期刊文献+

前列腺酸性磷酸酶在慢性痛大鼠脊髓背角和背根神经节的表达变化 被引量:2

Changes of the expression of prostatic acid phosphatase in spinal dorsal horn and dorsal root ganglion in different chronic pain models of the rat
下载PDF
导出
摘要 目的:观察前列腺酸性磷酸酶(prostatic acid phosphatase,PAP)在多种慢性痛大鼠脊髓背角(spinaldorsal horn,SDH)和背根神经节(dorsal root ganglion,DRG)内的表达变化。方法:应用免疫组织化学染色法以及免疫荧光多重染色技术在多种慢性痛模型大鼠观察PAP的表达变化。结果:在正常大鼠,PAP阳性反应产物主要位于DRG的中、小型的非肽能神经元,PAP阳性神经元约占DRG神经元总数的64±4.3%;在脊髓背角,PAP阳性纤维和终末主要位于Ⅱ层。在神经病理性痛模型大鼠,术侧脊髓背角Ⅱ层的PAP阳性初级传入终末较对侧减少甚至消失,DRG内PAP阳性神经元较对侧明显减少。在慢性炎性痛模型大鼠,双侧脊髓背角和DRG内PAP的表达未见明显改变。结论:PAP特异地定位于DRG神经元以及脊髓背角Ⅱ层,可能与神经病理性痛信号的传递和加工密切相关。 Objective: To observe the expression changes of prostatic acid phosphatase(PAP) in the spinal dorsal horn(SDH) and dorsal root ganglion(DRG) in different chronic pain models of the rat.Methods: Immunohistochemistry combined with multiple immunofluorescent histochemical technique was employed to detect the expression changes of PAP in different chronic pain models.Results: In the intact normal rats,PAP was principally located in small-to medium-sized non-peptidergic neurons in the DRG,and the number of PAP-immunoreactive(PAP-ir) neurons was about 64±4.3% to the total number of the DRG neurons.In the SDH,only PAP-ir fibers and terminals but not PAP-ir neurons were exclusively observed in lamina I and II,especially in lamina II.In a model of neuropathic pain rat,PAP immunoreactivities were markedly decreased,or even vanished in the SDH and DRG ipsilateral to the nerve injury side.There were no remarkable changes of the PAP expression on the side contralateral to the nerve injury.In an inflammatory pain model induced by CFA injection into the rat hindpaw,however,there were no obvious expression changes of PAP-ir neurons,fibers and terminals in bilateral SDHs and DRGs.Conclusion: PAP is specifically expressed in the SDH and DRG.It might play important roles in the transduction and process of the signals of the neuropathic pain.
出处 《神经解剖学杂志》 CAS CSCD 北大核心 2012年第1期1-6,共6页 Chinese Journal of Neuroanatomy
基金 国家自然科学基金(30900772)
关键词 前列腺酸性磷酸酶 慢性痛 脊髓背角 背根神经节 prostatic acid phosphatase chronic pain spinal dorsal horn dorsal root ganglion
  • 相关文献

参考文献13

  • 1Casals-Diaz L, Vivo M, Navarro X. Nociceptive responses and spinal plastic changes of afferent C-fibers in three neuropathic pain models induced by sciatic nerve injury in the rat [ J ]. Exp Neurol, 2009, 217:84-95.
  • 2Silverman JD, Kruger L. Acid phosphatase as a selective marker for a class of small sensory ganglion cells in several mammals: spinal cord distribution, histochemical properties, and relation to fluoride- resistant acid phosphatase ( FRAP ) of rodents [ J ]. Somatosens Res, 1998, 5:219-246.
  • 3Zylka MJ, Sowa NA, Taylor-Blake B, et al. Prostatic acid phospha- tase is an ectonucleotidase and suppresses pain by generating adenosine [J]. Neuron, 2008, 60:111 -122.
  • 4Zylka MJ. Nonpeptidergic circuits feel your pain [ J ]. Neuron, 2005, 47:771 -778.
  • 5Hong Y, Liu Y, Chabot JG, et al. Upregulation of adrenomedullin in the spinal cord and dorsal root ganglia in the early phase of CFA- induced inflammation in rats [ J]. Pain, 2009, 146 : 105 - 113.
  • 6Bennett GJ, Xie YK. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in mall [J]. Pain, 1988, 33 : 87 - 107.
  • 7lsabelle D, Woof CJ. Spared nerve injury : an animal model of persistent peripheral neuropathic pain [ J ]. Pain, 2000, 87 : 149 - 158.
  • 8Kim SH, Chung JM. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat [ J ]. Pain, 1992, 50:355 - 363.
  • 9Reif AE, Schlesinger RM, Fish CA, et al. Acid phosphatase is enzymes in cancer of the prostate [J]. Cancer, 1973. 31: 689- 699.
  • 10Quintero IB, Araujo CL, Pulkka AE, et al. Prostatic acid phosphatase is not a prostate specific target [ J]. Cancer Res, 2007, 67: 6549 - 6554.

同被引文献26

  • 1王毅,王芳,宿晓云,原田守,山田亮,伊东恭悟,颜炜群.前列腺酸性磷酸酶在非前列腺腺癌中的表达[J].第四军医大学学报,2007,28(19):1775-1777. 被引量:5
  • 2Obrosova IG.Diabetic painful and insensate neuropahty pathogenesis and potential treatments[J].Neurotherapeuties,2009,6(4):638-647.
  • 3Edwards JL,Vincent AM,Cheng HT,et al.Diabetic neuropathy:mechanisms to management[J].Pharmacol Ther,2008,120(1):1-34.
  • 4Sadosky A,Schaefer C,Mann R,et al.Burden of illness associated with painful diabetic peripheral neuropathy among adults seeking treatment in the US:results from a retrospective chart review and cross-sectional survey[J].Diabetes Metab Syndr Obes,2013,6:79-92.
  • 5Zylka MJ,Nathaniel AS,Bonnie TB,et al.Prostatic acid phosphatase is an ectonucleotidase and suppresses pain by generating adenosine[J].Neuron,2008,60(1):111-22.
  • 6Cui Y,Xu H,Wu H,et al.Spatio-temporal expression and functional involvement of transient receptor potential vanilloid 1in diabetic mechanical allodynia in rats[J].PLoS One,2014,9(7):e102052.
  • 7Sun W,Miao B,Wang X,et al.Gastrodin inhibits allodynia and hyperalgesia in painful diabetic neuropahty rats by decreasing excitability of nociceptive primary sensory neurons[J].PLoS One,2012,7(6):e39647.
  • 8Wu H,Yin J,Zhang T,et al.Inhibiting spinal neuronastrocytic activation correlates with synergistic analgesia of dexmedetomidine and ropivacaine[J].PLoS ONE,2014,9(3):e92374.
  • 9Solin T,Kontturi M,Pohlmann R,et al.Gene expression and prostate specificity of humanprost atic acid phosphatase(PAP):evaluation by RNA blot analyses[J].Biochim Biophys Acta,1990,1048(1):72-77.
  • 10Quintero IB,Araujo CL,Pulkka AE,et al.Prostatic acid phosphatase is not a prostate specific target[J].Cancer Res,2007,67(14):6549-54.

引证文献2

二级引证文献1

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