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Introduction

Cardiovascular disease is a challenging disease with high morbidity and mortality worldwide (1). Myocardial ischemia/reperfusion (MI/R) injury is the primary risk factor in the pathological process of heart disease. Although reperfusion is the most efficient way to mimic tissue damage, the re-establishment of the blood supply is known to induce various adverse events (2). In addition, MI/R also induces endoplasmic reticulum (ER) stress and activates apoptosis-related signaling pathways (3).

The ER serves a number of roles in protein synthesis, lipid biosynthesis and detoxification. When normal ER function is disrupted by various cellular disturbances, unfolded and misfolded proteins accumulate, resulting in a condition known as ER stress (4). The alteration of redox homeostasis results in excessive generation of reactive oxygen species (ROS), which subsequently causes ER stress (5). ER stress promotes the dissociation of the ER chaperone glucose-regulated protein 78 (GRP78) from transmembrane proteins and triggers their activation (6). Protein kinase R-like endoplasmic reticulum kinase (PERK) is one of transmembrane proteins and dimerizes under ER stress, which phosphorylates eukaryotic translation initiation factor 2 subunit α (eIF2α) (7). eIF2α mediates the transcription of activating transcription factor-4 (ATF4), which interacts with the pro-apoptotic factor C/EBP homologous protein (CHOP) (8). Additionally, ER stress induces cell apoptosis by activating the caspase family cascade (9).

NAD-dependent protein deacetylase sirtuin-1 (SIRT1), known as one of the mammalian homologues of yeast Sir2, is a histone deacetylase and regulates various biological processes, such as the inflammatory reaction, oxidative stress and apoptosis (10,11). A previous study demonstrated that SIRT1 overexpression protects cardiomyocytes against MI/R injury from ER stress (12). The protective effect is due to the activation of the PERK/eIF2α pathway, which is associated with cardiomyocyte apoptosis. Hence, SIRT1 may be a potential target to treat cardiac pathologies by attenuating ER stress.

Inonotus obliquus (IO) is a fungus belonging to the Hymenochaetaceae family of Basidiomycetes, which grows on birch trees (13). The main bioactive compounds of IO are polysaccharides, polyphenols, melanin and triterpenes (14). IO exerts various biological functions, including anti-inflammatory, antitumor and immunomodulatory effects (15,16). However, its effects on cardiovascular diseases has been rarely studied. The current study was designed to investigate the role of IO extract (IOE) in MI/R injury and determine the exact molecular mechanisms.

Materials and methods

Ethanol extraction of IO

IO was collected from Jilin Province, Northeastern China and identified by Professor GuangShu Wang (Jilin University). A total of 2,500 g IO powder was weighed, soaked in 12.5 l distilled water overnight at room temperature and extracted at 80°C for 2.5 h. The supernatant was collected after filtration using three layers of gauze, and the extraction was repeated twice in the same manner. The filtrate was concentrated by rotary evaporation, dried at 60°C, crushed and passed through an 80-mesh sieve to obtain the preliminary extract. Next, 12.5 l 70% ethanol was added to the preliminary extract obtained from water extraction (extracted at 75°C for 2.5 h). The supernatant was gathered by filtering through three layers of gauze, and the extraction was repeated twice in the same manner. The filtrates were collected and concentrated by rotary evaporation, then dried at 60°C, crushed and passed through an 80-mesh sieve, and 127.9 g IOE was obtained. The extraction rate of IOE was 5.12% according to the following formula: Extraction rate = weight of IOE/weight of IO powder. Meanwhile, the main composition of IOE was assessed using a T-6 Series UV–Vis spectrophotometer (Beijing Purkinje General Instrument Co., Ltd.). The contents of total flavonoid, total saponin, polysaccharide and polyphenol were calculated using respective standard curves (y=0.0117×+0.0554, R2=0.9998; y=0.0301×+0.0871, R2=0.9992; y=16.253×+0.1019, R2=0.9999 and y=97.266×+0.1984, R2=0.9996) with the percentage of 1.76, 1.06, 0.57 and 1.07%.

