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Clin Exp Immunol ; 115(1): 32-41, 1999 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9933418

RESUMO

A recently developed compound, a multivalent guanylhydrazone (CNI-1493) that inhibits TNF-alpha production by suppressing TNF-alpha translational efficiency, was administered in an experimental model of collagen type II-induced arthritis in DA rats. CNI-1493 was injected daily intraperitoneally either before the onset of arthritis or after the establishment of clinical disease. Prophylactic treatment with CNI-1493 significantly prevented or delayed the onset and suppressed the severity of arthritis in a dose-dependent manner. Therapeutic intervention with CNI-1493 in established joint disease also resulted in a significant reduction of clinical signs of arthritis in treated animals. No severe side-effects were noted when animals were treated with daily CNI-1493 doses up to 5 mg/kg. An immunohistochemical study was performed which demonstrated that CNI-1493 led to a reduced expression of TNF-alpha at the site of disease activity. Thus, CNI-1493 with documented inhibitory effects on TNF-alpha synthesis, has proven successful in ameliorating the course of arthritis in CIA. We believe that the use of a compound such as CNI-1493 with a defined mode of action provides a useful tool for dissecting and understanding important pathogenic mechanisms operating in the development of chronic arthritis.


Assuntos
Anti-Inflamatórios não Esteroides/uso terapêutico , Artrite Experimental/tratamento farmacológico , Colágeno , Hidrazonas/uso terapêutico , Animais , Anticorpos/sangue , Artrite Experimental/induzido quimicamente , Artrite Experimental/prevenção & controle , Colágeno/imunologia , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Masculino , Nitritos/sangue , Ratos , Ratos Endogâmicos , Fator de Necrose Tumoral alfa/antagonistas & inibidores
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