期刊文献+

壳聚糖对大鼠脊髓损伤后小胶质细胞/巨噬细胞的影响 被引量:3

Effect of Chitosan on Microglia/Macrophages after Rats' Spinal Cord Injury
下载PDF
导出
摘要 目的观察应用壳聚糖治疗大鼠胸髓完全横断损伤后,损伤区及其周围小胶质细胞/巨噬细胞的变化情况。方法35只成年雌性Wistar大鼠随机分成假手术组(n=5)、单纯损伤组(n=15)、壳聚糖治疗组(n=15)。分别于术后1d、3d、7d、2周和4周通过免疫组织化学方法,检测小胶质细胞/巨噬细胞的变化情况。结果单纯损伤后小胶质细胞/巨噬细胞在1d时即活化增殖,3d时达高峰,之后迅速减少;应用壳聚糖治疗后,7d达高峰,2~4周时仍有OX42阳性小胶质细胞/巨噬细胞存在。结论壳聚糖可更长时间地募集小胶质细胞/巨噬细胞到损伤区及其周围脊髓组织。 Objective To observe the response of activated microglia/macrophages within and around the lesion site after rats' spinal cord injury treated with chitosan. Methods 35 adult female Wistar rats were randomly divided into the sham group (n=5), completely transection group (n= 15) and chitosan treated group (n= 15). The responses of activated microglia/macrophages on the 1st day, 3rd day, 7th day, and in the 2nd week and 4th week after surgery were examined by immunohistochemistry. Results Microglia/ macrophages were fully activated and the number of these cells increased and got the highest level on the 3rd day post injury, then quickly decreased. In the chitosan treated animals, the microglia/macrophages were fully activated and the number increased to peak on the 7th day, then quickly decreased, there were still a few microglia/macrophages around the wound in the 2nd to 4th week after the treatment. Conclusion Microglia/macropbages could be recruited within and around the lesion area longer when treated by chitosan.
出处 《中国康复理论与实践》 CSCD 2009年第4期321-323,共3页 Chinese Journal of Rehabilitation Theory and Practice
基金 "十一五"863计划生物和医药技术领域干细胞与组织工程重大项目(No.2006AA02A129)
关键词 脊髓损伤 壳聚糖 小胶质细胞/巨噬细胞 soinal cord iniurv, chitosan, microglia/macroohages
  • 相关文献

参考文献12

  • 1Dougherty KD, Dreyfus CF, Black IB. Brain-derived neurotrophic factor in astrocytes, oligodendroeytes, and microglia/macrophages after spinal cord injury [J]. Neurobiol Dis,2000,7(6 Pt B) :574--585.
  • 2Bomstein Y, Marder JB, Vitner K, et al. Features of skincoincubated macrophages that promote recovery from spinal cord injury[J]. J Neuroimmunol,2003,142(1-2) : 10--16.
  • 3Grill R, Murai K, Blesch A, et al. Cellular delivery of neurotrophin-3 promotes corticospinal axonal growth and partial functional recovery after spinal cord injury[J]. J Neurosci, 1997,17 (14) : 5560--5572.
  • 4Chou TC, Fu E, Shen EC. Chitosan inhibits prostaglandin E2 formation and cyclooxygenase-2 induction in lipopolysaccharide-treated RAW 264.7 macrophages[J]. Biochem Biophys Res Commun, 2003,308 (2) : 403--407.
  • 5Carlson SL, Parrish ME, Springer JE, et al. Acute inflammatory response in spinal cord following impact injury[J]. Exp Neurol,1998,151(1) :77--88.
  • 6Popovich PG, Wei P, Stokes BT, et al. Cellular inflammatory response after spinal cord injury in sprague-dawley and lewis rats[J]. J Comp Neurol,1997,377(3):443--464.
  • 7Wu GJ, Tsai GJ. Chitooligosaccharides in combination with interferon-7 increase nitric oxide production via nuclear factor-kB activation in murine RAW264. 7 macrophages[J]. Food Chem Toxicol, 2007,45 (2) : 250--258.
  • 8Rapalino O, Lazarov Spiegler O, Agranov E, et al. Implantation of stimulated homologus macrophages results in patial recovery of paroplegic rats[J]. Nat Med,1998,4(7):814-- 821.
  • 9Schwartz M. T cell mediated neuroprotection is a physiological response to central nervous system insults[J]. J Mol Med, 2001,78:594--597.
  • 10Bakalash S, Shlomo GB, Aloni E, et al. T cell-based vaccination for morphological and functional neuroprotection in a rat model of chronically elevated intraocular pressure[J]. J Mol Med,2005,83:904--916.

同被引文献43

引证文献3

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部