Evaluation of immunomodulatory activity of tenoxicam in mice

0Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

Purpose: The present study was conducted to evaluate the effect of tenoxicam on cellular and humoral immunity. Methods: Tenoxicam (2.5-10mg/kg) was administered at three different doses to three groups of mice and the cellular immune responses were studied using delayed hypersensitivity response (DTH) and cyclophosphamide-induced neutropenia while the humoral immune response was evaluated using hemagglutination test and mice mortality ratio. Normal saline and cyclophosphamide were used as negative and positive controls, respectively. Results: DTH assay resulted in a significant reduction in skin thickness (p < 0.05) for tenoxicam treated groups when compared to the negative control group at 24 h, 48 h and 72 h after administration of challenging dose of dinitrochlorobenzene (DNCB). Cyclophoshamide induced neutropenia showed a significant percentage reduction in total leukocyte count (TLC) and differential leukocyte count (DLC) i.e. lymphocytes and neutrophils (p< 0.05), but an increase in monocytes in all the treatment groups in the following order: 10 mg>5 mg >2.5 mg> negative control group. A dose dependent reduction response was observed (p<0.05) in haemagglutination assay (HA). In mice lethality test mortality ratios of 2.5 mg, 5 mg, 10 mg tenoxicam were 60 %, 80% and 100 %, respectively, compared to 20 % and 100 % for normal saline group and cyclophosphamide, respectively Conclusion: The results suggest that tenoxicam suppresses both cellular and humoral immunity in mice.

Cite

CITATION STYLE

APA

Nasim, F., Javeed, A., Ashraf, M., & Ghafoor, A. (2018). Evaluation of immunomodulatory activity of tenoxicam in mice. Tropical Journal of Pharmaceutical Research, 17(9), 1811–1816. https://doi.org/10.4314/tjpr.v17i9.19

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free