The effects and mechanism of ginsenoside Rg1 on myocardial remodeling in an animal model of chronic thromboembolic pulmonary hypertension
© Li et al.; licensee BioMed Central Ltd. 2013
Received: 15 January 2013
Accepted: 17 May 2013
Published: 5 June 2013
Recent studies haveshown that ginsenoside Rg1, extracted from the dry roots of Panax notoginseng as a traditional Asian medicine, plays an anti-fibrosis role in myocardial remodeling. However, the mechanism still remains unclear. In the present study, we investigate the effect of ginsenoside Rg1on the collagenic remodeling of myocardium in chronic thromboembolic pulmonary hypertension (CTEPH), and its potential mechanism.
A rat model of CTEPH was established by injecting thrombi through the jugular vein wice in2 weeks. Four weeks later, four groups (Group A: normal rats + normal saline; Group B: normal rats + Rg1; Group C: CTEPH model + normal saline; Group D: CTEPH model + Rg1) were established. Normal saline and Rg1 were administrated by intraperitoneal injection. Ineach group, we measured the hemodynamic parameters, as well as the right ventricle to left ventricle (RV/LV) thickness ratio. Myocardial tissue sections of the RV were stained by hematoxylin-eosin +gentian violet and the morphological characteristics were observed by light microscopy. The matrix metalloproteinases (MMP) -2 and −9 were detected by the western blot.
Compared with Group A and Group B, the right ventricular systolic pressure was significantly increased in Group C and significantly decreased in Group D. Compared with Group A and Group B, the RV/LV thickness ratio of the rats was significantly higher in Group C and Group D. There was significant fibrosis with collagen in Group C compared with Group A and Group B, and less significant changes in Group D were observed compared with those in Group C. The expression of MMP-2 and MMP-9 exhibited a significant decrease in Group C and was also significantly decreased in Group D compared withGroup A and Group B. Also, a negative linear relationship was shown between collagen-I and the expression of MMP-2 and MMP-9.
Our animal study showed that ginsenoside Rg1 positively affects myocardial remodeling and pulmonary hemodynamics in CTEPH. Upregulation of the expression of MMP-2 and MMP-9 could explain the beneficial effects of ginsenoside Rg1 in CTEPH.
KeywordsPanax notoginseng saponins Ginsenoside Rg1 Chronicthromboembolic pulmonary hypertension Myocardial remodeling Matrix metalloproteinases
This study aimed to investigate the changes in collagen during right ventricular remodeling and its regulatory mechanism in a rat model of chronic thromboembolic pulmonary hypertension (CTEPH) treated with ginsenoside Rg1 so that we can provide a new approach in the treatment of anti-myocardial remodeling.
Healthy male Sprague Dawley (SD) rats, weighing 250 g to 300 g at the age of 2 months, were provided by the Experimental Animal Center of Chongqing Medical University, China. The animals were allowed to drink and eat freely, caged at 18°C to 20°C and in 65% to 70% relative humidity. All experimental procedures were conducted in accordance with the Guiding Principles for the Care and Use of Animals in Research and Teaching, approved by the Institutional Animal Care and Use Committee of Chongqing Medical University, China.
Reagents and instruments
The experiments used rabbit anti-matrix metalloproteinase (MMP)-2 polyclonal antibodies (Sigma, USA), anti-MMP-9 polyclonal antibodies (Santa Cruz, USA), DAB reagent (Boster Company, China), gentian violet (GV) dye (Department of Histology and Embryology, Chongqing Medical University, China), protein lysate (Beijing Zhongshan Golden Bridge Biological, China), goat anti-rabbit IgG-HRP (Sigma,USA), mouse anti-β-actin monoclonal antibodies (Santa Cruz, USA), ginsenoside Rg1 (Chinese National Institute for the Control of Pharmaceutical and Biological Products, China), an optical imaging system (Olympus, Japan), a medical pathology image processing system (Axioskop40,ZEISS) and a multi-biological signals lead recorder (Chengdu Optical biotechnology company, China).
From a total of 32 SD rats, 16 were used to establish the rat model of CTEPH. The preparationof the CTEPH rat model was modified from that described before . The day before embolization, a sample of 0.2 ml blood was collected from the tail vein and placed in a sterile tube under a 37°C water bath overnight. A thrombus was placed in sterilized petri dishes and divided into 3 mm × 1 mm emboli. Rats were injected intraperitoneally with 10% chloral hydrate (0.3 gkg-1) for anesthesia. The rats were fixed on the operating table and their right external jugular vein was exposed after a neck incision. The rats were injected with a mixture of about 15 thrombotic emboli in 2 ml saline injected at a speed of 0.5 ml.min-1. The rats showed symptoms of cyanosis and shortness of breath after injection. The needle was pulled out after injection and the neck was sutured after hemostasis. The CTEPH rat model was determined by chest radiographs. The experiment was repeated twice in 2 weeks in the same way for a total of 4 weeks. Anti-fibrinolytic tranexamic acid (12.5 mg.kg-1.d-1) was injected into the whole peritoneum. Besides the 32 SD rats, an additional two rats were killed in the pre-experiment to identify the anesthetic dose of chloral hydrate used in our study.
