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International Journal of Vascular Medicine
Volume 2013 (2013), Article ID 915983, 8 pages
http://dx.doi.org/10.1155/2013/915983
Research Article

Chronic NaHS Treatment Is Vasoprotective in High-Fat-Fed ApoE−/− Mice

1School of Medical Sciences and Health Innovations Research Institute, RMIT University, Bundoora, VIC 3083, Australia
2Department of Pharmacology, Monash University, Clayton, VIC 3800, Australia

Received 22 March 2013; Accepted 12 June 2013

Academic Editor: Karl A. Illig

Copyright © 2013 Asha Ford et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Hydrogen sulfide is emerging as an important mediator of vascular function that has antioxidant and cytoprotective effects. The aim of this study was to investigate the role of endogenous H2S and the effect of chronic exogenous H2S treatment on vascular function during the progression of atherosclerotic disease. ApoE−/− mice were fed a high-fat diet for 16 weeks and treated with the H2S donor NaHS or the cystathionine-γ-lyase (CSE) inhibitor D,L-propargylglycine (PPG), to inhibit endogenous H2S production for the final 4 weeks. Fat-fed ApoE−/− mice displayed significant aortic atherosclerotic lesions and significantly impaired endothelial function compared to wild-type mice. Importantly, 4 weeks of NaHS treatment significantly reduced vascular dysfunction and inhibited vascular superoxide generation. NaHS treatment significantly reduced the area of aortic atherosclerotic lesions and attenuated systolic blood pressure. Interestingly, inhibiting endogenous, CSE-dependent H2S production with PPG did not exacerbate the deleterious vascular changes seen in the untreated fat-fed ApoE−/− mice. The results indicate NaHS can improve vascular function by reducing vascular superoxide generation and impairing atherosclerotic lesion development. Endogenous H2S production via CSE is insufficient to counter the atherogenic effects seen in this model; however exogenous H2S treatment has a significant vasoprotective effect.

1. Introduction

Hydrogen sulfide is a recently identified gasotransmitter reported to have numerous physiological effects in diverse processes including metabolism, inflammation, the nervous system, and the cardiovascular system [1]. The cardiovascular effects of this molecule are currently of major interest and include vascular relaxation, cardioprotection, and vasculoprotective effects [2, 3].

In mammalian cells, H2S is produced primarily by 2 pyridoxyl-5′-phosphate-dependent enzymes, cystathionine-β-synthase (CBS), and cystathionine-γ-lyase (CSE). Additionally, a role for 3-mercaptopyruvate sulfurtransferase in concert with cysteine aminotransferase has been identified in the vasculature [4]. With respect to vasoregulation, CSE is of particular interest as it is reported to be present in a range of vascular beds and its expression has been clearly identified in vascular smooth muscle cells. CSE has also been located in endothelial cells and additionally it is reported to contribute to endothelium-dependent vasorelaxation [5, 6]. Inhibition of CSE with the irreversible inhibitor D,L-propargylglycine (PPG) leads to an elevation of blood pressure in vivo [7] and increased vascular tone in vitro [8]. Importantly, mice deficient in CSE are hypertensive compared to their wild-type controls [5]. Collectively, these reports point to a role for H2S in the regulation of vascular function.

Atherosclerosis is the most common underlying cause in the development of coronary artery disease, a leading cause of death and morbidity worldwide. Atherosclerosis is a chronic immunoinflammatory, fibroproliferative disease caused by lipid accumulation, affecting large- and medium-sized arteries [9, 10]. Atherosclerosis has a multifactorial pathogenesis, involving vascular inflammation, including increased reactive oxygen species generation which leads to impairment of vascular endothelial function, by reducing NO bioavailability [11].

A number of previous studies have indicated that H2S has many properties that may lead to the inhibition of atherogenesis (for review see [12]). These properties include inhibition of proliferation [13], induction of apoptosis [14] in vascular cells, inhibition of oxidative damage, and decreased production of reactive oxygen species (ROS) [15, 16]. These effects are all cytoprotective, and additionally H2S treatment leads to decreased foam cell production [17], a reduction in adhesion molecule expression [18] decreased chemokine signalling [19] and decreased platelet aggregation [20]. H2S is also reported to have antiinflammatory [21] and anti-remodelling effects [22], in addition to vasorelaxant effects in both large [8, 2325] and small [2628] blood vessels which could also be beneficial in preventing the progression of vascular disease.

This study focuses on the anti-oxidant properties of H2S that suggest that it may be a useful agent in the treatment or prevention of vascular dysfunction in atherosclerosis. Thus, our hypothesis was that H2S will act as a vascular protective factor, due to inhibitory effects on superoxide production and action in the vasculature. The specific aims of this study were to examine the role of both endogenously produced H2S and chronic exogenous H2S treatment in vivo on a lesion development, vascular superoxide generation, and endothelial function in the fat-fed mouse model of atherosclerosis.

