- Open Access
Inhaled tolafentrine reverses pulmonary vascular remodeling via inhibition of smooth muscle cell migration
© Pullamsetti et al. 2005
- Received: 17 August 2005
- Accepted: 01 November 2005
- Published: 01 November 2005
The aim of the study was to assess the chronic effects of combined phosphodiesterase 3/4 inhibitor tolafentrine, administered by inhalation, during monocrotaline-induced pulmonary arterial hypertension (PAH) in rats.
CD rats were given a single subcutaneous injection of monocrotaline to induce PAH. Four weeks after, rats were subjected to inhalation of tolafentrine or sham nebulization in an unrestrained, whole body aerosol exposure system. In these animals (i) the acute pulmonary vasodilatory efficacy of inhaled tolafentrine (ii) the anti-remodeling effect of long-term inhalation of tolafentrine (iii) the effects of tolafentrine on the expression profile of 96 genes encoding cell adhesion and extracellular matrix regulation were examined. In addition, the inhibitory effect of tolafentrine on ex vivo isolated pulmonary artery SMC cell migration was also investigated.
Monocrotaline injection provoked severe PAH (right ventricular systolic pressure increased from 25.9 ± 4.0 to 68.9 ± 3.2 after 4 weeks and 74.9 ± 5.1 mmHg after 6 weeks), cardiac output depression and right heart hypertrophy. The media thickness of the pulmonary arteries and the proportion of muscularization of small precapillary resistance vessels increased dramatically, and the migratory response of ex-vivo isolated pulmonary artery smooth muscle cells (PASMC) was increased. Micro-arrays and subsequent confirmation with real time PCR demonstrated upregulation of several extracellular matrix regulation and adhesion genes, such as matrixmetalloproteases (MMP) 2, 8, 9, 10, 11, 12, 20, Icam, Itgax, Plat and serpinb2. When chronically nebulized from day 28 to 42 (12 daily aerosol maneuvers), after full establishment of severe pulmonary hypertension, tolafentrine reversed about 60% of all hemodynamic abnormalities, right heart hypertrophy and monocrotaline-induced structural lung vascular changes, including the proportion of pulmonary artery muscularization. The upregulation of extracellular matrix regulation and adhesion genes was reduced by nearly 80% by inhalation of the tolafentrine. When assessed in vitro, tolafentrine blocked the enhanced PASMC migratory response.
In conclusion, we demonstrate for the first time that inhalation of combined PDE3/4 inhibitor reverses pulmonary hypertension fully developed in response to monocrotaline in rats. This "reverse-remodeling" effect includes structural changes in the lung vascular wall and key molecular pathways of matrix regulation, concomitant with 60% normalization of hemodynamics.
- Pulmonary Hypertension
- Pulmonary Arterial Hypertension
- Mass Median Aerodynamic Diameter
- Migratory Response
- Ventricular Systolic Pressure
Pulmonary arterial hypertension (PAH) is a severe disabling disease characterized by elevation of pulmonary artery pressure and death attributable to right heart failure . It is a progressive, proliferative vascular disorder resulting from persistent vasoconstriction and structural remodeling of pulmonary vessels. The structural changes include endothelial cell injury, neovascularization of small arteries, smooth muscle cell (SMC) migration and proliferation, and abnormal accumulation of extracellular matrix proteins associated with activation of matrix metalloproteinases (MMPs) .
The MMPs are a family of matrix-degrading enzymes that have been implicated in two important processes in vessel wall repair: cellular migration , and regulating extracellular matrix composition and content . Based on their substrate specificity, MMPs were subdivided into four groups: i) interstitial collagenases (MMP 1, MMP 8 and MMP 13) that degrade fibrillary collagens; ii) type IV collagenases (MMP 2 and MMP 9) that degrade basement membrane components; iii) stromelysins (MMP 3, MMP 10 and MMP 11) that degrade proteoglycans, fibronectin, laminin, gelatin and the globular proteins of the type IV collagen; and iv) membrane type-MMPs (MT-1, MMP 15, MMP 16 and MMP 17), possessing a broad spectrum of activities.
