Huperzine A ameliorates damage induced by acute myocardial infarction in rats through antioxidant, anti-apoptotic and anti-inflammatory mechanisms

  • Authors:
    • Xizhong Sui
    • Changqing Gao
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  • Published online on: November 1, 2013     https://doi.org/10.3892/ijmm.2013.1546
  • Pages: 227-233
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Abstract

Huperzine A (HupA), an alkaloid used in traditional Chinese medicine and isolated from Huperzia serrata, has been shown to possess diverse biological activities. The present study was undertaken to evaluate the cardioprotective potential of HupA in myocardial ischemic damage using a rat model of acute myocardial infarction. HupA significantly diminished the infarct size and inhibited the activities of myocardial enzymes, including creatine kinase (CK), the MB isoenzyme of creatine kinase (CK-MB), lactate dehydrogenase (LDH) and cardiac troponin T (cTnT). A significantly reduced activity of malondialdehyde (MDA) and elevated activities of superoxide dismutase (SOD), of the non-enzymatic scavenger enzyme, glutathione (GSH), as well as of glutathione peroxidase (GSH-PX) were found in the HupA-treated groups. Furthermore, decreased protein levels of caspase-3 and Bax, and increased levels of Bcl-2 were observed in the infarcted hearts of the rats treated with various concentrations of HupA. In addition, treatment with HupA markedly inhibited the expression of the nuclear factor-κB (NF-κB) subunit p65, tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). These findings suggest that the cardioprotective potential of HupA is associated with its antioxidant, anti-apoptotic and anti-inflammatory properties in acute myocardial infarction in rats.

Introduction

Myocardial infarction is one of the most common ischemic heart diseases and a major cause of morbidity and mortality worldwide. It is a clinical syndrome arising from the sudden and persistent interruption of the myocardial blood supply, eventually leading to the loss of cardiomyocytes. Although a number of drugs, including angiotensin-converting enzyme inhibitors, calcium channel blockers and angiotensin II receptor antagonists, has been widely used to treat myocardial ischemia in western medicine, the usefulness of these drugs has been limited due to their serious adverse effects, such as cardiac depression or even, proarrhythmic effects (1). There is great interest in the development of new types of cardioprotective drugs, which may attenuate the effects of myocardial infarction in clinical practice.

Cumulative evidence has demonstrated that cell death in myocardial infarction is mainly mediated by reactive oxygen species (ROS). A previous study demonstrated that the accumulation of oxygen free radicals following ischemia not only destroyed cellular structures, but further caused mitochondrial dysfunction, activating apoptotic signaling cascades (2). The fatty acids are attacked by an excess of free radicals in myocardial membranes. This causes a chain reaction of lipid peroxidation, which has a harmful effect on the myocardium during acute myocardial infarction (3). In addition, oxidative stress is intimately involved in the occurrence of myocardial ischemia. Therefore, the reduction of ROS may attenuate the effects of acute myocardial infarction.

Apoptosis has been shown to participate in the pathogenesis of myocardial injuries during myocardial infarction. Caspase-3 serves as an ‘apoptotic effector’ in response to apoptotic stimuli (4). It has previously been reported that a dramatic elevation of caspase-3 can cause damage in isoproterenol-induced Wistar rats with acute myocardial infarction (5). In addition, proteins of the Bcl-2 family have been shown to play a central role in the regulation of cellular apoptosis. Bcl-2 is a cytosolic protein and serves as an anti-apoptotic molecule, whereas another member of the family, Bax, functions as a pro-apoptotic protein (6). These findings suggest that the regulation of caspase-3, Bcl-2 and Bax proteins may attenuate the cardiac damage occuring in myocardial infarction.

Nuclear factor-κB (NF-κB), which is found among most eukaryotes, is the hub of the related signal transduction pathway and is present in myocytes. Its levels can reflect the pathological changes occuring during acute myocardial infarction (7,8). The activation of NF-κB can lead to the release of pro-inflammatory cytokines, such as tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). During myocardial infarction, high levels of NF-κB p65, TNF-α and IL-1β in cells can promote myocardial necrosis and cellular apoptosis, eventually leading to serious heart failure. Thus, drugs that suppress the NF-κB signaling pathway and the release of pro-inflammatory factors may be used for the treatment of diverse cardiac disorders.

