Metformin modulates cardiac endothelial dysfunction, oxidative stress and inflammation in irradiated rats: A new perspective of an antidiabetic drug.
Heba M KaramRasha R RadwanPublished in: Clinical and experimental pharmacology & physiology (2019)
Cardiovascular disease is one of the most pivotal disorders after radiotherapy. The aim of this study investigates the possible protective effect of metformin against gamma radiation-induced heart damage in male rats. Group 1 (control) received saline, group 2 was whole body gamma-irradiated 5 Gy, group 3 was orally administered metformin 50 mg/kg/day for 2 weeks, group 4 received metformin 50 mg/kg/day for 1 week, then exposed to whole-body gamma radiation at a dose of 5 Gy and continued with metformin for further 1 week. The results revealed that the administration of metformin to irradiated rats significantly ameliorated the changes in cardiac biomarkers (LDH and CK-MB) compared with irradiated group. Heart catalase and SOD activities showed normal level when compared with the irradiated group. Also, NF-κB, IL-6 and TNF- α levels were markedly decreased compared with the corresponding values of irradiated group. Consequently, metformin reduced E-selectin as well ICAM and VCAM-1. These results confirmed by histopathological examination. In conclusion, concomitant administration of metformin during radiotherapy acts as a potent heart protector from oxidative stress, inflammatory mediators and endothelial dysfunction induced damages. Results thus hold a great promise for a new implication of an antidiabetic drug (metformin) as adjunct to radiotherapy.
Keyphrases
- oxidative stress
- radiation induced
- cardiovascular disease
- radiation therapy
- early stage
- diabetic rats
- heart failure
- atrial fibrillation
- left ventricular
- rheumatoid arthritis
- dna damage
- signaling pathway
- clinical trial
- machine learning
- metabolic syndrome
- coronary artery disease
- immune response
- endothelial cells
- single cell
- high glucose
- cardiovascular risk factors
- anti inflammatory
- heat stress
- placebo controlled
- heat shock protein