Animals

Wistar rats (female, 250–280 g) were purchased from Changchun Yisi Experimental Animal Co., Ltd., and raised in a controlled environment (22–24°C; 55–60% humidity and 12/12-h light/dark cycle) with free access to food and water. Animals were treated according to the Guide for the Care and Use of Laboratory Animals (US National Institutes of Health) (17) and the Committee for the Care and Use of Laboratory Animals of Jilin University (Changchun, China). The animal experiments of the present study were approved by the Ethical Committee for Experimental Animals, School of Pharmaceutical Sciences, Jilin University (approval no. 20190049).

Experimental design

A total of 150 female rats were randomly assigned into five groups (n=30): i) Non-MI/R sham group (Sham); ii) MI/R group (MI/R); iii) MI/R+IOE 150 mg/kg group (MI/R-IOE150); iv) MI/R+IOE 300 mg/kg group (MI/R-IOE300) and v) MI/R+IOE 600 mg/kg group (MI/R-IOE600). The animals in the treatment groups were intragastrically administered with IOE (150, 300 or 600 mg/kg) for 7 consecutive days. The rats of the Sham and MI/R groups were intragastrically administered with 0.5% carboxymethylcellulose sodium for 7 consecutive days. Surgical procedures were performed on rats in the Sham group, but without left anterior descending (LAD) coronary artery ligation. In other groups, LAD ligation was performed on the hearts for 2 h and then reperfused for 2 h.

Experimental model establishment

At day 7, 3% sodium pentobarbital (30 mg/kg body weight, intraperitoneal injection) was used to anesthetize the rats after 1 h of administration. Rat hearts were exteriorized via open-chest surgery. A 6/0 nylon suture was put to make a slip knot around the LAD coronary artery and induce myocardial ischemia. After 2 h of ligation, the ligature was loosened to restore myocardial blood supply for myocardial reperfusion. Rats in the Sham group were subjected to the same procedure, but without ligation. Reperfusion was performed for 2 h. The rats were anesthetized by intraperitoneal injection with 3% sodium pentobarbital (30 mg/kg body weight). Then, ~8 ml volume of blood was taken from the abdominal aorta of the unconscious rats for painless euthanasia. Death was confirmed when respiratory and cardiac arrest was observed, following which, cardiac tissues were harvested for further experiments.

Cardiac function assessment

After 2 h of reperfusion, 3% sodium pentobarbital (30 mg/kg body weight, intraperitoneal injection) was used to anesthetize the rats. Once anesthetized, the thoracic area was shaved and covered with ultrasonic transmission gel. A portable echocardiography machine (GE Vivid I; GE Healthcare) was used to evaluate the cardiac function of rats. The left ventricular (LV) ejection fraction (EF), LV fractional shortening (FS), LV internal dimensions at diastole (LVIDd) and LV internal diameter systole (LVIDs) were evaluated. An observer who was blinded to the experimental design measured these parameters in three consecutive cardiac cycles.

Determination of myocardial infarction size (MIS)

After 2 h of reperfusion, the heart tissues were excised to perform MIS measurements. Five pieces of the left ventricle parallel to the atrioventricular groove were transected, immersed in 0.5% nitro blue tetrazolium chloride (NBT) phosphate buffer and stained for 1 min in a 37°C water bath. Normal myocardial tissues were stained dark red, while ischemic myocardial tissues were pale. The ischemic myocardial tissue was excised and weighed. The MIS was calculated as follows: Ischemic myocardial weight/wet weight of the left ventricle ×100%.

Determination of cardiac enzymes

A total of 2 ml blood was collected after 2 h of reperfusion. Serum was separated from the blood samples by centrifugation (2,000 × g, 10 min, 4°C) and used for the evaluation of creatine kinase-MB (CK-MB; cat. no. H197; Nanjing Jiancheng Bioengineering Institute), aminotransferase (AST; cat. no. C010-1-1; Nanjing Jiancheng Bioengineering Institute) and lactate dehydrogenase (LDH; cat. no. A020-2-2; Nanjing Jiancheng Bioengineering Institute) activities using respective diagnostic kits in accordance with the manufacturer's instructions.

