Drug Res (Stuttg) 2019; 69(10): 572-578
DOI: 10.1055/a-0956-673
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Non-steroidal Anti-inflammatory Drugs in Tonic, Phasic and Inflammatory Mouse Models

Hugo F. Miranda
1   Neuroscience Department, Faculty of Medicine, Universidad de Chile, Santiago, Chile
,
Viviana Noriega
2   Cardiovascular Department, Clinical Hospital, Universidad de Chile, Santiago, Chile
,
Fernando Sierralta
3   Pharmacology Program, ICBM, Faculty of Medicine, Universidad de Chile, Santiago, Chile
,
Paula Poblete
1   Neuroscience Department, Faculty of Medicine, Universidad de Chile, Santiago, Chile
,
Nicolas Aranda
1   Neuroscience Department, Faculty of Medicine, Universidad de Chile, Santiago, Chile
,
Juan Carlos Prieto
2   Cardiovascular Department, Clinical Hospital, Universidad de Chile, Santiago, Chile
3   Pharmacology Program, ICBM, Faculty of Medicine, Universidad de Chile, Santiago, Chile
› Author Affiliations
Further Information

Publication History

received 16 April 2019

accepted 06 June 2019

Publication Date:
28 June 2019 (online)

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Abstract

The principal mechanism of action of non-steroidal anti-inflammatory drugs (NSAIDs) is the inhibition of ciclooxigenases. In this study was evaluated if NSAIDs could induce antinociceptive differences according to the type of murine pain model. Male mice were injected intraperitoneally with meloxicam, diclofenac, piroxicam, metamizol, ibuprofen, naproxen and paracetamol in the writhing, tail flick and formalin orofacial tests and dose-response were analyzed to obtain the ED50 of each drugs. Administration of NSAIDs produced in a dose-dependent antinociception with different potency in the tests. The relative potency of NSAIDs among the tests shows a value of 5.53 in the orofacial formalin test in phase I and 6.34 in phase II between meloxicam and paracetamol; of 7.60 in the writhing test between meloxicam and paracetamol and of 8.46 in the tail flick test between ibuprofen and paracetamol. If the comparison is made for each NSAID in the different tests, the minimum value was 0.01 for between writhing and phase II of the orofacial formalin. Meanwhile, the highest power ratio was 11.71 for diclofenac between writhing and tail flick tests. In conclusion, the results suggests that intraperitoneal NSAIDs administration induce antinociceptive activity depending on the type of pain. The results support that NSAIDs administration, induce a wide variety of antinociceptive effect, depending on the type of pain. This suggest the participation of different mechanisms of action that can be added to the simple inhibition of COXs controlled by NSAIDs.