Of the MMPs, expression of MMP 2 and MMP 9 in particular, which degrade type IV collagen of basement membranes, are increased in the pulmonary vascular bed, during both monocrotaline (MCT) and hypoxia-induced experimental PAH . In addition, MMP 1, an interstitial collagenase, is upregulated in MCT-induced PAH . In recent years, several pharmacological interventions in PAH, including MMP inhibitors, endothelin antagonist, angiotensinogen inhibitors and phosphodiesterase (PDE) inhibitors that target either the MMP cascades or endogenous vascular elastases, proved to be beneficial in experimental PAH models, with most of these agents being applied prior to full establishment of the disease [7–11]. Suppression of vessel wall remodeling was assumed to largely contribute to these beneficial effects.
The phosphodiesterases (PDEs) are a large family of intracellular enzymes that degrade cyclic nucleotides [12, 13]. Because of their potential for altering a variety of cellular responses, PDEs are appealing targets for the treatment of PAH [14, 15]. Phosphodiesterase 3 and 4 isoenzymes are the essential players co-regulating cAMP catabolism in many organs, including the lung, and were shown to be upregulated in experimental PAH models. Inhibitors of PDE 3 and 4 synergistically promoted the acute pulmonary vasodilation evoked by prostacyclin or its stable analogues in experimental models of PAH [16–18]. Recently, inhalation of the combined -selective PDE3/4 inhibitor tolafentrine has been shown to amplify the vasodilatory effect of inhaled iloprost in patients with PAH . However, no data are currently available regarding effects of long-term inhalation of tolafentrine on hemodynamics and pulmonary vascular remodeling in PAH models.
In the present investigation, we employed monocrotaline (MCT), a toxin derived from plants of the Crotalaria species , for pulmonary artery smooth muscle cell hypertrophy and severe pulmonary hypertension in rats . In this model we examined (i) the acute pulmonary vasodilatory efficacy of inhaled tolafentrine (ii) the anti-remodeling effect of long-term inhalation of tolafentrine (iii) the inhibitory effect of tolafentrine on pulmonary artery SMC cell migration, and (iv) the effect of the PDE inhibitor on the expression profile of 96 genes encoding cell adhesion and extracellular matrix regulation. To mimic clinical conditions, inhalation of tolafentrine commenced after pulmonary hypertension was already fully established. Essentially, we found that inhaled tolafentrine reverses hemodynamic abnormalities as well as structural changes, SMC migration and proliferation and matrix remodeling, representing the key features of MCT induced PAH.
Experiments were performed on male CD rats 300 – 350 g body weight, Charles River, Sulzfeld, Germany). Pulmonary hypertension was induced by a single subcutaneous injection of monocrotaline (MCT, 60 mg/kg, Sigma, Deishofen, Germany), dissolved in 0.1 M NaOH, adjusted to pH 7.4 with 0.1 M HCl, according to the previous reports [7, 10, 21, 22].
The experiments were performed in accordance with the National Institutes of Health Guidelines on the Use of Laboratory Animals. Both the University Animal Care Committee and the Federal Authorities for Animal Research of the Regierungspräsidium Giessen (Hessen, Germany) approved the study protocol.
The animals were classified into the following four groups: 1) rats injected with saline sacrificed after 28 days (Control, n = 8); 2) MCT-injected rats sacrificed after 28 days (MCT[28d], n = 12); 3) MCT-injected sacrificed after 42 days, with nebulized vehicle being administered from day 28 to day 42 (MCT[42d], n = 14); 4) MCT-injected rats sacrificed after 42 days, with nebulized tolafentrine being administered from day 28 to day 42 (MCT[42d]/Tola, n = 10). For acute hemodynamic studies 12 MCT[28d] rats (MCT injected for 28 days) were used (inhalation of saline, n = 6; and inhalation of tolafentrine in two different doses, n = 6 each).
