Skip to main content

Intimal Hyperplasia in Balloon Dilated Coronary Arteries is Reduced by Local Delivery of the NO Donor, SIN-1 Via a cGMP-Dependent Pathway



To elucidate the mechanism by which local delivery of 3-morpholino-sydnonimine (SIN-1) affects intimal hyperplasia after percutaneous transluminal coronary angioplasty (PTCA).


Porcine coronary arteries were treated with PTCA and immediately afterwards locally treated for 5 minutes, with a selective cytosolic guanylate cyclase inhibitor, 1 H-(1,2,4)oxadiazole(4,3-alpha)quinoxaline-1-one (ODQ) + SIN-1 or only SIN-1 using a drug delivery-balloon. Arteries were angiographically depicted, morphologically evaluated and analyzed after one and eight weeks for actin, myosin and intermediate filaments (IF) and nitric oxide synthase (NOS) contents.


Luminal diameter after PCI in arteries treated with SIN-1 alone and corrected for age-growth was significantly larger as compared to ODQ + SIN-1 or to controls (p < 0.01). IF/actin ratio after one week in SIN-1 treated segments was not different compared to untreated segments, but was significantly reduced compared to ODQ + SIN-1 treated vessels (p < 0.05). Expression of endothelial NADPH diaphorase activity was significantly lower in untreated segments and in SIN-1 treated segments compared to controls and SIN-1 + ODQ treated arteries (p < 0.01). Restenosis index (p < 0.01) and intimal hyperplasia (p < 0.01) were significantly reduced while the residual lumen was increased (p < 0.01) in SIN-1 segments compared to controls and ODQ + SIN-1 treated vessels.


After PTCA local delivery of high concentrations of the NO donor SIN-1 for 5 minutes inhibited injury induced neointimal hyperplasia. This favorable effect was abolished by inhibition of guanylyl cyclase indicating mediation of a cyclic guanosine 3',5'-monophosphate (cGMP)-dependent pathway. The momentary events at the time of injury play crucial role in the ensuring development of intimal hyperplasia.

Peer Review reports


Endothelial injury after PTCA results in denudation or even rupture of the internal elastic lamina, causing damage to smooth muscle cells (SMC) and release of signal substances, which in turn contribute to neointimal formation and often restenosis [1].

Endothelial-derived NO reduces these events and modulates several physiological processes in the vasculature, including vascular tone, SMC migration, leukocyte adhesion, platelet adhesion and aggregation [2]. The biologic response of SMC and endothelial cells to NO differs. NO inhibits SMC proliferation and can increase apoptotic SMC cell death [3]. On the contrary NO in physiological concentrations enhances endothelial proliferation and reduces endothelial cell apoptosis [47]. NO exerts its effects both by a cGMP-dependent and a cGMP-independent pathway [8].

Orally or intravenously administered NO precursors and donors have been shown to moderately affect intimal hyperplasia after arterial injury in animal and human studies [912]. These studies have been hampered by the fast degradation rate of NO in blood, which allows only minimal amounts of NO, if any, to reach the injured area. However, intrapericardial delivery of NO has been shown to inhibit PTCA induced restenosis [13]. The NO donor SIN-1 has recently been shown to reduce intimal hyperplasia after PTCA, and may be advantageous as it releases NO by fast and spontaneous degradation[14].

The aim of the present study was to evaluate the effect of locally delivered NO on intimal hyperplasia after PTCA, and to investigate whether the NO donor SIN-1 affects intimal hyperplasia via a cGMP dependent pathway.


Animal care and handing followed guidelines in the National Institutes of Health (NIH publication No 85-23, revised 1996). The local ethical committee for animal care approved the study. Twenty-nine domestic pigs weighing 21.5 ± 0.6 kg were premedicated with azaperone 2 mg/kg intramuscularly 30 minutes before the procedure. After induction of anesthesia with thiopental 5-25 mg/kg the animals were orally intubated with cuffed endotracheal tubes. A slow infusion of 1.25 μl/mL Fentanyl in Ringer-acetate was started at a rate of 1.5 mL/min and adjusted as needed. Mechanical ventilation was then established with a Siemens-Elema 300 B ventilator with a mixture of nitrous oxide (70%) and oxygen (30%). Hypnosis was complemented with small intermittent doses of 5 mg meprobamat as needed.

