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Introduction

The mechanism underlying acute myocardial infarction involves the occurrence of atherosclerosis, followed by atherosclerotic plaque rupture, hemorrhage and thrombosis or coronary artery spasm, leading to complete or incomplete coronary occlusion (1). The recurrence and mortality rates of acute myocardial infarction are high in China, at ~10 and 16%, respectively. Following an initial myocardial infarction, the mortality rate of second relapse increases to >38% (2).

Inducible nitric oxide synthase (iNOS) is important in angiogenesis and its generation. Nitric oxide generated by iNOS catalysis may, in addition to inducing endothelial cell migration and proliferation, mediate angiogenic action of growth factors, including vascular endothelial growth factor, fibroblast growth factor and transforming growth factor (3). Liu et al reported that tirofiban reduces the size of the no-reflow and infarct of acute myocardial infarction through suppression of iNOS activity (4). Zaitone et al provided evidence that rosuvastatin promotes angiogenesis in acute myocardial infarction via the control of iNOS in rats (5).

Nuclear factor-κB (NF-κB) is present in almost all cells, including neuronal and glial cells, as well as brain endothelial cells and other cells, which can be combined specifically with gene promoters or enhancer sequences of other cells to promote transcription and expression, and are closely associated to the inflammatory response, immune response, and the proliferation, differentiation and apoptosis of cells (6,7). Sui et al suggested that huperzine A ameliorates the damage induced by acute myocardial infarction through inhibition of the expression of the NF-κB subunit p65 in rats. Qiao et al demonstrated that anesthetic preconditioning protects rat hearts from ischemia/reperfusion (I/R) injury through the attenuation of NF-κB activation (8).

Monocyte chemotactic protein-1 (MCP-1) promoter sequence analysis has revealed that there is an activating protein-1 (AP-1) binding site in the promoter region and NF-κB binding sites, indicating that AP-1 activation is involved in regulating the expression of MCP-1 (9). Interleukin-1β (IL-1β) induces the expression of MCP-1 through the activation of NF-κB and AP-1, while the proteasome inhibitor induces the expression of MCP-1 by the AP-1 signaling pathway (10). Valen et al reported that NF-κB and AP-1 regulate the inflammatory genes in the hearts of patients with unstable angina (11), and Xie et al suggested that activation of the AP-1 transcription pathway may be important in ventricular remodeling of myocardial infarction (12).

Several studies (13–15) have demonstrated the close association between heat shock protein 72 (HSP7) and myocardial protection, and the extent of HSP72 induction and myocardial protection intensity presents a positive correlation (13). However, as the induction of the endogenous expression of HSP72 requires sublethal stress, it cannot be used clinically (11). Tanonaka et al suggested that trandolapril increases tolerance against heat stress-induced deterioration of acute myocardial infarction through HSP72 and HSP73 (13), and Valen et al reported that unstable angina activates myocardial infarction through the activation of HSP72, and the suppression of NF-κB and AP-1 (11).

Candesartan is an angiotensin II receptor antagonist, belonging to diphenyl imidazole, with a similar effect to losartan. The binding force of candesartan with angiotensin receptor 1 is 80 times higher, compared with that of losartan (16,17). Candesartan restores reperfusion injury through HSP72 in hereditary insulin-resistant rats (18). The present study aimed to estimate the potential effects of candesartan against acute myocardial infarction, examine whether candesartan can treat acute myocardial infarction and further investigate the mechanism underlying its effects.

