WJPPS Citation

Login

Search

News & Updation

  • Journal web site support Internet Explorer, Google Chrome, Mozilla Firefox, Opera, Saffari for easy download of article without any trouble.
  •  
  • Updated Version
  • WJPPS introducing updated version of OSTS (online submission and tracking system), which have dedicated control panel for both author and reviewer. Using this control panel author can submit manuscript
  • Call for Paper
    • WJPPS  Invited to submit your valuable manuscripts for Coming Issue.
  • ICV
  • WJPPS Rank with Index Copernicus Value 84.65 due to high reputation at International Level

  • Scope Indexed
  • WJPPS is indexed in Scope Database based on the recommendation of the Content Selection Committee (CSC).

  • WJPPS: New Impact Factor 2026
  • WJPPS Impact Factor has been Increased to 8.485 for Year 2026.

  • WJPPS: AUGUST ISSUE PUBLISHED
  • AUGUST 2026 Issue has been successfully launched on 1 AUGUST 2026.

Abstract

PROTECTIVE EFFECT OF DAPANSUTRILE AGAINST METHOTREXATE-INDUCED TESTICULAR TOXICITY IN RATS

Haider H. Motlak, Mahmoud Elshal, Marwa S. Serrya*

ABSTRACT

Background: Methotrexate (MTX) is a widely used therapy for the treatment of malignancies and autoimmune diseases; however, its use is limited by adverse effects such as testicular toxicity and impairment of male fertility. Objective: This study aimed to evaluate the protective effect of dapansutrile (DAPA) against methotrexate (MTX)-induced testicular toxicity in rats. Methods: Twenty-four adult male rats were divided into four groups: control, MTX, MTX + DAPA (10 mg/kg), and MTX + DAPA (20 mg/kg). Testicular toxicity was first assessed by measuring relative testicular weight, sperm count, and sperm viability, in addition to histopathological examination of testicular tissue. Results: Administration of MTX resulted in a non-significant decrease in relative testicular weight; however, it caused a significant reduction in sperm count and viability. In addition, marked histopathological alterations were observed,including degeneration of seminiferous tubules and disruption of spermatogenesis. Co-administration of DAPA with MTX produced a mild, dose-dependent improvement, where DAPA-treated groups showed a significant recovery in sperm parameters and partial restoration of testicular histoarchitecture. Conclusion: DAPA effectively attenuated MTX-induced testicular toxicity, preserving both testicular structure and function in a mild, dose-dependent manner. These findings suggest its potential role as a protective agent against chemotherapy-induced reproductive toxicity.

Keywords: Dapansutrile; Methotrexate; Testicular toxicity; Spermatogenesis; Sperm count; Sperm viability; Histopathology; Rat model.


[Download Article]     [Download Certifiate]

Call for Paper

World Journal of Pharmacy and Pharmaceutical Sciences (WJPPS)
Read More

Online Submission

World Journal of Pharmacy and Pharmaceutical Sciences (WJPPS)
Read More

Email & SMS Alert

World Journal of Pharmacy and Pharmaceutical Sciences (WJPPS)
Read More