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Article

Sodium Hydrosulfide Prevents Myocardial Dysfunction through Modulation of Extracellular Matrix Accumulation and Vascular Density

by
Li-Long Pan
1,
Xian-Li Wang
1,
Xi-Ling Wang
1 and
Yi-Zhun Zhu
1,2,*
1
Shanghai Key Laboratory of Bioactive Small Molecules, Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China
2
Institute of Biomedical Sciences, Fudan University, Shanghai 200032, China
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2014, 15(12), 23212-23226; https://doi.org/10.3390/ijms151223212
Submission received: 23 September 2014 / Revised: 16 November 2014 / Accepted: 26 November 2014 / Published: 12 December 2014
(This article belongs to the Section Biochemistry)
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Abstract

:
The aim was to examine the role of exogenous hydrogen sulfide (H2S) on cardiac remodeling in post-myocardial infarction (MI) rats. MI was induced in rats by ligation of coronary artery. After treatment with sodium hydrosulfide (NaHS, an exogenous H2S donor, 56 μM/kg·day) for 42 days, the effects of NaHS on left ventricular morphometric features, echocardiographic parameters, heme oxygenase-1 (HO-1), matrix metalloproteinases-9 (MMP-9), type I and type III collagen, vascular endothelial growth factor (VEGF), CD34, and α-smooth muscle actin (α-SMA) in the border zone of infarct area were analyzed to elucidate the protective mechanisms of exogenous H2S on cardiac function and fibrosis. Forty-two days post MI, NaHS-treatment resulted in a decrease in myocardial fibrotic area in association with decreased levels of type I, type III collagen and MMP-9 and improved cardiac function. Meanwhile, NaHS administration significantly increased cystathionine γ-lyase (CSE), HO-1, α-SMA, and VEGF expression. This effect was accompanied by an increase in vascular density in the border zone of infarcted myocardium. Our results provided the strong evidences that exogenous H2S prevented cardiac remodeling, at least in part, through inhibition of extracellular matrix accumulation and increase in vascular density.

1. Introduction

Peripheral artery disease is an important healthcare problem in the world and is associated with increased risk for coronary artery events, such as myocardial infarction (MI) [1,2]. Adverse cardiac remodeling following MI remains a significant cause of congestive heart failure [3]. Cardiac remodeling is characterized by significant changes in left ventricle size, shape, and function [4]. This myocardial remodeling sets in motion a number of cellular and extracellular matrix events. Particularly, the extracellular matrix turnover in the non-ischemic myocardium is considered to be maladaptive and contributes to the pathophysiology of myocardial remodeling and progression to heart failure [5,6]. In addition, induction and/or activation of matrix metalloproteinases (MMPs) in the surrounding viable myocardium accelerate extracellular matrix turnover and a failure of mature scar formation [7]. Therefore, pharmacological approaches for intervening excessive deposition of extracellular matrix and MMP may be therapeutic strategies for cardiac remodeling.
As a third endogenously produced gaseous signaling molecule, hydrogen sulfide (H2S) has emerged as a potentially important mediator in cardiovascular homeostasis and cardioprotection [8,9,10]. H2S production has been attributed to three key enzymes in the cysteine biosynthesis pathway, cystathionine β-synthase [11] and cystathionine γ-lyase (CSE), and 3-mercaptopyruvate sulfurtransferase [12,13]. Moreover, CSE is the main H2S-generating enzyme that has been identified in cardiovascular system, including heart [14]. H2S has seen considerable interest in modulating many physiological and pathophysiological processes [6,15]. Significant reduction of CSE expression or deprivation of endogenous H2S generation may lead to the development of various cardiovascular diseases [8,16]. Similar to other gaseous signaling molecules, H2S plays several roles in cardiovascular system which include regulation of vessel diameter, protection of endothelium from redox stress, ischemia reperfusion injury and chronic inflammation [17]. The salubrious effects of H2S are attributed to its various biological activities, including anti-oxidative [18], anti-inflammatory [19], proangiogenic [15], and vasodilating [20] capacities. Recently, our group reported that the administration of NaHS inhibited apoptosis of myocardial myocytes via protection of mitochondrial function in a model of heart failure [21]. Furthermore, several groups, including our own, have demonstrated that administration of H2S played a protective role in the process of fibrosis in the injured myocardium and failing heart [6]. Although the physiological and cardioprotective effects of H2S have previously been documented, the effects and molecular mechanisms of H2S on remodeling and neovascularization after myocardial ischemia (MI) have not been fully evaluated.
Therefore, the aim of this study was to demonstrate that long-term sodium hydrosulfide (NaHS, a H2S donor) [6] therapy impeded MI-induced cardiac dysfunction and extracellular matrix turnover in the non-ischemic myocardium. In addition, we showed that exogenous H2S supplementation modulated CSE and HO-1 expression, which contributed to new vessels growth in the border zone of infarct area.