2. Materials and Methods

2.1. Animals and Ethics

All experimental procedures involving the use of animals were carried out in accordance with the “Guide for the Care and Use of Laboratory Animals” published by the US National Institutes of Health and the project was approved by the RMIT University Animal Ethics Committee prior to the commencement. All animals were housed in the RMIT Animal Facility, RMIT University, Bundoora West Campus, on a 12-hour day/night cycle at room temperature of . Male mice with a C57BL/6J background ( ) and male C57BL/6J wild-type (WT) mice were purchased from the Animal Resource Centre, Western Australia. From 5 weeks of age mice were fed a high-fat diet containing 22% fat, 0.15% cholesterol (Specialty Feeds, Western Australia) for 16 weeks.

2.2. Treatments

During the final four weeks of fat feeding, mice were assigned to 4 groups: (1) untreated, (2) treated with NaHS to deliver H2S at 10 μmol/kg/day, (low NaHS), (3) NaHS 100 μmol/kg/day (high NaHS), or (4) D,L-propargylglycine (PPG) 30 mg/kg/day. All treatments were administered daily by intraperitoneal injection. Adult male C57 mice ( ), aged 16 weeks and fed on standard rodent chow, were also used as a wild-type (WT) control group.

2.3. Systolic Blood Pressure Measurement

Systolic blood pressure was measured at weeks 12 and 16 (before and after treatment), using the noninvasive tail-cuff apparatus (ADInstruments, Sydney). Systolic blood pressure was averaged from four to six consecutive measurements taken at intervals of 1-2 mins.

2.4. Tissue Collection

Mice were culled in a humane manner via CO2 asphyxiation (95% CO2, 5% O2), followed by cervical dislocation and decapitation. The aorta and liver were dissected out and washed in ice-cold oxygenated Krebs’ solution (composition in mM: NaCl 119, KCl 4.7, MgSO4 1.17, NaHCO3 25, KH2PO4 1.18, CaCl2 2.5, glucose 5.5, EDTA 0.026, and pH 7.4). Aortic arches (for oil red O staining) and abdominal aorta segments (for endothelial function assays) were used immediately. Blood plasma samples were snap frozen in N2 for later use.

2.5. Plasma Lipid Measurements

Total plasma cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), and triglyceride levels were measured with a Konelab 20XTi Random Access Analyser.

2.6. Measurement of Lesion Formation

Development of atherosclerotic lesions across the aortae was assessed using en face staining with Oil Red O. The aortae were dissected free of connective tissue and stained with oil red O then washed in 60% isopropyl alcohol. Longitudinal segments were then photographed with a digital camera. Image J was used for analysis of total tissue to lesion area ratio via manual tracing with measurements based on a calibration image of 1 mm. Lesion area was expressed as a percentage of the total luminal area.

2.7. Endothelial Function Assay

Abdominal aortic rings were mounted in myograph chambers, where they were maintained in Krebs’ solution at 37°C, continuously supplied with carbogen (95% CO2, 5% O2). The aortic rings were allowed to equilibrate for 20 min under zero force, then a 5 mM resting tension was applied. Changes in isotonic tone were recorded using Myograph Interface model 610 M (ADInstruments, Sydney) and the myodac data acquisition system. Concentration response curves to the endothelium-dependent dilator acetylcholine (ACh) were constructed in vessels preconstricted with the thromboxane analogue U46619. Precontraction to U46619 was submaximal and not significantly different between groups. At the end of the ACh curve, 10 μM of the endothelium-independent dilator levcromakalim (LKM) was added to test vascular smooth muscle cell function.

2.8. Measurement of Vascular Superoxide Generation

Superoxide anion production in the aorta was determined by lucigenin-enhanced chemiluminescence assay as previously described [29, 30]. Briefly, sections of abdominal aorta (3 mm long) were preincubated for 45 min at 37°C in Krebs-HEPES buffer (composition (mM): NaCl 99.9, KCl 4.7, KH2PO4 1.0, MgSO4·7H2O 1.2, D-glucose 11.0, NaHCO3 25.0, CaCl2·2H2O 2.5, Na HEPES 20.0, and pH 7.4) containing diethyldithiocarbamic acid (1 mM) to inactivate superoxide dismutase and NADPH (100 μM) as a substrate for NADPH oxidase. 300 μL of Krebs-HEPES buffer, containing lucigenin (5 μM) with and without the flavoprotein inhibitor diphenylene iodonium (DPI, 1 μM) to inhibit NADPH oxidase, was placed into a 96-well OptiPlate, which was loaded into a POLARstar Optima photon counter (BMG Labtech, Melbourne, VIC, Australia) to measure background photon emission at 37°C. After background counting was completed, a single ring of aorta was added to each well and photon emission was recounted. The background reading was subtracted from the superoxide anion counts and normalized with dry tissue weight.

2.9. Data Analysis

Results are expressed as mean ± standard error of the mean (SEM) with the number of experiments denoted by . Concentration response curves to ACh were expressed as a percentage reversal of the U46619 precontraction. These data were computer fitted to a sigmoidal curve using nonlinear regression (GraphPad Prism, version 5.0) to calculate the sensitivity of the vasorelaxation response (pEC50). Statistical analysis was performed using either unpaired -tests or by 1-way analysis of variance (ANOVA) with post hoc tests applied as appropriate and as stated in the text (GraphPad Prism, Version 5, Graphpad Software Incorporated). was considered statistically significant.

2.10. Drugs and Reagents Used

All drugs and reagents were purchased from Sigma-Aldrich (St. Louis, MO, USA). All drugs were dissolved in dH2O, with the exception of LKM, which was dissolved in methanol.

