Hydroxysafflor Yellow A Alleviates Acute Myocardial Ischemia/Reperfusion Injury in Mice by Inhibiting Ferroptosis via the Activation of the HIF-1 & alpha;/SLC7A11/GPX4 Signaling Pathway

Ferroptosis is closely associated with the pathophysiology of myocardial ischemia. Hydroxysafflor yellow A (HSYA), the main active ingredient in the Chinese herbal medicine safflower, exerts significant protective effects against myocardial ischemia/reperfusion injury (MI/RI). The aim of this study was to investigate the protective effects of HSYA against MI/RI and identify the putative underlying mechanisms. An in vivo model of acute MI/RI was established in C57 mice. Subsequently, the effects of HSYA on myocardial tissue injury were evaluated by histology. Lipid peroxidation and myocardial injury marker contents in myocardial tissue and serum and iron contents in myocardial tissue were determined using biochemical assays. Mitochondrial damage was assessed using transmission electron microscopy. H9C2 cardiomyocytes were induced in vitro by oxygen-glucose deprivation/reoxygenation, and ferroptosis inducer erastin was administered to detect ferroptosis-related indicators, oxidative-stress-related indicators, and expressions of ferroptosis-related proteins and HIF-1a. In MI/RI model mice, HSYA reduced myocardial histopathological damage, ameliorated mitochondrial damage in myocardial cells, and decreased total cellular iron and ferrous ion contents in myocardial tissue. HSYA increased the protein levels of SLC7A11, HIF-1a, and GPX4 and mitigated erastin- or HIF-1a siRNA-induced damage in H9C2 cells. In summary, HSYA alleviated MI/RI by activating the HIF-1a/SLC7A11/GPX4 signaling pathway, thereby inhibiting ferroptosis.

Automated summary

This study investigated the protective effects of Hydroxysafflor yellow A (HSYA) against myocardial ischemia/reperfusion injury (MI/RI) and identified the underlying mechanisms. HSYA reduced myocardial histopathological damage, ameliorated mitochondrial damage, and decreased iron contents in myocardial tissue. It activated the HIF-1a/SLC7A11/GPX4 signaling pathway to inhibit ferroptosis, thereby alleviating MI/RI.