2. Results and Discussion

2.1. NaHS Inhibited Fibrosis in the Border Zone of Infarcted Myocardium

Interstitial fibrosis in the border zone of infarcted myocardium is commonly observed in failing hearts and contributes to functional impairment [22]. The degree of fibrosis and chamber remodeling were assessed on 42 days after post MI. As shown in Figure 1A,B, scarce fibrosis of myocardial wall was observed in the sham group. In contrast, significant area of fibrosis occurred in the vehicle group. In agreement with our previous study showing that NaHS administration could reduce the fibrosis size in heart failure rats [21], the extent of fibrosis significantly reduced in the NaHS treatment group (15.0% ± 3.2%) compared with vehicle group (32.8% ± 1.4%) ( 1C, p < 0.05). These findings suggested that NaHS might attenuate extracellular matrix accumulation in the border zone of infarcted myocardium.
Ijms 15 23212 g001a 1024Ijms 15 23212 g001b 1024
Figure 1. Sodium hydrosulfide (NaHS) inhibited fibrosis in the border zone of infarcted myocardium. (A) Representative Masson’s staining of cardiac fibrosis; (B) High-magnification microphotographs of Masson-stained sections showed the extent of cardiac fibrosis. Scale bar = 25 μM; and (C) Quantitative analysis of fibrosis area (percentage of left ventricular (LV) area) at 42 days post MI. n = 6, # p < 0.01 vs. sham-operated rats; * p < 0.01 vs. vehicle-treated rats.
Figure 1. Sodium hydrosulfide (NaHS) inhibited fibrosis in the border zone of infarcted myocardium. (A) Representative Masson’s staining of cardiac fibrosis; (B) High-magnification microphotographs of Masson-stained sections showed the extent of cardiac fibrosis. Scale bar = 25 μM; and (C) Quantitative analysis of fibrosis area (percentage of left ventricular (LV) area) at 42 days post MI. n = 6, # p < 0.01 vs. sham-operated rats; * p < 0.01 vs. vehicle-treated rats.
Ijms 15 23212 g001aIjms 15 23212 g001b

2.2. NaHS Mitigated Type I and III Collagen as well as Matrix Metalloproteinases-9 (MMP-9) Expression

Excessive extracellular matrix accumulation in the non-ischemic myocardium leads to myocardial fibrosis and ventricular dysfunction [23]. In agreement with previous findings that chronic MI induced myocardial fibrosis in rats 42 days post MI, the levels of collagen types I and III protein in the border zone of infarcted tissues were increased by 35% and 47% compared to sham group, respectively. NaHS treatment was associated with significant decreased collagen type I and type III expression in the border zone of infarcted tissues (14%) at 42 days post MI (Figure 2A,B, p < 0.05). Meanwhile, the effects of NaHS administration on collagen types III expression were also confirmed by immunofluorescence staining through specific antibodies (Figure 2C). Consistent with the protein expression by Western bot analysis, the cross-sectional views showed relative low level of collagen type III (bright, wavy appearance) presents in the border zone of infarcted tissues in those sections of sham rats. However, vehicle-treated MI rats exhibited marked increased collagen type III protein accumulation, which was significantly reduced by rats treated with NaHS. Furthermore, we also measured MMP-9 level, which was associated with an improvement of myocardial remodeling. As shown in Figure 2D, MMP-9 expression in vehicle-treated animals marked increased compared with sham-operated rats, whereas NaHS administration significantly attenuated this increase (p < 0.05).

2.3. NaHS Modulated CSE and Heme Oxygenase-1 Expression in the Border Zone of Infarcted Myocardium

Our previous study has shown that NaHS inhibited fibrotic response in vivo and in vitro via upregulation of heme oxygenase-1 (HO-1) [6]. To investigate the underlying mechanism of H2S on chronic-induced cardiac fibrosis, we examined the effects of NaHS on HO-1 expression in the border zone of infarcted tissues. Consistent with our previous report [6], therapy with NaHS significantly induced HO-1 expression compared with sham-operated rats (p < 0.05), but no significant change in HO-1 expression between sham-operated or vehicle-treated animals was observed (p < 0.05) (Figure 3A). We previously reported that a reduction in H2S plasma and tissue levels was observed in ischemic heart disease [9,21], therefore, the expression of H2S-generating enzyme CSE was also analyzed by western blot analysis. As shown in Figure 3B, a slight increase CSE expression in the border zone of infarcted tissues was observed in vehicle-treated animals compared to the sham-operated rats (p < 0.05). Interestingly, NaHS therapy markedly increased CSE protein expression in the border zone of infarcted tissues compared with sham-operated rats (p < 0.05).
Ijms 15 23212 g002 1024
Figure 2. NaHS mitigated type I and III collagen as well as matrix metalloproteinases-9 (MMP-9) expression. Western blot for (A) type I collagen; (B) type III collagen; and (C) MMP-9 expression. Bar graphs showed quantitative analysis of type I collagen, type III collagen, and MMP-9; GAPDH was used as loading control. Representative photomicrographs showing (D) type III collagen in the border zone of infarcted myocardium detected by fluorescence microscopy (×400 magnification). # p < 0.05 vs. sham-operated group; * p < 0.05 vs. vehicle-treated group; n = 6.
Figure 2. NaHS mitigated type I and III collagen as well as matrix metalloproteinases-9 (MMP-9) expression. Western blot for (A) type I collagen; (B) type III collagen; and (C) MMP-9 expression. Bar graphs showed quantitative analysis of type I collagen, type III collagen, and MMP-9; GAPDH was used as loading control. Representative photomicrographs showing (D) type III collagen in the border zone of infarcted myocardium detected by fluorescence microscopy (×400 magnification). # p < 0.05 vs. sham-operated group; * p < 0.05 vs. vehicle-treated group; n = 6.
Ijms 15 23212 g002
Ijms 15 23212 g003 1024
Figure 3. NaHS modulated cystathionine γ-lyase (CSE) and heme oxygenase-1 (HO-1) expression in the border zone of infarcted myocardium. Western blot for (A) CSE and (B) HO-1 expression. Bar graphs showed quantitative analysis of CSE and HO-1; GAPDH was used as loading control. # p < 0.05 vs. sham-operated rats; n = 6.
Figure 3. NaHS modulated cystathionine γ-lyase (CSE) and heme oxygenase-1 (HO-1) expression in the border zone of infarcted myocardium. Western blot for (A) CSE and (B) HO-1 expression. Bar graphs showed quantitative analysis of CSE and HO-1; GAPDH was used as loading control. # p < 0.05 vs. sham-operated rats; n = 6.
Ijms 15 23212 g003

