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- Title
Electroporation-mediated pain-killer gene therapy for mononeuropathic rats.
- Authors
Lin, C.-R.; Yang, L.-C.; Lee, T.-H.; Lee, C.-T.; Huang, H.-T.; Sun, W.-Z.; Cheng, J.-T.
- Abstract
The relatively low expression levels achieved from transferred genes have limited the application of nonviral vectors for gene transfer into the spinal cord in vivo. Thus, the aim of this study was to evaluate the efficacy of electroporationmediated pro-opiomelanocortin (POMC) gene therapy for neuropathic pain using an animal model of chronic constricrive injury (CCI). Firstly, the optimal pulse characteristics (voltage, pulse duration, number of shocks) were investigated for in vivo electroporation-mediated gene transfer into the spinal cord. The electroporation process makes use of plasmid DNA, which expresses the POMC gene. Expression levels were evaluated in this study by Western blot. We conclude that the optimal conditions for electroporation are a pulse voltage of 200 V, 75-ms duration, 925-ms interval, for five iterations. Secondly, electroporation treatment for neuropathic pain was attempted on CCl rats using plasmid DNA that expresses the POMC gene. Intrathecal administrations of the POMC vector elevated spinal beta-endorphin levels, as manifested in a significantly elevated pain threshold for the CCI limbs. This result suggests that gene therapy for neuropathic pain using this novel technique is very efficacious, and thus shows promise for further clinical trials.
- Subjects
PROOPIOMELANOCORTIN; GENETIC transformation; ELECTROPORATION
- Publication
Gene Therapy, 2002, Vol 9, Issue 18, p1247
- ISSN
0969-7128
- Publication type
Article
- DOI
10.1038/sj.gt.3301790