Huperzine A (HupA) is a compound found in the plant Qian Ceng Ta (Huperzia serrata), used in traditional Chinese medicine (9). It has been previously demonstrated to upregulate the cholinergic anti-inflammatory pathway and to inhibit immunosenescence and age-related disorders, such as Alzheimer’s disease, by suppressing acetylcholinesterase (AChE) activity (1013). Additionally, HupA has been reported to reduce oxidative damage in D-galactose-treated rats (14). However, it has not been well established whether HupA can protect against acute myocardial infarction in rats. Based on the above data, we hypothesized that HupA exerts cardioprotective effects in rats with acute myocardial infarction, and further explored the potential cardioprotective mechanisms involved.

Materials and methods

Ethics statement

The experimental protocols for animal handling were approved by the Animal Ethics Committee of the Medical School of Chinese PLA, Beijing, China.

Animals and induction of acute myocardial infarction

We purchased adult male Wistar rats (250–300 g) from the Beijing Animal Center (Beijing, China). The rats were housed in polypropylene cages under a controlled environment (12:12 h light/dark cycle, 50–70% humidity, 24°C) with free access to water and food. The rat model of acute myocardial infarction was established as previously described with minor modifications (15). Briefly, the animals were anesthetized intraperitoneally (i.p.) with sodium pentobarbital (40 mg/kg). They were then intubated and artificially ventilated with a respirator. The standard electrocardiogram (II) was procured by a transducer attached to a multi-channel recorder (BL-420F; Chengdu Tai Meng Science and Technology Co. Ltd., Chengdu, China), with electrodes subcutaneously inserted into the limbs of the animals. A 5–0 silk suture of 1–2 mm was selected to encircle the left anterior descending coronary artery under the left atrial appendage. The sham-operated animals underwent identical surgical procedures with the exception of the coronary artery ligation. Efforts were made to minimize the number of animals used and their suffering. Successful ligation was confirmed by an ST-segment elevation and regional cyanosis of the myocardial surface.

Drug administration

HupA (98% pure; Sigma-Aldrich, St. Louis, MO, USA) was dissolved in physiological saline solution. The rats were randomly divided into 4 groups, 2 referred to as contorl and 2 as treated: i) the control sham-operated group, in which the rats were injected with physiological saline (0.1 ml/100 g, i.p.) and underwent identical surgery with the exception of the coronary artery ligation; ii) the control vehicle-treated group, in which the rats were injected with physiological saline (0.1 ml/100 g, i.p.) and underwent the ligation of the left coronary artery; and iii) 2 HupA treatment groups, which were subjected to the ligation of the left coronary artery and treated with 167 and 500 μg/kg HupA, respectively. The rats were injected with physiological saline solution or HupA 7 consecutive days. Thirty minutes after the final injection, the rats underwent left coronary artery ligation.

Measurement of infarct size

The hearts were rapidly excised and the left ventricles were sliced into 2-mm thick sections from the apex to the atrioventricular groove 6 h after the coronary artery was ligated, followed by incubation with 1% triphenyltetrazolium chloride (TTC) (Sigma-Aldrich) solution at 3°C for 30 min. The normal myocardium was stained brick red, while the area without color corresponded to the ischemic heart muscle. The volume and weight of the rat hearts as a percentage of the left ventricle were used to calculate the size of the infarcted area.

Quantification of activities of cardiac marker enzymes

Six hours after the ligation of the coronary artery, the blood samples were collected in order to determine the activities of the myocardial-specific enzymes, creatine kinase (CK), the MB isoenzyme of creatine kinase (CK-MB), lactate dehydrogenase (LDH) and cardiac troponin T (cTnT). The colorimetric method was employed to determine the activities of CK, CK-MB and LDH following the manufacturer’s instructions (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Serum cTnT levels were measured using the Elecsys 2010 immunoassay (Roche Diagnostics GmbH, Mannheim, Germany).