2.4. NaHS Promoted the Growth of New Vessels in the Border Zone of Infarcted Myocardium

Immunohistochemical staining of CD34 was carried out to assess the capillary density in theborder zone of the infarct area. As shown in Figure 4A capillary density (CD34 cells) in the border zone of infarct area slightly increased compared with sham-operated animals. Interestingly, NaHS treatment significantly increased capillary density compared to vehicle group (Figure 4A). Meanwhile, NaHS administration, but not vehicle treatment, also markedly enhanced arteriolar density in the border zone of infarct area compared with sham-operated rats by immunohistochemical staining using specific artery marker antibody α-smooth muscle actin (α-SMA) (Figure 4B). Because vascular endothelial growth factor (VEGF) is a pivotal angiogenic factor, we next examined VEGF expression in the border zone of infarct area with or without the administration of NaHS using immunohistochemical staining and Western blot. NaHS, but not vehicle treatment, significantly augmented VEGF level in the border zone of infarct area compared with sham-operated rats as measured by Western blot (Figure 4C, p < 0.05). In addition, the similar VEGF expression in the border zone of infarct area among three groups was also identified by immunohistochemical staining (Figure 4D).
Ijms 15 23212 g004 1024
Figure 4. NaHS promoted the growth of new vessels in the border zone of infarcted myocardium. Representative photomicrographs showing capillary density (CD34 staining, black arrow and arrowheads indicated capillaries) (A); arteriolar density (α-SMA staining, black arrow indicated arteries) (B); and vascular endothelial growth factor (VEGF) protein (black arrow indicated VEGF expression) (C) in the border zone of infarcted myocardium detected by immunohistochemical staining. Scale bar = 25 μM; HPF, ×20 high-powered field; LPF, ×10 low-powered field; and (D) Western blot for VEGF expression. Bar graphs showed quantitative analysis of VEGF; GAPDH was used as loading control. # p < 0.05 vs. sham-operated rats; n = 6.
Figure 4. NaHS promoted the growth of new vessels in the border zone of infarcted myocardium. Representative photomicrographs showing capillary density (CD34 staining, black arrow and arrowheads indicated capillaries) (A); arteriolar density (α-SMA staining, black arrow indicated arteries) (B); and vascular endothelial growth factor (VEGF) protein (black arrow indicated VEGF expression) (C) in the border zone of infarcted myocardium detected by immunohistochemical staining. Scale bar = 25 μM; HPF, ×20 high-powered field; LPF, ×10 low-powered field; and (D) Western blot for VEGF expression. Bar graphs showed quantitative analysis of VEGF; GAPDH was used as loading control. # p < 0.05 vs. sham-operated rats; n = 6.
Ijms 15 23212 g004

2.5. NaHS Prevented Cardiac Dysfunction

The echocardiographic data was shown in Figure 5 and Table 1, 42 days post MI coursed chamber dilatation as detected by increased left ventricular internal dimension diastole (LVIDd) and left ventricular internal dimension systole (LVIDs) (p < 0.05) and cardiac dysfunction as assessed by decreased percentage of fractional shortening (FS) and ejection fraction (EF) (p < 0.05). However, NaHS therapy markedly prevented chamber dilatation and attenuated cardiac dysfunction as evidenced by increased percentage of FS and EF (p < 0.05). Heart rates were not significantly different among three groups.
Ijms 15 23212 g005 1024
Figure 5. NaHS prevented cardiac dysfunction. Echocardiography assessment of cardiac function. Representative images of echocardiography. n = 7.
Figure 5. NaHS prevented cardiac dysfunction. Echocardiography assessment of cardiac function. Representative images of echocardiography. n = 7.
Ijms 15 23212 g005
Table
Table 1. Echocardiographic Parameters.
Table 1. Echocardiographic Parameters.
ParametersSham (n = 7)Vehicle (n = 8)NaHS (n = 8)
LVIDd (cm)0.57 ± 0.020.73 ± 0.03 #0.71 ± 0.03
LVIDs (cm)0.3 ± 0.020.51 ± 0.06 #0.41 ± 0.05 *
R-R (s)0.15 ± 0.010.15 ± 0.010.16 ± 0.01
LVEDV (mL)0.42 ± 0.040.88 ± 0.05 #0.81 ± 0.14
LVESV (mL)0.07 ± 0.010.35 ± 0.06 #0.19 ± 0.05 *
EF (%)84.0 ± 0.3063.0 ± 0.20 #78.0 ± 0.30 *
FS (%)47.37 ± 3.4428.55 ± 1.17 #39.45 ± 3.11 *
HR (bpm)393 ± 16415 ± 16396 ± 13
LVIDd, left ventricular internal dimension diastole; LVIDs, left ventricular internal dimension systole; R-R, R-R intervals; LVEDV, left ventricular end-diastolic volume; LVESV, left ventricular end-systolic volume; EF, ejection fraction; FS, fractional shortening; HR, heart rate; # p < 0.05 vs. sham-operated animals; * p < 0.05 vs. vehicle-treated rats.

