Therapeutic Efficacy of Thymoquinone in Attenuating Obstructive Renal Fibrosis: A Dose-Response Analysis of Tumor Necrosis Factor-Alpha Suppression and Histopathological Remodeling

Authors

  • Edy Nur Rachman Trainee in Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  • Suprapti Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  • Muhammad Irsan Saleh Department of Biomedical, Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  • Ian Effendi Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  • Zulkhair Ali Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  • Novadian Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia

DOI:

https://doi.org/10.37275/bsm.v10i5.1583

Keywords:

Chronic kidney disease, Renal fibrosis, Thymoquinone, Tumor necrosis factor-alpha, Unilateral ureteral obstruction

Abstract

Background: Chronic kidney disease is characterized by progressive renal fibrosis, a maladaptive process driven by chronic inflammation and extracellular matrix accumulation. Tumor necrosis factor-alpha (TNF-α) plays a central role in this fibrogenic cascade. Thymoquinone (TQ), the primary bioactive compound of Nigella sativa, exhibits potent anti-inflammatory properties.

Methods: In this therapeutic intervention model, 107 male Wistar rats were subjected to Unilateral Ureteral Obstruction (UUO). To test TQ's ability to halt established fibrogenesis, treatment was delayed until day 7 post-obstruction. Rats were randomized to receive TQ intraperitoneally at 5, 10, or 20 mg/kg body weight for 14 days. Outcomes included renal function (urea/creatinine), tubulointerstitial injury (PAS staining), fibrosis area (Sirius Red staining), and localized TNF-α mRNA expression (reverse transcriptase PCR normalized to GAPDH). Data were analyzed using ANOVA followed by Tukey’s Honestly Significant Difference (HSD) test. 

Results: UUO induced significant structural injury and upregulated TNF-α expression compared to sham controls (p < 0.001). TQ intervention significantly reduced the tubulointerstitial injury score, with the greatest reduction at 20 mg/kg (p < 0.01). The positively stained fibrotic area exhibited a U-shaped response, maximally decreased at the 10 mg/kg dose (p < 0.01). Similarly, TNF-α mRNA relative expression was significantly suppressed by TQ, exhibiting a pharmacological ceiling effect at 10 mg/kg (p < 0.01). 

Conclusion: Thymoquinone administered therapeutically mitigates established structural renal fibrosis and tubulointerstitial injury by downregulating TNF-α-mediated inflammation. A 10 mg/kg dose represents the optimal therapeutic threshold for anti-fibrotic efficacy in obstructive nephropathy. 

Authors

  • Edy Nur Rachman1*
  • Suprapti2
  • Muhammad Irsan Saleh3
  • Ian Effendi2
  • Zulkhair Ali2
  • Novadian2
  1. 1Trainee in Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  2. 2Department of Nephrology and Hypertension, Dr. Mohammad Hoesin General Hospital/Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  3. 3Department of Biomedical, Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia

Corresponding author Edy Nur Rachman — edyrachmann@gmail.com

Article history

  1. Submitted
  2. Accepted
  3. Published

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Published

2026-03-12

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How to Cite

1.
Edy Nur Rachman, Suprapti, Muhammad Irsan Saleh, Ian Effendi, Zulkhair Ali, Novadian. Therapeutic Efficacy of Thymoquinone in Attenuating Obstructive Renal Fibrosis: A Dose-Response Analysis of Tumor Necrosis Factor-Alpha Suppression and Histopathological Remodeling. Bioscmed [Internet]. 2026 Mar. 12 [cited 2026 Aug. 13];10(5):1824-36. Available from: https://bioscmed.com/index.php/bsm/article/view/1583

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