Measurement of malondialdehyde (MDA), superoxide dismutase (SOD), glutathione (GSH) and glutathione peroxidase (GSH-PX) activities

The enzymatic activities of MDA, SOD, GSH and GSH-PX in the heart homogenates were measured according to the instructions provided with the relevant commercially-available assay kits (Nanjing Jiancheng Bioengineering Institute). The concentration of MDA, a presumptive marker of oxidant-mediated lipid peroxidation, was quantified using the thiobarbituric acid (TBA)-reacting substances assay, followed by measuring the absorbance at a wavelength of 532 nm. SOD activity was measured in the heart homogenates by calculating the rate of inhibition of nucleotide oxidation. The activities of GSH-PX and GSH were determined by quantifying the rate of oxidation of the reduced glutathione to the oxidized glutathione by H2O2. One unit of GSH-PX was represented as the quantity that reduced the level of GSH by 1 μM in 1 min/mg protein. Quantification of protein concentrations in the heart homogenates was performed using the Coomassie Brilliant Blue method and bovine serum albumin as the standard.

Caspase-3 activity assay

The cleavage of the chromogenic caspase substrate, acetyl-Asp-Glu-Val-Asp-p-nitroanilide (Ac-DEVD-pNA), by caspase-3 was used to measure the activity of the enzyme. The amount of caspase-3 was measured by the colorimetric approach using a commercial kit (Beyotime Institute of Biotechnology, Beijing, China). The protein samples from the heart muscles were acquired as described below in ‘Western blot analysis’. Approximately 50 μg of protein was added to the reaction buffer containing Ac-DEVD-pNA (2 mM), incubated at 37°C for 4 h, and the absorbance of yellow pNA was calculated by a spectrometer at a wavelength of 405 nm. The activity of caspase-3, normalized as to the total protein activity in heart muscle, was then expressed as a fold change, compared with the baseline caspase-3 activity of the control (sham-operated) group.

Western blot analysis

Western blot analysis was performed on the heart samples from each group. Briefly, heart muscle from different samples was homogenized in ice-cold RIPA buffer. Following centrifugation at 13,200 × g for 20 min at 4°C, the supernatant was collected and the total protein level was measured using a standard BCA method (Beyotime Institute of Biotechnology).

Proteins (50 μg) were separated in 8 or 10% SDS-polyacryl-amide gels and transferred onto nitrocellulose membranes (Millipore, Billerica, MA, USA). The membranes were blocked with 5% fat-free milk for 2 h at room temperature and then incubated with a primary antibody overnight at 4°C. The primary antibodies used were as follows: rabbit anti-caspase-3 (1:300), rabbit anti-Bcl-2 (1:200), rabbit anti-Bax (1:200) (all from Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) and mouse anti-GAPDH (1:2,000; Kang Chen, Shanghai, China). The membranes were then rinsed and incubated with horseradish peroxidase-conjugated goat anti-rabbit antibody (1:5,000) or goat anti-mouse antibody (1:5,000) (both from Santa Cruz Biotechnology, Inc.) for 2 h. The detection of immunolabeled protein bands was performed using an enhanced chemiluminescence (ECL) kit (Pierce, Rockford, IL, USA), followed by exposure to an X-ray film. GAPDH was used as the loading control. The quantification of protein band intensities was carried out using Quantity One software (Bio-Rad, Hercules, CA, USA).

Measurement of NF-κB, TNF-α and IL-1β levels

The nuclear levels of p65 may positively correlate with the activation of the NF-κB pathway. The NF-κB/p65 ActivELISA kit (Imgenex, San Diego, CA, USA) was used to measure the levels of NF-κB-free p65 in the nuclear lysates following the manufacturer’s instructions. The quantification of TNF-α and IL-β was carried out using the TNF-α and IL-1β Quantikine Rat immunoassay kits following the manufacturer’s instructions (R&D Systems, Minneapolis, MN, USA).

Statistical analysis

Data are expressed as the means ± SD from 6 rats in each group. Experimental results were analyzed using a one-way ANOVA followed by Dunnett’s test for individual comparisons between the means of each group. All statistical analyses were performed using SPSS 13.0 software. A value of P<0.05 was considered to indicate a statistically significant difference.

