Indian Journal of Animal Research
SCOPUSWeb of Science
  • Year: 2025
  • Volume: 59
  • Issue: 10

Galngin Mitigates Glycerol-induced Rhabdomyolysisassociated Acute Kidney Injury by Modulating Nf-κb-mediated Cytokine Pathways and Apoptotic Responses

  • Author:
  • F. Manal El-Khadragy1, Rewaida Abdel-Gaber2, H. Nourhan Mohamed3, H. Fatma Elzahraa Salem4,*
  • Total Page Count: 9
  • Page Number: 1672 to 1680

1Department of Biology, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia

2Department of Zoology, College of Science, King Saud University, P.O. 2455, Riyadh, 11451, Saudi Arabia

3Faculty of Medicine, Newgiza University, New Giza, Cairo, Egypt

4Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt, P.O. Box 11611, Egypt

*Corresponding Author: Fatma Elzahraa H. Salem, Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt, P.O. Box 11611, Egypt, Email: elzahraa.fatma@yahoo.com

Online published on 5 February, 2026.

Abstract

This study investigated the protective capabilities of galangin, a naturally occurring flavonoid found in galangal and propolis, against glycerol-induced acute kidney injury (AKI), a serious complication associated with rhabdomyolysis.

Rats were pre-treated with galangin (100 mg/kg) for 21 days before receiving a glycerol single injection (50%, 10 mg/kg, intramuscular) to induce AKI. According to the findings, the kidneys in the AKI group showed notable molecular and functional alterations.

Treatment with galangin notably reduced kidney relative weight and decreased serum levels of urea and creatinine, indicating preservation of renal function. Furthermore, the intervention lowered concentrations of lactate dehydrogenase (LDH) and creatine kinase (CK), key indicators of muscle breakdown associated with rhabdomyolysis. A remarkable finding was galangin's ability to enhance the endogenous antioxidant defence system. Treatment led to increased activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and glutathione reductase (GR), along with elevated levels of reduced glutathione (GSH). Concurrently, galangin treatment resulted in reduced malondialdehyde (MDA) and nitric oxide (NO) concentrations, demonstrating effective suppression of oxidative stress markers. Similarly, animals receiving galangin exhibited significantly reduced levels of pro-inflammatory mediators, including interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), myeloperoxidase (MPO) and nuclear factor kappa B (NF-κB). Simultaneously, there was an elevation in anti-inflammatory interleukin-10 (IL-10) compared to the untreated model group, in addition to a significant modulation of apoptotic pathways by decreased expression of pro-apoptotic proteins Bax and caspase-3, and increased in Bcl-2. The comprehensive findings from this study provide compelling evidence for galangin as a promising therapeutic agent against glycerol-induced acute kidney injury. Overall, galangin shows promise as a potential therapeutic agent for preventing or treating rhabdomyolysis-associated acute kidney injury.

Keywords

AKI, Antioxidant, Apoptosis, Galangin, Inflammation, Kidney, Rhabdomyolysis