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强力霉素诱导表达脑啡肽细胞株的构建及其对慢性神经痛大鼠的镇痛作用 被引量:2

ESTABLISHMENT OF AN IMMORTALIZED RAT ASTROCYTE STRAIN EXPRESSING ENKEPHALIN REGULATED BY DOXYCYCLINE AND ITS ANALGESIC EFFECT ON RAT CHRONIC NEUROPATHIC PAIN
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摘要 目的构建受强力霉素诱导表达脑啡肽的永生化大鼠星形胶质细胞株,并评价鞘内移植该细胞对慢性坐骨神经压榨性损伤(CCI)大鼠的镇痛效应。方法应用逆转录病毒转染法,建立受强力霉素调控表达人前脑啡肽原基因(hPPE)的永生化大鼠星形胶质细胞株(IAST/Tet-On/hPPE),实时定量PCR及放射免疫分析法检测强力霉素对该细胞株脑啡肽表达的定量调节。将IAST/Tet-On/hPPE细胞植入CCI大鼠蛛网膜下腔,观察腹腔注射强力霉素对其镇痛效应的影响及免疫组织化学检测脊髓背角Fos蛋白的表达。结果实时定量PCR及放射免疫分析结果显示,强力霉素可定量调控IAST/Tet-On/hPPE细胞株中脑啡肽的表达;IAST/Tet-On/hPPE植入CCI大鼠的蛛网膜下腔后,大鼠机械缩爪阈值升高(P<0.05),脊髓背角浅层Fos蛋白表达明显降低(P<0.05),且该镇痛效应受强力霉素调控。结论成功构建了可调控的定量表达脑啡肽的永生化星形胶质细胞株,其有望成为慢性疼痛治疗的新方法。 Objective To establish an immortalized rat astrocyte strain (IAST) expressing enkephalin regulated by doxycycline (Dox) and observe its analysesic effect on rat chronic neuropathic pain. Methods Retrovirus infection method was employed to develop an immortalized rat astrocyte strain expression enkephalin regulated by doxycycline, hPPE gene expression level of IAST/Tet-On/hPPE strain was detected by Real time-PCR and radioimmunoassay. Its analgesic potential was investigated by mechanical paw withdrawal thresholds after these cells were implanted into the subarachnoid space of chronic constrictive injury (CCI) rats. The expression of Fos protein in the dorsal horn of spinal cord was determined by immunohistochemistry. Results An immortalized rat astrocyte strain secreting enkephalin under the control of doxycycline was established successfully. After transplantation of IAST/Tet-On/hPPE cell into the subarachnoid space of chronic constrictive injury (CCI) rats, the sensitivity of mechanical allodynia and the expression of Fos protein were significantly decreased ( P 〈 0.05), so the transplantation of lAST/ Tet-On/hPPE cell alleviated significantly CCI-induced chronic neuropathic pain in rats and the analgesic effect was also able to be regulated by Dox. Conclusion An immortalized rat astrocyte strain expressing enkephalin regulated by Dox has been established, which may provide a new tool for regulatable gene therapy for chronic pain in the future.
出处 《解剖学报》 CAS CSCD 北大核心 2006年第6期617-621,共5页 Acta Anatomica Sinica
基金 国家自然科学基金资助项目(30170905) 杨森基金资助
关键词 人前脑啡肽原基因 慢性疼痛 星形胶质细胞 逆转录病毒转染法 细胞移植 大鼠 Human preproenkephalin gene Chronic pain Astrocyte Retrovirus infection method Cell transplantation Rat
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  • 1Kalso E,Edwards JE,Moore RA,et al.Opioids in chronic non-cancer pain:systematic review of efficacy and safety[J].Pain,2004,112(3):372-380. 被引量:1
  • 2Fink D,Mata M,Glorioso JC.Cell and gene therapy in the treatment of pain[J].Adv Drug Deliv Rev,2003,55(8):1055-1064. 被引量:1
  • 3Eaton MJ.Emerging cell and molecular strategies for the study and treatment of painful peripheral neuropathies[J].J Peripher Nerv Syst,2000,5(2):59-74. 被引量:1
  • 4Gossen M,Freundlieb S,Bender G,et al.Transcriptional activation by tetracyclines in mammalian cells[J].Science,1995,268(5218):1766-1769. 被引量:1
  • 5安珂,田玉科,杨辉,高峰,王鹏.猿肾病毒40大T抗原基因永生化大鼠星形胶质细胞株的构建[J].中华麻醉学杂志,2004,24(11):838-841. 被引量:11
  • 6徐颖,田玉科,田学愎,杨辉,安珂,高峰.携带可调控人前脑啡肽原基因逆转录病毒载体的构建及鉴定[J].中华麻醉学杂志,2005,25(7):511-514. 被引量:4
  • 7Bennett GJ,Xie YK.A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man[J].Pain,1988,33:87-107. 被引量:1
  • 8Eaton M,Martinez B,Frydel S,et al.Initial characterization of the transplant of irmortalized chromaffin cells for the attenuation of chronic neuropathic pain[J].Cell Transplant,2000,9(5):637-656. 被引量:1
  • 9Villetti G,Bergamaschi M,Bassani F,et al.Antinociceptive activity of the N-methyl-D-aspartate receptor antagonist N-(2-Indanyl)-glycinamide hydrochloride (CHF3381) in experimental models of inflammatory and neuropathic pain[J].J Pharmacol Exp Ther,2003,306(2):804-814. 被引量:1
  • 10Wilson SP,Yeomans DC,Bender MA,et al.Antihyperalgesic effects of infection with a preproenkephalin-encoding herpes virus[J].Proc Natl Acad Sci USA,1999,96(6):3211-3216. 被引量:1

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