Determination of oxidative stress levels in myocardial tissue

After 2 h of reperfusion, rat hearts were excised to prepare heart homogenates. Prepared myocardial tissues were excised and homogenized (10%) in ice-cold physiological saline solution using a Tissue-Tearor (Bio Spec Products, Inc.). The supernatant was separated from heart homogenates by centrifugation (3,500 × g, 15 min, 4°C) and used for the evaluation of superoxide dismutase (SOD; cat. no. A001-1-2; Nanjing Jiancheng Bioengineering Institute), malondialdehyde (MDA; cat. no. A003-1-1; Nanjing Jiancheng Bioengineering Institute), glutathione peroxidase (GSH-px; cat. no. A005-1-2; Nanjing Jiancheng Bioengineering Institute) and catalase (CAT; cat. no. A007-2-1; Nanjing Jiancheng Bioengineering Institute) levels using respective diagnostic kits in accordance with the manufacturer's instructions.

Histological examination

After 2 h of reperfusion, rat hearts were quickly harvested. and the blood was expelled. Hearts were fixed in 4% paraformaldehyde solution for 24 h at room temperature. After rinsing with water, heart tissues were dehydrated with gradient ethanol solution and embedded in paraffin. Subsequently, heart tissues were cut into 3–5 µm-thick slices and stained using a hematoxylin and eosin (H&E) kit for 3 min at room temperature. An optical microscope was used to observe morphological changes. The degree of cardiac damage was assessed by an independent researcher blind to the experimental design.

TUNEL assay

Myocardial apoptosis was evaluated using a TUNEL assay kit (cat. no. 11684817910; Sigma-Aldrich; Merck KGaA). Heart tissue was fixed in 4% paraformaldehyde solution for 24 h at room temperature, embedded in paraffin, then sectioned on slides at 3–5 µm-thickness. TUNEL (1:9 mixed in equilibration buffer) staining of apoptotic cells (green fluorescence). DAPI (5 µg/ml) was used to dye the nuclei for 5 min (blue fluorescence). The slides were then sealed with 50% glycerin. Five randomly selected fields of view were observed and apoptotic cells of each section were counted under an ECLIPSE 80i fluorescence microscope (Nikon Corporation). The cardiomyocyte apoptotic index (AI) was counted as follows: Number of TUNEL-positive nuclei/the number of total nuclei ×100%.

Reverse transcription-quantitative (RT-q)PCR

Total RNA was extracted from cardiac tissues using TRIzol® reagent (Invitrogen; Thermo Fisher Scientific, Inc.), quantified with the T-6 Series UV–VIS spectrophotometer (Beijing Purkinje General Instrument Co., Ltd.) and reverse transcribed into cDNA using a Hifair® II First Strand cDNA Synthesis Kit (cat. no. 11120ES60; Shanghai Yeasen Biotechnology Co., Ltd.). RT was carried out at 42°C for 15 min, then 85°C for 15 sec. Subsequently, qPCR was performed with sequence-specific primers using the SYBR Green Master Mix kit (cat. no. 11202ES03; Shanghai Yeasen Biotechnology Co., Ltd.). The thermocycling conditions consisted of 40–50 cycles at 95°C for 10 sec, 55°C for 20 sec and 72°C, 20 sec. The following primer pairs were used for qPCR: Caspase-12 forward, 5′-CAGCACATTCCTGGTGTTTAT-3′ and reverse, 5′-GACTCTGGCAGTTACGGTTGTT-3′ and β-actin forward, 5′-GCACCGCAAATGCTTCTAGG-3′ and reverse, 5′-AAAGGGTGTAAAACGCAGCTC-3′. Data were calculated using the 2−∆∆Cq method (18) with the mRNA levels of β-actin as an internal control.