Results

Effects of HupA on myocardial infarct size in a rat model of acute myocardial infarction

The chemical structure of HupA is illustrated in Fig. 1. The infarct size in the vehicle-treated group was 39.31±2.78%. Following treatment with HupA at concentrations of 167 and 500 μg/kg, the size of the infarcted area significantly decreased to 31.77±1.74% (P<0.01) and 26.21±1.91% (P<0.01), respectively, in comparison with the vehicle-treated group (Fig. 2).

Effects of HupA on serum CK, CK-MB, LDH and cTnT levels in a rat model of acute myocardial infarction

The measurements of serum CK, CK-MB, LDH and cTnT levels in the control and treated groups are summarized in Table I. The rats with acute myocardial infarction showed a significant increase in serum levels of CK, CK-MB, LDH and cTnT (P<0.01) as compared with the sham-operated control group. Pre-treatment with 167 and 500 μg/kg HupA significantly decreased (P<0.01) the serum levels of CK, CK-MB, LDH and cTnT in the rats subjected to myocardial infarction vs. the vehicle-treated group.

Table I

Effects of HupA on serum levels of CK, CK-MB, LDH and cTnT in rats subjected to acute myocardial infarction.

Table I

Effects of HupA on serum levels of CK, CK-MB, LDH and cTnT in rats subjected to acute myocardial infarction.

GroupCKCK-MBLDHcTnT
Sham-operated group0.24±0.0578.08±2.611838±405.690.058±0.03
Vehicle-treated group0.58±0.07a186.16±6.11a3748.5±398.27a0.3±0.05a
HupA (167 μg/kg)0.41±0.06b115.87±7.29b 3165.67±405.44b0.19±0.05b
HupA (500 μg/kg)0.29±0.08b93.45±7.42b2455.5±319.19b0.17±0.04b

a P<0.01 vs. sham-operated group;

b P<0.01 vs. vehicle-treated group.

{ label (or @symbol) needed for fn[@id='tfn3-ijmm-33-01-0227'] } HupA, huperzine A; CK, creatine kinase; CK-MB, MB isoenzyme of creatine kinase; LDH, lactate dehydrogenase; cTnT, cardiac troponin T. Data are presented as the means ± SD (n=6).

Effects of HupA on the activities of MDA, SOD, GSH-PX and GSH in a rat model of acute myocardial infarction

Table II demonstrates the activities of MDA, SOD, GSH-PX and GSH in the rat hearts from the control and treated groups. Rats subjected to acute myocardial infarction exhibited a marked increase in MDA levels, an indicator of lipid peroxidation, as compared with the sham-operated control rats (P<0.01). The administration of 167 and 500 μg/kg HupA to the rats with myocardial infarction significantly reduced ischemia-mediated lipid peroxidation in comparison with the vehicle-treated group (P<0.01 for both HupA concentrations). Furthermore, the activities of antioxidants and antioxidative enzymes were measured in the heart homogenates from the control and treated groups. Rats with acute myocardial infarction showed a significant reduction in SOD, GSH-PX and GSH activities (P<0.01) vs. the control rats. However, following treatment with HupA (167 or 500 μg/kg), a significant elevation in the activities of SOD, GSH-PX and GSH was observed in the infarcted rat heart as compared with the vehicle-treated group (P<0.01 for both HupA concentrations).

Table II

Effects of HupA on MDA, SOD, GSH-PX and GSH activities in the hearts of rats subjected to acute myocardial infarction.

Table II

Effects of HupA on MDA, SOD, GSH-PX and GSH activities in the hearts of rats subjected to acute myocardial infarction.

GroupMDASODGSH-PXGSH
Sham-operated group25.19±1.076.29±0.736.29±0.7334.81±2.69
Vehicle-treated group16.29±0.80a3.34±0.18a3.34±0.18a23.61±2.15a
HupA (167 μg/kg)20.90±1.00b4.87±0.48b4.87±0.48b28.85±1.79b
HupA (500 μg/kg)22.22±1.24b5.25±0.25b5.25±0.25b30.54±2.21b

a P<0.01 vs. sham-operated group;

b P<0.01 vs. vehicle-treated group.