Grouping and administration
Sixteen normal rats (8 in Group A and 8 in Group B) and 16 CTEPH model rats (8 in Group C and 8 in Group D) were given intraperitoneal injections of 0.9% saline (2 ml.d-1) or PNS (100 mg.kg-1.d-1). The groups were: Group A: normal rats + 0.9% saline; Group B: normal rats + Rg1; Group C: CTEPH model rats + 0.9% saline; Group D: CTEPH model rats + Rg1. The injections were givenonce daily for a total of 4 weeks.
Detection of hemodynamics in rats
The rats were injected intraperitoneally with 10% chloral hydrate with a concentration of 0.3 g.kg-1 and were fixed in a supine position. After4 weeks of intraperitoneal injections, the right external jugular vein was isolated and exposed after a center-right incision through the neck. A PE-50 PVC catheter was inserted into the right external jugular vein slowly at 1 cm to 2 cm from the superior vena cava, 2 cm to 3 cm from the right atrium, and 4 cm from the right ventricle. The biological signal acquisition system was connected to record the right ventricular systolic pressure according to the catheter position judged bychanges of the pressure curve waveform.
Determination of ventricularfree-wall thickness
Animals were sacrificed by an overdose of chloral hydrate after the determination of the right ventricular pressure. The heart was removed with saline rinse. The right ventricular (RV) and left ventricular (LV) free wall were cut from the heart. Through a cross section along the mitral valve leaflets, the RV and LVfree-wall thicknesses were measured by microscope and the RV/LV free-wall thickness ratio was calculated as an indicator for right ventricular hypertrophy.
Hematoxylin-eosinexamination of myocardial tissue
From the tip of the right ventricle, 1 cm × 0.3 cm of free myocardial tissue was taken and immersed in a 10% methanol fixture, then embedded in a paraffin section. Butterfly shaped sections of 5-mm thickness were cut and placed on glass microscope slides stained with hematoxylin and eosin (HE) for histological analysisusing the pathological image processing system.
Gentian violetstainingof myocardial tissue
To determinethe collagen deposition in myocardial tissues, GV staining was used in the study. Myocardial tissues were first dehydrated through a graded ethanol series, dewaxed using xylene, immediately dehydrated with 95% alcohol and 100% alcohol, GV dyed for 3 min to 5 min and were mountedusing a neutral xylene resin. Images wereacquired by an optical microscope (magnification 400×) and five random fields in each section were analyzed. GV staining was determinedusing the Image Pro PLUS software.
From the tip of the RV, a sample of 1 cm × 0.3 cm of free myocardial tissue was taken and cut into pieces. A protein lysis buffer was added and the samples were quantified using Coomassie brilliant blue. Then 20-μg protein samples were added to the sample buffer for sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), the polyvinylidene fluoride (PVDF) membranes were transferred and samples were incubated with anti-MMP-2 antibodies (1:300) and anti-MMP-9 antibodies (1:500) at 4°C overnight. The membranes were incubated with anti-rabbit HRP-IgG antibodies (1:2,000) at room temperature for 1 h and were colored by diaminobenzidine (DAB) after the membrane had been washed repeatedly. Fluorescence band integrated optical density values were collected and the intensity of the bandswas readusing the relative integral optical density. Western blot images were analyzed by Bio-Rad’s Quantitive One software and corrected using mouse anti-β-actin monoclonal antibodies.
Measurement dataare presented as mean ± standard error of the mean. Differences between groups were analyzed by one-way ANOVA. A level of P < 0.05 was considered statistically significant. Statistical analysis was done using the SPSSl0.0 statistical software.
