Possible beneficial effects of benfotiamine, a thiamine derivative, in isoproterenol-induced myocardial infarction in rats /
الدور المفيد المحتمل للبنفوتيامين: مشتق الثيامين: فى علاج إحتشاء عضلة القلب الناجم عن إيزوبروتيرينول فى الجرذان
Omnia Farouk Abdelmonem Hassan ; Supervised Aiman Saad Elkhatib , Lamiaa Ahmed Ahmed , Omneya Osama Galal
- Cairo : Omnia Farouk Abdelmonem Hassan , 2020
- 134 P. : charts , facimiles ; 25cm
Thesis (Ph.D.) - Cairo University - Faculty of Pharmacy - Department of Pharmacology and Toxicology
Acute myocardial infarction (AMI) remains the most common cause of morbidity and mortality worldwide.The present study was directed to investigate the beneficial effects of pre- and post-treatments with benfotiamine in isoproterenol (ISO)-induced MI in rats. Myocardial heart damage was induced by subcutaneous injection of ISO (150 mg/kg) once daily for two consecutive days. Benfotiamine (100 mg/kg/day) was given orally for two weeks before or after ISO treatment. ISO administration revealed significant changes in electrocardiographic recordings, elevation of levels of cardiac enzymes; creatinine kinase (CK-MB) and troponin-I (cTn-I), and perturbation of markers of oxidative stress; nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, malondialdehyde (MDA), reduced glutathione (GSH), superoxide dismutase (SOD) and glutathione peroxidase (GPx) and markers of inflammation; protein kinase C (PKC), nuclear factor-kappa B (NF-B) and metalloproteinase-9 (MMP-9).The apoptotic markers (caspase-8 and p53) were also significantly elevated in ISO groups in addition to histological alterations. Groups treated with benfotiamine pre- and post-ISO administration showed significant decrease in cardiac enzymes levels and improvement of oxidative stress, inflammatory and apoptotic markers compared to the ISO groups. The current study highlights the potential role of benfotiamine as a promising agent for prophylactic and therapeutic interventions in myocardial damage in several cardiovascular disorders via NADPH oxidase inhibition