Materials and methods

Drug administration

The chemical structure of candesartan (Sigma-Aldrich; purity 98%) is indicated in Fig. 1, which was dissolved in physiological saline. The casein kinase (CK; cat. no. GA-PM0252MO; GenAsia Biotech, Co., Ltd., Shanghai China), the MB isoenzyme of creatine kinase (CK-MB; cat. no. E-EL-R1327c; Elabscience Biotechnology Co., Ltd., Wuhan, China), lactate dehydrogenase (LDH; cat. no. E-EL-R0338c, Elabscience Biotechnology Co., Ltd.) and cardiac troponin T (cTnT; cat. no. E-EL-R0151c; Elabscience Biotechnology Co., Ltd.) commercial kits, and iNOS (cat. no. E-EL-R0520c; Elabscience Biotechnology Co., Ltd.), NF-κB p65 (cat. no. ybA467Ge; Shanghai Yantuo Biotechnology) and MCP-1 (cat. no. E-EL-R0633c, Elabscience Biotechnology Co., Ltd.) commercial enzyme linked immunosorbent assay (ELISA) kits were purchased from Beyotime Institute of Biotechnology (Nanjing, China). TRIzol reagent was purchased from Invitrogen Life Technologies (Carlsbad, CA, USA). A PrimeScript RT reagent kit was purchase from Takara Biotechnology, Co., Ltd. (Dalian, China). The Bicinchoninic Acid protein assay and caspase-3 and caspase-9 activities colorimetric kits were purchased from Sangon Biotech Co., Ltd. (Shanghai, China).

Figure 1 Chemical structure of candesartan.

Animals

A total of 30 male Wistar rats (8-week-old; 280-300 g) were purchased from The Animal Center of Xi'an Jiaotong University, and animal experiments were performed in accordance with the Guide for the Care and Use of Laboratory Animals (19), and approved by the ethics committee of the Xi'an Jiaotong University (Xi'an, China). These rats were provided with access to water and rodent chow ad libitum, and were housed under a 12 h/12 h light/dark cycle at 22–24°C.

Myocardial infarction induction and experimental groups

Initially, all rats were anesthetized with sodium pentobarbitone (40 mg/kg; Sigma-Aldrich) prior to surgery being performed. The myocardial infarction rat model was induced by ligating the left anterior descending coronary artery, as described previously (20,21). The myocardial infarction rat model was confirmed by regional cyanosis of the myocardial surface with measurement of ST-segment elevation.

Briefly, the rats were divided into the following three groups, one group per cage: Control group (n=10), comprising normal rats administered with saline solution (0.1 ml/100 g); vehicle group (n=10), comprising the myocardial infarction rat model administered with saline solution (0.1 ml/100 g); candesartan treatment group (n=10), comprising the myocardial infarction rat model administered with candesartan 0.25 mg/kg for 2 weeks via the caudal vein, on the basis of the previous report (18). Surgery was performed on the rats in the myocardial infarction group by occlusion of the coronary artery 30 mins following the final administration.

Measurement of the activities of CK, CK-MB, LDH and the level of cTnT

Following treatment with candesartan for 2 weeks, whole bloods samples were collected from the rats in each group following occlusion of the coronary artery for 6 h. Subsequently, the supernatants were centrifuged at 12,000 g for 10 min at 4°C and were stored for subsequent measurement at −20°C. According to the manufacturer's instructions (Beyotime Institute of Biotechnology), the activities of CK, CK-MB and LDH, and the level of cTnT in the rats were determined using a suite of commercial kits according to the manufacturer's instructions at 37°C.

Infarct size measurement

Following treatment with candesartan for 2 weeks, three rats from each group were sacrificed using decollation, then the hearts of the rats were immediately harvested and washed with physiological saline. The hearts of the rats were immediately washed with physiological saline, and the infarct size was measured. The left ventricle was placed at −80°C for 10 min following ligation of the coronary artery for 6 h. Infarct size was measured following the addition of 1% 2,3,5-triphenyltetrazolium chloride (1.5%; Sigma-Aldrich) at 37°C for 30 min in the dark (22,23). The size of the infarct area was measured by the volume and weight, as a percentage of the left ventricle. The heart areas exhibiting a brick red color were considered to be normal myocardium, whereas the areas without color were considered to be ischemic heart muscles.

