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J Clin Invest ; 114(1): 49-56, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15232611

RESUMO

Thrombolysis is widely used to intervene in acute ischemic stroke, but reestablishment of circulation may paradoxically initiate a reperfusion injury. Here we describe studies with mice lacking protein kinase Cdelta (PKCdelta) showing that absence of this enzyme markedly reduces reperfusion injury following transient ischemia. This was associated with reduced infiltration of peripheral blood neutrophils into infarcted tissue and with impaired neutrophil adhesion, migration, respiratory burst, and degranulation in vitro. Total body irradiation followed by transplantation with bone marrow from PKCdelta-null mice donors reduced infarct size and improved neurological outcome in WT mice, whereas marrow transplantation from WT donors increased infarction and worsened neurological scores in PKCdelta-null mice. These results indicate an important role for neutrophil PKCdelta in reperfusion injury and strongly suggest that PKCdelta inhibitors could prove useful in the treatment of stroke.


Assuntos
Encéfalo/enzimologia , Ataque Isquêmico Transitório/fisiopatologia , Neutrófilos/enzimologia , Proteína Quinase C/sangue , Traumatismo por Reperfusão/sangue , Animais , Encéfalo/patologia , Éxons , Ataque Isquêmico Transitório/sangue , Ataque Isquêmico Transitório/genética , Camundongos , Camundongos Knockout , Proteína Quinase C/deficiência , Proteína Quinase C/genética , Proteína Quinase C-delta , Recombinação Genética , Traumatismo por Reperfusão/enzimologia
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