An 8 F introducer sheath (Cordis, USA) was inserted into the left carotid artery and 10,000 IU Heparin given. After an angiogram, PTCA was performed in the left anterior descending artery (LAD) and in the left circumflex artery (LCX). The artery was dilated at 8 atm with a 20 × 3.0 or 3.5 mm dilation balloon (Boston Scientific, USA) using balloon: artery ratios 1.3:1. Before each balloon inflation the pig was given intra-cardially 100 μg nitro-glycerine to avoid spasm and to obtain consistent epicardial artery dilation. Inflation time was 30 s, and immediately after deflation a corresponding 3 or 3.5 × 20 mm drug delivery catheter (Dispatch, Boston Scientific, USA) was inserted into the PTCA-treated site and inflated at 8 - 10 atm. Effort was taken to minimize the time from balloon angioplasty to the time of drug treatment (approximately 1 minute), in order to avoid thrombus formation. Infusion with 10-5 M ODQ, a selective inhibitor of NO-sensitive guanylyl cyclase activity (Tocris Cookson, UK.) was performed at a rate of 1 ml/min. for 5 minutes. The Dispatch balloon was flushed with 1 ml saline and continued with infusion of 5 ml 10-4 M SIN-1 for 5 minutes. The selected high dose has been used in earlier studies, and we have recently demonstrated an inhibiting effect on intimal hyperplasia after 10 minutes [1517]. A 0.5-mm over-dilation was performed for 30 seconds in the corresponding, still untreated LAD or LCX, which were thereafter treated only with SIN-1. In five animals arteries used as controls, underwent PTCA and were treated with NaCl 1 ml/min for 10 minutes. Treatment of the arteries was randomized.

During coronary artery occlusion perfusion pressure was increased by a dopamine infusion and small doses of noradrenaline (10 μ g). Xylocain, 10 mg/kg was injected i.v. before releasing the occlusion to prevent the occurrence of malignant arrhythmias during reperfusion.

The catheters were withdrawn after a final angiogram. The left carotid artery was surgically reconstructed, and the skin sutured. Postoperatively, the pigs received 0.15 mg buprenorphine and 5 ml Streptocillin Vet. The pigs were given 250 mg aspirin daily starting at the day of the procedure.

One week after the angioplasty, one group of eleven pigs was sedated and euthanized with an intra-cardiac injection of 40-mmol potassium chloride. The treated segments were harvested immediately, using micro-surgical technique and cut into a proximal, a medial and a distal segment. An untreated segment was also obtained distal to the treated area. The vessel segments were analyzed electrophoretically for the following proteins actin, myosin and intermediate filaments (IF) and histochemically for NADPH diaphorase in order to visualize the presence of NOS.

Eight weeks postoperatively a second group of sixteen pigs was euthanized as described above. Coronary angiograms were performed and the arteries perfusion-fixated at 100 mmHg with 4% formaldehyde before harvesting. The arteries were examined by routine histology and NADPH histochemistry. A perfusion-fixated vessel segment distal to each of the treated areas was harvested as well.

Angiographic examination

Fluoroscopic video recordings and angiographic stills were examined. Using the guide catheter as reference, luminal diameter was calculated before, immediately after treatment, and at 8 weeks. Pigs grow fast in 8 weeks, in order to determine the growth of the artery; the diameter of the proximal reference segment, approximately 1 cm proximal to the treated area, was measured at the time of treatment and after 8 weeks. Artery growth was thus calculated as the difference in diameter of the arterial reference segments.

The absolute diameter of the treated segments at 8 weeks was reduced by age growth, in order to measure the angiographic late loss without the influence of natural growth in this non-stent model.

Electrophoretic examination

To investigate the relative content of actin, myosin and intermediate filament protein (IF) in smooth muscle cells (SMC's), the proteins were separated on one-dimensional SDS polyacrylamide gel electrophoresis (SDS-PAGE). The vascular preparations were homogenized in an SDS-buffer (composition: 25 mM tris (hydroxymethyl) aminomethane HCl (pH 6.8), 2% SDS, 5% mercaptoethanol and 10% glycerol) at a concentration of 50 μl/mg tissue wet weight. The homogenate was then boiled for 2 minutes and centrifuged at 10,000 rpm for 5 minutes. The supernatant was removed and stored at -20°C before electrophoretic analysis. The SDS-PAGE was performed essentially as described by Malmqvist et al. [18] using 8% polyacrylamide gels in a BioRad minigel system. The gels were stained with Coomassie blue, destained and scanned using a GS-300 densitometer (Hoeffer Scientific Instruments, USA). The areas under the myosin heavy chains, actin and intermediate filament bands were evaluated. The ratios of actin/myosin and intermediate filaments/actin were calculated from these areas.

