXPERIMENTAL NEUROLOGY,1998,(01):74-87.
  • 3孙为增,王新家.脊髓损伤后细胞因子的变化及作用[J].实用医学杂志,2009,25(8):1337-1338. 被引量:5
  • 4Sufium S,Lahav R,Han J. Leukaemia inhibitory factor is required for normal inflammatory responses to injury in the peripheral and central nervous systems in vivo and is chemotactic for macrophages in vitro[J].{H}European Journal of Neuroscience,2000,(02):457-466.
  • 5Mukaino M,Nakamura M,Okada S. Role of IL-6 in regulation of inflammation and stem cel differentiation in CNS trauma[J].{H}Nihon Rinsho Meneki Gakkai Kaishi,2008,(02):93-98.
  • 6Kang MK,Kang SK. Interleukin-6 induces proliferation in adult spinal cord derived neural progenitors via the JAK2/STAT3 pathway with EGf-indued MAPK phosphorylation[J].Cel Prolif,2008,(03):377-392.
  • 7Mil igan ED,Soderquist RG,Malone SM. Intrathecal polymer-based interleukin-10 gene delivery for neuropathic pain[J].{H}NEURON GLIA BIOLOGY,2006,(04):239-308.
  • 8Bethea JR,Dietrich WD. Targeting the host inflammatory response in traumatic spinal cord injury[J].J Curr Opin Neurol,2002,(03):355-360.
  • 9Plukett JA,Yu CG,Easton JM. Effects of interleukin-10(IL-10)on pain behavior and gene expression fol owing excitotoxic spinal cord injury in the rat[J].J Exp Neurol,2001,(01):144-154.
  • 10周华,刘华,黄坚,吴思荣,肖接承.IL-10对脊髓损伤后细胞凋亡和CD95作用的初步探讨[J].苏州大学学报(医学版),2005,25(3):395-397. 被引量:6

二级参考文献25

  • 1周华,刘华,黄坚,吴思荣,肖接承.IL-10对脊髓损伤后细胞凋亡和CD95作用的初步探讨[J].苏州大学学报(医学版),2005,25(3):395-397. 被引量:6
  • 2Bartholdi D, Schwab M E. Expression of pro-inflammatory cytokine and chemokine mRNA upon experimental spinal cord injury in mouse: an in situ hybridization study [J]. Eur J Neurosci, 1997,9 (7) : 1422-1438.
  • 3Pan J Z, Ni L, Sodhi A, et al. Cytokine activity contributes to induction of inflammatory cytokine mRNAs in spinal cord following contusion [J]. J Neurosci Res, 2002,68 (3) : 315-322.
  • 4Wang C X, Olschowka J A, Wrathall J R. Increase of interleukin-lbeta mRNA and protein in the spinal cord following experimental traumatic injury in the rat [J]. Brain Res, 1997,759(2): 190-196.
  • 5Nesic O, Xu G Y, McAdoo D, et al. IL-1 receptor antagonist prevents apoptosis and caspase-3 activation after spinal cord injury [J]. J Neurotrauma,2001,18 (9) : 947-956.
  • 6LiuS, XuGY, JohnsonKM, etal. Regulation of interleukin-lbeta by the interleukin-1 receptor antagonist in the glutamate-injured spinal cord : Endogenous neuroprotection [J]. Brain Res,2008,1231 : 63-74.
  • 7Streit W J, Semple-Rowland S L, Hurley S D, et al. Cytokine mRNA profiles in contused spinal cord and axotomized facial nucleus suggest a beneficial role for inflammation and gliosis [J]. Exp Neurol, 1998,152( 1 ) :74-87.
  • 8Sugiura S, Lahav R, Han J, et al. Leukaemia inhibitory factor is required for normal inflammatory responses to injury in the peripheral and central nervous systems in vivo and is chemotaetic for macrophages in vitro [J]. Eur J Neurosei,2000,12(2) : 457-466.
  • 9Mukaino M, Nakamura M, Okada S, et al. Role of IL-6 in regulation of inflammation and stem cell differentiation in CNS trauma [J]. Nihon Rinsho Meneki Gakkai Kaishi, 2008,31 (2) : 93-98.
  • 10Kang M K, Kang S K. Interleukin-6 induces proliferation in adult spinal cord-derived neural progenitors via the JAK2/ STAT3 pathway with EGF-induced MAPK phosphorylation [J]. Cell Prolif,2008,41 (3) : 377-392.

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