2.6. Discussion

The results presented in this study demonstrated that supplementation with exogenous H2S attenuated myocardial remodeling and prevented cardiac dysfunction post MI. These structural and functional changes were associated with reduced extracellular matrix accumulation (types I and III collagen, MMP-9 expression) and induced new vessels growth. In addition, modulation of CSE and HO-1 levels by exogenous H2S supplementation might contribute to anti-fibrotic and pro-angiogenic effects in the border zone of infarct area.
Several groups, including our own, have demonstrated that both exogenously H2S and endogenously derived H2S exhibit potent cardioprotective effects in models of acute MI and ischemia-induced heart failure [6,21,24,25]. However, the role and mechanism of H2S in ischemia-induced myocardial remodeling remains elusive. In our previous studies, endogenous H2S level in plasma significantly decreased after acute MI [26]. Exogenous H2S supplementation exerted cardioprotective effects through modulation of intracellular redox balance and reduction of cardiomyocytes loss during acute MI [27]. Recently, various studies have demonstrated that lower circulating H2S levels suffering from cardiac remodeling correlated negatively with the severity of the disease in models of heart failure or in patients [24,28]. However, in concert with previous studies [6,21], a slight increase of CSE expression was observed in the chronic ischemia myocardium in the present study. Meanwhile, we found that exogenous H2S therapy attenuated cardiac dysfunction and remodeling post MI. These findings are consistent with previous studies, which demonstrated H2S therapy attenuated left ventricular remodeling and dysfunction [21,24]. The upregulation of CSE in chronic ischemia myocardium may thus be a compensatory attempt to counterregulate the decreased level of endogenous H2S in chronic ischemia myocardium [10]. Herein, we found that exogenous H2S therapy modulated CSE expression in the border zone of infarct area and finally prevented cardiac remodeling and modulated CSE expression, which indicated that modulation of CSE expression contributed to attenuate cardiac remodeling post MI by inducing angiogenesis and directly inhibiting cardiac fibroblasts activation [6,24]. The mechanisms involved in the post MI myocardial remodeling may include complex pathways other than the CSE/H2S-mediated process. The above effects were suggested to be partly attributable to H2S-mediated compromised systemic changes, which may affect the disease process or outcome.
Excessive deposition of extracellular matrix, predominantly collagen, in peri-infarcted area represents myocardial stiffness leading to relaxation abnormalities and progressive dysfunction culminating in heart failure [29,30]. Therefore, reduction of excessive interstitial fibrosis in border infarcted area exerts a beneficial role in cardiac remodeling post MI [6]. Meanwhile, MMP-9 is involved in extracellular matrix degradation and cardiac remodeling and MMP-9 inhibition improves outcomes [3,31]. Activation post-infarction inflammation may promote cardiac remodeling through several distinct mechanisms, such as enhancing MMP activities, and increasing matrix degradation [32]. Our previous findings have demonstrated that H2S not only exerted anti-inflammatory activity but also inhibited pro-fibrotic response under acute MI in rats [6,21]. To further confirm whether exogenous H2S inhibited myocardial fibrosis in the border zone of infarct area, we examined the effects of exogenous H2S on extracellular matrix (types I and III collagen) deposition and MMP-9 expression, which play critical roles in the process of myocardial remodeling post MI. Intriguingly, our results demonstrated that pharmacologic supplementation of exogenous H2S substantially inhibited types I and III collagen as well as MMP-9 expression in peri-infarct area after MI. It was associated with decreased myocardial fibrosis and prevented cardiac dysfunction. Therefore, inhibition of extracellular matrix accumulation and MMP-9 expression by exogenous H2S might contribute to its anti-fibrotic effect after MI.
H2S is also a pro-angiogenic agent and promotes new vessel formation in the setting of ischemic diseases [33,34,35]. VEGF, a potent angiogenic cytokine, plays a central role in coronary vascular network growth under ischemic conditions [36]. In the present study, exogenous H2S therapy increased VEGF expression post MI. This was associated with increased vascular density in the exogenous H2S-treated hearts, as evidenced by the increase in the expression of CD34 and α-SMA. Various studies have reported that HO-1 induction is an important cardioprotective adaptation that opposes pathological myocardial remodeling through production of its metabolites such as carbon monoxide, bilirubin, and free iron [6,37,38]. HO-1 has also been reported to play a role in mediating VEGF-induced angiogenesis [39,40]. Although HO-1 and H2S signaling have traditionally been considered to operate via distinct pathways, there is evidence of cross-talk between the two pathways. For instance, The HO-1 positively modulates VEGF synthesis and promotes angiogenesis via activation of several intracellular signal pathways [41]. While, the increase in VEGF expression is amplified via a positive feedback loop, where VEGF-induced S-nitrosylation of Keap1 promotes Nrf2-dependent HO-1 induction [26,42]. In agreement with our previous reports [6,19], we found that exogenous H2S therapy dramatically induced HO-1 expression in the border zone of the infarct area. We also found that the upregulation of HO-1 by exogenous H2S partly contributed to ameliorating detrimental remodeling, as evidenced by reducing extracellular matrix accumulation and impeding cardiac dysfunction. Obviously, both biological molecules do not always work independently, but rather can cross-modulate each other’s biological activity in the vasculature. Although, a slight increase in VEGF and HO-1 expression and new vascular formation were observed in vehicle-treated hearts, which might be due to negative feedback caused by the reparative mechanisms of the body. These evidences suggested that exogenous H2S stimulated the angiogenic processes post MI via a positive feedback loop between HO-1 and VEGF axes. This effect was accompanied by an increase in vascular density and reduced myocardial fibrosis in the border zone of infarct area. Collectively, the induction of angiogenesis via VEGF-HO-1 signaling afforded by H2S contributed to prevent the adverse remodeling and improve cardiac function post MI.

3. Methods

3.1. Animal Care

All animals used in this study received humane care and in compliance with the principles of laboratory animal care formulated by Fudan University for Medical Research and Guide for the Care and Use of Laboratory Animals.

3.2. Chemicals and Antibodies

NaHS was purchased from Sigma–Aldrich (St. Louis, MO, USA). Antibodies against GAPDH, VEGF, HO-1, and CSE were from Santa Cruz Biotechnology (Santa Cruz, CA, USA); antibodies against collagen type I and type III, MMP-9 were purchased from Calbiochem (Dermstadt, Germany); antibodies against CD34 and α-SMA were from Abcam (Shanghai, China).