NADPH histochemistry

The vascular segments were fixed overnight in a mixture of 2% formaldehyde and 0.2% picric acid in phosphate buffer (pH 7.2) or in buffered 4% formaldehyde, followed by rinsing in Tyrode's solution containing 10% sucrose. Specimens were frozen on dry ice and cut in a cryostat at a thickness of 10 μm. NADPH diaphorase activity was rendered visible by incubation of the sections for 45 minutes in 0.1 M Tris-HCl (pH 7.2) containing 1 mM NADPH (Sigma, USA), 0.2% Triton X-100 at 37°, followed by washing in Tris-HCl [19].

Each segment was cut into multiple sections, examined under a light microscope and photographed with maximum of light, creating a completely yellow photograph where only NADPH cells stained dark blue. The images obtained were transferred to a CD-ROM in Kodak format and imported into Photoshop 5.5 (Adobe Inc., USA). These photographs were subtracted into a black and white image. Due to the gray scale practically only the NADPH-stained endothelial cells were black. A 45 × 15 mm representative portion of the cross sectional screen-area consisting of endothelium and media was selected. From the histogram menu, the percentage of black pixels in the photo was registered as percentage of the total number of pixels in the selection.

Histo-morphological examination

Each sample was cut further into 4-14 sections, which were stained with haematoxylin-eosin for routine histological evaluation. A similar number of sections was cut and stained with van Gieson elastica and used for morphological measurements. Measurements were performed without knowledge of the treatment of the segments.

The intimal (I), medial (M), and luminal (L) areas as well as the internal elastic lamina (IEL) circumference and the IEL fracture length (F) were measured using computerized digital planimetry with a video microscope (Olympus BX 50 F4, Japan) and customized software (Analysis 3.0, Soft Imaging System, Germany). Vessel size was assessed by measuring the area circumscribed by the outer border of the external elastic lamina (EEL area). Injury index = F/IEL, was calculated as fracture length of the IEL normalized for the size of the artery by the circumference of the IEL. Intimal hyperplasia was also normalized for the total artery wall area: I/(I+M). The restenosis index = ((I/(I+M))/(F/IEL) could then be calculated taking into account the degree of injury. Changes in vessel geometry after injury and repair denoted the residual lumen and were defined as L/(L+I) [20, 21].

Summary of the study design

A total of 29 pigs were treated with local drug delivery in the LAD as well as the LCX with either SIN-1 alone or ODQ + SIN-1, except for the control pigs were only NaCl was used. After 7 days 11 pigs were sacrificed and the treated segments examined by electrophoresis and NADPH histochemistry. 56 days later the rest were sacrificed, 5 control animals and 11 pigs were examined by NADPH, angiography, electrophoresis, histochemistry, and histo-morphology


One-way ANOVA with Bonferroni post hoc test was used to compare multiple means. Mann-Whitney test was used for comparison between two groups. p values < 0.05 were considered significant. Data are presented as mean ± SD.


Two pigs, which were excluded from the study, died peri-procedurally due to ischemic events. The remaining pigs survived the procedure without complications. The pigs weighed at baseline 21.5 ± 0.64; after 7 days 23.1 ± 1.28 and increased to 41.5 ± 2.14 Kg at 56 days. Blood pressure was stable throughout the drug delivery procedure.

Angiographic examination

The diameters of the proximal reference segments, used for calculating age growth, were 3.24 ± 0.40 mm at day 0 and 3.73 ± 0.44 mm at 8 weeks resulting in 0.55 ± 0.31 mm diameter growths (17%). There was no significant difference in growth between treatment groups.

The angiographic results are presented in (Table 1). With or without age correction SIN-1 treated arteries had significantly larger diameter compared to control (p < 0.01). Following ODQ + SIN-1 treatment vascular diameter was not changed significantly compared to control.

Table 1 Angiographic characteristics

Late loss occurring in treated segments after 8 weeks was calculated as the artery diameter after PTCA at day 0 minus the diameter at 8 weeks adjusted for growth.

Electrophoretic examination

Biochemical analysis of the effect of SIN-1 on intermediate filament proteins one week after treatment is presented in (Figure 1). The ratio of IF/actin in SIN-1 treated segments did not differ significantly from the corresponding ratios in untreated segments. PTCA followed by ODQ prior to SIN-1 treatment caused a significant increase in the IF/actin ratio compared to untreated arteries as well as SIN-1 treated vessels. IF/myosin ratio was not affected by SIN-1 whereas PTCA followed by ODQ+ SIN-1 treatment non-significantly increased the ratio (p = 0.06) (Figure 2). We could not detect any statistically significant changes in the relative amount of myosin heavy chain normalized to actin.

