The Effect of Descurainia Sophia Seed Extract on Nephrotoxicity Markers Induced by Acetaminophen in Mice

Authors

  • Maryam Iman Dept. of Pharmaceutics, Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran
  • Pedram Moshaie-Nezhad Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
  • Seyed Mohammad Zarei Dept. of Pharmacognosy, Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran
  • Zahra Bahari Dept. of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran
  • Zohreh Jangravi Dept. of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran
Abstract:

    Background & Objective:  Acetaminophen is known as the most common agent which causes hepatic and renal toxicity in human and experimental animals at supra-therapeutic doses. The current study investigated the protective effects of Descurainia sophia seed extract on the acetaminophen-induced nephrotoxicity markers in male mice.  Materials & Methods:  Experimental male mice (n=60, Swiss albino mice) were divided into six groups as follows: Group A (control group), Group B (acetaminophen group), and treatment groups including T1, T2, T3, and T4 (D. sophia seed extract groups). Toxicity was induced by acetaminophen (500 mg/kg). The mice administered D. sophia seed extract for 7 days in doses of 50, 100, 200, and 300 mg/kg. In the next step, animals were euthanized 24 hours after acetaminophen administration. Blood samples were collected. Serum levels of blood urea nitrogen (BUN), creatinine, and uric acid were analysed. Furthermore, kidney tissues were removed for histopathological examination via haematoxylin and eosin staining.  Results:  Our data revealed that acetaminophen increased the levels of BUN, creatinine and uric acid (P<0.05). Pre-treatment of D. sophia seed extract decreased the serum BUN, creatinine and uric acid significantly compared to the acetaminophen group (P<0.05). Additionally, in histopathological examination, D. sophia extract had restored acetaminophen-induced nephrotoxicity, particularly in the dose of 300 mg/kg.   Conclusion:   The present findings suggested that oral administration of D. sophia seed extract has protective effect against acetaminophen nephrotoxicity in mice.     

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Journal title

volume 29  issue 134

pages  2- 2

publication date 2021-04

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