3.3. Generation of Chronic MI and Drug Treatment

Male Sprague-Dawley rats weighing between 200 and 250 g were anesthetized with sodium pentobarbital (50 mg/kg i.p. (intraperitoneal injection)). MI was induced in rats by ligation of left anterior descending artery (LAD) as described previously [6,22]. Rats were either subjected to left coronary artery ligation (n = 30) or sham surgery (n = 10). During ligation of the LAD, rats were randomized to one of two groups; Vehicle group: this group consisted of rats with myocardial ischemia that received saline (n = 15); NaHS group: MI rats infused with NaHS (56 μM/kg·day, n = 15). All treatments were intraperitoneally injected after LAD and were continued thereafter (once per day for seven days per week). The experimental period was 6 weeks. NaHS was employed as an exogenous H2S donor and the dose used in the present study was selected on the basis of our previous publications [6,21].

3.4. Echocardiography

Echocardiographic studies were performed at 42 days after operation. The rat was lightly anesthetized with sodium pentobarbital (50 mg/kg, i.p.), and transthoracic echocardiography was performed using an echocardiographic system (SONOS 7500; Philips Medical System, Best, The Netherlands) equipped with a 12.0-MHz phased-array transducer. Two-dimensional short-axis views of the left ventricle and M-mode tracings were recorded to measure LVIDd, LVIDs, left ventricular end-diastolic volume (LVEDV), left ventricular end-systolic volume (LVESV), EF, and FS.

3.5. Sample Preparation for Histological and Morphometric Analysis

After cardiac function evaluation, hearts were collected and embedded in OCT compound (Tissue Tek; Miles Inc., Elkhart, IN, USA), frozen in liquid nitrogen-cooled and stored at −80 °C. The samples were sectioned to a thickness of 5 µm. Percentage of fibrosis was determined with Masson’s trichrome stained tissue sections using Image J software (National Institutes of Health, Bethesda, MD, USA).

3.6. Immunohistochemistry and Immunofluorescence Analysis

The samples from 42-day treatment (n = 6 in each group) were fixed with 4% buffered formalin, and embedded in paraffin. Fibrosis area and total LV area were expressed as the percentage of the area of fibrosis. To assess neovascularization, cryosections from 42-day samples were incubated with antibodies against VEGF, CD34, and α-SMA, respectively. The slides were washed and incubated with biotinylated, affinity-purified goat anti-mouse IgG as the secondary antibody. After avidin-biotin amplification, the slides were incubated with 3,3'-diaminobenzidine and counterstained with hematoxylin. Sections were examined with a microscope (Nikon ECLIPSE TE200, Tokyo, Japan). Three representative microscopic images of each sections were digitally captured and analyzed for capillary density (CD34-positive structures) and arteriolar density (α-SMA-positive structures) and analyzed using Image J software.
For immunofluorescence staining, the sections were blocked with 5% BSA for 1 h and incubated with the primary antibody against collagen type III. Subsequently, sections were incubated with fluorescein isothiocyanate conjugated anti-rabbit antibody (Invitrogen, Carlsbad, CA, USA), and counterstained for nuclei with DAPI. Immunofluorescence was visualized using a fluorescent microscope (Carl Zeiss Inc., Jena, Germany). The results were based on three independent analyses.

3.7. Western Blot Analysis

The border zone of infarcted tissues (defined as 1 mm of myocardium surrounding the infarct zone) was isolated as described elsewhere [21,22]. Protein concentration was determined with a BCA protein assay kit (Biocolor Biotechnology, Shanghai, China). Western blot analysis was carried out as our previously described elsewhere [6]. Equal amounts (30 μg) of protein were separated on SDS-polyacrylamide gels, transferred to a nitrocellulose membrane (GE Healthcare, Buckingham, UK), and incubated with the appropriate primary antibodies in 5% fat-free milk in Tris-buffered saline with 0.1% Tween, followed by HRP-conjugated anti-mouse or anti-rabbit IgG (1:5000; ICL Lab, Newberg, OR, USA). The immunoreactive bands were visualized by enhanced chemoluminescence with a camera-based imaging system (Alpha Innotech, Santa Clara, CA, USA). The density of the signals was quantified with the AlphaEase software. The primary antibodies were used as follows: CSE (1:500), HO-1(1:1000), VEGF (1:500), Collagen I (1:500), Collagen III (1:500), MMP-9 (1:1000), and GAPDH (1:2000).

3.8. Statistical Analysis

Data were expressed as mean ± standard error of the mean (mean ± SEM). All data analysis was performed with the use of GraphPad Prism 5 software (GraphPad-Prism Software Inc., San Diego, CA, USA). Differences between mean values of multiple groups were analyzed by one-way analysis of variance with Tukey’s test for post hoc comparisons. Statistical significance was considered at p < 0.05.

4. Conclusions

In summary, this study highlights the role of exogenous H2S supplementation in MI-induced myocardial remodeling and cardiac dysfunction, and has shown that exogenous H2S therapy suppresses extracellular matrix accumulation and induces new vessels growth in the border zone of infarct area, at least in part, through modulation of HO-1 and CSE expression. The cardioprotective effect of exogenous H2S suggests that H2S supplementation may be a promising candidate for ventricular remodeling post MI.

Acknowledgments

This work was supported by grants from National Natural Science Foundation of China (Nos: 81202528; 81102435; 81470164; 81330080), and Fundamental Research Funds for Central-Owned Universities (Nos: 20520133185, 20520133219).

Author Contributions

Li-Long Pan and Yi-Zhun Zhu designed the experiments; Li-Long Pan, Xian-Li Wang, and Xi-Ling Wang did the experiments; Li-Long Pan and Xian-Li Wang analyzed the experiment data; and Li-Long Pan and Yi-Zhun Zhu wrote the manuscript.

