Introduction
Green tea has been known for a long time to have antioxidant [1], antimicrobial [2], anti-inflammatory [3], antiallergic [4], and anticarcinogenic [5] properties, and there is a great deal of interest in its bioregulatory effects. Green tea has vasodilatory effects [6], can inhibit the development of arteriosclerosis [7], and there is evidence that it reduces the incidence of cardiac diseases [8].
The main bioactive substances of green tea consist of (-)-epigallocatechin-3-gallate (EGCG), (-)-epigallocatechin (EGC), (-)-epicatechin-3-gallate (ECG), and (-)-epicatechin (EC)-like polyphenolic epicatechin. EGCG is the most abundant catechin in green tea, and has the highest biological activity [9]. In animal models, EGCG administration has been shown to inhibit the cerebral and renal ischemic injury [10,11].
Recently, it has been reported that EGCG can protect the heart from cardiac ischemic injury [12]. However, in actual clinical cases, acute myocardial infarction patients already have cardiac ischemic injury when they are admitted to the hospital, and it is impossible to administer therapeutic drugs before an unexpected acute myocardial infarction occurs. Therefore, practical treatment of acute myocardial infarction would include administration after acute coronary artery occlusion or during reperfusion. The administration of EGCG during reperfusion has been reported to reduce cardiac reperfusion injury [13]; however, there have not yet been any studies on the extent that EGCG reduces myocardial necrosis, an indicator of reperfusion injury.
In this study, EGCG was administered to isolated rat hearts during coronary artery reperfusion, and the effects of EGCG on myocardial necrosis and cardiac hemodynamics were analyzed.
Materials and Methods
Isolated heart perfusion using the Langendorff system
The proposed study was approved by the ethics committee of our institution. Coronary perfusion by the Langendorff system with modified Krebs-Henseleit (KH) buffer solution, containing 118.5 NaCl, 4.7 KCl, 1.2 MgSO4, 1.8 CaCl2, 24.8 NaHCO3, 1.2 KH2PO4, and 10 glucose (in mM), was performed. KH buffer was freshly prepared and filtered through a 2.0 µm microfilter (Nalge Nunc International Corp., Rochester, NY, USA). The KH buffer was added to the Langendorff apparatus, and 30 min before the experiment, the buffer was bubbled with 95% O2 and 5% CO2, so that pH would be about 7.4. The Langendorff system was maintained at 38℃ by a water circulation pump.
Male Wistar rats (Korea Taconic Co., Daegu, Korea) weighing 280-330 g were anesthetized by an intraperitoneal injection of 100 mg/kg pentobarbital sodium (Entobar®, Hanlim Pharceuticals, Yongin, Korea), and 300 IU heparin was also administered. After each rat was anesthetized and no longer responsive to noxious stimulus to the tail, a median thoracotomy was performed. Within 1 min of heart removal, the heart was immediately connected to the Langendorff system via the aorta, and perfused with modified KH buffer solution, allowing for coronary flow. The perfusion pressure was set at 100 cmH2O above the heart.
Drainage of coronary perfusate from the right side of the heart was collected in a graduated cylinder to measure coronary perfusion. To measure ventricular function, a balloon was inserted into the left ventricle (LV) through the left atrium. The balloon was coupled to a graded threaded micro-syringe and balloon volume was adjusted to give a left ventricular end-diastolic pressure (LVEDP) of 5-10 mmHg at the beginning of the experiment. The left ventricular developed pressure (LVDP) was calculated from the difference between the left ventricular systolic pressure (LVSP) and LVEDP. The rate-pressure product (RPP) was calculated by multiplying the heart rate by the LVDP. Hemodynamic parameters, including +dP/dtmax and -dP/dtmin, were determined using an MP150 pressure transducer (BioPac Systems, Santa Barbara, CA, USA).
Inducing regional ischemia
Ischemia was induced after the heart had been connected to the Langendorff system and a minimum of 30 min of stabilization had elapsed. To induce regional ischemia, a 6-0 polypropylene suture was looped around the proximal segment of the left coronary artery, and both ends of the suture were threaded through a 1 cm PE50 tube to form a snare loop. Ischemia was triggered by pulling the thread of the snare and blocking coronary artery flow. Reperfusion was induced by relaxing the snare. After reperfusion, if ventricular fibrillation (VF) occurred, there was usually spontaneous reversion to normal sinus rhythm within 30 sec. If the duration of VF was longer than 30 sec, the heart was treated with finger flick cardioversion until a perfusing rhythm was obtained.
