Betaine Protects Mice from Cardiotoxicity Triggered by Sodium Arsenite Through Antioxidative and Anti-inflammatory Pathways.
Saeedeh ShariatiMaryam ShiraniReza AzadnasabLayasadat KhorsandiMohammad Javad KhodayarPublished in: Cardiovascular toxicology (2024)
NaAsO 2 is known as a harmful pollutant all over the world, and many chronic heart diseases can be attributed to its prolonged exposure in NaAsO 2 -contaminated water. Therefore, considering the anti-inflammatory and antioxidant effects of betaine (BET), in this study, our team investigated the cardioprotective effects of this phytochemical agent on sodium arsenite (NaAsO 2 )-induced cardiotoxicity. Forty male mice were randomly divided into 4 groups: (I) Control; (II) BET (500 mg/kg); (III) NaAsO 2 (50 ppm); and (IV) NaAsO 2 + BET. NaAsO 2 was given to the animals for 8 weeks, but BET was given in the last two weeks. After decapitation, inflammatory factors and biochemical parameters were measured, and Western blot analyses were performed. BET decrease the activity level of alanine aspartate aminotransferase, creatine kinase MB, thiobarbituric acid reactive substances level, inflammatory factors (tumor necrosis factor-α) content, and nuclear factor kappa B expression. Furthermore, BET increased cardiac total thiol and activity levels of catalase, superoxide dismutase, and glutathione peroxidase and nuclear factor erythroid-2 expression. Hence, the administration of BET ameliorated the deleterious effects stemming from the imbalance of oxidative and antioxidant pathways and histopathological alterations observed in NaAsO 2 -intoxicated mice, thereby attenuating oxidative stress-induced damage and inflammation.
Keyphrases
- nuclear factor
- anti inflammatory
- oxidative stress
- toll like receptor
- poor prognosis
- diabetic rats
- heart failure
- drinking water
- heavy metals
- rheumatoid arthritis
- immune response
- type diabetes
- atrial fibrillation
- metabolic syndrome
- left ventricular
- binding protein
- quality improvement
- inflammatory response
- tyrosine kinase
- skeletal muscle
- endothelial cells
- high glucose
- wild type