Pol Olga, Murtra Patricia, Caracuel Laura, Valverde Olga, Puig Margarita M, Maldonado Rafael
Department of Anesthesiology, Hospital del Mar, IMIM, Universitat Autònoma de Barcelona, Spain.
Neuropharmacology. 2006 Jan;50(1):123-32. doi: 10.1016/j.neuropharm.2005.11.002. Epub 2005 Dec 15.
The development of neuropathic pain is associated with multiple changes in gene expression occurring in the dorsal root ganglia (DRG) and spinal cord. The goal of this study was to evaluate whether the disruption of CB1 cannabinoid receptor gene modulates the changes induced by neuropathic pain in the expression of mu- (MOR), delta- (DOR) and kappa-opioid receptors (KOR) mRNA levels in the DRG and spinal cord. The induction of c-fos expression in the lumbar and sacral regions of the spinal cord was also evaluated in these animals. Opioid receptors mRNA levels were determined by using real-time PCR and Fos protein levels by immunohistochemistry. Nerve injury significantly reduced the expression of MOR in the DRG and the lumbar section of the spinal cord from CB1 cannabinoid knockout (KO) mice and wild-type littermates (WT). In contrast, mRNA levels of DOR and KOR were not significantly changed in any of the different sections analysed. Furthermore, sciatic nerve injury evoked a similar increase of c-fos expression in lumbar and sacral regions of the spinal cord of both KO and WT. In all instances, no significant differences were observed between WT and KO mice. These data revealed specific changes induced by neuropathic pain in MOR expression and c-fos levels in the DRG and/or spinal cord that were not modified by the genetic disruption of CB1 cannabinoid receptors.
神经性疼痛的发展与背根神经节(DRG)和脊髓中发生的基因表达的多种变化相关。本研究的目的是评估CB1大麻素受体基因的破坏是否调节神经性疼痛诱导的DRG和脊髓中μ-(MOR)、δ-(DOR)和κ-阿片受体(KOR)mRNA水平表达的变化。还评估了这些动物脊髓腰段和骶段中c-fos表达的诱导情况。通过实时PCR测定阿片受体mRNA水平,通过免疫组织化学测定Fos蛋白水平。神经损伤显著降低了CB1大麻素基因敲除(KO)小鼠和野生型同窝小鼠(WT)的DRG和脊髓腰段中MOR的表达。相比之下,在分析的任何不同节段中,DOR和KOR的mRNA水平均未发生显著变化。此外,坐骨神经损伤在KO和WT小鼠脊髓的腰段和骶段均引起了类似的c-fos表达增加。在所有情况下,WT和KO小鼠之间均未观察到显著差异。这些数据揭示了神经性疼痛在DRG和/或脊髓中诱导的MOR表达和c-fos水平的特定变化,这些变化未因CB1大麻素受体的基因破坏而改变。