Inhalation of tolafentrine
Four weeks after a single MCT injection, rats were subjected to inhalation of tolafentrine or sham nebulization in an unrestrained, whole body aerosol exposure system as described . For assessment of chronic effects of inhaled saline or tolafentrine (dose deposited in the lungs ~ 120 μg/kg day), 15 min nebulization maneuvers using a jet nebulizer with a constant flow rate of 6 l/min (Pari LC Star, Pari, Starnberg, Germany) were repeated twelve times per day for 2 weeks (day 28 – 42). Particles generated by the jet nebulizer were characterized by a mass median aerodynamic diameter (MMAD) of 2.8 μm and a geometric standard deviation (GSD) of 2.5 (determined by laser difractometric measurements, as described . Preliminary experiments with nebulization of 99Tc-DTPA determined the total lung deposition of nebulized material to range at 0.5 %, in accordance with previous studies in this model .
To assess the acute effects of inhaled tolafentrine, hemodynamic testing in response to the drug was performed in animals that had previously received a MCT injection 4 weeks prior to study. Hemodynamics were measured before and after a single inhalation of the tolafentrine (130 and 650 μg/kg min for 10 min) by an ultrasonic nebulizer with MMAD of 4.0 μm and GSD of 2.1 as described previously [22, 23, 25].
Surgical Preparation, measurement of hemodynamics and tissue preparation
For measurement of hemodynamic parameters, rats were anaesthetized with an i.p. injection of ketamine (9 mg/kg body mass) and medetomidine (100 μg/kg body mass), followed by an i.m. injection of atropine (250 μg/kg body mass). The rats were tracheotomized and ventilated with a frequency of 60 breaths/min. Positive end expiratory pressure was set at 1 cm H2O. A polyethylene catheter was inserted into the left carotid artery to measure arterial pressure. A right heart catheter (PE 50 tubing) was inserted into the right ventricle through the right jugular vein for measurement of right ventricular systolic pressure with fluid-filled force transducers [10, 11]. Cardiac output (CO) was measured by thermodilution technique as described [10, 11]. Briefly, a thermistor (1.5 F) was placed into the ascending thoracic aorta via the right carotid artery for the measurement of transpulmonary thermodilution cardiac output (Cardiotherm 500-X, Hugo-Sachs Electronic – Harvard Apparatus GmbH, March-Hugstetten, Germany). The CO was averaged from three consecutive determinations and indexed to the weight of the animal to obtain cardiac index (CI). After exsanguination, the left lung was fixed for histology in 10% neutral buffered formalin and the right lung was snap frozen in liquid nitrogen.
Right ventricular hypertrophy
The RV was dissected from the left ventricle (LV) and the septum (S) and weighed to determine the extent of RV hypertrophy as follows: RV/ (LV+S).
Histological examination of the lungs
Paraffin lung sections (3 μm) were double-stained with anti-α-smooth muscle actin antibody (dilution 1:900, clone 1A4, Sigma, Saint Louis, Missouri) and anti-human von Willebrand factor antibody (vWF, dilution 1:900, Dako, Hamburg, Germany). Sections were counterstained with hematoxylin and examined by light microscopy using a computerized morphometric system (Qwin, Leica, and Wetzlar, Germany) for assessing the degree of muscularization of small peripheral pulmonary arteries [10, 11, 23]. In addition, lung sections were stained for Elastin-Nuclear Fast Red to assess the medial wall thickness.
Categorization of pulmonary arteries based on the degree of muscularization and on the external diameter and the percentage of medial wall thickness were performed as previously described [10, 11, 23].
Microarray and data analysis
Total RNA extraction was performed using the Trizol reagent (Burlington, Ontario, Canada) according to the instructions given by the manufacturer from control, monocrotaline (MCT[42d]) and monocrotaline plus tolafentrine (MCT[42d]/Tola) treated lungs. Samples were treated with DNase I according to the RNase-free DNase set (QIAGEN, Hilden, Germany). Total RNA (5 μg) from each sample was used to generate Biotin-16-dUTP labeled cDNA and hybridized to the extracellular matrix and adhesion molecules gene array (GEArray Q series, Superarray, MD, USA). After hybridization, the membranes were developed according to the manufacturer's recommendations to yield luminescent signals, which were then captured on X-ray film.
The resulting image data were analyzed for differential gene expression patterns using GE Array Analyzer 1.2 (Super Array Bioscience Corp., Frederick, MD) software. Loading was adjusted on the basis of the intensity of hybridization signals relative to the housekeeping gene GAPDH.