3. Results

3.1. Systolic Blood Pressure Measurements

Systolic blood pressure measurements were recorded from fat-fed mice in each treatment group at weeks 12 and 16 (before and after treatment) and in age-matched WT controls at 16 weeks. Measurements collected before treatment showed no significant difference between groups. Fat-fed mice had significantly higher systolic blood pressure than the age-matched WT controls. Fat-fed mice treated with either 10 or 100 μmol/kg/day NaHS had a significant reduction in systolic pressure compared to untreated mice (Figure 1). PPG treatment had no significant effect on systolic blood pressure.

915983.fig.001
Figure 1: Systolic blood pressure (SBP) measured by the tail-cuff method in WT (open bar) and fat-fed mice (shaded bar). Fat-fed mice had a significantly higher SBP than age matched WT controls. SBP was significantly reduced in fat-fed mice treated with either 10 or 100 μmol/kg/day NaHS. Treatment with PPG 30 mg/kg/day had no effect on SBP. , -test WT versus fat-fed mice, , ANOVA, untreated versus treated, .
3.2. Plasma Lipid Levels

Plasma lipid profiles were collected from fat-fed mice in each treatment group and also from an age matched WT control group. High-fat-fed mice had significantly greater total cholesterol, and LDL levels when compared to WT controls (Table 1). There was no difference in HDL or plasma triglyceride levels across all groups. Treatment with either 10 or 100 μmol/kg/day NaHS had no effect on plasma lipid profile nor did treatment with PPG (30 mg/kg/day).

tab1
Table 1: Effect of chronic treatment with NaHS or PPG on plasma lipid profile.
3.3. Assessment of Atherosclerotic Lesion Area

Atherosclerotic lesion development was assessed using en face oil red O staining. The luminal surfaces of the aortic arches from the high-fat-fed mice in each treatment group were examined for total atherosclerotic lesion area. Mice treated with NaHS (10 μmol/kg/day) showed a significant 8% decrease in lesion area when compared with the untreated high-fat-fed mice. Treatment with PPG had no significant effect on total lesion area (Figure 2).

fig2
Figure 2: Representative sections of aorta from (a) untreated and (b) NaHS (10 μmol/kg/day) treated fat-fed mice. (c) Group data for analysis of total lesion area in fat-fed mice chronically treated with NaHS 10 or 100 μmol/kg/day or PPG 30 mg/kg/day. , ANOVA, untreated versus treated, .
3.4. Assessment of Endothelial Function

Isolated abdominal aorta from high-fat-fed mice displayed marked endothelial dysfunction compared to WT mice as sensitivity and maximum vasorelaxation responses ( ) to the endothelium-dependent dilator ACh were significantly impaired (Table 2, Figure 3). Chronic treatment with either dose of NaHS significantly improved endothelial function compared to untreated fat-fed mice, as both and pEC50 values for these groups were significantly improved and comparable to WT controls. The group treated with PPG had a suppressed and also displayed impairment in sensitivity to ACh which was similar to that in untreated fat-fed . Relaxation responses to the NO donor sodium nitroprusside (SNP 10 μM) were maximal and of equivalent sensitivity in all treatment groups (data not shown).

tab2
Table 2: Effect of chronic treatment with NaHS or PPG on endothelial function.
915983.fig.003
Figure 3: Concentration-response curves to the endothelium-dependent vasodilator acetylcholine (ACh) in aorta from WT (○) and fat-fed mice. mice are untreated (●) or chronically treated with 10 (▲) or 100 (▾) μmol/kg/day NaHS or PPG 30 mg/kg/day (◆). Untreated fat-fed mice had significantly attenuated response to ACh ( and EC50) ( , -test, WT versus fat-fed ). Fat-fed treated with NaHS at either dose had improved relaxation responses ( and EC50) to ACh ( , ANOVA untreated, versus treated), .
3.5. Vascular Superoxide Anion Generation

Aortic rings from WT and mice from each treatment group were collected for determination of vascular superoxide generation. Fat-fed mice had significantly greater vascular superoxide production than age-matched controls. There was a significant inhibition of superoxide production in the 10 and 100 μmol/kg/day NaHS-treated groups (Figure 4). PPG treatment had no significant effect on vascular superoxide generation.

915983.fig.004
Figure 4: Superoxide generation in aorta from WT control (open bar) and fat-fed mice (shaded bar) treated with either NaHS (10 or 100 μmol/kg/day) or PPG (30 mg/kg/day). Vascular superoxide generation was significantly increased in fat-fed mice ( , -test, WT versus , ). Vascular superoxide production was significantly impaired in the groups treated with either 10 or 100 μmol/kg/day NaHS. ( , ANOVA, versus untreated group, ). PPG treatment had no effect. The flavoprotein inhibitor DPI, used to inhibit NADPH oxidase, virtually abolished the vascular superoxide signal (black bars).

4. Discussion

The primary finding of this study is that chronic NaHS treatment in vivo has a vasoprotective effect in mice under conditions of high-fat diet and genetic dyslipidaemia. This is the first study to show that chronic exogenous NaHS treatment in vivo can cause a reduction in vascular superoxide anion generation, which has the effect of protecting the endothelium from damage thereby preserving endothelial function. In addition, these data show the benefits of NaHS treatment also extend to inhibiting the development of vascular lesions and reducing systolic blood pressure.