{ label (or @symbol) needed for fn[@id='tfn6-ijmm-33-01-0227'] } HupA, huperzine A; MDA, malondialdehyde; SOD, superoxide dismutase; GSH-PX, glutathione peroxidase; GSH, glutathione. Data are presented as the means ± SD (n=6).

Effects of HupA on caspase-3 activity in a rat model of acute myocardial infarction

In order to explore whether HupA attenuates the apoptotic damage induced by myocardial infarction, the activity of caspase-3, an effector of the apoptotic signaling pathway, was determined by colorimetric analysis. Caspase-3 activity was markedly elevated by 319.92% (P<0.01) in the vehicle-treated group as compared with the sham-operated group (Fig. 3). In the HupA-treated (167 and 500 μg/kg) groups, there was a significant reduction in caspase-3 activity by 39.80% (P<0.01) and 47.03% (P<0.01), respectively, as compared with the vehicle-treated group.

Effects of HupA on the protein expression of caspase-3, Bcl-2 and Bax in a rat model of acute myocardial infarction

To corroborate the fact that HupA prevents cardiac damage induced by acute myocardial infarction in rats, western blot analysis was carried out to determine the expression levels of the apoptosis-related proteins, caspase-3, Bcl-2 and Bax, in the rat hearts. Western blot analysis with caspase-3 antibody exhibited a specific band of 20 kDa, characteristic of caspase-3 (Fig. 4A). The protein expression of caspase-3 in the vehicle-treated group with myocardial infarction was markedly increased in the rat hearts as compared with the sham-operated control group (P<0.01). Nevertheless, upon treatment with HupA (167 or 500 μg/kg) a marked reduction in caspase-3 protein expression was observed in the infarcted rats (P<0.01 for both HupA concentrations) in comparison to the vehicle-treated group (Fig. 4B). Thus, these results further confirmed that HupA treatment reduced the caspase-3 protein level in a rat model of acute myocardial infarction, in line with the caspase-3 activity measurements. In addition, proteins of the Bcl-2 family, such as Bcl-2 and Bax, are considered to play a pivotal role in the regulation of apoptotic cascades. Fig. 4A shows that these proteins were detected in bands of 26 kDa for Bcl-2 and 23 kDa for Bax. The statistical comparison revealed a statistically significant reduction in Bcl-2 and a marked elevation in Bax protein levels in the vehicle-treated rats (P<0.01) as compared with the sham-operated group. However, upon treatment with HupA (167 or 500 μg/kg), we observed strikingly elevated and markedly decreased levels of Bcl-2 and Bax, respectively (P<0.01 for both HupA concentrations) in the infarcted rat hearts as compared with the vehicle-treated group (Fig. 4C and D).

Effects of HupA on protein expression of NF-κB p65, TNF-α and IL-1β in a rat model of acute myocardial infarction

Table III shows the effects of HupA on the protein levels of the inflammatory response molecules, NF-κB p65, TNF-α and IL-1β, in a rat model of acute myocardial infarction. It was found that the levels of NF-κB p65 (P<0.01), TNF-α (P<0.01) and IL-1β (P<0.01) were markedly increased in the vehicle-treated group with myocardial infarction. However, treatment with HupA (167 or 500 μg/kg) induced a reduction in NF-κB p65 (P<0.01), TNF-α (P<0.01) and IL-1β (P<0.01) levels in comparison to the group subjected to myocardial infarction.

Table III

Effects of HupA on NF-κB p65, TNF-α and IL-1β levels in the hearts of rats subjected to acute myocardial infarction.

Table III

Effects of HupA on NF-κB p65, TNF-α and IL-1β levels in the hearts of rats subjected to acute myocardial infarction.

GroupNF-κB p65TNF-αIL-1β
Sham-operated group13.17±1.1284.47±2.332.16±0.13
Vehicle-treated group45.32±1.02a410.92±8.56a6.25±0.27a
HupA (167 μg/kg)35.17±0.71b377.76±15.74b4.20±0.23b
HupA (500 μg/kg)25.98±0.88b254.73±7.29b3.54±0.26b

a P<0.01 vs. sham-operated group;

b P<0.01 vs. vehicle-treated group.