Real-time polymerase chain reaction
Quantitative real-time PCR was performed as described . Briefly, total RNA was isolated from frozen lungs using Trizol Reagent according to the manufacturer's instructions. For the generation of cDNA, equal amounts of RNA from each sample were used as templates for reverse transcription of first-strand cDNA using the qPCR™ Mastermix (Euro-genetec, Seraing, Belgium) according to the manufacturer's protocol. For quantitative real-time RT-PCR analysis, 2 μl cDNA was placed into 50 μl reaction volume containing SYBR Green PCR mix and sequence-specific oligonucleotide primers. The thermal cycle conditions used for all reactions were as follows: activation, 50°C for 2 min; denaturation, 95°C for 10 min; and cycle, 95°C for 10 s and 60°C for 5 s (40 times). Specific primers used for sequence detection were: rGAPDH,5'-GTG ATG GGT GTG AAC CAC GAG-3' (forward) and5'-CCA CGA TGC CAA AGT TGT CA-3'(reverse); forMMP2,5'-ATC TGC AAG CAA GAC ATT GTC TT-3'(forward)and 5'-GCC AAA TAA ACC GAT CCT TGA A-3' (reverse);for MMP8, 5'-CGG GAA GAC ATA CTC TTC GAA-3'(forward)and 5'-CAT GGA TCT TCT TTG ATT GTC G-3' (reverse);for MMP9, 5'-GTA ACC CTG GTC ACC GGA CTT -3'(forward)and 5'-ATA CGT TCC CGG CTG ATC AG-3' (reverse); for MMP10, 5'- GGA GAT GCT CAC TTC GAT GAT-3' (forward)and 5'-CAG CAA CCA GGA ATA AAT TGG-3' (reverse); for MMP11, 5'-TTC TGA GAT TGA TGC TGC TTT C-3'(forward)and 5'-TGT CCA CGA AGG AAG TAG GC-3' (reverse); for MMP12, 5'-GCT GTC ACA ACA GTG GGA GA-3' (forward)and 5'-GTA ATG TTG GTG GCT GGA CTC-3' (reverse); for MMP20, 5'-GAA TAA ACT CTG GGG AAG CAG A-3'(forward)and 5'-TGA TTG GAT TAA GGC CTC GT-3' (reverse); for Icam, 5'-CAG CTG CGC TGT GTT TTG-3'(forward)and 5'-GGA TGG GAG CTG AAA AGT TG-3' (reverse); For Itgax, 5'-GCC TCG AGA CTG GAG ATC AT-3'(forward)and 5'-GGA GAG CTG GGA GCC AGT-3' (reverse);for Ncam1, 5'-ACC ATG AGC TGG ACA AAG GA-3'(forward)and 5'-CAC TGA AGA TGT GCT TCT CGT C-3' (reverse); for Plat, 5'-AAT GAA GGG AGA GCT GTT GTG-3'(forward) and 5'-TCC TCT TCT GAA CCT CCT GTG-3' (reverse); for Serpinb2, 5'-CGA AAG GGA TTT TGT GAT GTC-3' (forward)and 5'-GTG GGA AAT GGG AAT TCG T-3' (reverse). All real-time reactions were carried on an ABI 7700 sequence Detection System (Applied Biosystems, Foster City, CA, USA), and analysis was performed with the accompanying software. At the end of the PCR cycle, a dissociation curve was generated to ensure the amplification of a single product and the threshold cycle time (Ct values) for each gene was determined. Relative mRNA levels were calculated based on the Ct values and normalized to house keeping gene GAPDH.
Pulmonary artery smooth muscle cell (PASMC) migration was examined in Transwell cell culture chambers with gelatin-coated polycarbonate membranes as described previously . For this assay, control and MCT-treated rat PASMCs were isolated and added to the upper well of a Transwell (Corning Costar, Cambridge, MA) at 2 × 105 cells/well. The platelet-derived growth factor – BB (PDGF-BB) was added to the lower chamber at a concentration of 25 ng/ml and cells were allowed to migrate for 8 and 24 hours. In experiments with the combined selective PDE3/4 inhibitor tolafentrine (0.05, 0.1 and 0.3 μM), MCT-treated rat PASMCs were pre-incubated with tolafentrine in the upper well of a Transwell for 30 min before the addition of PDGF-BB into the lower chamber. Migration was quantified by staining the cells with crystal violet (Sigma, Deishofen, Germany) following microscopic cell counts on five random fields in each well. Experiments were performed in triplicate and were repeated at least three times.