Test substances
Green tea extracts were made using dried commercial green tea leaves (Boseung green tea Myeongga, Gwangju, Korea). Ten milliliters of water containing 0.2 g green tea were heated to 60℃ and stirred for 5 min. The leaves were then removed by filtering, and the solution was freeze-dried to obtain the green tea extract (GT) used in the experiment. GT and EGCG (Sigma-Aldrich Chemical Co., St. Louis, MO, USA) were each dissolved in distilled water to make less than 2.5 mM stock solutions. The test stock solutions were stored at 4℃ and diluted on the day of the experiment with KH buffer to the final concentrations.
Test protocols
The duration of all episodes of regional ischemia induced in isolated hearts was 30 min and reperfusion was performed for 2 h. There were 2 experiments, and hearts were randomly assigned to 3 groups for each experiment. For each experiment, either GT or EGCG were administered 5 min before coronary reperfusion to 30 min after reperfusion for a total of 35 min.
The first experiment was to determine the effects of green tea itself, which is not a pure epicatechin. GT at 0.5 µM (GT-0.5, n = 7) and 1 µM (GT-1, n = 8) was administered to isolated rat hearts. After the hearts had undergone 2 h of reperfusion, the myocardial infarction was compared to the control group where GT was not administered (GT-0, n = 8).
The second experiment was to determine the effects of EGCG, the main component of green tea. EGCG at 1 µM (EGCG-1, n = 8) and 10 µM (EGCG-10, n = 8) was administered as described, and the myocardial infarction was then compared to the control group where EGCG was not administered (EGCG-0, n = 9). There were no differences in the body weight and heart weight among the groups (Table 1).
Measurement of area at risk and area of necrosis
Measurements of the areas at risk (AR) and areas of necrosis (AN) were performed in the same manner as in our previous study [14]. After 2 h of reperfusion, the snare around the left coronary artery was reoccluded, and 3 mL of diluted fluorescent polymer microspheres (Duke Scientific Corp., Palo Alto, CA, USA) were slowly infused into the aorta. The hearts were then removed from the Langendorff system, drained, and weighed. They were then frozen for 1-3 h at -20℃. An acrylic rodent heart matrix (Zivic Instruments, Pittsburgh, PA, USA) was used to make 2 mm transverse sections. The sections were soaked for 20 min at 37℃ in 1% 2,3,5-triphenyltetrazolium chloride (TTC). Colored viable tissue by TTC was distinguished from the noncolored area of myocardial necrosis using 10% formalin. For each LV, AR, and AN, the volume (cm3) was calculated by multiplying the area by the width of each specimen (2 mm). The area of myocardial necrosis was defined as AN/AR. All measurements were performed in a blinded fashion. There were no differences in the volumes of LV, AR, or AR/LV values among the groups (Table 1).
Statistical analysis
The means ± S.E. were determined for the data. One-way ANOVA, as well as least significant difference tests for later verification, were performed. Values of P < 0.05 were considered to be statistically significant. Data analysis was performed using SPSS for Windows, version 12.0.
Results
A total of 51 rat hearts were used in the experiments. Three hearts were excluded from analysis; 1 heart had an LVDP less than 80 mmHg and 2 hearts had continuous arrhythmias during the stabilization period. Therefore the results of 48 rat hearts were compared.
In the GT experiment, the AN/AR value for group GT-0.5 was 26.0 ± 1.2% and for group GT-0 was 27.4 ± 1.1%. There was no significant difference. However, the AN/AR for group GT-1 was 10.3 ± 2.1%, which was significantly lower than either group GT-0 or GT-0.5 (P < 0.001) (Fig. 1).
In the EGCG experiment, 3 hearts from each of the 3 groups developed VF immediately after reperfusion, but immediately reverted to normal sinus rhythm. There were no significant differences in the hemodynamic indicators, LVDP, RPP, +dP/dtmax, and -dP/dtmin during the stabilization period (Table 2). Hemodynamic recoveries in terms of percent changes measured during stabilization and 2 h after reperfusion were determined in the EGCG groups. The percent change of LVDP for group EGCG-0 and group EGCG-1 were 42.8 ± 7.0% and 48.0 ± 3.3%, respectively, and there was no significant difference between the two groups. However the LVDP for group EGCG-10 was 72.0 ± 10.5%, which was significantly higher than the LVDP of either group EGCG-0 or group EGCG-1 (P = 0.01, P = 0.036, respectively) (Fig. 2). The RPP for group EGCG-0 was 38.8 ± 7.9%; for group EGCG-1 was 46.1 ± 3.6%; and for group EGCG-10 was 63.9 ± 9.9%, which was significantly higher than the RPP in group EGCG-0 (P = 0.016).
