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Calcium dobesilate ameliorates hepatorenal injury induced by carbon tetrachloride in mice

OBJECTIVE(S): Calcium dobesilate (CaD) has anti-oxidant, anti-inflammatory, and anti-apoptotic effects. In this study, the protective effects of CaD against hepatorenal damage induced by carbon tetrachloride (CCl(4)) in mice were evaluated. MATERIALS AND METHODS: Thirty male mice were randomly divid...

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Detalles Bibliográficos
Autores principales: Hakimizadeh, Elham, Kaeidi, Ayat, Rahmani, Mohammadreza, Allahtavakoli, Mohammad, Hassanshahi, Jalal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124530/
https://www.ncbi.nlm.nih.gov/pubmed/35655592
http://dx.doi.org/10.22038/IJBMS.2022.61499.13606
Descripción
Sumario:OBJECTIVE(S): Calcium dobesilate (CaD) has anti-oxidant, anti-inflammatory, and anti-apoptotic effects. In this study, the protective effects of CaD against hepatorenal damage induced by carbon tetrachloride (CCl(4)) in mice were evaluated. MATERIALS AND METHODS: Thirty male mice were randomly divided into five groups: Control, CaD 100 mg/kg, CCl(4), CCl(4)+CaD 50 mg/kg, and CCl(4)+CaD 100 mg/kg. CaD (50 and 100 mg/kg) was administered orally once a day for 4 weeks. The liver and kidney indices (serum creatinine, blood urine nitrogen, alanine aminotransferase, and aspartate aminotransferase levels) were determined. Also, liver and kidney tissue oxidant/anti-oxidant markers (glutathione peroxidase, malondialdehyde, total anti-oxidant capacity, and superoxide dismutase) were measured. Cleaved caspase-3, Bax, cytochrome-c, and Bcl-2 protein levels were measured by immunoblotting method in the liver and kidney tissues. The liver and kidney histopathological changes were evaluated by the Hematoxylin and Eosin (H&E) staining method. RESULTS: CCl(4) induced significant oxidative stress and apoptosis in kidney and liver tissues that was concomitant with histopathological abnormalities in these organs in the CCl(4) group versus the control (P<0.05). However, CaD (100 mg/kg) could significantly improve the histopathological change in the liver and kidney tissues of CCl(4)+CaD 100 mg/kg mice versus the CCl(4) group (P<0.05). In addition, CaD (100 mg/kg) attenuated the pro and anti-apoptotic markers in the liver and kidney tissues of CCl(4)+CaD 100 mg/kg mice versus the CCl(4) group (P<0.05). CONCLUSION: CaD (100 mg/kg) has a protective effect against hepatorenal injury induced by CCl(4) at least via its anti-apoptotic and anti-oxidant properties.