Xanthohumol Protects the Rat Myocardium against Ischemia/Reperfusion Injury-Induced Ferroptosis

Ferroptosis is an iron-dependent form of cell death caused by the inactivation of glutathione peroxidase 4 (GPX4) and accumulation of lipid peroxides. Ferroptosis has been found to participate in the ischemia-reperfusion (I/R) injury, leading to heart dysfunction and myocardial cell death. Xanthohumol (XN), a prenylated flavonoid isolated from Humulus lupulus, has multiple pharmacological activities, such as anti-inflammatory and antioxidant. This study is aimed at investigating whether XN could attenuate the I/R-induced ferroptosis in cardiomyocytes and the underlying mechanisms. Cardiomyocytes were treated with Fe-SP and RSL3, and the rat hearts were treated with I/R. The results from the present study show that XN was able to protect cardiomyocytes against Fe-SP- and RSL3-induced ferroptotic cell death by decreasing the production of lipid peroxidation and ROS, chelating iron, reducing the NRF2 protein level, and modulating the protein levels of GPX4. Moreover, XN significantly decreased the mRNA levels of ferroptosis markers, Ptgs2 and Acsl4, and the protein levels of ACSL4 and NRF2 and modulated the protein levels of GPX4 in I/R-treated hearts. The findings from the present study suggest that XN might have the therapeutic potential for the I/R-induced ferroptosis injury.


Introduction
According to the World Health Organization, ischemic heart disease is the first leading cause of death worldwide [1]. Currently, reperfusion is the definitive treatment for acute ischemic heart disease [2]. However, there is no effective therapy to prevent heart damage caused by ischemia-reperfusion (I/ R) injury (IRI). IRI may cause massive cardiomyocyte death, which is a major cause of cardiac dysfunction, leading to cardiac arrhythmias, heart failure, and death [3]. Oxidative stress has been demonstrated to consider a key initiator of IRI in clinical [4]. In addition, the deregulation of iron homeostasis has an important contribution to increasing intracellular free iron in cardiac cells [5]. The iron ion can enhance the generation of reactive oxygen species (ROS) by Fenton reaction, subsequently increasing cell damage through the attack of lipids to induce ferroptosis, which differs from apoptosis, necrosis, or autophagy [6].
Ferroptosis is an iron-dependent form of cell death caused by inactivation of glutathione peroxidase 4 (GPX4) and accumulation of lipid peroxides [7]. GPX4 not only catalyzes the peroxidation of hydrogen peroxide (H 2 O 2 ) but also detoxifies the lipid peroxides by reducing glutathione [8]. Jang et al. reported that ferroptotic stimuli reduce mitochondrial bioenergetics, glutathione depletion, and GPX4 inactivation, leading to ferroptosis in cardiomyocytes [9]. Park et al. indicated that downregulation of GPX4 during myocardial infarction contributes to ferroptotic cell death in cardiomyocytes upon metabolic stress [10]. Feng et al. reported that the liproxstatin-1 (Lip-1), a ferroptosis inhibitor, protects the myocardium against IRI by protecting mitochondrial structural integrity and function and restoring the GPX4 level to reduce heart damage [11].
Under physiological conditions, almost all iron is tightly bound to iron-protein, such as transferrin and ferritin, which control iron reactivity. During ischemia, however, a large amount of iron is released from iron-protein and then participates in the generation of free radicals [12]. Previous studies have shown that iron chelators can protect the heart from IRI. Tang et al. showed that deferoxamine, an iron chelator, significantly attenuated myocardial injury in the I/Rtreated rat hearts [13]. Fang et al. demonstrated that inhibition of ferroptosis by dexrazoxane, an iron chelator, or ferrostatin-1 (Fer-1), a ferroptosis inhibitor, reduces the myocardial infarct size through maintaining mitochondrial function [14].
Safe and effective natural products play a vital role in drug discovery, especially for cardiovascular diseases [15][16][17][18]. Flavonoids are naturally presented in a variety of fruit, vegetables, and plant-based food products. Flavonoids can not only inhibit lipid peroxidation and chelate redoxactive metals but also improve cardiac function and attenuate myocardial infarction [19][20][21]. Recently, it has been reported that flavonoids can suppress erastin-induced ferroptosis in human pancreatic ductal adenocarcinoma cells [22]. In addition, epidemiological studies have shown a positive correlation between the diet of flavonoid-rich foods and cardiovascular health [23]. Xanthohumol (XN), a prenylated flavonoid isolated from Humulus lupulus, has multiple bioactivities, such as anti-inflammatory, antioxidant, and antilipid peroxidation, as well as antiatherosclerosis, antiadipogenesis, and anticancer [24]. However, the mechanisms underlying XN-induced protection against ferroptosis remain unclear. The object of the present study was to investigate whether XN could attenuate the I/R-induced ferroptosis in cardiomyocytes and the underlying mechanisms of its action.