Figure 1
figure 1

Artery wall ratio of intermediate filaments/actin after PTCA with ODQ prior to SIN-1 treatment or SIN-1 alone. Legend: Figure 1 depicts the ratio of intermediate filaments to actin in treated and untreated segments. ODQ + SIN-1 caused a significant increase in the ratio compared to untreated segments and segments treated only with SIN-1 (p < 0.05). All groups summarize data from six animals. Data presented as mean ± SD. Mann-Whitney test.

Figure 2
figure 2

Artery wall ratio of intermediate filaments/myosin after PTCA with ODQ prior to SIN-1 treatment or SIN-1 alone. Legend: Figure 2 depicts the ratio of intermediate filaments to myosin in treated and untreated segments. ODQ + SIN-1 caused a non-significant increase in the ratio compared to untreated segments and segments treated only with SIN-1 (p = 0.06). All groups summarize data from six animals. Data presented as mean ± SD. Mann-Whitney test.

NADPH histochemistry

At 8 weeks saline treated controls showed significant increase in NADPH staining compared to untreated vessels (p < 0.01) as a normal response to artery injury. The increase was inhibited after PTCA with SIN-1treatment, whereas PTCA with ODQ prior to SIN-1 treatment resulted in significant elevation of NADPH staining (p < 0.01) (Figure 3).

Figure 3
figure 3

NADPH stained pixels 8 weeks after PTCA treated with ODQ prior to SIN-1 or SIN-1 alone. Legend to figure 3: NADPH staining at 8 weeks was significantly deceased in SIN-1 treated arteries compared to controls (p < 0.01). There was no significant difference between SIN-1 treated and untreated segments. NADPH staining in control segments and ODQ + SIN-1 treated segments was increased compared to untreated arteries. There was no difference in NADPH staining between controls and ODQ + SIN-1 treated vessels. All groups summarize data from six animals. Data presented as mean ± SD. * indicates p < 0.05 One-way ANOVA with Bonferroni post hoc test.

The increase in NADPH staining after ODQ + SIN-1 application was detectable one week after treatment (Figure 4).

Figure 4
figure 4

NADPH stained pixels 1 week after PTCA treated with ODQ prior to SIN-1 or SIN-1 alone. Legend to figure 4: At one week there was no significant difference in NADPH staining between the SIN-1 treated arteries compared to untreated vessels. NADPH staining was significantly higher in ODQ + SIN-1 treated segments compared to SIN-1 treated as well as untreated vessels (p < 0.01). All groups summarize data from six animals. Data presented as mean ± SD. * indicates p < 0.05 Mann-Whitney test.

Changes in NADPH diaphorase activity were circumscribed to treated segments while there were no changes observed in correlating matched distal untreated segments.

Histo-morphological examination

8 weeks after treatment all arteries were patent. There were no statistically significant differences in the internal elastic lamina fracture lengths inflicted to the arteries. In the SIN-1 treated segments, the restenosis index (0.60 ± 0.65) was 72% less and the amount of intimal hyperplasia (0.07 ± 0.06) 71% reduced compared to controls. The residual lumen (0.92 ± 0.08) was 26% larger in SIN-1 segments and there were no differences in EEL compared to controls. Intimal hyperplasia is significantly decreased after SIN-1 treatment compared to controls (p < 0.01). Addition of ODQ prior to SIN-1 treatment resulted in response to injury similar to the response of controls (NaCl) (Table 2).

Table 2 Histo-pathological characteristics of PTCA injured coronary arteries 8 weeks after treatment with ODQ + SIN-1 and SIN-1 and control


This study shows that delivery of the NO donor SIN-1 at the site of a PTCA injury for 5 minutes decreases significantly intimal hyperplasia/restenosis. Inhibition of guanylyl cyclase by ODQ attenuated the beneficial effect of NO delivery indicating the involvement of a cGMP dependent pathway. In this experiment additional ODQ to the delivery system did not increase intimal hyperplasia compared with controls.

Application of a NO donor was chosen in the present study, since NO interferes with the restenotic process at several levels. NO has three major properties in the vascular system: anti-ischemic/anti-hypertensive, anti-atherosclerotic and anti-thrombotic. Nitric oxide interferes with most intracellular messengers because it diffuses rapidly and isotopically through tissues [2].

The action of NO in regulating growth and migration of vascular smooth muscle cells is mainly mediated through a cGMP-dependent mechanism [22, 23]. Activated platelets participate by adhering to endothelial ulcerations and releasing mitogens and cytokines, which induce SMC migration and proliferation. SMCs in the vascular lesion change their phenotype from contractile to secretory [8]. In the present study we examined whether the beneficial effect of an externally applied NO donor in a high concentration could be modified by a guanylyl cyclase inhibitor, as an indication for the implication of a cGMP dependent pathway in the development of intimal hyperplasia/restenosis.