Hydrogen sulfide has emerged as an important cardiovascular mediator that has been shown to modulate vascular tone and blood pressure. Deficiency of endogenous H2S is reported to play a role in the development of hypertension in spontaneously hypertensive rats [7] and CSE-deficient mice are reported to be hypertensive [5]. The reduction in systolic blood pressure seen in the present study is modest, but significant, and likely results from the vasorelaxant effects of NaHS. These have been attributed primarily to actions at KATP channels [31], but other K+ channel subtypes [8, 23, 26, 32], Ca2+ channels [33] and other mechanisms involving PDE and [34] PKG [35] are also implicated.

A most important finding from this study is that chronic NaHS treatment elicits protection of endothelial function. Endothelium dependent vasorelaxation is significantly impaired in mice fed a high-fat diet, with both sensitivity and maximal relaxation significantly attenuated. Indeed, endothelial dysfunction is a feature of early blood vessel disease and occurs before the development of atherosclerotic lesions. Chronic treatment with NaHS restores endothelial function to the same level as in the wild-type mice. This probably indicates a protection of NO bioavailability since acetylcholine initiated endothelium-dependent vasorelaxation is primarily mediated by NO in mouse aorta [36] and interestingly, the protective effects of NaHS on endothelial function occur at the same dose as the inhibition of vascular superoxide production, suggesting a link between these two events, and consistent with the fact that increased superoxide is known to inhibit NO bioavailability.

A key aspect of the biology of H2S is its anti-oxidant effects. H2S is a potent one-electron chemical reductant and nucleophile that is theoretically capable of scavenging free radicals by single electron or hydrogen atom transfer [37]. Thus, H2S may participate in many reactions [38] and is reported to readily scavenge reactive oxygen and nitrogen species such as peroxynitrite [39], superoxide [40], hydrogen peroxide [41], hypochlorous acid [42] and lipid hydroperoxides [37]. Additionally it has been demonstrated that H2S can inhibit the activity and expression of NADPH-oxidase [16], the major vascular source of superoxide.

It is well known that reactive oxygen species contribute to the pathogenesis of cardiovascular diseases [43]. The parent reactive oxygen species is the free radical superoxide produced by several oxidases including NADPH oxidase, xanthine oxidase, cyclooxygenase and endothelial nitric oxide synthase (eNOS) in its uncoupled state [44]. Overproduction of reactive oxygen species, in particular superoxide from NADPH oxidase, is implicated as a key mediator of endothelial dysfunction and loss of NO bioavailability is associated with many cardiovascular diseases, including diabetic vascular disease, hypertension and atherosclerosis [45]. That oxidative stress apparent in atherosclerosis was affirmed in this study as the fat-fed ApoE−/− mice had significantly greater vascular superoxide generating capacity than the wild-type controls. The lucigenin-based assay employed here showed that the presence of the flavoprotein inhibitor DPI, used to inhibit NADPH oxidase, almost abolished the vascular superoxide production, strongly suggesting that the source of superoxide was an NADPH oxidase. Previous work has shown that NaHS inhibits activity and expression of NADPH-oxidase [16, 46] in cultured vascular smooth muscle cells however the present study extends this finding suggesting an in vivo effect of NADPH oxidase inhibition by chronic NaHS treatment and offers a likely molecular mechanism for the vasculoprotective effect of chronic NaHS treatment in this study.

NaHS treatment had no effect on the plasma lipid profile of these mice. This is not surprising as the fat feeding regime used provides a gross excess of dietary cholesterol. In this model of atherosclerosis, advanced lesions covering nearly 40% of the lumen of the aorta were observed in mice fat-fed for 16 weeks. This is in line with previous studies using this model [4749]. These vascular lesions were substantially reduced with NaHS treatment for the final 4 weeks of fat feeding, suggesting that the treatment may not just inhibit the progression of lesion development but may also cause regression of lesions. This effect is possibly related to the inhibition of inflammatory responses involving NF-κB and adhesion molecule expression [18]. Additionally, this effect may be due to suppression of vascular superoxide production, since previous studies in this model show a link between atheroprotection and reduced vascular superoxide with consequent increased NO bioavailability [4850].

D,L-propargylglycine is a widely used inhibitor of CSE, despite quite poor selectivity and cell permeability [51]. The dose of PPG used in this study is the same as that used previously in mice [18] and is maximal as further increases in dose can elicit nephrotoxicity [52]. In the current study CSE activity in the liver, the richest tissue source of the enzyme, was shown to be markedly suppressed in the PPG-treated group (data not shown), suggesting that vascular CSE would also be suppressed, although we did not test this directly. On the basis of using PPG as an inhibitor of CSE, endogenous H2S is reported to be involved in the regulation of basal blood vessel tone [8] and indeed blood pressure [7]. Previous studies examining the progression of atherosclerosis in mice found that CSE activity and endogenous H2S production were inhibited in this model [18], results that concur with other data showing an inverse relationship between plasma H2S levels and cardiovascular disease. Furthermore Wang et al. [18] found that treatment with PPG exacerbated the atherogenesis in their mouse model. The present results are in some contrast to this. PPG did not have any exacerbating effect, suggesting that CSE-derived H2S does not ameliorate the deleterious effects of the combination of the atherogenic diet and genetic dyslipidemia on blood pressure or vascular dysfunction in this model of atherosclerosis. A simple explanation for this is that endogenous H2S would be overwhelmed by the atherogenic insult of the model, which adds a high-fat diet to the genetic dyslipidaemia, a significant enhancement of the atherogenic potency. It is also possible that other non-CSE sources of H2S, are upregulated under conditions of CSE inhibition, to replace CSE-derived H2S these may include H2S derived from cystathionine-beta synthase or 3-mercaptopyruvate transferase and further studies would be required to investigate this possibility.