Western blot analysis of the protein expression levels of iNOS and HSP-72

Following treatment with candesartan for 2 weeks, cardiac cytosolic samples were collected from each group following occlusion of the coronary artery for 6 h. The samples were incubated with 100 µl tissue lysis buffer [1% (w/v) Triton, 0.1% SDS, 0.5% deoxycholate, 1 mmol/l EDTA, 20 mmol/l Tris (pH 7.4), 150 mmol/l NaCl, 10 mmol/l NaF; Beyotime Institute of Biotechnology] for 20 min on ice. Subsequently, the supernatants were centrifuged at 12,000 g for 10 min at 4°C and were stored for subsequent measurement at −20°C. The protein concentrations were determined using a Bicinchoninic Acid protein assay kit (Sangon Biotech Co., Ltd.). An equal quantity of total protein (30 µg) was fractioned on 12% sodium dodecyl sulfate-polyacrylamide gels (Beyotime Institute of Biotechnology), and transferred electrophoretically onto polyvinylidene fluoride membranes (0.22 mm; EMD Millipore, Billerica, MA, USA). The membranes were blocked with phosphate-buffered saline (PBS) with 5% non-fat milk to block nonspecific binding sites. Following blocking, the membranes were incubated with monoclonal rabbit anti-human anti-iNOS (1:1,500; cat. no. sc-49055; Santa Cruz Biotechnology, Inc., Dallas, TX, USA), monoclonal rabbit anti-HSP-72 (1:1,000; cat. no. sc-59570; Santa Cruz Biotechnology, Inc.) and monoclonal rabbit anti-β-actin (1:3,000; cat. no. D110007; Sango Bioscience, Beijing, China) overnight at 4°C. The following day, the membrane was detected by incubation with sheep anti-rabbit IgG (1:10,000; cat. no. C000944; Sango Bioscience), conjugated with horseradish peroxidase at 37°C for 2 h. The relative band intensity was determined using Chem Image 5500 software (UVP, Upland, CA, USA).

ELISA to determine the activities of iNOS and NF-κB p65

Following treatment with candesartan for 2 weeks, whole bloods samples were collected from the rats in each group, following occlusion of the coronary artery for 6 h. Subsequently, the supernatant were centrifuged at 12,000 × g for 10 min at 4°C and were stored for subsequent measurement at −20°C. According to the manufacturer's instructions (Beyotime Institute of Biotechnology), the activities of iNOS and NF-κB p65 in the rats were performed using a suite of commercial ELISA kits according to the manufacturer's instructions at 37°C.

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) analyses of the gene expression levels of MCP-1 and AP-1

Following treatment with candesartan for 2 weeks, cardiac cytosolic samples were collected from each group following occlusion of the coronary artery for 6 h. Total RNA was obtained from the myocardial samples using TRIzol reagent (Invitrogen Life Technologies). RNA (1 µg) was reverse transcribed into cDNA using a One Step PrimeScript miRNA cDNA Synthesis kit (Takara Bio, Inc.), according to the manufacturer's instructions. The gene expression levels of MCP-1 and AP-1 were measured by RT-qPCR using a CFX96 Touch Real-Time PCR system (Bio-Rad Laboratories, Inc., Hercules, CA, USA) and a PrimeScript RT reagent kit, according to manufacturer's instructions. The sequences of the AP-1 primers were as follows: Forward 5′-AAC TGA AGC TCG CAC TCTCG-3′ and reverse 5′-TCA GCA CAG ATC TCC TTGGC-3′. The sequences of the MCP-1 primers were as follows: Forward 5′-AAG TGT GAT GAC TCA GGT TTG CCC TGA-3′ and reverse 5′-AAG TGT GAT ATC TCA GGT TTG CCC TGA-3′. The GAPDH primer sequences were as follows: Forward 5′-GCA CCG TCA AGG CTG AGAAC-3′ and reverse 5′-TGG TGA AGA CGC CAG TGGA-3′. The reaction was conducted with the following conditions: 95°C for 5 min, 40 cycles of 95°C for 30 sec, 60°C for 30 sec and 72°C for 30 sec.

