Quercetin Alleviates Renal Ischemia/Reperfusion-Induced Acute Kidney Injury by Modulating IL-1β, Caspase-3, and Glutathione Signaling in Rats

Authors

  • hassan alaasam Department of Pharmacology and Therapeutics, Faculty of Pharmacy, University of Kufa, Najaf, Iraq
  • Suhad traiji zamil Department of Pharmacology and Therapeutics, Faculty of Pharmacy, University of Kufa, Najaf, Iraq

Keywords:

Renal ischemia reperfusion; Quercetin; Nephroprotection; Oxidative stress; Inflammation; Apoptosis

Abstract

Abstract

Background
Renal ischemia/reperfusion injury (IRI) is a leading contributor to acute kidney injury, involving complex pathophysiological mechanisms such as excessive oxidative stress, inflammatory activation, and dysregulation of cell survival pathways. Quercetin, a naturally occurring flavonol, is well recognized for its strong antioxidant and anti-inflammatory activities. The present study was designed to investigate the potential nephroprotective role of quercetin in an experimental rat model of renal ischemia/reperfusion injury.

Materials and Methods
Twenty-eight adult male Sprague–Dawley rats were randomly allocated into four experimental groups: sham-operated, ischemia/reperfusion (I/R) control, vehicle-treated (DMSO), and quercetin-treated groups. Renal ischemia/reperfusion injury was experimentally induced by subjecting both kidneys to ischemia for 30 minutes, followed by 2 hours of reperfusion. Quercetin was administered intraperitoneally at a dose of 50 mg/kg, 30 minutes prior to the induction of ischemia. Renal tissue levels of interleukin-1β (IL-1β), caspase-3, and glutathione (GSH) were determined using commercially available sandwich ELISA kits. in addition to the assessment of renal histopathological changes.

Results
Renal ischemia/reperfusion injury induced a significant increase in IL-1β and caspase-3 levels, along with a marked depletion of GSH, in comparison with the sham group, reflecting pronounced inflammatory activation, apoptotic signaling, and oxidative stress. In contrast, quercetin pretreatment effectively mitigated renal injury by suppressing inflammatory and apoptotic responses and restoring antioxidant capacity, as evidenced by reduced IL-1β and caspase-3 levels and normalization of GSH content relative to the I/R control and vehicle groups. and attenuating renal histological damage.

Conclusion
Quercetin confers pronounced nephroprotective effects against renal ischemia/reperfusion injury, largely mediated through its antioxidant, anti-inflammatory, and antiapoptotic properties.

 

Keywords
Renal ischemia/reperfusion injury; Quercetin; Nephroprotection; Oxidative stress; Inflammation; Apoptosis

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Author Biography

  • Suhad traiji zamil, Department of Pharmacology and Therapeutics, Faculty of Pharmacy, University of Kufa, Najaf, Iraq
     

    Dr. Suhad Traiji Zamil is an Assistant Professor in the Department of Pharmacology and Therapeutics, Faculty of Pharmacy, University of Kufa, Iraq. Her research focuses on pharmacology, oxidative stress, inflammation, experimental disease models, and the molecular mechanisms underlying drug action.

Published

2026-07-31

Issue

Section

Articles

How to Cite

alaasam, hassan, & zamil, S. (2026). Quercetin Alleviates Renal Ischemia/Reperfusion-Induced Acute Kidney Injury by Modulating IL-1β, Caspase-3, and Glutathione Signaling in Rats. Kufa Journal of Pharmaceutical Sciences, 3(2). https://journal.uokufa.edu.iq/index.php/kjps/article/view/23990

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