More work is still required to examine the pharmacokinetics of NaHS and the distribution, sequestration, and metabolism of H2S donated from any of the reported H2S donor compounds. It is noted that the present results are obtained from a single daily ip dose of NaHS for a relatively short period. NaHS rapidly forms H2S when dissolved [53], and it has been shown that intravenously administered NaHS is rapidly removed from the plasma [54]. H2S is rapidly consumed in oxygenated tissues [55], so it was not expected that plasma concentrations of sulfide would be different between groups. Plasma H2S levels were not measured in this study since we reasoned that they were unlikely to be different between groups and there is controversy over the methods available for doing this [55]. Despite this, previous studies indicate that treatment with similar doses of NaHS in mice does indeed increase plasma H2S levels [18]. That aside, in this study the administered NaHS certainly causes an acute effect which then has longer-term consequences. There is evidence that sulfide donors can cause sulfhydration of specific proteins [56], and though speculative, this is a potential mechanism that would be the starting point for further investigation.

In the present study a dose dependence of NaHS effect is not apparent for any of the parameters investigated. The beneficial effects of NaHS in reducing blood pressure, improved endothelial function, decreased lesion area and vascular superoxide production were all observed at a dose of 10 μmol/kg/day and this effect was preserved but not enhanced at 100 μmol/kg/day for the SBP data, endothelial function data, and reduced vascular superoxide production, suggesting that the effects on blood vessel tone, endothelial protection, and vascular superoxide production may be linked. These data also indicate that there is a tight therapeutic window for the effects of a sulfide donor in this condition, an observation that is supported by several previous studies (see [57]). The field of H2S biology is plagued with a lack of tools, in particular selective and specific blockers of H2S-producing enzymes, consistent and stable donors and reliable scavengers. Improvements in these will be most useful for advances in the study of the physiological and pathophysiological effects of H2S.

In conclusion, this is the first study to show in an in vivo model an inhibition of vascular superoxide generation with chronic NaHS treatment. This effectively protects endothelial function from the oxidative stress induced by the atherogenic diet and renders the vessels resistant to the development of atherosclerotic lesions. An additional beneficial effect of chronic NaHS treatment is a reduction in systolic blood pressure, probably due to vasorelaxant effects. In conclusion, these data show that NaHS donors may be a useful prevention and treatment for vessel damage caused by oxidative stress.

Conflicts of Interests

The authors report no conflict of interests.

Acknowledgments

Dr. Hart was the recipient of an Australian NHMRC Peter Doherty Fellowship and an Honorary Research Fellow in the Department of Pharmacology, Monash University, Australia. The authors wish to thank Professor Owen Woodman, Ms. Mirna Boujaoude. Ms. Hooi Ng for assistance with the lucigenin assays, and RDDT for the plasma lipid measurements and they acknowledge the help of the staff in the RMIT animal facility. Grant support for this project was from the NHMRC of Australia, Ramaciotti Foundation, William Buckland Foundation, and the School of Medical Sciences, RMIT University.