Measurement of caspase-3 and caspase-9 activities

Following treatment with candesartan for 2 weeks, cardiac cytosolic samples were collected from the rats in each group following occlusion of the coronary artery for 6 h. A total of 50 µg protein was incubated in solution buffer (Ac-DEVD-pNA for caspase-3; Ac-LEHD-pNA for caspase-9; BD Biosciences, San Jose, CA, USA) at 37°C for 30 min in the dark. According to the manufacturer's instructions (Sangon Biotech Co., Ltd.), the activities of caspase-3 and caspase-9 were measured at an absorbance of 405 nm using a Bio-Rad 680 microplate reader (Bio-Rad Laboratories, Inc.).

Statistical analysis

All data were analyzed using SPSS 17.0 software (SPSS, Inc., Chicago, IL, USA) and are presented as the mean ± standard deviation. Statistical analyses were performed using one-way analysis of variance, followed by Dunnett's test. P<0.05 was considered to indicate a statistically significant difference.

Results

Candesartan suppresses the activities of CK, CK-MB and LDH, and the level of cTnT in a rat model of acute myocardial infarction

To determine the protective effects of candesartan on the heart of the acute myocardial infarction rat model, the present study examined the activities of CK, CK-MB and LDH, and the level of cTnT in a rat model of acute myocardial infarction. The measurements of serum levels of CK, CK-MB, LDH and cTnT in the control group, vehicle group and candesartan treatment group (0.25 mg/kg) are summarized in Table I. The activities of CK, CK-MB and LDH, and the level of cTnT were significantly increased in the serum of the vehicle group, compared with the control group. Pretreatment with candesartan at a dose of 0.25 mg/kg markedly reduced the activities of CK, CK-MB and LDH, and the level of cTnT in the serum of the rat model of acute myocardial infarction, compared with that in the vehicle group (Table I).

Table I Candesartan suppresses the activities of CK, CK-MB and LDH, and the level of cTnT in a rat model of myocardial infarction.

Table I

Candesartan suppresses the activities of CK, CK-MB and LDH, and the level of cTnT in a rat model of myocardial infarction.

Group	CK (U/ml)	CK-MB (IU/l)	LDH (U/l)	cTnT (U/ml)
Control	0.24±0.02	86.74±6.83	1711.14±353.58	0.08±0.03
Vehicle	0.91±0.05a	205.39±9.32a	5854.12±431.04a	0.57±0.05a
CAN (0.25)	0.43±0.03b	112.38±7.56b	3252.37±326.77b	0.25±0.03b

{ label (or @symbol) needed for fn[@id='tfn1-mmr-12-06-8193'] } Data are presented as the mean ± standard deviation.

a P<0.01, vs. control group;

b P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats.

Candesartan suppresses infarct size in a rat model of acute myocardial infarction

The infarct size in the vehicle group was 42.56±1.23%. Following treatment with candesartan (0.25 mg/kg), the infarct size of the acute myocardial infarction group was significantly reduced to 31.89±2.11%, compared with the vehicle group (Fig. 2).

Figure 2 Candesartan suppresses infarct size in an acute myocardial infarction rat model. Data are presented as the mean ± standard deviation. #P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats.

Candesartan inhibits the expression and activity of iNOS in a rat model of acute myocardial infarction

To more directly determine whether candesartan (0.25 mg/kg) inhibited nitric oxide in the rat model of acute myocardial infarction, the protein expression of iNOS in the rat model of acute myocardial infarction was evaluated using western blot analysis in the present study. The protein expression of iNOS in the vehicle group was significantly increased in the rat model of acute myocardial infarction, compared with the control group (Fig. 3A and B). However, following treatment with candesartan at a dose of 0.25 mg/kg, a marked reduction in the protein expression of iNOS was noted in the rat model of acute myocardial infarction, compared with that in the vehicle group (Fig. 3A and B). In addition, the activity of iNOS in the vehicle group was markedly elevated, compared with the control group (Fig. 3C). In the candesartan treatment groups (0.25 mg/kg), the activity of iNOS was significantly decreased, compared with that in the control group (Fig. 3C).

