Abstract
Tanshinone ⅡA (TSA), a component of traditional Chinese medicine, effectively protects
against myocardial injury. However, its clinical application is limited by poor water
solubility and a short half-life. In this study, we report on four TSA derivatives
designed and synthesized by our research group. The protective activity against hypoxia-reoxygenation
injury in cells was evaluated, and derivative Ⅰ-3 was selected for in vivo experiments to verify its myocardial protective activity in rats with myocardial
infarction. The results demonstrated that these four compounds could protect neonatal
rat cardiomyocytes from hypoxia-reoxygenation injury. Among the derivatives, Ⅰ-3 showing
superior protective effects, we found that Ⅰ-3 has enhanced metabolic stability and
an extended half-life. Ⅰ-3 exhibited superior biological activity, effectively reducing
the heart infarction area, alleviating myocardial hypertrophy, and enhancing cardiac
pumping function. Ⅰ-3 reported in
the present work represents a novel and effective derivative of TSA, showing great
potential for the treatment of myocardial ischemia (MI).
Keywords
Salvia miltiorrhiza
- Lamiaceae - Tanshinone ⅡA - derivatives - myocardial ischemia - coronary artery
ligation - cardiomyocytes - hemodynamic