References

  1. R. Wang, “Two's company, three's a crowd: can H2S be the third endogenous gaseous transmitter?” FASEB Journal, vol. 16, no. 13, pp. 1792–1798, 2002. View at Publisher · View at Google Scholar · View at Scopus
  2. J. L. Hart, “Role of sulfur-containing gaseous substances in the cardiovascular system,” Frontiers in Bioscience, vol. 3, pp. 736–749, 2011. View at Scopus
  3. E. Streeter, H. H. Ng, and J. L. Hart, “Hydrogen sulfide as a vasculoprotective factor,” Medical Gas Research, vol. 3, no. 1, p. 9, 2013.
  4. N. Shibuya, Y. Mikami, Y. Kimura, N. Nagahara, and H. Kimura, “Vascular endothelium expresses 3-mercaptopyruvate sulfurtransferase and produces hydrogen sulfide,” Journal of Biochemistry, vol. 146, no. 5, pp. 623–626, 2009. View at Publisher · View at Google Scholar · View at Scopus
  5. G. Yang, L. Wu, B. Jiang, et al., “H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine γ-lyase,” Science, vol. 322, no. 5901, pp. 587–590, 2008. View at Publisher · View at Google Scholar · View at Scopus
  6. R. Wang, “Hydrogen sulfide: a new EDRF,” Kidney International, vol. 76, no. 7, pp. 700–704, 2009. View at Publisher · View at Google Scholar · View at Scopus
  7. H. Yan, J. Du, and C. Tang, “The possible role of hydrogen sulfide on the pathogenesis of spontaneous hypertension in rats,” Biochemical and Biophysical Research Communications, vol. 313, no. 1, pp. 22–27, 2004. View at Publisher · View at Google Scholar · View at Scopus
  8. M. R. Al-Magableh and J. L. Hart, “Mechanism of vasorelaxation and role of endogenous hydrogen sulfide production in mouse aorta,” Naunyn-Schmiedebergs Archives of Pharmacology, vol. 383, no. 4, pp. 403–413, 2011. View at Publisher · View at Google Scholar · View at Scopus
  9. J. Fan and T. Watanabe, “Inflammatory reactions in the pathogenesis of atherosclerosis,” Journal of Ptherosclerosis and Thrombosis, vol. 10, no. 2, pp. 63–71, 2003. View at Scopus
  10. C. Weber and H. Noels, “Atherosclerosis: current pathogenesis and therapeutic options,” Nature Medicine, vol. 17, no. 11, pp. 1410–1422, 2011. View at Publisher · View at Google Scholar · View at Scopus
  11. C. P. Judkins, H. Diep, B. R. S. Broughton, et al., “Direct evidence of a role for Nox2 in superoxide production, reduced nitric oxide bioavailability, and early atherosclerotic plaque formation in ApoE/ mice,” American Journal of Physiology, vol. 298, no. 1, pp. H24–H32, 2010. View at Publisher · View at Google Scholar · View at Scopus
  12. E. G. Lynn and R. C. Austin, “Hydrogen sulfide in the pathogenesis of atherosclerosis and its therapeutic potential,” Expert Review of Clinical Pharmacology, vol. 4, no. 1, pp. 97–108, 2011. View at Publisher · View at Google Scholar · View at Scopus
  13. J. Du, Y. Hui, Y. Cheung, et al., “The possible role of hydrogen sulfide as a smooth muscle cell proliferation inhibitor in rat cultured cells,” Heart and Vessels, vol. 19, no. 2, pp. 75–80, 2004. View at Publisher · View at Google Scholar · View at Scopus
  14. G. Yang, L. Wu, and R. Wang, “Pro-apoptotic effect of endogenous H2S on human aorta smooth muscle cells,” FASEB Journal, vol. 20, no. 3, pp. 553–555, 2006. View at Publisher · View at Google Scholar · View at Scopus
  15. H. Laggner, M. K. Muellner, S. Schreier, et al., “Hydrogen sulphide: a novel physiological inhibitor of LDL atherogenic modification by HOCl,” Free Radical Research, vol. 41, no. 7, pp. 741–747, 2007. View at Publisher · View at Google Scholar · View at Scopus
  16. S. Muzaffar, N. Shukla, M. Bond, et al., “Exogenous hydrogen sulfide inhibits superoxide formation, NOX-1 expression and Rac1 activity in human vascular smooth muscle cells,” Journal of Vascular Research, vol. 45, no. 6, pp. 521–528, 2008. View at Publisher · View at Google Scholar · View at Scopus
  17. Z. Z. Zhao, Z. Wang, G. H. Li, et al., “Hydrogen sulfide inhibits macrophage-derived foam cell formation,” Experimental Biology and Medicine, vol. 236, no. 2, pp. 169–176, 2011. View at Publisher · View at Google Scholar · View at Scopus
  18. Y. Wang, X. Zhao, H. Jin, et al., “Role of hydrogen sulfide in the development of atherosclerotic lesions in apolipoprotein E knockout mice,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 29, no. 2, pp. 173–179, 2009. View at Publisher · View at Google Scholar · View at Scopus
  19. H. Zhang, C. Guo, D. Wu, et al., “Hydrogen sulfide inhibits the development of atherosclerosis with suppressing CX3CR1 and CX3CL1 expression,” PLoS One, vol. 7, no. 7, article e41147, 2012.
  20. G. Zagli, R. Patacchini, M. Trevisani, et al., “Hydrogen sulfide inhibits human platelet aggregation,” European Journal of Pharmacology, vol. 559, no. 1, pp. 65–68, 2007. View at Publisher · View at Google Scholar · View at Scopus