Figure 3 Candesartan inhibits the expression and activity of iNOS in a rat model of acute myocardial infarction. (A) Protein expression of iNOS was measured using western blot analysis. (B) Statistical analysis of protein levels of iNOS. (C) Statistical analysis of the activity of iNOS. Data are presented as the mean ± standard deviation. *P<0.01, vs. control group; #P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats; iNOS, inducible nitric oxide synthase.

Candesartan inhibits the activity of NF-κB in a rat model of acute myocardial infarction

In order to corroborate the protection of candesartan on NF-κB p65 activity in a rat model of acute myocardial infarction, the activity of NF-κB p65 in the rat model of acute myocardial infarction was determined using a commercial ELISA kit. The results demonstrated that the activity of NF-κB p65 in the vehicle group increased, compared with the control group (Fig. 4). Notably, treatment with candesartan (0.25 mg/kg) reversed the effects of increased NF-κB p65 activity, which were observed in the vehicle group (Fig. 4).

Figure 4 Candesartan inhibits the expression of NF-κB in a rat model of acute myocardial infarction. Data are presented as the mean ± standard deviation. *P<0.01, vs. control group; #P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats; NF-κB, nuclear factor κB.

Candesartan inhibits the expression of AP-1 in a rat model of acute myocardial infarction

The present study aimed to investigate whether candesartan (0.25 mg/kg) had protective effects on the expression of AP-1 in the rat model of acute myocardial infarction, The present study examined the gene expression of AP-1 using RT-qPCR. In the left ventricle, the gene expression of AP-1 in the vehicle group was markedly elevated, compared with that in the control group (Fig. 5). Ppretreatment with candesartan (0.25 mg/kg) was observed to reduce the gen expression of AP-1, compared with that in the vehicle group (Fig. 5).

Figure 5 Candesartan inhibits the expression of AP-1 in a rat model of acute myocardial infarction. Data are presented as the mean ± standard deviation. *P<0.01, vs. control group; #P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats; AP-1, activating protein-1.

Candesartan inhibits the expression of MCP-1 in a rat model of acute myocardial infarction

The present study further analyzed the protective effects of candesartan on the activity of MCP-1 in the rat model of acute myocardial infarction, by determining the gene expression levels of MCP-1 using RT-qPCR. In the vehicle group, the gene expression of MCP-1 was remarkably increased, compared with that in the control group (Fig. 6). However, following treatment with candesartan (0.25 mg/kg) for 2 weeks, the gene expression of MCP-1 was decreased significantly, compared with that in the vehicle group (Fig. 6).

Figure 6 Candesartan inhibits the expression of MCP-1 in a rat model of acute myocardial infarction. Data are presented as the mean ± standard deviation. *P<0.01, vs. control group; #P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats; MCP-1, monocyte chemotactic protein-1.

Candesartan restores the expression of HSP-72 in a rat model of acute myocardial infarction

To more directly determine whether candesartan restores the expression of HSP-72 in a rat model of acute myocardial infarction, the protein expression of HSP-72 was determined using western blot analysis the present study. The protein expression of HSP-72 in the vehicle group was markedly decreased, compared with that in the control group (Fig. 7A and B). By contrast, pretreatment with candesartan (0.25 mg/kg) increased the protein expression of HSP-72, compared with that in the vehicle group (Fig. 7A and B).