NO, derived from endothelial cells, modulates SMC migration and reduces production of extracellular matrix [24, 25]. In physiological concentrations NO contributes to human endothelial cell survival, whereas in high concentrations NO induces endothelial cell apoptosis [26, 27]. SIN-1 spontaneously releases NO, which can further react with superoxide and at high concentrations form peroxynitrite (ONOO-) [28]. NO scavenges superoxide anion directly and independent of cGMP. Peroxynitrite is a selective oxidant [29] causing nitration of structural proteins [28]. SIN-1 in concentrations of 400 μM has been shown to result in necrosis of cell cultures due to peroxynitrite. However, concentrations of 200 μM SIN-1 caused cellular apoptosis [30]. In the present study it is plausible that production of peroxynitrite at a concentration of 100 μM SIN-1, affected our results. However, since the effect of SIN-1 on intimal hyperplasia was inhibited in the presence of ODQ, a cytosolic guanylyl cyclase inhibitor, this assumption seems unlikely.

PTCA treatment causes intimal hyperplasia [20]. In the present study we have shown angiographically increased artery diameter after local delivery of SIN-1. A clinical multicenter study (ACCORD) indentified modest improvement of restenosis after intravenous or oral administration of sydnonimines [11]. Yet, a recent randomized trial of 166 patients failed to show benefit of 8 mg/day controlled release tablets for 6 month on restenosis after PTCA [12]. Site-specific delivery of SIN-1 affects more potently intimal thickening as in this case the biological action of NO is not circumscribed by immediate degradation upon exposure oxyhaemoglobin. Exposure of vascular tissue to NO delivery for a very short interval (5 minutes) has been proven in this and a previous study to exert long-lasting effects on tissue remodelling and patency [14]. These effects are of outmost clinical relevance in everyday treatment of arthrosclerosis.

Biochemical analysis of the arterial wall proteins actin, myosin and intermediate filaments was performed one week postoperatively, as histological examination is uncertain at this time point. The SMC cytoskeleton contains a high amount of IF but IF can be found in all types of cells. The function of IF in SMC is not established, but IF is increased in hypertrophy and hyperplasia [31]. The content of actin is not changed in smooth muscle in intimal hyperplasia when related to total tissue weight [32]. Since SMC adaption is associated with an increase in IF while the amount of actin is unchanged, we chose to use the IF/actin ratio as a measurement of PTCA induced adaption to arterial injury.

We found that SIN-1 treatment after PTCA affects the structural IF system in the SMC in a pronounced way. NO released by SIN-1 and applied to the injured area inhibits the increase of the IF/actin and IF/myosin ratios. On the contrary when the cGMP dependent NO-pathway is blocked by ODQ, IF/actin increase significantly, indicating a rapid turnover of IF proteins and cell growth after injury.

It cannot be excluded that the increased IF/actin and IF/myosin ratios seen after ODQ+SIN-1 treatment represents an increase in the number of non-SMC, activated at the time of injury. The present results suggest a possible role for NO in SMC remodeling in response to injury, as exposure to SIN-1 significantly reduced the IF/actin ratio, which directly correlated to the degree of neointimal formation at 8 weeks. Interestingly, a recent study has demonstrated that hematopoietic stem cells give rise to SMC after angioplasty [33]. If this is the case our results indicate that NO may influence stem cells.

In the heart, nitric oxide synthase (NOS) is found almost exclusively in vessels [30]. Practically none is found in the endocardium, valves or cardiac muscle fibers. Most NOS in the heart is in the form of the endothelial isoform (eNOS). Recently, it has been suggested that eNOS localized in the endothelial caveolae may act as a mechanosensor to couple NO release to long time hemodynamic changes that regulate extracellular matrix turnover, endothelial and SMC proliferation, migration and responsiveness to growth factors; events ultimately responsible for artery remodeling [8, 24, 25]. The inducible isoform (iNOS) is only found after injury [34]. In an attempt to establish the amount of NOS in the endothelium after PTCA treatment with SIN-1 or ODQ+SIN-1, NADPH diaphorase histochemistry of the arteries was performed. This histochemical reaction is sensitive to temperature and fixation-time. For this reason treated segments were always matched and compared with their distal untreated segment, which was harvested simultaneously. Although NADPH also marks other enzymes such as cytochrome P450 reductase, NADPH oxidase and non-specific phosphatases these enzymes are predominantly found in the liver [35, 36]. This response was inhibited by SIN-1. We attributed this effect to the release of NO as addition of ODQ abolished the favorable result of SIN-1 application. Events modulating endothelial NOS appeared early after vascular injury as changes in NADPH diaphorase staining were present already at one week. The present findings suggest that NO down-regulates the expression of NOS in newly formed endothelial cells to normal levels and implicate a long lasting change in the mRNA expression of endothelial cells [37]. A plausible alternative explanation may be that the local delivery of SIN-1, leads to a greater degree of local endothelial loss, which is not recovered at later time-points as compared with NaCl treated animals. However, in this case one would expect decreased NADPH activity whenever SIN-1 is applied even in the presence of ODQ. Our results do not show decrease when ODQ is used, indicating that the SIN-1 effect is mediated through the cGMP dependent NO pathway, which requires functioning endothelium.

