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作 者:肖兴鹏[1] 曹菲[1] 许爱军[1] 高峰[1] 田学愎[1] 田玉科[1]
机构地区:[1]华中科技大学同济医学院附属同济医院麻醉科教研室
出 处:《临床麻醉学杂志》2010年第5期424-426,共3页Journal of Clinical Anesthesiology
基 金:高等学校博士学科点专项科研基金资助项目(20060487046);国家自然科学基金资助项目(30672027)
摘 要:目的 观察鞘内注射蛋白激酶Cγ(PKCγ)基因短发夹RNA(shRNA)慢病毒载体pLV-PKC2对骨癌痛大鼠痛觉的影响,探讨PKCγ基因shRNA对骨癌痛的镇痛效果.方法 选取成年雌性Wistar大鼠24只,随机分为四组:PKC组、骨癌痛组(CIBP组)、磷酸缓冲液组(PBS组)和对照组(C组),每组6只.于骨癌痛模型制作前1 d、模型制作后每隔3天测定大鼠机械缩爪阈值和机械缩爪持续时间.使用免疫组织化学法检测大鼠脊髓背角PKCγ的表达.结果 PKC组大鼠鞘内注射慢病毒载体pLV-PKC2模型制作12 d后,各时点机械缩爪阈值较CIBP、PBS、C组明显升高;持续时间明显缩短(P〈0.05).PKC组大鼠脊髓背角PKCγ蛋白表达量显著低于CIBP组(P〈0.05).结论 慢病毒pLV-PKC2能明显降低骨癌痛大鼠脊髓背角PKCγ的蛋白表达量,同时具有显著的镇痛效应.Objective To investigate the analgesic effect of intrathecal injection of protein kinase C garnma(PKCT)-short hair(sh)RNA lentivirus in rats with cancer-induced bone pain(CIBP). Methods After establishernent of rats CIBP model, 24 female Wistar rats were randomly divided into PKC group, CIBP group, PBS group and Control group with 6 rats each. The changes of nociceptive behaviors including mechanical withdrawal threshold(MWT) and mechanical withdrawal duration(MWD) were assessed before injection and every other 3 days after injection. After completion of pain assessments, the rats were sacrificed and the spinal cord of [urnhar 4-6 segments was taken for detecting the expression of PKC~' by irnmunohistochemistry. Results The MWT of PKC group significantly increased and the MWD evidently prolonged compared to CIBP, PBS, C group on the 5th day after injection of lentivims pLV-PKC2 (the12th day after establishement of model). The PKC7 expression in PKC group significantly reduced compared to that in CIBP group(P〈0. 05). Conclusion Lentivims pLV-PKCe can both evidently decrease the expression of PKC2 and significantly produce analgesic effect.
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