The +dP/dtmax for group EGCG-0 was 44.1 ± 6.8%; for group EGCG-1 was 49.1 ± 3.8%; and for group EGCG-10 was 73.9 ± 10.4%, which was significantly higher than the +dP/dtmax in groups EGCG-0 and EGCG-1 (P = 0.009, P = 0.029, respectively). The -dP/dtmin for group EGCG-0 was 40.2 ± 4.6%; for group EGCG-1 was 46.7 ± 2.4%; and for group EGCG-10 was 59.4 ± 7.9%, which was significantly higher than the -dP/dtmin for group EGCG-0 (P = 0.019).
For groups EGCG-0, EGCG-1, EGCG-10, the AR/LV values were 58.2 ± 2.9%, 57.8 ± 3.8%, and 58.2 ± 4.5%, respectively. There were no significant differences among the groups in the development of regional ischemia in the LV (Fig. 3). The AN/AR value for group EGCG-0 was 27.2 ± 1.4%; for group EGCG-1 was 20.3 ± 2.9%; and for group EGCG-10 was 13.2 ± 4.0%, which was significantly lower compared to group EGCG-0 (P = 0.002). The AN/LV values for groups EGCG-0, EGCG-1, and EGCG-10 were 15.9 ± 1.2%, 12.0 ± 2.3%, and 8.7 ± 3.1%, respectively. Compared to group EGCG-0, the AN/LV in group EGCG-10 was significsantly lower (P = 0.028).
Discussion
GT of 1 µM administered during reperfusion in isolated rat hearts effectively reduced post-reperfusion myocardial necrosis. Ten µM of EGCG, the most abundant catechin in green tea, effectively reduced post-reperfusion myocardial necrosis, and improved cardiac hemodynamics, namely the recoveries of LVDP, RPP, +dP/dtmax and -dP/dtmin.
Townsend et al. [12] first reported that 100 µM of EGCG administered during ischemia successfully reduced myocardial necrosis and prevented ischemic injury in isolated rat hearts. The effects of EGCG administered during reperfusion were first reported by Aneja et al. [13]. In an in vivo experiment, EGCG administered during reperfusion caused a decrease in myeloperoxidase activity, which is a marker of neutrophil accumulation, an indicator of inflammatory response. They also reported that EGCG reduced plasma creatine phosphokinase activity. In cardiac tissue stained with hematoxylin and eosin, heart tissue trauma and necrosis were decreased in rats receiving EGCG. In the presented study, in which TTC stain was used to measure the degree of myocardial necrosis, 10 µM EGCG administered during reperfusion caused significant decreases in AN/AR and AN/LV values compared to other groups.
Although 1 µM of green tea extract was shown to effectively decrease myocardial necrosis, 1 µM EGCG had no effect in reducing myocardial necrosis in this study. However, 10 µM EGCG was effective. Although the exact reason for this result is not known, there are other catechins besides EGCG in green tea, such as EGC, ECG, and EC, which may also have cardioprotective effects. The discovery that EGCG has inotropric effects on isolated rat hearts supports this possibility. It has been reported that when green tea leaves are heated, the epimerization of EGCG produces (-)-gallocathechin-3-gallate (GCG), which like EGCG, protects the heart after reperfusion [16]. This may be why 1 µM green tea reduced myocardial necrosis, even though in the present study, 1 µM EGCG had no effect. Further research is required to resolve this issue.