Effect of ginsenoside Rg1 on hemodynamics and RV/LV ratio in rats
Histopathological examinationusing hematoxylin and eosin and gentian violet staining
Effect of ginsenoside Rg1 on the expression of MMP-2 and MMP-9 in myocardial tissue
Correlationbetween the expression of MMP-2 or MMP-9 and collagen-I
A myocardial collagen networkmainly composed of collagen-I/III, relies on the connection between myocardial structure and a direct correlation to the heart’s global systolic and diastolic function, and this was first proposed by Borg in 1981. Studies have found that the deposition of collagenI/III and the imbalance of collagenI/III are the main components of myocardial collagen network remodeling [3, 16]. The mechanism for impaired heart function due to interstitial fibrosis reconstruction is that myocardial collagen remodeling leads to collagen deposition, an increase in wall stiffness (decreased compliance), ventricular filling limitation, stroke volume reduction, severe interstitial fibrosis, restriction in the natural movement of myocardial cells, myocardial capillary bed reduction, residual myocardial ischemia and, ultimately, systolic and diastolic dysfunction . Therefore, promoting the degradation of collagen plays an important role in the reduction of ventricular remodeling.
The major finding of the present study is that right ventricular hypertrophy, disorganized myocardial cells, myocardial cell hypertrophy, inflammatory cell infiltration, a significant increase in interstitial pink collagen and significant fibrosis in the rat heart model of CTEPH, were all improved significantly by a daily supplement of ginsenoside Rg1. That is, ginsenoside Rg1 partially reversed right ventricular remodeling in CTEPH rats. The changes in myocardial collagen were very obvious in right ventricular remodeling. Although this observation is similar to those made in a recent study, where daily administration of ginsenoside Rg1 restored morphological change of myocardial fibrosis , this is the first study to show the beneficial effect of ginsenoside Rg1, the use of which is based on a previous study that used an experimental model of hepatic fibrosis . This study also partially reveals the mechanisms that are involved in the protective effect of ginsenoside Rg1 on attenuating myocardial remodeling.
It is believed that myocardial remodeling is to restore the structural architecture and cardiac function, which go in parallel with an increased expression and activity of MMPs . MMPs are typical enzymes involved in myocardial remodeling, of which MMP-2 and MMP-9 play the mostimportant role . MMP-2 and MMP-9 are gelatinases, which can degrade gelatin and normal collagen, causing the normal myocardial interstitium to be replaced by a fibrous myocardial interstitium, enlarging the ventricles and decreasing cardiac function.They haverecently aroused wide attention fortheir possible involvement in myocardial remodeling [19, 20].
MMP-9has an important effect on myocardial remodeling [3, 18]. Clinical studies have also found that MMP-2 activityis closely related to ventricular remodeling and heart dysfunction [21, 22]. This study showed that the expression of MMP-2 and MMP-9 was low butdetectable in normal myocardial tissue, where they have an important role in the maintenance of the normal metabolism of myocardial interstitial homeostasis and the structural integrity of cardiomyocytes and the interstitium.
When the rats suffered from CTEPH and right ventricular hypertrophy, the expression of MMP-2 and MMP-9 in Group C was significantly lower than that in Group A, B and D, and was accompanied by significant myocardial collagen deposition Pearson’s correlation showed that the expression of MMP-2 and MMP-9 had a negative linear correlation with the expression of collagen-I, which is consistent with previous findings . This finding indicated that decreased expression of MMP-2 and MMP-9 could be one of the mechanisms leading to collagen remodeling when rats had CTEPH and right ventricular hypertrophy. After ginsenoside Rg1 intervention, the expression of MMP-2 and MMP-9 in Group D was significantly higher than in Group C. The changein the expression of MMP-2 and MMP-9 suggested that ginsenoside Rg1 deterred right ventricular remodeling in CTEPH, which was possibly achieved by the upregulation of expression of MMP-2 and MMP-9.
In addition, the beneficial effects of ginsenoside Rg1 on myocardial remodeling need to be furtherstudied due to the small sample size. The probable side effects of the compound are unclear in thetreatment of myocardial remodeling and its mechanism still needs to be proved in future studies.
In summary, our results from this study showed that daily supplementation with ginsenoside Rg1 potently attenuated right ventricular hypertrophy and myocardial remodeling in the rat model of CTEPH. Ginsenoside Rg1 also upregulated MMP-2 expression in myocardial tissue. The protective effect of ginsenoside Rg1 on myocardial remodeling may be partly associated with the upregulation of MMP-2 expression. Although our present study was performed in an experimental model, which does not directly predict a response to therapy in humans, it provides a potentially new therapeutic target for patients with CTEPHthrough ginsenoside Rg1 treatment.
Chronic thromboembolic pulmonary hypertension
Hematoxylin and eosin
Panax notoginseng saponins
Sodium dodecyl sulfate polyacrylamide gel electrophoresis.
This work was supported by grants from the National Nature Science Foundation of China (No. 30971303). We thank Hyun Billy Bae, MD, from Richmond University Medical Center, New York Medical College, Staten Island, NY 10310, USA, for reviewing the manuscript.
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