  21. N. R. Sodha, R. T. Clements, J. Feng, et al., “Hydrogen sulfide therapy attenuates the inflammatory response in a porcine model of myocardial ischemia/reperfusion injury,” Journal of Thoracic and Cardiovascular Surgery, vol. 138, no. 4, pp. 977–984, 2009. View at Publisher · View at Google Scholar · View at Scopus
  22. X. Zhao, L. K. Zhang, C. Y. Zhang, et al., “Regulatory effect of hydrogen sulfide on vascular collagen content in spontaneously hypertensive rats,” Hypertension Research, vol. 31, no. 8, pp. 1619–1630, 2008. View at Scopus
  23. W. S. Cheang, W. T. Wong, B. Shen, et al., “4-Aminopyridine-sensitive K+ channels contributes to NaHS-induced membrane hyperpolarization and relaxation in the rat coronary artery,” Vascular Pharmacology, vol. 53, no. 3-4, pp. 94–98, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. S. W. Lee, Y. Cheng, P. K. Moore, and J. S. Bian, “Hydrogen sulphide regulates intracellular pH in vascular smooth muscle cells,” Biochemical and Biophysical Research Communications, vol. 418, no. 4, pp. 1142–1147, 2012. View at Publisher · View at Google Scholar · View at Scopus
  25. L. Kiss, E. A. Deitch, and C. Szabo, “Hydrogen sulfide decreases adenosine triphosphate levels in aortic rings and leads to vasorelaxation via metabolic inhibition,” Life Sciences, vol. 83, no. 17-18, pp. 589–594, 2008. View at Publisher · View at Google Scholar · View at Scopus
  26. E. Streeter, J. Hart, and E. Badoer, “An investigation of the mechanisms of hydrogen sulfide-induced vasorelaxation in rat middle cerebral arteries,” Naunyn-Schmiedeberg's Archives of Pharmacology, vol. 385, no. 10, pp. 991–1002, 2012. View at Publisher · View at Google Scholar
  27. W. Zhao and R. Wang, “H2S-induced vasorelaxation and underlying cellular and molecular mechanisms,” American Journal of Physiology, vol. 283, no. 2, pp. H474–H480, 2002. View at Scopus
  28. Y. Cheng, J. F. Ndisang, G. Tang, K. Cao, and R. Wang, “Hydrogen sulfide-induced relaxation of resistance mesenteric artery beds of rats,” American Journal of Physiology, vol. 287, no. 5, pp. H2316–H2323, 2004. View at Publisher · View at Google Scholar · View at Scopus
  29. C. H. Leo, A. Joshi, J. L. Hart, and O. L. Woodman, “Endothelium-dependent nitroxylmediated relaxation is resistant to superoxide anion scavenging and preserved in diabetic rat aorta,” Pharmacological Research, vol. 66, no. 5, pp. 383–391, 2012.
  30. C. H. Leo, J. L. Hart, and O. L. Woodman, “3′,4′-dihydroxyflavonol reduces superoxide and improves nitric oxide function in diabetic rat mesenteric arteries,” PLoS ONE, vol. 6, no. 6, article e20813, 2011. View at Publisher · View at Google Scholar · View at Scopus
  31. W. Zhao, J. Zhang, Y. Lu, and R. Wang, “The vasorelaxant effect of H2S as a novel endogenous gaseous KATP channel opener,” EMBO Journal, vol. 20, no. 21, pp. 6008–6016, 2001. View at Publisher · View at Google Scholar · View at Scopus
  32. O. Jackson-Weaver, J. Osmond, M. A. Riddle, et al., “Hydrogen sulfide dilates rat mesenteric arteries by activating endothelial large-conductance Ca2+-activated K+channels and smooth muscle Ca2+ sparks,” American Journal of Physiology, vol. 304, no. 11, pp. H1446–H1454, 2013. View at Publisher · View at Google Scholar
  33. G. H. Liang, Q. Xi, C. W. Leffler, and J. H. Jaggar, “Hydrogen sulfide activates Ca2+ sparks to induce cerebral arteriole dilatation,” The Journal of Physiology, vol. 590, no. 11, pp. 2709–2720, 2012. View at Publisher · View at Google Scholar
  34. M. Bucci, A. Papapetropoulos, V. Vellecco, et al., “Hydrogen sulfide is an endogenous inhibitor of phosphodiesterase activity,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 30, no. 10, pp. 1998–2004, 2010. View at Publisher · View at Google Scholar · View at Scopus
  35. M. Bucci, A. Papapetropoulos, V. Vellecco, et al., “cGMPDependent protein kinase contributes to hydrogen sulfide-stimulated vasorelaxation,” PLoS One, vol. 7, no. 12, article e53319, 2012.
  36. G. J. Waldron, H. Ding, F. Lovren, P. Kubes, and C. R. Triggle, “Acetylcholine-induced relaxation of peripheral arteries isolated from mice lacking endothelial nitric oxide synthase,” British Journal of Pharmacology, vol. 128, no. 3, pp. 653–658, 1999. View at Publisher · View at Google Scholar · View at Scopus
  37. S. Carballal, M. Trujillo, E. Cuevasanta, et al., “Reactivity of hydrogen sulfide with peroxynitrite and other oxidants of biological interest,” Free Radical Biology and Medicine, vol. 50, no. 1, pp. 196–205, 2011. View at Publisher · View at Google Scholar · View at Scopus
  38. A. Stasko, V. Brezova, M. Zalibera, S. Biskupic, and K. Ondrias, “Electron transfer: a primary step in the reactions of sodium hydrosulphide, an H2S/HS- donor,” Free Radical Research, vol. 43, no. 6, pp. 581–593, 2009. View at Publisher · View at Google Scholar · View at Scopus
