Liraglutide pretreatment mitigated isoprenaline-induced cardiac dysfunction, reduced serum markers of myocardial injury, and induced antioxidative protection in rats.
Does liraglutide pretreatment prevent isoprenaline-induced myocardial injury in rats?
Liraglutide pretreatment provides antioxidative protection and alleviates isoprenaline-induced myocardial injury in a rat model.
Type 2 diabetes mellitus (T2DM) increases the risk of cardiovascular disease, especially myocardial injury. Due to their hypoglycemic effects, glucagon-like peptide-1 receptor agonists (GLP-1RAs) are efficiently used for T2DM management. GLP-1RAs also have anti-inflammatory and antioxidative effects and can improve cardiac function. The aim of this study was to investigate the cardioprotective effects of liraglutide, a GLP-1RA, on isoprenaline-induced myocardial injury in rats. The study included four groups of animals. They were pretreated with saline for 10 days + saline on days 9 and 10 (control), saline for 10 days + isoprenaline on days 9 and 10 (isoprenaline group), liraglutide for 10 days + saline on days 9 and 10 (liraglutide group), and liraglutide for 10 days, and on days 9 and 10 isoprenaline was administered. This study evaluated ECG, myocardial injury markers, oxidative stress markers, and pathohistological changes. The results showed that liraglutide mitigated the isoprenaline-induced cardiac dysfunction recorded by ECG. Liraglutide reduced serum markers of myocardial injury such as high-sensitive troponin I, aspartate aminotransferase, alanine aminotransferase, reduced thiobarbituric acid reactive substances, increased catalase and superoxide dismutase activity, increased reduced glutathione level, and improved lipid profile. Liraglutide induced antioxidative protection and alleviated isoprenaline-induced myocardial injury.
Bajić et al. (2023) studied Isoprenaline-induced myocardial injury. Liraglutide vs. Saline was evaluated on ECG, myocardial injury markers, oxidative stress markers, and pathohistological changes. Liraglutide pretreatment mitigated isoprenaline-induced cardiac dysfunction, reduced serum markers of myocardial injury, and induced antioxidative protection in rats.