Sinapic acid attenuates cyclophosphamide-induced liver toxicity in mice by modulating oxidative stress, NF-κB, and caspase-3 | ||
| Iranian Journal of Basic Medical Sciences | ||
| مقاله 5، دوره 26، شماره 5، مرداد 2023، صفحه 526-531 اصل مقاله (500.21 K) | ||
| نوع مقاله: Original Article | ||
| شناسه دیجیتال (DOI): 10.22038/ijbms.2023.68579.14960 | ||
| نویسندگان | ||
| Shiva Rezaei1، 2؛ Seyed Jalal Hosseinimehr3؛ Mehryar Zargari4؛ Abbasali Karimpour Malekshah1؛ Mansooreh Mirzaei1؛ Fereshteh Talebpour Amiri* 1 | ||
| 1Department of Anatomy, Faculty of Medicine, Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran | ||
| 2Student Research Committee, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran | ||
| 3Department of Radiopharmacy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran | ||
| 4Department of Biochemistry, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran | ||
| چکیده | ||
| Objective(s): Cyclophosphamide (CP) as an antineoplastic drug is widely used in cancer patients, and liver toxicity is one of its complications. Sinapic acid (SA) as a natural phenylpropanoid has anti-oxidant, anti-inflammatory, and anti-cancer properties. Materials and Methods: The purpose of the current study was to determine the protective effect of SA versus CP-induced liver toxicity. In this research, BALB/c mice were treated with SA (5 and 10 mg/kg) orally for one week, and CP (200 mg/kg) was injected on day 3 of the study. Oxidative stress markers, serum liver-specific enzymes, histopathological features, caspase-3, and nuclear factor kappa-B cells were then checked. Results: CP induced hepatotoxicity in mice and showed structural changes in liver tissue. CP significantly increased liver enzymes and lipid peroxidation, and decreased glutathione. The immunoreactivity of caspase-3 and nuclear factor kappa-B cells was significantly increased. Administration of SA significantly maintained histochemical parameters and liver function enzymes in mice treated with CP. Immunohistochemical examination showed SA reduced apoptosis and inflammation. Conclusion: The data confirmed that SA with anti-apoptotic, anti-oxidative, and anti-inflammatory activities was able to preserve CP-induced liver injury in mice. | ||
| کلیدواژهها | ||
| Apoptosis؛ Cyclophosphamide؛ Liver injury؛ Inflammation؛ Oxidative stress؛ Sinapic acid | ||
| مراجع | ||
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