Abbreviation

CSE
cystathionine γ-lyase
MI
myocardial infarction
MMPs
matrix metalloproteinases
HO-1
heme oxygenase-1
VEGF
vascular endothelial growth factor
NaHS
Sodium hydrosulfide
H2S
Hydrogen sulfide
LVIDd
left ventricular internal dimension diastole
LVIDs
left ventricular internal dimension systole
LVEDV
left ventricular end-diastolic volume
LVESV
left ventricular end-systolic volume
EF
ejection fraction
FS
fractional shortening

Conflicts of Interest

There are no conflict of interest to declare.

References

  1. Inglis, S.C.; Bebchuk, J.; Al-Suhaim, S.A.; Case, J.; Pfeffer, M.A.; Solomon, S.D.; Hou, Y.R.; Pitt, B.; Dargie, H.J.; Ford, I.; et al. Peripheral artery disease and outcomes after myocardial infarction: An individual-patient meta-analysis of 28,771 patients in CAPRICORN, EPEHESUS, OPTIMAAL and VALIANT. Int. J. Cardiol. 2013, 168, 1094–1101. [Google Scholar]
  2. Golomb, B.A.; Dang, T.T.; Criqui, M.H. Peripheral arterial disease: Morbidity and mortality implications. Circulation 2006, 114, 688–699. [Google Scholar] [CrossRef] [PubMed]
  3. Halade, G.V.; Jin, Y.F.; Lindsey, M.L. Matrix metalloproteinase (MMP)-9: A proximal biomarker for cardiac remodeling and a distal biomarker for inflammation. Pharmacol. Ther. 2013, 139, 32–40. [Google Scholar] [CrossRef] [PubMed]
  4. Saparov, A.; Chen, C.W.; Beckman, S.A.; Wang, Y.; Huard, J. The role of antioxidation and immunomodulation in postnatal multipotent stem cell-mediated cardiac repair. Int. J. Mol. Sci. 2013, 14, 16258–16279. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Konstam, M.A.; Kramer, D.G.; Patel, A.R.; Maron, M.S.; Udelson, J.E. Left ventricular remodeling in heart failure: Current concepts in clinical significance and assessment. JACC Cardiovasc. Imaging 2011, 4, 98–108. [Google Scholar] [CrossRef] [PubMed]
  6. Pan, L.L.; Liu, X.H.; Shen, Y.Q.; Wang, N.Z.; Xu, J.; Wu, D.; Xiong, Q.H.; Deng, H.Y.; Huang, G.Y.; Zhu, Y.Z. Inhibition of NADPH oxidase 4-related signaling by sodium hydrosulfide attenuates myocardial fibrotic response. Int. J. Cardiol. 2013, 168, 3770–3778. [Google Scholar] [CrossRef] [PubMed]
  7. Spinale, F.G.; Villarreal, F. Targeting matrix metalloproteinases in heart disease: Lessons from endogenous inhibitors. Biochem. Pharmacol. 2014, 90, 7–15. [Google Scholar] [CrossRef] [PubMed]
  8. Pan, L.L.; Liu, X.H.; Gong, Q.H.; Yang, H.B.; Zhu, Y.Z. Role of cystathionine γ-lyase/hydrogen sulfide pathway in cardiovascular disease: A novel therapeutic strategy? Antioxid. Redox Signal. 2012, 17, 106–118. [Google Scholar] [CrossRef] [PubMed]
  9. Zhu, Y.Z.; Wang, Z.J.; Ho, P.; Loke, Y.Y.; Zhu, Y.C.; Huang, S.H.; Tan, C.S.; Whiteman, M.; Lu, J.; Moore, P.K. Hydrogen sulfide and its possible roles in myocardial ischemia in experimental rats. J. Appl. Physiol. 2007, 102, 261–268. [Google Scholar] [CrossRef] [PubMed]
  10. Wang, Y.; Zhao, X.; Jin, H.; Wei, H.; Li, W.; Bu, D.; Tang, X.; Ren, Y.; Tang, C.; Du, J. Role of hydrogen sulfide in the development of atherosclerotic lesions in apolipoprotein E knockout mice. Arterioscler. Thromb. Vasc. Biol. 2009, 29, 173–179. [Google Scholar] [CrossRef] [PubMed]
  11. Zhao, W.; Zhang, J.; Lu, Y.; Wang, R. The vasorelaxant effect of H2S as a novel endogenous gaseous KATP channel opener. EMBO J. 2001, 20, 6008–6016. [Google Scholar] [CrossRef] [PubMed]
  12. Szabo, C. Hydrogen sulphide and its therapeutic potential. Nat. Rev. Drug Discov. 2007, 6, 917–935. [Google Scholar] [CrossRef] [PubMed]
  13. Hibuya, N.; Koike, S.; Tanaka, M.; Ishigami-Yuasa, M.; Kimura, Y.; Ogasawara, Y.; Fukui, K.; Nagahara, N.; Kimura, H. A novel pathway for the production of hydrogen sulfide from d-cysteine in mammalian cells. Nat. Commun. 2013, 4, 1366–. [Google Scholar] [CrossRef] [PubMed]
  14. Kimura, H. Signaling molecules: Hydrogen sulfide and polysulfide. Antioxid. Redox Signal. 2014. [Google Scholar] [CrossRef]
  15. Polhemus, D.J.; Kondo, K.; Bhushan, S.; Bir, S.C.; Kevil, C.G.; Murohara, T.; Lefer, D.J.; Calvert, J.W. Hydrogen sulfide attenuates cardiac dysfunction after heart failure via induction of angiogenesis. Circ. Heart Fail. 2013, 6, 1077–1086. [Google Scholar] [CrossRef] [PubMed]