Western blot assay

Myocardial tissues were homogenized in lysis buffer (cat. no. P0013; Beyotime Institute of Biotechnology) and protease inhibitor cocktail on ice and purified by centrifugation at 14,000 × g for 15 min at 4°C. The protein concentration was determined using the BCA method. A total of 40 µg protein was loaded onto 10–12% gels and resolved via SDS-PAGE. Separated proteins were then transferred to a PVDF membrane for 2 h. PVDF membranes were blocked for 1.5 h in 5% bovine serum albumin (cat. no. P0252; Beyotime Institute of Biotechnology) at room temperature and washed three times with TBS+0.2% Tween-20. Membranes were incubated overnight at 4°C with the following primary antibodies (all from Affinity Biosciences): SIRT1 (1:2,000; cat. no. DF6033), GRP78 (1:800; cat. no. AF5366), eIF2α (1:1,000; cat. no. AF6087; Affinity Biosciences), phosphorylated (p)-eIF2α (Ser52) (1:1,500; cat. no. AF3087), PERK (1:1,000; cat. no. AF5304), p-PERK (Thr982) (1:1,500; cat. no. DF7576), CHOP (1:1,500; cat. no. DF6025), caspase-12 (1:1,500; cat. no. AF5199), pro-caspase-3 (1:1,500; cat. no. AF6311), pro-caspase-9 (1:1,500; cat. no. AF6348) or anti-β-actin (1:5,000; cat. no. AF7018). A goat anti-rabbit secondary antibody (1:5,000; cat. no. IH-0011; Beijing Dingguo Changsheng Biotechnology Co., Ltd.) was used to observe primary antibody binding, and then bands were visualized using an ECL western blotting substrate (cat. no. KF001; Affinity Biosciences). Densitometric analysis of the bands was conducted using ImageJ software (version 1.5.1k; National Institutes of Health).

Statistical analysis

All data are presented as the mean ± SD and were analyzed using SPSS 22.0 (IBM Corp.). Data were analyzed using one-way ANOVA followed by Tukey's Honest Significant Difference test. P<0.05 was considered to indicate a statistically significant difference.

Results

IOE improves cardiac function

The cardiac function of post-surgical hearts was evaluated by echocardiography. As shown in Fig. 1A-E, deterioration of cardiac function was induced in the MI/R group, LVIDd and LVIDs increased to 6.13±0.99 and 4.25±0.46 mm, respectively, whereas LVEF and LVFS decreased to 51.75±6.39 and 24.13±5.00%, respectively, compared with the Sham group (P<0.01). IOE pretreatment increased the recovery of cardiac function in the impaired hearts, which was demonstrated by increased LVEF and LVFS, as well as decreased LVIDd and LVIDs, compared with the M/R group (P<0.05 or P<0.01).

Figure 1. IOE improves cardiac function. (A) Echocardiography images of each group. Bar graphs of (B) LVIDd, (C) LVIDs, (D) LVEF and (E) LVFS. Data are presented as the mean ± standrd deviation. n=10. ##P<0.01 vs. Sham. *P<0.05 and **P<0.01 vs. MI/R. IOE, Inonotus obliquus extract; LV, left ventricular; LVIDd, LV internal dimensions at diastole; LVIDs, LV internal diameter systole; LVEF, LV ejection fraction; LVFS, LV fractional shortening; MI/R, myocardial ischemia/reperfusion.

IOE decreases infarct size and attenuates MI/R Injury

NBT staining was used to observe the effects of IOE on the infarction scale. As shown in Fig. 2A, the infarct size reached up to 36.42±6.67% in the MI/R group. IOE (150, 300 and 600 mg/kg) significantly decreased the infarct size compared with the MI/R group (P<0.01). Furthermore, the activities of myocardial enzymes (LDH, CK-MB and AST) were significantly increased following MI/R injury compared with the Sham group, which further caused myocardial injury (P<0.01; Fig. 2B-D). IOE attenuated MI/R injury through inhibiting the activities of myocardial enzymes in MI/R-IOE groups (P<0.01).

