Allium jesdianum Attenuates Oxidative Stress and Inflammatory Responses in the Liver of Cyclophosphamide-Treated Mice | ||
| Pathobiology Reserach | ||
| Volume 28, Issue 4, Autumn 2025, Pages 63-70 PDF (501.51 K) | ||
| Document Type: Original Research | ||
| DOI: 10.48311/mjms.2025.117248.82609 | ||
| Authors | ||
| KOBRA SHIRANI* 1; Alireza Rezaei2; Bahareh Sadat yousefsani3; Ameneh Omidi4 | ||
| 1Department of Toxicology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. | ||
| 21. Department of Toxicology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. | ||
| 33. Department of Traditional Medicine, School of Persian Medicine, Iran University of Medical Sciences, Tehran, Iran. | ||
| 4Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. | ||
| Abstract | ||
| Introduction The liver is essential for drug metabolism and detoxification, and cyclophosphamide (CTX) can trigger hepatotoxicity via oxidative stress and inflammatory responses. Allium jesdianum has antioxidant and anti-inflammatory effects that may mitigate CTX-induced liver injury. This study investigates whether the antioxidant properties of A. jesdianum can protect organ function in a CTX-treated animal model, with implications for potential adjunctive strategies in CTX therapy. Methods and materials Twenty male NMRI mice divided randomly into 4 groups (n=5 per group): normal saline for 14 days (oral), A. jesdianum extract at 200 mg/kg daily for 14 days (oral), CTX at 20 mg/kg intraperitoneal (IP) for 5 days, and A. jesdianum extract at 200 mg/kg (oral) daily for 14 days + CTX at 20 mg/kg IP during the last 5 days. Tissue samples were collected and analyzed for lipid peroxidation, antioxidant enzyme activity, and inflammatory cytokines. Results: CTX increased thiobarbituric acid reactive substances (TBARS), which were attenuated by A. jesdianum (P < 0.001). Antioxidant enzymes such as catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px) were adversely modulated by CTX and markedly ameliorated by A. jesdianum pretreatment (p < 0.001). Pro-inflammatory cytokines (interleukin-6 (IL-6), interleukin-1β (IL-1β), and tumor necrosis factor-alpha (TNF-α) were increased in the CTX group, which was significantly decreased by A. jesdianum (p < 0.001, p < 0.001, and p < 0.01, respectively). Conclusion A. jesdianum suggests attenuating CTX-associated liver toxicity by dampening oxidative stress and inflammatory responses, thereby supporting its prospective role as a natural cytoprotective adjunct in chemotherapy regimens. | ||
| Keywords | ||
| Allium jesdianum; Liver; Pro-inflammatory cytokines; Antioxidant enzymes | ||
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