Porcine coronary arteries respond to injury with constrictive remodeling, elastic recoil and tissue proliferation, in a manner similar to human arteries [38, 39]. Development of intimal hyperplasia is related to the degree of injury [20] and events at the onset [14]. There was no significant difference in the IEL fracture length inflicted to the arteries, but the arteries treated with SIN-1 had a 72% lower restenosis index, 71% less intimal hyperplasia compared to controls, and 26% larger residual lumen. This effect is apparently due to NO since it is abolished in the presence of ODQ.


Events at the onset of injury are crucial to the process of neointimal formation. Intimal hyperplasia/restenosis is significantly reduced by application of SIN-1 immediately after PTCA. The mechanism underlying the effect of SIN-1 was shown to rely on NO release, which is inhibited by guanylyl cyclase, both in SMC as well as in endothelial cells.



Percutaneous transluminal coronary angioplasty


left anterior coronary artery


Left circumflex coronary artery




1 H-(1,2,4)oxadiazole(4,3-alpha)quinoxaline-1-one


intermediate filaments


nitric oxide synthetase


cyclic guanosine 3',5'-monophosphate


smooth muscle cells


intimal vascular layer


medial vascular layer


luminal area


internal elastic lamina


fracture length of the IEL


Injury index


Intimal hyperplasia


restenosis index


residual lumen


endothelial isoform


inducible isoform


  1. Libby P: Inflammation in atherosclerosis. Nature. 2002, 420 (6917): 868-874. 10.1038/nature01323.

    Article  CAS  PubMed  Google Scholar 

  2. Pacher P, Beckman JS, Liaudet L: Nitric oxide and peroxynitrite in health and disease. Physiol Rev. 2007, 87: 315-424. 10.1152/physrev.00029.2006.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Sarkar K, Sharma SK, Sachdeva R, Romeo F, Mehta JL: Coronary artery stenosis: vascular biology and emerging therapeutic strategies. Expert Rev Cardiovasc Ther. 2006, 4 (4): 543-556. 10.1586/14779072.4.4.543.

    Article  CAS  PubMed  Google Scholar 

  4. Sarkar R, Gordon D, Stanley JC, Webb RC: Dual cell cycle-specific mechanism mediate the antimitogenic effects of nitric oxide in vascular smooth muscle cells. Hypertens. 1997, 15: 275-283. 10.1097/00004872-199715030-00009.

    Article  CAS  Google Scholar 

  5. Münzel T: Recent findings on nitrates: their action, bioactivation and development of tolerance. Dtsch Wochensch. 2008, 133 (44): 2277-2282. 10.1055/s-0028-1091272.

    Article  Google Scholar 

  6. Kim YM, Bombeck CA, Billiar TR: Nitric oxide as a bifunctional regulator of apoptosis. Circ.Res. 1999, 84: 253-256.

    Article  CAS  PubMed  Google Scholar 

  7. Rabkin SW: Nitric oxide-induced cell death in the heart. The role of autophagy. Autophagy. 2007, 3 (4): 347-349.

    Article  CAS  PubMed  Google Scholar 

  8. Maxell AJ: Mechanisms of dysfunction of the nitric oxide pathway in vascular disease. Nitric Oxide. 2002, 6 (2): 101-124. 10.1006/niox.2001.0394.

    Article  Google Scholar 

  9. Shiraki T, Takamura A, Oka T, Saito D: Effect of short-term administration of high dose L-Arginine on restenosis after percutaneous coronary angioplasty. J Cardiol. 2004, 44 (1): 13-20.

    PubMed  Google Scholar 

  10. Yoon J, Wu C-j, Homme J, Tuch TJ, Wolff RG, Topol EJ, Lincoff AM: Local delivery of nitrix oxide from a eluting stent to inhibit neointimal thickening in a porcine coronary injury model. Yonsei Medical Journal. 2002, 43 (2): 242-251.

    Article  CAS  PubMed  Google Scholar 

  11. Lablanche J-M, Grollier G, Lusson J-R, et al: Effect of direct nitric oxide donors Linsidomine and Molsidomine on angiographic restenosis after coronary balloon angioplasty. The ACCORD study. Circulation. 1997, 95 (1): 83-89.