  16. Snijder, P.M.; Frenay, A.S.; de Boer, R.A.; Pasch, A.; Hillebrands, J.; Leuvenink, H.G.; van Goor, H. Exogenous administration of thiosulfate, a donor of hydrogen sulfide, attenuates Angiotensin II-induced hypertensive heart disease in rats. Br. J. Pharmacol. 2014. [Google Scholar] [CrossRef]
  17. Polhemus, D.J.; Lefer, D.J. Emergence of hydrogen sulfide as an endogenous gaseous signaling molecule in cardiovascular disease. Circ. Res. 2014, 114, 730–737. [Google Scholar] [CrossRef] [PubMed]
  18. Shen, Y.; Guo, W.; Wang, Z.; Zhang, Y.; Zhong, L.; Zhu, Y. Protective effects of hydrogen sulfide in hypoxic human umbilical vein endothelial cells: A possible mitochondria-dependent pathway. Int. J. Mol. Sci. 2013, 14, 13093–13108. [Google Scholar] [CrossRef] [PubMed]
  19. Pan, L.L.; Liu, X.H.; Gong, Q.H.; Wu, D.; Zhu, Y.Z. Hydrogen sulfide attenuated tumor necrosis factor-α-induced inflammatory signaling and dysfunction in vascular endothelial cells. PLoS One 2011, 6, e19766. [Google Scholar] [CrossRef] [PubMed]
  20. Mustafa, A.K.; Sikka, G.; Gazi, S.K.; Steppan, J.; Jung, S.M.; Bhunia, A.K.; Barodka, V.M.; Gazi, F.K.; Barrow, R.K.; Wang, R.; et al. Hydrogen sulfide as endothelium-derived hyperpolarizing factor sulfhydrates potassium channels. Circ. Res. 2011, 109, 1259–1268. [Google Scholar]
  21. Wang, X.; Wang, Q.; Guo, W.; Zhu, Y.Z. Hydrogen sulfide attenuates cardiac dysfunction in a rat model of heart failure: A mechanism through cardiac mitochondrial protection. Biosci. Rep. 2011, 31, 87–98. [Google Scholar] [CrossRef]
  22. Liu, X.H.; Pan, L.L.; Deng, H.Y.; Xiong, Q.H.; Wu, D.; Huang, G.; Gong, Q.H.; Zhu, Y.Z. Leonurine (SCM-198) attenuates myocardial fibrotic response via inhibition of NADPH oxidase 4. Free Radic. Biol. Med. 2013, 54, 93–104. [Google Scholar] [CrossRef] [PubMed]
  23. Dobaczewski, M.; Gonzalez-Quesada, C.; Frangogiannis, N.G. The extracellular matrix as a modulator of the inflammatory and reparative response following myocardial infarction. J. Mol. Cell. Cardiol. 2010, 48, 504–511. [Google Scholar] [CrossRef] [PubMed]
  24. Kondo, K.; Bhushan, S.; King, A.L.; Prabhu, S.D.; Hamid, T.; Koenig, S.; Murohara, T.; Predmore, B.L.; Gojon, G., Sr.; Gojon, G., Jr.; et al. H2S protects against pressure overload-induced heart failure via upregulation of endothelial nitric oxide synthase. Circulation 2013, 127, 1116–1127. [Google Scholar]
  25. Wang, Q.; Liu, H.R.; Mu, Q.; Rose, P.; Zhu, Y.Z. S-propargyl-cysteine protects both adult rat hearts and neonatal cardiomyocytes from ischemia/hypoxia injury: The contribution of the hydrogen sulfide-mediated pathway. J. Cardiovasc. Pharmacol. 2009, 54, 139–146. [Google Scholar] [CrossRef] [PubMed]
  26. Shen, Y.; Shen, Z.; Miao, L.; Xin, X.; Lin, S.; Zhu, Y.; Guo, W.; Zhu, Y.Z. miRNA-30 family inhibition protects against cardiac ischemic injury by regulating cystathionine-γ-lyase expression. Antioxid. Redox Signal. 2014. [Google Scholar] [CrossRef]
  27. Calvert, J.W.; Jha, S.; Gundewar, S.; Elrod, J.W.; Ramachandran, A.; Pattillo, C.B.; Kevil, C.G.; Lefer, D.J. Hydrogen sulfide mediates cardioprotection through Nrf2 signaling. Circ. Res. 2009, 105, 365–374. [Google Scholar] [CrossRef] [PubMed]
  28. Kovacic, D.; Glavnik, N.; Marinsek, M.; Zagozen, P.; Rovan, K.; Goslar, T.; Mars, T.; Podbregar, M. Total plasma sulfide in congestive heart failure. J. Card. Fail. 2012, 18, 541–548. [Google Scholar] [CrossRef] [PubMed]
  29. Burchfield, J.S.; Xie, M.; Hill, J.A. Pathological ventricular remodeling Mechanisms: Part 1 of 2. Circulation 2013, 128, 388–400. [Google Scholar] [CrossRef] [PubMed]
  30. Heusch, G.; Libby, P.; Gersh, B.; Yellon, D.; Bohm, M.; Lopaschuk, G.; Opie, L. Cardiovascular remodelling in coronary artery disease and heart failure. Lancet 2014, 383, 1933–1943. [Google Scholar] [CrossRef] [PubMed]
  31. Ramirez, T.A.; Iyer, R.P.; Ghasemi, O.; Lopez, E.F.; Levin, D.B.; Zhang, J.; Zamilpa, R.; Chou, Y.M.; Jin, Y.F.; Lindsey, M.L. Aliskiren and valsartan mediate left ventricular remodeling post-myocardial infarction in mice through MMP-9 effects. J. Mol. Cell. Cardiol. 2014, 72, 326–335. [Google Scholar] [CrossRef] [PubMed]