Aneja et al. [13] has reported that when they administered EGCG during reperfusion, the RPP measured after reperfusion was not different between the groups where EGCG had been administered and where it had not been. In the present study, however, the RPP in the group in which 10 µM EGCG was administered, was significantly higher after 2 h of reperfusion compared to the group in which EGCG had not been administered. One reason for difference in results may be due to differences in methods of calculation. Aneja et al. [13] calculated the RPP using the product of the mean arterial pulse pressure and the heart rate; whereas the authors of this study used the product of LVDP and the heart rate. After reperfusion, compared to the other groups, in the group administered 10 µM EGCG, the LVSP was restored, and LVEDP decreased. This increased LVDP recovery, which triggered RPP recovery. Other reasons why the RPP results of the present study may differ from the RPP results of Aneja et al. [13] may be the different testing methods, different amounts of administered EGCG, and different administration times. However, the LVDP and RPP enhancements in the present study are similar to the results of Townsend et al. [12], where, during ischemia, they administered EGCG and stimulated LVDP recovery after reperfusion. EGCG administration, whether during ischemia or reperfusion, consequently enhances cardiac hemodynamics. However, in assessing the damage caused by cardiac ischemia and reperfusion, the cardiac hemodynamic indicies that reflect mechanical function may not be the suitable [17]. In evaluating reperfusion injury, measuring the degree of cardiac necrosis may be a more reliable indicator.
Most biological studies assessing EGCG used concentrations ranging from 10 µM to 100 µM. The present study observed the reduction of cardiac necrosis with administration of 10 µM. However, a human blood concentration of 10 µM EGCG can only be achieved if the subjects under fasting were to ingest 50-60 cups of green tea. In addition, even by ingesting 800 mg capsules of pure EGCG, it would be difficult to achieve a concentration greater than 5 µM [6]. Therefore, 10 µM EGCG, which proved to be effective in reducing cardiac necrosis, is impossible to achieve for human beings by just drinking green tea. Although not yet clinically feasible, therapeutic levels may be possible by intravenous administration.
Recently, there have been studies reporting that green tea has reduced the incidence of coronary artery disease and related deaths in human beings. Nakachi et al. [18] reported that drinking more than 10 cups of green tea reduced the likelihood of cardiovascular disease-related death. Sano et al. [19] reported that when patients undergoing coronary angiography were separated into groups with and without coronary occlusion, the group without coronary occlusion drank significantly much more green tea, about 6 glasses a day. Kuriyama [20] also showed in an epidemiological survey that drinking green tea reduced the risk of cardiovascular diseases. A long-term cohort study [21] on 40,000 subjects reported that green tea reduced death rates, especially deaths due to cardiovascular diseases. However, there are still no objective data on the exact amount of green tea needed to reduce the risk of cardiovascular diseases. However, it is unclear whether the effects of green tea may differ in relation to other factors such as race, culture, region, diabetes, hypertension, and hyperlipidemia. More research is required.
The studies on whether EGCG reduces the rates of ischemia- and reperfusion-related damage in animals and human beings so far have not yet been able to explain the mechanisms behind reduction. Townsend et al. [12] suggested that the cardioprotective effect of EGCG is due to the reduction of phosphorylation and activation of pro-apoptotic factors, and the signal transduction and activator of transcription (STAT)-1. Potenza et al. [22] stated that EGCG is cardioprotective, because it triggers the production of nitric oxide and activates phosphatidylinositol-3-OH kinase. Li et al. [15] believes that EGC, a green tea catechin, causes myocardial contraction due to protein kinase C epsilon. Although the activation of G protein-coupled receptors (GPCR) is involved in the mechanism of intracellular messaging in the prevention of reperfusion injury [23], the relationship between EGCG and GPCR activation has yet to be illuminated.
Recent discoveries have illuminated the main mechanisms involved in the cardioprotective effect after reperfusion injury, which include the ERK1/2 or PI3-kinase as the main intracellular control pathway [24,25]. However, Dreger et al. [26] reported in their study using cardiac muscle cells, that the activation of prosurvival signaling kinases and the upregulation of antioxidative enzymes had no effect on the cardioprotective activity of EGCG. Also, it has recently been discovered that during the first few minutes of reperfusion, the inhibition of the opening of the mitochondrial permeability transition pore (MPTP) is the final target of the cardioprotective mechanism of EGCG [27,28]. More detailed research on the intracellular control pathway of cardioprotection by EGCG, including the inhibition of the opening of MPTP is needed.
In conclusion, the results of this study show that EGCG, the primary bioactive substance of green tea, reduced reperfusion-induced cardiac necrosis rates in isolated mouse hearts. In addition, EGCG administered during reperfusion reduced stunning after reperfusion. However, detailed research on the intracellular pathways involved in the prevention of cardiac reperfusion damage by EGCG and on whether green tea is effective in reducing cardiac reperfusion damage in human beings, is needed.
PDF Links
PubReader
XML Download
Full text via DOI
Full text via PMC
Download Citation
Print