    Article  PubMed  Google Scholar 

  12. Wohrle J, Hoher M, Nusser T, Kocks M: No effect of highly dosed nitric oxide donor molsidomine on the angiographic restenosis after percutaneous coronary angioplasty: a randomized, placebo controlled double-blind trial. Can J Cardiol. 2003, 19 (5): 495-500.

    CAS  PubMed  Google Scholar 

  13. Baek SH, Hrabie JA, Keefer LK, Hou D, Fineberg N, Rhoades R, March KL: Augmentation of intrapericardial nitric oxide level by a prolonged-release nitric oxide donor reduces luminal narrowing after porcine coronary angioplasty. Circulation. 2002, 105: 2779-2784. 10.1161/01.CIR.0000017432.19415.3E.

    Article  CAS  PubMed  Google Scholar 

  14. Harnek J, Zoucas E, Sjuve R, Arner A, Ekblad E, Schou H, Perez de Sà V, Stenram U: Local infusion of the NO donor SIN-1 after angioplasty reduces intimal hyperplasia in porcine coronary arteries. Acta Radiol. 2003, 44 (4): 395-402.

    CAS  PubMed  Google Scholar 

  15. Palmer RMJ, Ferrige AG, Moncada S: Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor. Nature. 1987, 327: 524-526. 10.1038/327524a0.

    Article  CAS  PubMed  Google Scholar 

  16. Groves PH, Lewis MJ, Cheadle HA, Penny WJ: SIN-1 reduces platelet adhesion and platelet thrombus formation in a porcine model of balloon angioplasty. Circulation. 1993, 87: 590-597.

    Article  CAS  PubMed  Google Scholar 

  17. Furlong B, Henderson AM, Lewis MJ, Smith JA: Endothelium-derived relaxing factor inhibits in vitro platelet aggregation. Br. J. Pharmcol. 1987, 90 (4): 687-692.

    Article  CAS  Google Scholar 

  18. Malmqvist U, Arner A: Isoform distribution and tissue content of contractile and cytoskeletal proteins in hypertrophied smooth muscle from rat portal vein. Circ. Res. 1990, 66 (3): 832-845.

    Article  CAS  PubMed  Google Scholar 

  19. Hope B, Michael GJ, Knigge KM, Vincent SR: Neuronal NADPH diaphorase is a nitric oxide synthase. Proc Natl Acad Sci USA. 1991, 88: 2811-2814. 10.1073/pnas.88.7.2811.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Nugent HM, Rogers C, Edelman ER: Endothelial implants inhibit intimal hyperplasia after porcine angioplasty. Circ Res. 1999, 84: 384-391.

    Article  CAS  PubMed  Google Scholar 

  21. Bonan R, Paiement P, Scortichini D, Cloutier MJ, Leung TK: Coronary restenosis: Evaluation of a restenosis injury index in a swine model. Am Heart J. 1993, 126 (6): 1334-1340. 10.1016/0002-8703(93)90531-D.

    Article  CAS  PubMed  Google Scholar 

  22. Lee KW, Norell MS: Management of "no-reflow" complicating reperfusion therapy. Acute Card Care. 2008, 10 (1): 5-14. 10.1080/17482940701744318.

    Article  PubMed  Google Scholar 

  23. Pilz RB, Catsteel DE: Regulation of gene expression by cGMP. Circ Res. 2003, 93: 1034-1046. 10.1161/01.RES.0000103311.52853.48.

    Article  CAS  PubMed  Google Scholar 

  24. Rudic RD, Shesely EG, Nobuyo M, Maeda N, Smithies O, Segal SS, Sessa WC: Direct evidence for the importance of endothelium derived Nitric Oxide in vascular remodeling. J.Clin.Invest. 1998, 101 (4): 731-736. 10.1172/JCI1699.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Gratton JP, Bernatchez P, Sessa WC: Caveola and calveolins in the cardiovascular system. Circ.Res. 2004, 94: 1408-1417. 10.1161/01.RES.0000129178.56294.17.

    Article  CAS  PubMed  Google Scholar 

  26. Shen YH, Wang XL, Wilken DE: Nitric oxide induces and inhibits apoptosis through different pathways. FEBS Lett. 1998, 433 (1-2): 125-131. 10.1016/S0014-5793(98)00844-8.

    Article  CAS  PubMed  Google Scholar 

  27. Brüne B, von Knethen A, Sandau KB: Nitric oxide and its role in apoptosis. Eur.J.Pharmacol. 1998, 351: 261-272. 10.1016/S0014-2999(98)00274-X.