  32. Shinde, A.V.; Frangogiannis, N.G. Fibroblasts in myocardial infarction: A role in inflammation and repair. J. Mol. Cell. Cardiol. 2014, 70, 74–82. [Google Scholar] [CrossRef] [PubMed]
  33. Cai, W.J.; Wang, M.J.; Moore, P.K.; Jin, H.M.; Yao, T.; Zhu, Y.C. The novel proangiogenic effect of hydrogen sulfide is dependent on Akt phosphorylation. Cardiovasc. Res. 2007, 76, 29–40. [Google Scholar] [CrossRef] [PubMed]
  34. Kan, J.; Guo, W.; Huang, C.; Bao, G.; Zhu, Y.; Zhu, Y.Z. S-propargyl-cysteine, a novel water-soluble modulator of endogenous hydrogen sulfide, promotes angiogenesis through activation of signal transducer and activator of transcription 3. Antioxid. Redox Signal. 2014, 20, 2303–2316. [Google Scholar] [CrossRef] [PubMed]
  35. Bir, S.C.; Kolluru, G.K.; McCarthy, P.; Shen, X.; Pardue, S.; Pattillo, C.B.; Kevil, C.G. Hydrogen sulfide stimulates ischemic vascular remodeling through nitric oxide synthase and nitrite reduction activity regulating hypoxia-inducible factor-1alpha and vascular endothelial growth factor-dependent angiogenesis. J. Am. Heart Assoc. 2012, 1, e004093. [Google Scholar] [CrossRef] [PubMed]
  36. Sato, K.; Wu, T.; Laham, R.J.; Johnson, R.B.; Douglas, P.; Li, J.; Sellke, F.W.; Bunting, S.; Simons, M.; Post, M.J. Efficacy of intracoronary or intravenous VEGF165 in a pig model of chronic myocardial ischemia. J. Am. Coll. Cardiol. 2001, 37, 616–623. [Google Scholar] [CrossRef] [PubMed]
  37. Chen, T.M.; Li, J.; Liu, L.; Fan, L.; Li, X.Y.; Wang, Y.T.; Abraham, N.G.; Cao, J. Effects of heme oxygenase-1 upregulation on blood pressure and cardiac function in an animal model of hypertensive myocardial infarction. Int. J. Mol. Sci. 2013, 14, 2684–2706. [Google Scholar] [CrossRef] [PubMed]
  38. Wang, G.; Hamid, T.; Keith, R.J.; Zhou, G.; Partridge, C.R.; Xiang, X.; Kingery, J.R.; Lewis, R.K.; Li, Q.; Rokosh, D.G.; et al. Cardioprotective and antiapoptotic effects of heme oxygenase-1 in the failing heart. Circulation 2010, 121, 1912–1925. [Google Scholar]
  39. Penumathsa, S.V.; Koneru, S.; Zhan, L.; John, S.; Menon, V.P.; Prasad, K.; Maulik, N. Secoisolariciresinol diglucoside induces neovascularization-mediated cardioprotection against ischemia-reperfusion injury in hypercholesterolemic myocardium. J. Mol. Cell. Cardiol. 2008, 44, 170–179. [Google Scholar] [CrossRef] [PubMed]
  40. Kim, Y.M.; Pae, H.O.; Park, J.E.; Lee, Y.C.; Woo, J.M.; Kim, N.H.; Choi, Y.K.; Lee, B. S.; Kim, S R.; Chung, H.T. Heme oxygenase in the regulation of vascular biology: From molecular mechanisms to therapeutic opportunities. Antioxid. Redox Signal. 2011, 14, 137–167. [Google Scholar]
  41. Kim, J.H.; Lee, K.S.; Lee, D.K.; Kim, J.; Kwak, S.N.; Ha, K.S.; Choe, J.; Won, M.H.; Cho, B.R.; Jeoung, D.; et al. Hypoxia-responsive microRNA-101 promotes angiogenesis via heme oxygenase-1/vascular endothelial growth factor axis by targeting Cullin 3. Antioxid. Redox Signal. 2014, 21, 2469–2482. [Google Scholar]
  42. Kweider, N.; Fragoulis, A.; Rosen, C.; Pecks, U.; Rath, W.; Pufe, T.; Wruck, C.J. Interplay between vascular endothelial growth factor (VEGF) and nuclear factor erythroid 2-related factor-2 (Nrf2): Implications for preeclampsia. J. Biol. Chem. 2011, 286, 42863–42872. [Google Scholar] [CrossRef] [PubMed]

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MDPI and ACS Style

Pan, L.-L.; Wang, X.-L.; Wang, X.-L.; Zhu, Y.-Z. Sodium Hydrosulfide Prevents Myocardial Dysfunction through Modulation of Extracellular Matrix Accumulation and Vascular Density. Int. J. Mol. Sci. 2014, 15, 23212-23226. https://doi.org/10.3390/ijms151223212

AMA Style

Pan L-L, Wang X-L, Wang X-L, Zhu Y-Z. Sodium Hydrosulfide Prevents Myocardial Dysfunction through Modulation of Extracellular Matrix Accumulation and Vascular Density. International Journal of Molecular Sciences. 2014; 15(12):23212-23226. https://doi.org/10.3390/ijms151223212

Chicago/Turabian Style

Pan, Li-Long, Xian-Li Wang, Xi-Ling Wang, and Yi-Zhun Zhu. 2014. "Sodium Hydrosulfide Prevents Myocardial Dysfunction through Modulation of Extracellular Matrix Accumulation and Vascular Density" International Journal of Molecular Sciences 15, no. 12: 23212-23226. https://doi.org/10.3390/ijms151223212

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