H9c2
Cardiomyoblasts Culture. H9c2 cardiomyoblasts obtained from ATCC were cultured in Dulbecco's Modified Eagle Medium-high glucose (Gibco, Grand Island, NY) supplemented with 10% fetal bovine serum (Gibco) and 1% penicillin/streptomycin (Gibco). H9c2 cardiomyoblasts were seeded in 0.1% gelatin-coated plate and incubated at 37°C in a fully humidified atmosphere with 5% CO 2 , and the medium was changed every 2 days. After growing to 80% confluence, the cells were rinsed with phosphate-buffered saline (PBS) solution, detached using 0.25% trypsin-EDTA (Gibco), and then, neutralized by adding fresh medium. The cell suspension was centrifuged at 1,200 rpm for 5 min. The cell pellet was resuspended with the medium, and dispensed into a new 15 cm petri dish.
2.3. Preparation and Culture of Ventricular Myocytes. All laboratory animal protocol was approved by the Institution of Animal Care and Use Committee of the Hualien Tzu Chi Hospital (IACUC Approval No. 108-10). Two-day-old neonatal Sprague-Dawley rats (both sexes) were used as cardiomyocyte donors and sacrificed by decapitation according to a previous report [25]. Briefly, the isolated hearts were washed using Hank's buffer (Gibco). The tissues were minced and digested with 0.045% pancreatin (Sigma) and 0.01% collagenase II (Gibco) in Hank's buffer, and the enzyme was then inactivated with culture medium (F-12 medium supplemented with 10% fetal bovine serum, 10% horse serum, and 1% penicillin/streptomycin; Gibco). Cells were plated onto 10 cm petri dish and incubated for 1 h at 37°C in a fully humidified atmosphere with 5% CO 2 incubator to reduce fibroblast contamination. The ventricular myocytes were collected and seeded on 0.1% collagen-coated 6 cm petri dish in culture medium with 10 μM cytosine arabinoside, and the medium was daily changed.

Langendorff Heart Perfusion
System. Rats were anesthetized with urethane (1.5 g/kg, i.p.), then hearts were excised and arrested in Krebs Henseleit (KH) buffer as previously described [26]. Following 30 min equilibration, ischemia was induced by halting perfusion for 45 min. Reperfusion was followed with KH buffer and XN (5 or 10 μM) together for 60 min. Control hearts were not subjected to I/R. 2.5. Cell Viability Assay. H9c2 cardiomyoblasts and cardiomyocytes were seeded in 24-well plate. After 16 h, the medium was removed, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) (Sigma-Aldrich) solution (5 mg/mL in PBS) was added to each 24-well plate and incubated for 2 h at 37°C. Then, formazan salts were solubilized with DMSO and absorbance at 570 nm was measured using an ELISA plate reader (Multiskan EX; Thermo, Waltham, MA). The absorbance of each well was measured at 570 nm using an ELISA plate reader (Multiskan EX; Thermo, Waltham, MA).
2.6. Cell Death Analysis. First, the treated cells were trypsinized, collected and stained with Annexin V-FITC Apoptosis Detection Kit (BioVision, CA) in binding buffer, and detected by Gallios™ Flow Cytometer (Beckman Coulter, Brea, CA). The excitation/emission was detected at 488/ 525 nm wavelength, and PI emission was detected at 575 nm wavelength. Second, Hoechst 33342 (Sigma-Aldrich) and propidium iodide (PI) (Sigma-Aldrich) double staining were used to validate any changes in apoptosis, necrosis, and cell populations. Apoptosis was characterized by 2.11. Western Blot Analysis. Cells were washed twice with PBS and lysed in RIPA lysis buffer (Millipore) containing protease inhibitor (Calbiochem) and phosphatase inhibitor (Calbiochem). The lysates were clarified by centrifugation at 12,000 rpm for 15 min at 4°C, and the protein concentration was determined using a BSA protein assay kit (Bio-Red; Hercules, CA). Western blot analysis was performed according to a previous report [27]. Briefly, the sample containing 30 μg of protein was loaded into a 10% SDS-polyacrylamide gel and then transferred to PVDF membrane (Millipore).
The membrane was treated with 5% BSA to block the nonspecific binding of IgG and then incubated with the primary antibodies overnight at 4°C. Anti-GPX4 (Cat No. GTX54095), anti-FTH (Cat No. GTX101733), and anti-NRF2 (Cat No. GTX103322) purchased from GeneTex (Irvine, CA) were in 1,000 dilution. Anti-ACSL4 (Cat No. ab155282) purchased from Abcam (Cambridge) was in 1,000 dilution. Anti-β-actin (Cat No. MAB1501) purchased from Millipore was in 10,000 dilution. Anti-GAPDH (Cat No. GTX100118) purchased from GeneTex was in 10,000 dilution. After washing, the membrane was incubated with the secondary antibodies (peroxidase-conjugated goat antirabbit IgG or anti-mouse IgG) at a 1 : 5,000 dilution. The detected proteins were visualized with an ECL detection kit (Cat No. GERPN2232, GE Healthcare; Uppsala, Sweden) and UVP ChemStudio Plus touch (Analytik Jena; Jena, Germany). The resulting bands were analyzed using Image-Pro Plus 4.5 software (Media Cybernetics, Silver Spring, USA) and normalized using the level of β-actin or GAPDH. 2.13. Statistics. Experimental data were presented as means ± standard error of the mean (SEM). Comparisons were subjected to one-way ANOVA followed by Fisher's least significant difference test, and p values < 0.05 were considered significant.