    Article  PubMed  Google Scholar 

  28. Beckman JS, Koppenol WH: Nitric oxide, superoxide and peroxynitrite: The good, the bad and the ugly. Am.J.Physiol. 1996, 271: C1424-1437.

    CAS  PubMed  Google Scholar 

  29. Radi R, Beckman JS, Bush KM, Freeman BA: Peroxynitrite oxidation of sulfhydryls. The cytotoxic potential of superoxide and nitric oxide. J.Biol.Chem. 1991, 266 (7): 4244-4250.

    CAS  PubMed  Google Scholar 

  30. Kaji T, Kaieda I, Hisatsune T, Kaminogawa S: 3-Morpholinosydnonimine hydrochloride induces p53-dependent apoptosis in murine primary neural cells: A critical role for p21ras-MAPK-p19ARF pathway. Nitric Oxide. 2002, 6 (2): 125-134. 10.1006/niox.2001.0389.

    Article  CAS  PubMed  Google Scholar 

  31. Kocher O, Gabbiani G: Cytoskeletal features of normal and atheromatous human arterial smooth muscle cells. Hum Pathol. 1986, 17 (9): 875-880. 10.1016/S0046-8177(86)80637-2.

    Article  CAS  PubMed  Google Scholar 

  32. Gabbiani G, Kocher O, Bloom WS, Vandekerckhove J, Weber K: Actin expression in smooth muscle cells of rat aortic intimal thickening, human atheromatous plaque, and cultured rat aortic media. J Clin Invest. 1984, 73 (1): 148-152. 10.1172/JCI111185.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Sata M, Saiura A, Kunisato A, Tojo A, Okada S, Tokuhisa T, Hirai H, Makuuchi M, Hirata Y, Nagai R: Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis. Nat Med. 2002, 8 (4): 403-409. 10.1038/nm0402-403.

    Article  CAS  PubMed  Google Scholar 

  34. Ursell PC, Mayes M: Anatomic distribution of nitric oxide synthetase in the heart. Int J Cardiol. 1995, 50 (3): 217-223. 10.1016/0167-5273(95)02380-F.

    Article  CAS  PubMed  Google Scholar 

  35. Persson K, Poljakovic M, Johansson K, Larsson B: Morphological and biochemical investigation of nitric oxide synthetase and related enzymes in the rat and pig urothelium. J Histochem Cytochem. 1999, 47 (6): 739-750. 10.1177/002215549904700603.

    Article  CAS  PubMed  Google Scholar 

  36. Shi Y, Niculescu R, Wang D, Patel S, Davenpeck KL, Zalewski A: Increased NAD(P)H oxidase and reactive species in coronary arteries after balloon injury. Arterioscler Tromb Vasc Biol. 2001, 21: 739-745. 10.1161/01.ATV.21.5.739.

    Article  CAS  Google Scholar 

  37. Brüne B, Sandau K, Knethen A: Apoptotic cell death and nitric oxide: activating and antagonistic transducing pathways. Biochemistry (Mosc). 1998, 63 (7): 817-825.

    Google Scholar 

  38. Nobuyoshi M, Kimura T, Ohishi H, Horiuchi H, Nosaka H, Hamasaki N, Yokoi H, Kim K: Restenosis after percutaneous transluminal coronary angiography: pathologic observations in 20 patients. J Am Coll Cardiol. 1991, 17 (2): 433-439. 10.1016/S0735-1097(10)80111-1.

    Article  CAS  PubMed  Google Scholar 

  39. Mintz GS, Popma JJ, Hong MK, Pichard AD, Kent KM, Satler LF, Leon MB: Intravascular ultrasound to discern device-specific effects and mechanisms of restenosis. Am J Cardiol. 1996, 78 (3A): 18-22.

    Article  CAS  PubMed  Google Scholar 

Pre-publication history

Download references


The study was supported by the Swedish Medical Research Council (04X-8268 and 04X-13406). Catheters were granted by Boston Scientific Co. We are grateful for expert help with the biochemical assays from Mrs. Christina Persson and for copy editing by Dr Goran K. Olivecrona.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Jan Harnek.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

JH and EZ drafted the primary study protocol. EE carried out the NADPH histochemistry. AA did all the electrophoretic examination. We all participated in the design of the study and performed the statistical analysis. US did all the pathology. VP did the entire anesthetic. All Authors conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Harnek, J., Zoucas, E., de Sá, V.P. et al. Intimal Hyperplasia in Balloon Dilated Coronary Arteries is Reduced by Local Delivery of the NO Donor, SIN-1 Via a cGMP-Dependent Pathway. BMC Cardiovasc Disord 11, 30 (2011).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: