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Neurosci Lett ; 476(2): 62-5, 2010 May 31.
Artigo em Inglês | MEDLINE | ID: mdl-20381587

RESUMO

Lipid peroxidation (LP) is one of the most harmful mechanisms developed after spinal cord (SC) injury. Several strategies have been explored in order to control this phenomenon. Protective autoimmunity is a physiological process based on the modulation of inflammatory cells that can be boosted by immunizing with neural-derived peptides, such as A91. Since inflammatory cells are among the main contributors to lipid peroxidation, we hypothesized that protective autoimmunity could reduce LP after SC injury. In order to test this hypothesis, we designed two experiments in SC contused rats. First, animals were immunized with a neural-derived peptide seven days before injury. With the aim of inducing the functional elimination of CNS-specific T cells, for the second experiment, animals were tolerized against SC-protein extract and thereafter subjected to a SC injury. The lipid-soluble fluorescent products were used as an index of lipid peroxidation and were assessed after injury. Immunization with neural-derived peptides reduced lipid peroxidation after SC injury. Functional elimination of CNS-specific T cells avoided the beneficial effect induced by protective autoimmunity. The present study demonstrates the beneficial effect of immunizing with neural-derived peptides on lipid peroxidation inhibition; besides this, it also provides evidence on the neuroprotective mechanisms exerted by protective autoimmunity.


Assuntos
Peroxidação de Lipídeos , Proteína Básica da Mielina/uso terapêutico , Neuropeptídeos/uso terapêutico , Ovalbumina/uso terapêutico , Traumatismos da Medula Espinal/prevenção & controle , Animais , Autoimunidade , Imunização , Proteína Básica da Mielina/imunologia , Neuropeptídeos/imunologia , Ovalbumina/imunologia , Ratos , Ratos Sprague-Dawley , Traumatismos da Medula Espinal/imunologia , Traumatismos da Medula Espinal/metabolismo , Linfócitos T/imunologia
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