Effects of XN on Ferroptotic Cell
Death. Fe-SP (0.5 μM) and RSL3 (0.1 μM) have been reported to induce ferroptosis through generating the lipid-based ROS and suppressing the GPX4 activity, respectively [28,29]. Although H9c2 cardiomyoblasts were not able to beat, they still showed many similarities to primary cardiomyocytes, including membrane morphology, g-signaling protein expression, and electrophysiological properties [30]. In the present study, we used the H9c2 rat cardiomyoblast cell line, which has the advantage of being an animal-free alternative, to assess the cytoprotection effect of XN on the Fe-SPinduced H9c2 cardiomyoblasts ferroptosis using the MTT assay. As shown in Figure (Figure 1(f)). These results showed that XN ameliorated the ferroptosis-induced lipid peroxidation and protected H9c2 cardiomyoblasts against ferroptotic cell death.

Effects of XN on ROS Production and Iron Content.
Lipid peroxidation has been described as a process under which oxidants such as ROS, attack lipids [31]. In the present study, we examined the ROS production in the Fe-SP-and RSL3-treated H9c2 cardiomyoblasts. The specific ROS (H 2 O 2 and hydroxyl radical (·OH)) measuring dye (CM-H 2 DCFDA) was used to measure the intracellular ROS by flow cytometry or confocal microscopy. As demonstrated in (Figures 2(a) and 2(b)), ROS generation was increased in H9c2 cardiomyoblasts treated with Fe-SP (0.5 μM) or RSL3 (0.1 μM). Cotreatment with XN (10 or 20 μM) and Fe-SP or RSL3 significantly decreased the ROS generation as compared with the cells treated with Fe-SP or RSL3 alone. We also observed that phen, a ferrous ion chelator, significantly decreased the ROS generation in H9c2 cardiomyoblasts treated with Fe-SP or RSL3 (Figure 2(b)). ·OH has particularly strong oxidizability with a one-electron reduction potential to attack DNA, lipid, and proteins. In cells, ·OH can be generated by the ferrous iron-catalyzed decomposition of H 2 O 2 via the Fenton reaction [31]. However, the role of XN in ferroptosis remains unexplored. We used flow cytometry and PGSK to detect intracellular iron concentrations. The PGSK fluorescence was quenched upon interaction with iron. As shown in Figure 2( These results showed that the XN possesses potent antioxidation and chelated intracellular iron in Fe-SP-induced H9c2 cardiomyoblasts ferroptosis.

Effects of XN on Ferroptosis-Induced Myocardial Cell
Death. Neonatal cardiomyocytes have been considered as a very useful model for cardiac ventricular cells to study various cellular and molecular mechanisms. To verify our findings in the rat ventricular cell line H9c2, the cultured neonatal rat primary cardiomyocytes were subjected to Fe-SP and RSL3 to induce ferroptosis. Cardiomyocytes were treated with Fe-SP (2 μM) for 24 h in the absence or presence of XN and then subjected for MTT assay to examine the cell viability. As shown in These results indicate that Fe-SP-and RSL3-induced cardiomyocyte death was due to ferroptosis, but did not induce both apoptosis and necrosis.

Mechanism of XN on Fe-SP-Induced Ferroptosis in
Cardiomyocytes. Ferroptosis has been reported to the degree of unsaturation of polyunsaturated fatty acid in lipid bilayers, which are especially susceptible to peroxidation [32]. We examined whether XN could inhibit intracellular ROS production and decrease lipid ROS by confocal microscopy using the specific ROS dye CM-H 2 DCFDA and lipid ROS probe C11 BODIPY 581/591, respectively. As demonstrated in Figure 4, treatment with Fe-SP for 24 h significantly increased the intracellular ROS and lipid peroxidation level. Moreover, cotreatment with XN abolished intracellular ROS production (Figure 4(a)) and lipid peroxidation (Figure 4(b)) in cardiomyocytes. Recent studies showed that long-chain acyl-CoA synthetase 4 (ACSL4), which plays a key role in lipid biosynthesis and fatty acid degradation, is an essential enzyme for ferroptosis execution [33]. To further confirm the effect of XN on ferroptosis, we examine the protein level of ACSL4 detected by Western blot analyses. The results showed that the protein level of ACSL4 was significantly decreased in the XN-treated group as compared with the Fe-SP-treated group (Figure 4(c)). It has been reported that GPXs can use the glutathione system to prevent peroxides, of which GPX4 is the main neutralizer of lipid peroxides [34]. We further examined the protein levels of GPX4 by Western blot analyses. Treatment with Fe-SP significantly decreased the protein levels of GPX4, and this effect was prevented by cotreatment with XN (Figure 4(d)), whether XN also through changed iron-binding protein (ferritin heavy chain (FTH)) protect Fe-SP-induced ferroptosis. The results showed that treatment Fe-SP significantly    Oxidative Medicine and Cellular Longevity decreased the protein level of FTH, and this reduction was not significantly affected by cotreatment with XN ( Figure 4(e)). Nuclear factor-erythroid factor 2-related factor 2 (NRF2) is a stress-inducible transcription factor, such as RSL3 and iron can induce NRF2 expression in cancer cells and astrocytes, respectively [35,36]. Whether the ferroptosis inhibition effects of XN were caused by inhibition of NRF2 was further evaluated. Treatment with Fe-SP for 2 h signifi-cantly increased the protein level of NRF2, and this effect was eliminated by cotreatment with XN (Figure 4(f)).

XN Protects the Heart against Ischemia-Reperfusion-Induced Ferroptosis.
Since in vitro study demonstrated that XN can protect cardiomyocytes against ferroptosis, we used Langendorff isolated heart preparations to investigate whether XN can reduce ferroptosis caused by I/R. To 9 Oxidative Medicine and Cellular Longevity evaluate the effect of XN on I/R injury, the heart was subjected to 45 min of myocardial ischemia followed by 60 min reperfusion after TTC staining. The results showed that XN (5 μM) significantly attenuated infarct size (white area) in ex vivo rat hearts ( Figure 5(a)). In addition, XN (5 μM) improved I/R-induced decrease of left ventricular developed pressure (LVDP) of isolated rat hearts (Supplementary Figure 1). Next, we applied the quantitative-PCR technique to examine the mRNA levels of Acsl4 and Ptgs2, molecular markers of ferroptosis, in the ex vivo heart. The results showed that the mRNA levels of Acsl4 and Ptgs2 were significantly decreased in the heart cotreated with I/R and XN (10 μM) together as compared with the I/R-treated alone (Figures 5(b) and 5(c)). The protein levels of ACSL4 also decreased in the heart cotreated with I/R and XN together ( Figure 5(d)). GPX4 is a key enzyme, which protects cells from ferroptosis by removing lipid hydroperoxide [37]. We also observed that the protein levels of GPX4 were significantly increased in hearts cotreated with I/R and XN together as compared with the heart treated with I/R alone ( Figure 5(e)). In addition, I/R significantly decreased the protein level of FTH. However, cotreatment with XN and I/R together did not significantly affect the protein levels of FTH as compared with treatment with I/R alone ( Figure 5(f)). Similar to the results from the study conducted in cardiomyocytes, treatment with I/R and XN together significantly decreased the NRF2 protein level as compared with treatment with I/ R alone ( Figure 5(g)). Taken together, these results suggested that XN could regulate the protein levels of GPX4, thereby protecting against the I/R-induced ferroptotic cell death in the ex vivo heart.

