Electroporation-mediated pain-killer gene therapy for mononeuropathic rats

C. R. Lin, L. C. Yang, T. H. Lee, C. T. Lee, H. T. Huang, W. Z. Sun, J. T. Cheng

Research output: Contribution to journalArticlepeer-review

35 Citations (Scopus)


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 electroporation-mediated pro-opiomelanocortin (POMC) gene therapy for neuropathic pain using an animal model of chronic constrictive 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 CCI 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.

Original languageEnglish
Pages (from-to)1247-1253
Number of pages7
JournalGene Therapy
Issue number18
Publication statusPublished - 2002

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Molecular Biology
  • Genetics


Dive into the research topics of 'Electroporation-mediated pain-killer gene therapy for mononeuropathic rats'. Together they form a unique fingerprint.

Cite this