Startseite Piroxicam reduces acute and chronic pain response in type 1 diabetic rats
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Piroxicam reduces acute and chronic pain response in type 1 diabetic rats

  • Abbas Alimoradian , Fatemeh Samimi , Hadise Aslfalah , Seied Amirhossein Latifi , Mehdi Salehi , Maryam Khodaei und Jamal Amri EMAIL logo
Veröffentlicht/Copyright: 8. Februar 2021

Abstract

Objectives

Pain associated with various underlying pathologies is a major cause of morbidity and diminished life quality in diabetic patients. Effective control of pain requires the use of analgesics with the best efficacy and with minimal side effects. Therefore, our aim in this study was to investigate the effects of non-steroidal anti-inflammatory drugs (NSAIDs) on pain in diabetic rats.

Methods

In this study, we investigated the analgesic effects of drugs belonging to three different classes of NSAIDs in a rat model of diabetes. Four diabetic groups received normal saline, diclofenac, piroxicam and ketorolac, respectively, and four non-diabetic groups received normal saline, diclofenac, piroxicam and ketorolac. Type 1 diabetes was induced in rats by a single injection of streptozotocin (60 mg/kg bw). Formalin (50 µL of 2.5%) nociception assay was used to examine the effect of treatment with diclofenac, piroxicam and ketorolac on acute and chronic pain in healthy and diabetic rats.

Results

Piroxicam showed significant analgesic effects both in the acute phase of pain (5–10 min after injection of formalin into the left hind paw), and in the chronic phase (20–60 min after formalin injection) in healthy as well as diabetic rats. Diclofenac and ketorolac also reduced pain scores in healthy rats. However, these two drugs failed to diminish pain in diabetic rats.

Conclusion

Our data point for better efficacy of piroxicam in controlling pain in diabetes.


Corresponding author: Jamal Amri, Member, Traditional and Complementary Medicine Research Center, Faculty of Medicine, Arak University of Medical Sciences, Arak 3848176941, Iran; and Department of Clinical Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran, E-mail:

Funding source: Arak University of Medical Sciences

Acknowledgments

The authors would like to thank the Arak University of Medical Sciences, Arak, Iran for financial support.

  1. Research funding: This work was supported by funds from the Arak University of Medical Sciences (Grant number: 1033).

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

  4. Ethical approval: The present study was approved by Review Board and Ethics Committee of Arak University of Medical Sciences, Iran.

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Received: 2019-12-21
Accepted: 2020-09-10
Published Online: 2021-02-08

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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