Figure 2. IOE decreases infarct size and attenuates MI/R injury. (A) Representative images of heart tissues. Normal myocardial tissues are dark red and ischemic myocardial tissues are pale. The MIS was calculated as the ischemic myocardial weight/wet weight of left ventricle ×100%. The levels of (B) CK-MB, (C) LDH and (D) AST in serum. Data are presented as the mean ± standard deviation. n=10. ##P<0.01 vs. Sham. **P<0.01 vs. MI/R. IOE, Inonotus obliquus extract; MI/R, myocardial ischemia/reperfusion; CK-MB, creatine kinase MB, LDG, lactate dehydrogenase; AST, aminotransferase; MIS, myocardial infarction size.

IOE relieves myocardial tissue injury

Myocardial tissues showed partially disordered and disorderly arrangement of myocardial fiber stripes, and partial lysis of cardiomyocytes accompanied by interstitial edema in the MI/R group (Fig. 3). Following treatment with IOE, myocardial fibers and cell morphology notably improved to varying degrees.

Figure 3. IOE relieves the histopathological changes in myocardial tissue. Representative hematoxylin and eosin staining images of myocardial slices at ×200 magnification (upper panel; scale bar, 50 µm) and ×400 magnification (lower panel; scale bar, 25 µm). n=4. IOE, Inonotus obliquus extract; MI/R, myocardial ischemia/reperfusion.

IOE reduces oxidative stress

MDA content and antioxidant enzymes (SOD, GSH-px and CAT) are key molecules for evaluating the degree of oxidative stress. After MI/R, the activities of these antioxidant enzymes were significantly reduced (Fig. 4A, C and D). Meanwhile, the content of MDA was significantly higher compared with the Sham group (P<0.01; Fig. 4B). IOE pretreatment (150, 300 and 600 mg/kg) increased the activities of antioxidant enzymes and decreased MDA content compared with the MI/R group (P<0.01). These values indicated that IOE pretreatment protected cardiomyocytes against oxidative stress.

Figure 4. IOE protects cardiomyocytes against oxidative stress. The activity of (A) SOD, the content of (B) MDA, the activity of (C) GSH-px and the activity of (D) CAT. Data are presented as the mean ± standard deviation. n=10. ##P<0.01 vs. Sham. **P<0.01 vs. MI/R. IOE, Inonotus obliquus extract; SOD, superoxide dismutase; GSH-px, glutathione peroxidase; CAT, catalase; MDA, malondialdehyde; MI/R, myocardial ischemia/reperfusion.

IOE decreases cardiomyocyte apoptosis

The present study aimed to detect the role of IOE in cell death by TUNEL staining. MI/R injury induced a certain degree of cardiomyocyte apoptosis by increasing the percentage of apoptotic cells in the MI/R group compared with the Sham group (P<0.01; Fig. 5A and B). As expected, pretreatment with IOE (150, 300 and 600 mg/kg) significantly decreased the percentage of apoptotic cells (P<0.05 or P<0.01). Therefore, the data suggested that IOE could alleviate cardiomyocyte apoptosis after MI/R injury.

Figure 5. IOE decreases cardiomyocyte apoptosis. (A) Representative images of TUNEL staining (scale bar, 100 µm). (B) Cardiomyocyte apoptosis index. Data are presented as the mean ± standard deviation. n=4. ##P<0.01 vs. Sham. *P<0.05, **P<0.01 vs. MI/R. IOE, Inonotus obliquus extract; MI/R, myocardial ischemia/reperfusion.

IOE activates SIRT1 and downregulates the PERK/eIF2α/CHOP pathway

Considering the role of SIRT1 in cardioprotection, SIRT1 expression in heart tissue was examined. MI/R injury could suppress SIRT1 expression compared with the Sham group, which was then activated by IOE (P<0.01; Fig. 6A and B). Furthermore, upregulation of ER chaperone GRP78, p-PERK, p-eIF2α, CHOP and caspase-12 was observed after MI/R injury in the heart (P<0.01; Fig. 6A and C-G). Moreover, the changes in mRNA expression of caspase-12 were investigated. As shown in Fig. 6H, the mRNA levels of caspase-12 in the ischemic myocardium were also notably increased in the MI/R group compared with the Sham group (P<0.01). As expected, IOE inhibited ER stress by downregulating the expression of ER stress-related markers (GRP78, p-PERK, p-eIF2α, CHOP and caspase-12) compared with the MI/R group (P<0.05 or P<0.01). IOE decreased the mRNA levels of caspase-12 in the MI/R-IOE groups (P<0.01). Collectively, the aforementioned values suggested that IOE attenuated MI/R injury by suppressing ER stress, which may be associated with SIRT1 activation.

