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Provedor de dados:  BJMBR
País:  Brazil
Título:  Anti-inflammatory, antinociceptive and ulcerogenic activity of a zinc-diclofenac complex in rats
Autores:  Santos,L.H.
Feres,C.A.O.
Melo,F.H.
Coelho,M.M.
Nothenberg,M.S.
Oga,S.
Tagliati,C.A.
Data:  2004-08-01
Ano:  2004
Palavras-chave:  Diclofenac-zinc complex
Gastric lesions
Non-steroidal anti-inflammatory drugs
Ulcerogenesis
Antinociception
Resumo:  We investigated the anti-inflammatory, antinociceptive and ulcerogenic activity of a zinc-diclofenac complex (5.5 or 11 mg/kg) in male Wistar rats (180-300 g, N = 6) and compared it to free diclofenac (5 or 10 mg/kg) and to the combination of diclofenac (5 or 10 mg/kg) and zinc acetate (1.68 or 3.5 mg/kg). The carrageenin-induced paw edema and the cotton pellet-induced granulomatous tissue formation models were used to assess the anti-inflammatory activity, and the Hargreaves model of thermal hyperalgesia was used to assess the antinociceptive activity. To investigate the effect of orally or intraperitoneally (ip) administered drugs on cold-induced gastric lesions, single doses were administered before exposing the animals to a freezer (-18ºC) for 45 min in individual cages. We also evaluated the gastric lesions induced by multiple doses of the drugs. Diclofenac plus zinc complex had the same anti-inflammatory and antinociceptive effects as diclofenac alone. Gastric lesions induced by a single dose administered per os and ip were reduced in the group treated with zinc-diclofenac when compared to the groups treated with free diclofenac or diclofenac plus zinc acetate. In the multiple dose treatment, the complex induced a lower number of the most severe lesions when compared to free diclofenac and diclofenac plus zinc acetate. In conclusion, the present study demonstrates that the zinc-diclofenac complex may represent an important therapeutic alternative for the treatment of rheumatic and inflammatory conditions, as its use may be associated with a reduced incidence of gastric lesions.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2004000800011
Editor:  Associação Brasileira de Divulgação Científica
Relação:  10.1590/S0100-879X2004000800011
Formato:  text/html
Fonte:  Brazilian Journal of Medical and Biological Research v.37 n.8 2004
Direitos:  info:eu-repo/semantics/openAccess
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