  39. M. Whiteman, J. S. Armstrong, S. H. Chu, et al., “The novel neuromodulator hydrogen sulfide: an endogenous peroxynitrite ‘scavenger’?” Journal of Neurochemistry, vol. 90, no. 3, pp. 765–768, 2004. View at Publisher · View at Google Scholar · View at Scopus
  40. S. K. Yan, T. Chang, H. Wang, L. Wu, R. Wang, and Q. H. Meng, “Effects of hydrogen sulfide on homocysteine-induced oxidative stress in vascular smooth muscle cells,” Biochemical and Biophysical Research Communications, vol. 351, no. 2, pp. 485–491, 2006. View at Publisher · View at Google Scholar · View at Scopus
  41. M. Lu, L. F. Hu, G. Hu, and J. S. Bian, “Hydrogen sulfide protects astrocytes against H2O2-induced neural injury via enhancing glutamate uptake,” Free Radical Biology and Medicine, vol. 45, no. 12, pp. 1705–1713, 2008. View at Publisher · View at Google Scholar · View at Scopus
  42. M. Whiteman, N. S. Cheung, Y. Z. Zhu, et al., “Hydrogen sulphide: a novel inhibitor of hypochlorous acid-mediated oxidative damage in the brain?” Biochemical and Biophysical Research Communications, vol. 326, no. 4, pp. 794–798, 2005. View at Publisher · View at Google Scholar · View at Scopus
  43. S. Kobayashi, N. Inoue, H. Azumi, et al., “Expressional changes of the vascular antioxidant system in atherosclerotic coronary arteries,” Journal of Atherosclerosis and Thrombosis, vol. 9, no. 4, pp. 184–190, 2002. View at Scopus
  44. W. G. Land, “Emerging role of innate immunity in organ transplantation—part I: evolution of innate immunity and oxidative allograft injury,” Transplantation Reviews, vol. 26, no. 2, pp. 60–72, 2012. View at Publisher · View at Google Scholar · View at Scopus
  45. R. P. Brandes, N. Weissmann, and K. Schröder, “NADPH oxidases in cardiovascular disease,” Free Radical Biology and Medicine, vol. 49, no. 5, pp. 687–706, 2010. View at Publisher · View at Google Scholar · View at Scopus
  46. S. Muzaffar, J. Y. Jeremy, A. Sparatore, P. Del Soldato, G. D. Angelini, and N. Shukla, “H2S-donating sildenafil (ACS6) inhibits superoxide formation and gp91phox expression in arterial endothelial cells: role of protein kinases A and G,” British Journal of Pharmacology, vol. 155, no. 7, pp. 984–994, 2008. View at Publisher · View at Google Scholar · View at Scopus
  47. K. Fukao, K. Shimada, H. Naito, et al., “Voluntary exercise ameliorates the progression of atherosclerotic lesion formation via anti-inflammatory effects in apolipoprotein E-deficient mice,” Journal of Atherosclerosis and Thrombosis, vol. 17, no. 12, pp. 1226–1236, 2010. View at Scopus
  48. A. Vinh, R. E. Widdop, S. Y. Chai, and T. A. Gaspari, “Angiotensin IV-evoked vasoprotection is conserved in advanced atheroma,” Atherosclerosis, vol. 200, no. 1, pp. 37–44, 2008. View at Publisher · View at Google Scholar · View at Scopus
  49. S. Tesanovic, A. Vinh, T. A. Gaspari, D. Casley, and R. E. Widdop, “Vasoprotective and atheroprotective effects of angiotensin (1–7) in apolipoprotein E-deficient mice,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 30, no. 8, pp. 1606–1613, 2010. View at Publisher · View at Google Scholar · View at Scopus
  50. A. Vinh, R. E. Widdop, G. R. Drummond, and T. A. Gaspari, “Chronic angiotensin IV treatment reverses endothelial dysfunction in ApoE-deficient mice,” Cardiovascular Research, vol. 77, no. 1, pp. 178–187, 2008. View at Publisher · View at Google Scholar · View at Scopus
  51. C. Szabõ, “Hydrogen sulphide and its therapeutic potential,” Nature Reviews Drug Discovery, vol. 6, no. 11, pp. 917–935, 2007. View at Publisher · View at Google Scholar · View at Scopus
  52. R. Konno, M. Ikeda, K. Yamaguchi, Y. Ueda, and A. Niwa, “Nephrotoxicity of D-propargylglycine in mice,” Archives of Toxicology, vol. 74, no. 8, pp. 473–479, 2000. View at Publisher · View at Google Scholar · View at Scopus
  53. E. R. Deleon, G. F. Stoy, and K. R. Olson, “Passive loss of hydrogen sulfide in biological experiments,” Analytical Biochemistry, vol. 421, no. 1, pp. 203–207, 2012. View at Publisher · View at Google Scholar · View at Scopus
  54. L. Li, M. Whiteman, Y. Y. Guan, et al., “Characterization of a novel, water-soluble hydrogen sulfide-releasing molecule (GYY4137): new insights into the biology of hydrogen sulfide,” Circulation, vol. 117, no. 18, pp. 2351–2360, 2008. View at Publisher · View at Google Scholar · View at Scopus
  55. K. R. Olson, “A practical look at the chemistry and biology of hydrogen sulfide,” Antioxid Redox Signal, vol. 17, no. 1, pp. 32–44, 2012.
  56. B. D. Paul and S. H. Snyder, “H2S signalling through protein sulfhydration and beyond,” Nature Reviews Molecular Cell Biology, vol. 13, no. 8, pp. 499–507, 2012.
  57. J. W. Calvert, W. A. Coetzee, and D. J. Lefer, “Novel insights into hydrogen sulfide-mediated cytoprotection,” Antioxidants and Redox Signaling, vol. 12, no. 10, pp. 1203–1217, 2010. View at Publisher · View at Google Scholar · View at Scopus