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Vaccination with a neural-derived peptide plus administration of glutathione improves the performance of paraplegic rats

  • S. Martiñon
    ,
  • E. García
    ,
  • N. Flores
    ,
  • I. Gonzalez
    ,
  • T. Ortega
    ,
  • M. Buenrostro
  • Instituto Mexicano del Seguro Social
    ,
  • Universidad Nacional Autónoma de México
    ,
  • Instituto Nacional de Pediatria
Research Output: Contribution to journal Article Peer-review

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 403-412 (10 pages)

Journal (Volume, Issue Number)

European Journal of Neuroscience (Volume 26, Issue 2)

Publication milestones

  • Published - 01/07/2007

Publication status

Published - 01/07/2007

ISSN

0953-816X

Publication IDs

  • Scopus: 34447625768
  • PubMed: 17623024

Abstract

After damage to the central nervous system (CNS) the body is protected by an adaptive immune response which is directed against myelin-associated proteins. Active immunization with nonpathogenic derivatives of CNS-associated peptides (DCAP) reduces the degeneration of neurons and promotes motor recovery after spinal cord injury (SCI) in rats. In order to improve even more the neurological outcome obtained with this therapy, either a combination of DCAP immunization plus glutathione monoethyl ester (GSHE) or a double DCAP immunization were performed. GSHE is a cell-permeant derivative of glutathione, a potent antioxidant agent that significantly inhibits lipid peroxidation after SCI. After a contusive or compressive SCI, the combination of GSHE + DCAP immunization, induced better motor recovery, a higher number of myelinated axons and better rubrospinal neuron survival than immunization alone. On the other hand, double-DCAP immunization counteracted the protective effect of DCAP therapy. Motor recovery and neuronal survival of double-immunized rats were similar to those observed in control animals (PBS-treated). Further studies revealed that double immunization was not encephalitogenic but inhibited the proliferative response of T-cells specific to the DCAP-immunized peptide. This clonal dysfunction was probably secondary to anergy. GSHE improves the protective effect induced by DCAP immunization while double immunization, reverts it.