Figure 7 Candesartan restores the expression of HSP-72 in a rat model of acute myocardial infarction. (A) Protein expression level of HSP-72 was measured using western blot analysis. (B) Statistical analysis of protein levels of HSP-72. Data are presented as the mean ± standard deviation. *P<0.01, vs. control group; #P<0.01, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats; HSP-72, heat shock protein-72.

Candesartan alters the activities of caspase-3 and caspase-9 in a rat model of acute myocardial infarction

To investigate the mechanism of candesartan on acute myocardial infarction, the activities of caspase-3 and caspase-9 were examined using colorimetric kits in the present study. The activities of caspase-3 and caspase-9 in the vehicle group were markedly increased, compared with those in the control group (Fig. 8A and B). However, these activities were not altered following treatment with candesartan (0.25 mg/kg) in the candesartan treatment group, compared with the vehicle group (Fig. 8A and B).

Figure 8 Effects of candesartan on the levels of caspase-3 and caspase-9 in a rat model of acute myocardial infarction. The activities of (A) caspase-3 and (B) caspase-9 were determined in the different treatment groups. Data are presented as the mean ± standard deviation. *P<0.01, vs. control group; ##P>0.05, vs. vehicle group. Control, saline-treated normal rats; Vehicle, saline-treated infarction model rats; CAN (0.25), candesartan (0.25 mg/kg)-treated infarction model rats.

Discussion

With economic developments in society and the improvement of living standards, more individuals are being found to exhibit high blood pressure, high cholesterol and high blood sugar, and patients with angina pectoris and myocardial infarction are also following an increasing trend (24). The irreversible necrosis caused by myocardial ischemic myocardial disease results in repeated episodes of heart failure, which is the leading cause of mortality worldwide (25). In the present study, the activities of CK, CK-MB and LDH, and the level of cTnT were observed to increase in the serum of a rat model of acute myocardial infarction following candesartan (0.25 mg/kg) treatment. In addition, the size of the acute myocardial infarction was significantly reduced in these rats. Suzuki et al reported that candesartan is more effective than angiotensin-converting enzyme inhibitors in preventing left ventricular remodeling following acute myocardial infarction (26).

There are two types of NOS for endothelial cells and cardiomyocytes: Primary NOS of calcium/calmodulin-dependence and iNOS of calcium/calmodulinnon-dependence (27). Endothelial cells synthesize a small quantity of nitric oxide under physiological conditions by primary NOS, which is important in the diffusion of nitric oxide into vascular smooth muscle cells, vascular relaxation through cyclic guanosine monophosphate pathway; entering the bloodstream to inhibit the activation, adhesion and aggregation of platelets and leukocytes; reducing the generation of superoxide radicals through direct inhibition of reduced nicotinamide adenine dinucleotide phosphate oxidase in neutrophils; and regulating the expression of adhesion molecules in neutrophils and endothelial cells (28). Following acute myocardial infarction, the basic function of coronary artery endothelial cells and the release function of nitric oxide stimulation by acetylcholine are impaired, and neutrophil-endothelial cell adhesion is promoted. The present study found that the protein expression and activity of iNOS were significantly reduced in a rat model of acute myocardial infarction. Bian et al reported the association between the effects of candesartan and NOS in spontaneous hypertensive rats (29), and Miller et al identified that candesartan attenuates diabetic retinal vascular pathology by the reduction of iNOS (30).

NF-κB has a central regulatory role in a variety of tissue and organ injuries (31). As a nuclear transcription factor with multi-directional regulation effect, NF-κB regulates the expression of a number of important immune factors, and may be involved in the promotion of inflammatory cytokine and chemokine generation, the proliferation differentiation of fibroblasts, extracellular matrix crosslinking and apoptosis, and is involved in the process of acute myocardial infarction, promoting the progression of acute myocardial infarction disease (7,32,33). Therefore its role in the development of acute myocardial infarction cannot be ignored. In the present study, candesartan was observed to attenuate NF-κB p65 activity in the rat model of acute myocardial infarction. Furthermore, Hadi et al reported that candesartan significantly attenuates atherosclerotic lesions and significantly reduces NF-κB activity in rabbits (34). In addition, Ishrat et al demonstrated that candesartan reduces hemorrhage in rat embolic stroke through a reduction in NF-κB activity (35).