Discussion
In the present study, we identified XN as a potent natural compound that protects cardiomyocytes from ferroptosis inducers-and I/R-induced ferroptotic cell death. XN protects H9c2 cardiomyoblasts from oxidative stress (lipid peroxidation and ROS) when they are exposed to RSL3-and Fe-SP-induced ferroptosis. XN is a powerful inhibitor of iron accumulation in Fe-SP-induced H9c2 cardiomyoblasts. Mechanistically, XN prevents the protein levels of GPX4 reduction and decreases the protein levels of NRF2 in the Fe-SP-treated cardiomyocytes. Furthermore, XN reduced the heart infarct size up to 95% when the rat hearts were exposed to I/R, likely due to reduction of the mRNA levels of Ptgs2 and Acsl4 as well as the protein levels of ACSL4 and NRF2 and modulation of the protein levels of GPX4 to attenuate cardiac I/R-induced ferroptosis. Additionally, a large number of compelling pieces of experimental evidence indicated the protective role of XN for cardiovascular diseases. For example, XN plays a potential protective effect in the aged cardiovascular system [38]. Another study suggests that XN attenuated isoprenaline-induced cardiac hypertrophy and fibrosis [39]. In the past few years, XN has been found to protect against IRI in the liver and brain, suggesting that this natural substance can be as a potential candidate for preventing the IRI in the heart [40,41].
RSL3, a ferroptosis inducer, directly acts on GPX4 and inhibits its activity. Although RSL3 can increase the levels of ROS, lipid peroxidation, and Ptgs2 mRNA to induce ferroptosis in H9c2 cardiomyoblasts, Fe-SP can induce intracellular iron overload, but not RSL3 in our study. Intracellular iron accumulation is considered a contribution to the execution of ferroptosis during cardiac I/R. In the present study, using neonatal cardiomyocytes treated with Fe-SP to mimic the pathophysiology of myocardial I/R injury in vitro, we evaluated the contribution of XN to prevent ferroptosis. In addition, Park et al. showed that undifferentiated C2C12 and H9c2 cells were highly sensitive to RSL3-induced ferroptosis, while differentiated C2C12 cells and neonatal rat cardiomyocytes were relatively resistant to ferroptosis. This is because myocyte differentiation induces some changes in cell signaling pathways to acquire resistance to RSL3-induced ferroptosis [10].
GPX4, a key antioxidant enzyme in the regulation of ferroptosis, can directly detoxify lipid hydroperoxides generated by ROS. In a previous study, it has been reported that downregulation of GPX4 during the early and middle stages of myocardial infarction contributes to ferroptosis in cardiomyocytes upon metabolic stress such as cysteine deprivation. Depletion or inhibition of GPX4 using specific siRNA or RSL3, respectively, resulted in accumulation of lipid peroxide, leading to ferroptosis in H9c2 cardiomyoblasts [10]. Besides, ectonucleotide pyrophosphatase/phosphodiesterase 2, a lipid kinase involved in lipid metabolism, overexpression protects H9c2 cardiomyoblasts from erastin-induced ferroptosis through modulating GPX4, ACSL4, and NRF2 expression [42]. Evidence has shown that NRF2 regulates ferroptosis primarily by directly affecting the GPX4 synthesis and function [43]. It is consistent with our findings that Fe-SP-induced cardiomyocytes and I/R-induced hearts lead to an increase in the protein levels of NRF2 and a decrease in the protein levels of GPX4, and these effects can be abolished by XN, although XN has been demonstrated to be active of antioxidants through the NRF2/heme oxygenase-1 signaling pathway. However, a study found that doxorubicin-induced cardiomyopathy results in the accumulation of nonheme iron via heme degradation by NRF2-mediated upregulation of heme oxygenase-1 [14]. Recent studies have indicated that heme oxygenase-1 plays a positive association role in ferroptosis by iron accumulation [14,44].
Some flavonoids efficiently chelate trace metals like copper and iron which are potential enhancers of ROS [45]. In the present study, we found that one of the mechanisms of action of XN in preventing ferroptosis is iron chelation. Consistent with our results, a study shows that XN can reduce iron accumulation in opisthorchis viverrini-induced cholangiocarcinogenesis [46]. In addition, Gao et al. found that inhibition of ferroptosis by deferoxamine, an iron chelator, can reduce the release of lactate dehydrogenase, improve cardiac function, and protect heart tissue from IRI [47]. Another iron chelator, dexrazoxane, can protect the heart against IRI-induced ferroptosis [14]. In the present study, we showed that XN can reduce iron accumulation and inhibit ROS production in the Fe-SP-treated H9c2 cardiomyoblasts. 10 Oxidative Medicine and Cellular Longevity

