Potentiation of diclofenac-induced anti-inflammatory response by aminoguanidine in carrageenan-induced acute inflammation in rats: the role of nitric oxide

• Published in: Inflammation research Vol. 52; no. 9; pp. 378 - 382
• Main Authors: Al-Majed, A A, Khattab, M, Raza, M, Al-Shabanah, O A, Mostafa, A M
• Format: Journal Article
• Language: English
• Published: Switzerland Springer Nature B.V 01.09.2003
• Subjects: Acute Disease; Animals; Anti-Inflammatory Agents, Non-Steroidal - pharmacology; Carrageenan - adverse effects; Diclofenac - pharmacology; Drug Synergism; Edema - chemically induced; Guanidines - pharmacology; Inflammation - chemically induced; Inflammation - metabolism; Inflammation - pathology; Male; Nitric Oxide - metabolism; Nitric Oxide Synthase - metabolism; Nitric Oxide Synthase Type II; Nitroprusside - pharmacology; Rats; Rats, Wistar; Time Factors
• ISSN: 1023-3830; 1420-908X
• DOI: 10.1007/s00011-003-1189-1

To investigate whether aminoguanidine (AG) treatment enhances the anti-inflammatory effect of diclofenac in an acute inflammation model in rats. In 48 rats carrageenan-induced paw edema was used as an acute inflammation model. Inflammatory activity was assessed at 1.5, 3 and 6 h after sub-planter injection of carrageenan (0.1 ml of a 1% solution in 0.85% saline). The anti-inflammatory effect of diclofenac (25 mg/kg, i.p.) was studied in comparison to that of the selective inducible nitric oxide synthase (iNOS) inhibitor, AG, and of nitric oxide donor, sodium nitroprusside (SNP). AG, failed to inhibit inflammation during the first 3 h following carrageenan administration, but caused a slight, although statistically insignificant inhibition at 6 h. Diclofenac significantly reduced the carrageenan-induced edema in rat paw at all the time points studied. Administration of diclofenac after AG pretreatment caused significant (P < 0.001) reduction in edema that was double that of diclofenac alone 6 h after carrageenan injection. Administration of SNP as a single dose after AG pretreatment prevented any potentiation of anti-inflammatory response that was observed in the case of AG combined with diclofenac treatment. These results show that AG markedly potentiates the anti-inflammatory activity of diclofenac at 6 h and this potentiation effect is nitric oxide-dependent.