Figure 6. Expression of SIRT1, GRP78, p-PERK, p-eIF2α, CHOP, caspase-12 and the mRNA levels of caspase-12 in the myocardium. (A) Representative blots of SIRT1, GRP78, p-PERK, p-eIF2α, CHOP and caspase-12. Semiquantitative analysis of (B) SIRT1, (C) GRP78, (D) p-PERK, (E) p-eIF2α, (F) CHOP and (G) caspase-12. (H) The mRNA levels of caspase-12 in the myocardium. Data are presented as the mean ± standard deviation. n=3. ##P<0.01 vs. Sham. *P<0.05 and **P<0.01 vs. MI/R. IOE, Inonotus obliquus extract; SIRT1, NAD-dependent protein deacetylase sirtuin-1; GRP78, glucose-regulated protein 78; PERK, protein kinase R-like endoplasmic reticulum kinase; eIF2α, eukaryotic translation initiation factor 2 subunit α; CHOP, C/EBP homologous protein; p, phosphorylated; MI/R, myocardial ischemia/reperfusion.

IOE suppresses ER stress-induced apoptosis

To evaluate the condition of cardiomyocyte apoptosis, the expression of pro-caspase-9 and pro-caspase-3 in ischemic hearts were measured. MI/R injury significantly decreased the expression of pro-caspase-9 and pro-caspase-3 compared with the Sham group (P<0.01; Fig. 7A-C). By contrast, IOE increased the expression of pro-caspase-9 and pro-caspase-3 in ischemic heart tissue compared with the MI/R group (P<0.05 or P<0.01). The data indicated that IOE protected the heart from MI/R injury via suppressing ER stress-induced cardiomyocyte apoptosis.

Figure 7. Expression of pro-caspase-9 and pro-caspase-3 in the myocardium. (A) Representative blots of pro-caspase-9 and pro-caspase-3. Semiquantitative analysis of (B) pro-caspase-9 and (C) pro-caspase-3. Data are presented as the mean ± standard deviation. n=3. ##P<0.01 vs. Sham. **P<0.01 vs. MI/R. MI/R, myocardial ischemia/reperfusion; IOE, Inonotus obliquus extract.

Discussion

IO possesses various pharmacological and biological properties, including antitumor, antimicrobial and antioxidant activities (19). It was previously reported that IO inhibited lipid peroxidation in hyperlipidemic rats (20). In the present study, IOE exerted cardioprotective effects by attenuating oxidative damage and suppressing ER stress-induced apoptosis.

Redox signaling is crucial in the regulation of cell function, including defense against invading microorganisms and gene expression for physiological activity. MI/R induces excessive generation of redox signaling of ROS to break redox homeostasis, which results in oxidative stress (21). The severity of reversible and irreversible cellular injury within cardiomyocytes is proportional to the level of ROS activation (22). ROS can induce lipid peroxidation, protein oxidation and nitration, mitochondrial permeability transition and DNA damage, causing cardiomyocyte death following MI/R (23). To keep the redox state in balance, redundant ROS is typically eliminated by several enzymes, such as SOD, GSH-px and CAT (24). Several therapeutic strategies can protect cardiomyocytes by inhibiting oxidative stress, for example, pre-conditioning, pro-conditioning and antioxidants (23). Our previous study revealed that ginsenoside Rg2 protected cardiomyocytes from MI/R injury by inhibiting oxidative stress and inflammation (25). In the present study, MI/R injury induced downregulation of GSH-px, SOD and CAT activities and upregulation of MDA content, which were counteracted by IOE. These results indicated that IOE pretreatment protected cardiomyocytes against oxidative stress.