{ label (or @symbol) needed for fn[@id='tfn9-ijmm-33-01-0227'] } HupA, huperzine A; NF-κB, nuclear factor-κB; TNF-α, tumor necrosis factor-α; IL-1β, interleukin-1β. Data are presented as the means ± SD (n=6).

Discussion

To our knowledge, the results of the present study revealed for the first time that: i) HupA has the potential to decrease the myocardial infarct size and the activities of CK, CK-MB, LDH in serum, as well as those of cTnT in a rat model of acute myocardial infarction; ii) HupA markedly inhibited lipid peroxidation (MDA production), but increased the activities of endogenous antioxidant enzymes (SOD and GSH), as well as those of the non-enzymatic scavenger, GSH-PX, in a rat model of acute myocardial infarction; iii) HupA treatment of rats with myocardial infarction resulted in a marked decrease in caspase-3 and Bax levels, and in an elevated Bcl-2 expression at the protein level; iv) HupA inhibited the protein expression of the major inflammatory factors, NF-κB p65, TNF-α and IL-1β, in the infarcted rat hearts. These findings support the hypothesis that the cardioprotective effects induced by HupA are associated with its antioxidant, anti-apoptotic and anti-inflammatory properties.

HupA, which is isolated from numerous plants of the Lamiaceae family, is a major phenolic monoterpene and has various pharmacological actions. It has been widely used in the food industry and clinical dentistry. The present study extended the spectrum of the therapeutic effects of HupA and demonstrated its potential as a potent cardioprotective agent in a rat model of acute myocardial infarction.

In ischemic heart disease, the infarct size and the activities of myocardial-specific enzymes, such as CK, CK-MB, LDH and cTnT, are known as important parameters for evaluating cardiac injury. Previous studies have demonstrated a prominent elevation of infarct size and of the activities of myocardial-specific enzymes, including CK, CK-MB and LDH, in rats with acute myocardial infarction (5,16). The activity of serum cTnT is a very specific and sensitive indicator of myocardial infarction. cTnT is a contractile protein that is rarely found in serum but is abundantly released when myocardial necrosis occurs (17). Consistent with previous reports, the present study illustrated that the infarct size and the activities of CK, CK-MB, LDH and cTnT significantly increased in rats subjected to myocardial infarction. Moreover, the activities of these enzymes were significantly reduced following treatment with HupA, demonstrating the cardioprotective effects of HupA.

It is well established that the excessive generation of oxygen free radicals is a pivotal factor that exacerbates cellular damage during ischemic attack. Under normal conditions, the generation of oxygen free radicals is kept under homeostatic control by endogenous antioxidant enzymes, such as SOD and GSH-PX, and by low-molecular weight antioxidants. The first line of cellular defense against oxidative injury may be the anti-oxidative system. A number of drugs based on antioxidants and radical scavengers has been shown to contribute to a favorable outcome in the therapy of ischemic diseases (18,19). Furthermore, the liberation of lipid aldehydes and peroxides is facilitated by cellular membrane damage. MDA is synthesized during the oxidation of fatty acids within myocardial membranes and causes a ripple effect of lipid peroxidation. Therefore, MDA may serve as an indicator of structural oxidative injury of cell membranes. The present study demonstrated that HupA induced a significant reduction in MDA, as well as in SOD, GSH and GSH-PX activities in the infarcted rat hearts. This result indicated that the cardioprotective effects of HupA against acute myocardial infarction are associated with its antioxidant properties.