Oxidative Medicine and Cellular Longevity
Lipid peroxidation is the key downstream feature of ferroptosis. Various lipids, such as phosphatidylcholine and phosphatidylethanolamine, are responsible for ferroptosisinduced lipid peroxidation. Peroxidized phosphatidylethanolamine species have been identified as predictive biomarkers for ferroptosis. Recent studies have shown that using gas cluster ion beam secondary ion mass spectrometry imaging can map PEox at ferroptotic H9c2 cardiomyoblasts [48]. In addition, LC-MS/MS analysis revealed a dramatic increase in PEox species in mitochondria in response to RSL3 and cardiac I/R [9]. A previous study showed that XN markedly decreases the level of lipid peroxidation and ROS production in rat liver [49]. Consistent with our results shown that XN inhibited RSL3-and Fe-SP-induced lipid peroxidation, MDA, and ROS enhancements in H9c2 cardiomyoblasts as well as Fe-SP-induced lipid peroxidation in cardiomyocytes. In addition, ACSL4 acts as an essential component for ferroptosis execution and dictates ferroptosis sensitivity by shaping cellular lipid composition. In the present study, we found that XN inhibited Fe-SP-and I/R-induced upregulation of ACSL4 in cardiomyocytes and ex vivo hearts. A study has shown that XN possesses glutathione levels and glutathione peroxidase activities to reduce lipid peroxidation on carbon tetrachloride-induced acute liver injury in rats [50]. Another report has shown that XN markedly reduced 4hydroxynonenal and increased glutathione levels in the hepatic I/R-injury in mice [40]. In the present study, we found that XN can modulate the protein levels of GPX4 from the Fe-SP-induced cardiomyocytes and the I/Rinduced hearts. Altered expression of GPX4 may play an important role in the protection of cardiomyocytes against ferroptosis.
Ferroptosis induced by I/R or ferroptosis inducer may show some biochemical characteristics as well as changes in protein and gene levels. The lipid peroxidation requires ACSL4-mediated conversion of arachidonic acid (AA) to AA-CoA. Importantly, the upregulation of ACSL4 levels is a biomarker of ferroptosis sensitivity [6]. Some studies have indicated that degradation of GPX4 protein can also be observed in ferroptosis-sensitive cells in response to erastin and RSL3 [51,52]. In addition, the upregulation of Ptgs2 mRNA is used as a biomarker of ferroptosis in mice exposed to erastin or RSL3. However, the upregulation of PTGS2 is also observed under nonferroptotic conditions, such as inflammation [53]. Moreover, some biochemical hallmarks of ferroptosis are used to distinguish ferroptosis and other types of cell death, such as accumulation of cellular iron or induction of lipid peroxidation. Unfortunately, the biomarkers of ferroptosis are also present in other types of cell death or pathological conditions. Therefore, more specific biomarkers are needed to detect ferroptotic cell death in the future [54].

Conclusions
Our results suggest that XN could chelate iron and inhibit ROS and lipid peroxidation in the Fe-SP-or RSL3-induced ferroptotic cell death in cardiomyocytes. Moreover, our ex vivo data support that XN can prevent ferroptosis during cardiac I/R by reducing the expression of Acsl4 and Ptgs2 mRNA, reducing the expression of ACSL4 and NRF2 protein, and modulating the expression of GPX4 protein.

Data Availability
All materials are available by the corresponding author.

Conflicts of Interest
The authors declare no conflicts of interest.

Supplementary Materials
Supplementary Figure 1: xanthohumol (XN) tended to suppress the I/R-induced decrease of left ventricular developed pressure (LVDP) of isolated rat heart. A latex balloon filled with Milli-Q water was inserted into the LV to record LV pressure. LV pressure was recorded by Power Lab system and Chart 8 software (ADInstruments, New South Wales, Australia). LVDP was calculated as the difference between maximal systolic and end-diastolic pressures. The hearts were exposed to 45