Ischemia and reperfusion activate a variety of cell death programs, categorized as apoptosis, necrosis or autophagy-associated cell death (26). ER stress plays a vital role in the pathogenesis of cardiac diseases and may be a therapeutic target to protect cardiomyocytes. In the MI/R process, ER stress occurs due to diverse stimuli, and then triggers the unfolded protein response (UPR). Overproduction of ROS disrupts protein folding and results in amplified UPR signaling (27). Previous evidence has suggested that UPR is initially activated by three endoplasmic reticulum stress sensors, serine/threonine-protein kinase/endoribonuclease IRE1, PERK and ATF6 (28). GRP78, an immunoglobulin binding protein, physically binds to these proteins and inhibits their activities under a steady state (29). PERK, also known as eukaryotic initiation factor 2α protein kinase 3, interacts with and phosphorylates eIF2α (30). Under ER stress, PERK dissociates from GRP78 and induces the phosphorylation of eIF2α. The PERK/eIF2α signaling pathway can limit protein translation and induce apoptosis by inducing CHOP expression (31). Caspase-12 localizes in the ER and is a critical mediator in ER stress-induced apoptosis by activating other caspases (32). Caspase-12 specifically clears pro-caspase-9 for activation and caspase-9 is active. Subsequently, caspase-9 ultimately activates caspase-3, the major effector caspase for apoptosis (33). In the present study, MI/R injury induced ER stress in rat cardiomyocytes. It was found that IOE pretreatment significantly decreased the expression of GRP78, p-PERK, p-eIF2α, CHOP and caspase-12 and the mRNA levels of Caspase-12. The present study also found that ER stress-induced apoptosis by MI/R injury was alleviated by IOE. Above all, the cardioprotective effects of IOE are based on the suppression of ER stress-induced cardiomyocyte apoptosis.

SIRT1 is a highly conserved histone deacetylase, which can deacetylate various transcription factors (34). It has been demonstrated that SIRT1 activation has protective effects in myocardial ischemia. SIRT1 and ER stress are involved in various pathologies, including diabetes, obesity, cancer and cardiovascular diseases (4,35,36). Resveratrol, a SIRT1 activator, inhibits ER stress via SIRT1 activation in vitro (37). Previous studies have indicated that SIRT1 may regulate eIF2α phosphorylation via regulating its acetylation process, thereby affecting its activity (38,39). SIRT1 inhibition has been demonstrated to cause the hyperactivation of the PERK/eIF2α pathway, which induces cardiomyocyte apoptosis by sustaining CHOP expression (12). The present study revealed that IOE notably increased SIRT1 expression in the ischemic myocardium. IOE also suppressed ER stress-induced apoptosis by mediating the PERK/eIF2α/CHOP signaling pathway. The present results demonstrated that IOE-induced SIRT1 activation may suppress ER stress-induced cardiomyocyte apoptosis, thereby reducing the infarct size in vivo. However, there is a complex interaction between SIRT1 and ER stress. SIRT1 activation has been reported to inhibit ER stress and apoptosis of cardiomyocytes by promoting autophagic clearance and decreasing the expression of the protein disulfide isomerase and S-nitrosylation (40,41). The role of IOE in these mechanisms need to be further studied.

In conclusion, the present findings showed that IOE pretreatment protected cardiomyocytes from MI/R injury by attenuating oxidative damage and suppressing ER stress-induced apoptosis. IOE may suppress ER stress-induced cardiomyocyte apoptosis via the PERK/eIF2α/CHOP pathway by the activation of SIRT1. Therefore, IO may be a potential therapeutic candidate in cardiovascular diseases.

Acknowledgements

Not applicable.

Funding

This project was supported by the Jilin Scientific and Technological Development Program (grant no. 20190701056GH).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

YX and WF conceived the study. YW, HC, YZ, PY, YL, DW, YX and WF performed the experiments. HC, YZ, PY, YL and DW analyzed the data. YW, YX and WF wrote the manuscript. YX and WF improved the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The animal experiments of this study were approved by the Ethical Committee for Experimental Animals, School of Pharmaceutical Sciences Jilin University (approval no. 20190049; Changchun, China).

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References