MCP-1 is a chemokine of CC-type cells, involved as signaling molecules. There are NF-κB and AP-1 binding sites in the gene promoter site, which can be combined with the DNA binding sequence of NF-κB, thus activating the transcription of the gene. Experiments have demonstrated that MCP-1 can protect neonatal myocardial cells of mice from hypoxic death, and its cytoprotective and chemotaxis effects are achieved through different signaling mechanisms. In the present study, the gene expression of MCP-1 was decreased by candesartan treatment. Candesartan has also been observed to inhibit LPS-induced gene expression through the suppression of MCP-1 protein concentrations in human renal tubular epithelial cells (36). Hadi et al reported that candesartan retards the progression of atherosclerosis via reducing MCP-1, NF-κβ and oxidative pathways (34).

The AP-1 transcription factor is an important target of intracellular c-Jun N-terminal kinase/stress-activated protein kinase protein products, encoded by immediate early genes in the nucleus, c-fos and c-Jun, from Fos and Jun family proteins respectively, which form homogenous or heterogeneous dimers through combination in a leucine zipper structure, to constitute the AP-1 transcription factor (11). The results of the present study demonstrated that candesartan reduced the gene expression of AP-1 in a rat model of acute myocardial infarction. Tharaux et al indicated that AP-1-receptor antagonism by candesartan activates the collagen I gene through the mitogen-acitvated protein/extracellular-signal regulated kinase pathway (37).

Previous studies have reported that HSP70 is an important cardioprotective protein, which is involved in delayed myocardial protection. (38,39) It has been demonstrated that heat shock for 24 h can increase myocardial tolerance to I/R injury, manifested by a reduction in infarct size (18). There are two types of method known to increase HSP72 content in cardiomyocytes. The first is the induction of the endogenous expression of HSP72, usually realized by heat stress at sublethal doses or by other harmful stimulating factors, including ischemia, hypoxia, ethanol, heavy metal salts and infection (40). The second is to guide exogenous HSP70 genes, to increase the expression levels of cardiac HSP72 by transgenic technology (11). The present study demonstrated that candesartan increased the protein expression of HSP-72 in a rat model of acute myocardial infarction. Taniguchi et al also suggested that candesartan protects against reperfusion injury in hereditary insulin-resistant rats through recovery of the expression of HSP72 (18).

Previous studies have revealed that candesartan improves peak systolic pressure, however, it does not alter the level of apoptosis or the expression of caspase-3 (41–43). Therefore, the present study examined the association between the protective effect of candesartan on acute myocardial infarction and the apoptosis of myocardial cells. In the present study, candesartan had no affect on cell apoptosis in acute myocardial infarction, or on the activities of caspase-3 and caspase-9 in the rat model of acute myocardial infarction. These results indicated that the protective effect of candesartan on acute myocardial infarction may involve several pathways. In conclusion, the present study demonstrated that the protective effect of candesartan ameliorated acute myocardial infarction in rats and revealed that its activity regulated iNOS, NF-κB, MCP-1, AP-1 and HSP72 in the rat model of acute myocardial infarction. Further investigations are required to clarify the other key signaling pathways of the interaction between the protective effect of candesartan and acute myocardial infarction.

Further investigations are required to clarify the other signaling pathways underlying the interaction between the protective effects of candesartan and acute myocardial infarction for clinical application.

Acknowledgments

This study was supported by the Key Program of the National Natural Science Foundation of China (grant no. 30830051), the '13315' Scientific and Technological Innovation Project of Shaanxi Province (grant no. 2008ZDKG-62) and the Scientific and Technological Projects for Social Development of Shaanxi Province (grant no. 2015SF024).

References