The cardiac impairment of ischemic patients occurs via oxidative stress and could lead to mitochondrial dysfunction and hence, activate an apoptotic cascade. To further explore the protective effects of HupA against cardiac injury induced by acute myocardial infarction in rats, we measured the levels of apoptosis-related proteins in the rat hearts. Caspases are evolutionarily conserved cysteinyl proteases with a central role in the apoptotic signaling pathway; among them, caspase-3 is a critical molecule in the caspase-dependent apoptotic cascade. Caspase-3 has previously been reported to activate a variety of substrates that presumably cause DNA fragmentation and cell death (20). An increasing number of studies has revealed the upregulation of caspase-3 following acute myocardial infarction (5,15). The present study demonstrated that treatment with HupA markedly reduced caspase-3 activity in the infarcted rat hearts. In agreement with our findings, Wang and Tang (9) also reported that HupA significantly decreased the expression level of caspase-3 in Alzheimer’s disease. In addition to caspases, proteins of the Bcl-2 family have been shown to be involved in the modulation of ischemia-induced apoptosis in rat myocytes. Bcl-2 itself acts as a repressor of apoptosis, while another member of the family, Bax, functions as a promoter of cell death (6). It has previously been reported that myocardial infarction induces a marked reduction in the expression of the anti-apoptotic protein, Bcl-2, and an increase in the expression of the apoptotic-promoting molecule, Bax (21,22). In agreement with previous studies, our findings demonstrated a significant downregulation of Bcl-2 and an upregulation of Bax in rats subjected to acute myocardial infarction. However, the alterations in the levels of Bcl-2 and Bax caused by ischemic damage were prevented by the administration of HupA. In addition, our results demonstrated a reduction in caspase-3 activity in the rats subjected to myocardial infarction treated with HupA, suggesting that the cadioprotective effects of HupA are associated with its anti-apoptotic properties in acute myocardial infarction in rats.

Previous studies have suggested that the inflammatory response participates in the pathogenesis of ischemic heart diseases, and NF-κB is regarded as an important factor in this respect (23,24). The activation of NF-κB leads to the release of pro-inflammatory cytokines, such as TNF-α and IL-1β. The inhibition of the NF-κB pathway has previously been reported to improve adverse left ventricular remodeling and cardiac dysfunction following myocardial infarction (25). Our study revealed that HupA inhibited the excessive activation of NF-κB p65 and reduced the release of TNF-α and IL-1β in rats subjected to myocardial infarction. Consistently, Ruan et al (14) found that HupA exerted anti-inflammatory effects against D-galactose-treated rats. In addition, a previous study illustrated that HupA inhibited the nuclear translocation of NF-κB and decreased the expression of pro-inflammatory factors following transient focal cerebral ischemia (26). Taken together, these findings suggest that HupA exerts cardioprotective effects against acute myocardial infarction through anti-inflammatory mechanisms.

In conclusion, the present study demonstrates that HupA attenuates the damage induced by acute myocardial infarction. The cardioprotective effects of HupA may be associated with its antioxidan, anti-apoptotic and anti-inflammatory properties. To our knowledge, our study presents the first evidence of the potential cardioprotective profile and related mechanisms of action of HupA. Our results also support the hypothesis that HupA may be a promising cardioprotective agent for the treatment of acute myocardial infarction. However, more detailed studies are required to fully elucidate its effects and mechanisms of action.

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2014-January
Volume 33 Issue 1

Print ISSN: 1107-3756
Online ISSN:1791-244X

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Copy and paste a formatted citation
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Spandidos Publications style
Sui X and Sui X: Huperzine A ameliorates damage induced by acute myocardial infarction in rats through antioxidant, anti-apoptotic and anti-inflammatory mechanisms. Int J Mol Med 33: 227-233, 2014
APA
Sui, X., & Sui, X. (2014). Huperzine A ameliorates damage induced by acute myocardial infarction in rats through antioxidant, anti-apoptotic and anti-inflammatory mechanisms. International Journal of Molecular Medicine, 33, 227-233. https://doi.org/10.3892/ijmm.2013.1546
MLA
Sui, X., Gao, C."Huperzine A ameliorates damage induced by acute myocardial infarction in rats through antioxidant, anti-apoptotic and anti-inflammatory mechanisms". International Journal of Molecular Medicine 33.1 (2014): 227-233.
Chicago
Sui, X., Gao, C."Huperzine A ameliorates damage induced by acute myocardial infarction in rats through antioxidant, anti-apoptotic and anti-inflammatory mechanisms". International Journal of Molecular Medicine 33, no. 1 (2014): 227-233. https://doi.org/10.3892/ijmm.2013.1546