All data are given as mean ± SEM. Differences between the groups were assessed by analysis of variance (one-way ANOVA) and Student-Newman-Keuls test for multiple comparisons with a p value < 0.05 regarded to be significant.
Acute vasodilatory effects of aerosolized tolafentrine in MCT treated (28d) rats
Chronic effects of aerosolized tolafentrine: hemodynamics
Chronic effects of aerosolized tolafentrine: right ventricular hypertrophy
Chronic effects of aerosolized tolafentrine: survival
In this study, rats were randomized to receive vehicle or inhaled tolafentrine beginning four weeks after MCT treatment. In the MCT[28d] group a survival of 78% was noted, while survival decreased to 60% in the MCT[42d] group. In the MCT[42d]/Tola 80 % survived the treatment protocol. However, due to insufficient number of experiments the significant effects on this parameter were not shown in detail.
Chronic effects of aerosolized tolafentrine: histopathology
Most impressively, both, medial wall thickness (22.5 ± 0.65%) and percentage of fully muscularized pulmonary arteries (32.5 ± 5) were significantly reduced by long term treatment of aerosolized tolafentrine, while the percentage of non-muscularized pulmonary arteries significantly increased.
Comparison of migratory responses of control- and MCT-PASMCs
Effect of tolafentrine: PDGF-Induced MCT- PASMCs migration
Effects of tolafentrine: expression of matrix-degrading proteases
Several adhesion molecules were also differentially expressed at the mRNA level. We observed a significantly increased expression of Icam and Itgax (4.34 ± 1.22 and 3.44 ± 0.33 fold). In contrast, Ncam was not changed upon MCT treatment. An upregulation of tissue plasminogen activator (plat) by 3.74 ± 0.83 and plasminogen activator inhibitor-2 (Serpinb2) by 2.68 ± 0.83 foldwith MCT treatment was also observed.
Most impressively, virtually all alterations in extracellular matrix and adhesion molecule gene expression induced by monocrotaline were fully or partially abrogated by tolafentrine (12 genes given in Figure 10).
In the present study, we demonstrate that daily repetitive tolafentrine inhalation significantly improved pulmonary hemodynamics and reversed structural and molecular changes underlying MCT induced PAH in rats. Notably, the inhalative therapy was commenced after full establishment of pulmonary hypertension, 4 weeks after application of monocrotaline. Similar to the abnormalities in human PAH, monocrotaline treatment in rats is known to provoke endothelial injury, proliferation, migration and hypercontraction of vascular smooth muscle cells, as well as inflammatory sequelae [28, 29]. The animals die due to a progressive increase in precapillary lung vascular resistance with subsequent right heart failure.
A recent study by our group showed that intravenous infusion of the combined selective PDE 3/4 inhibitor (tolafentrine) prevented the development of pulmonary hypertension and right ventricular hypertrophy in response to monocrotaline . However, the complexity and complications associated with the intravenous application of an agent exerting at the same time pulmonary and systemic vasodilation prompted us to evaluate the inhalative route of application in the present study. Moreover, the therapeutic potential of tolafentrine, i.e. its efficacy after full establishment of severe pulmonary hypertension, and its impact on molecular mechanisms closely linked with the structural wall changes were not addressed in the previous study.
For the inhalation therapy, aimed to achieve a selective pulmonary vasodilation, a 15 fold lower dose compared with the intravenous route of application was employed (120 μg/kg day versus 2 mg/kg day). This low inhaled dosage exerted per se no acute effects on systemic hemodynamics but demonstrated selective pulmonary vasodilation as has been demonstrated for several other compounds [16, 17]. Further increase in dose results in spill over of the compound in the systemic circulation and systemic side effects as demonstrated by the higher dose of 650 μg tolafentrine/kg min in this study. Since PDE 3 and 4 are expressed in smooth muscle cells throughout the cardiovascular system, tolafentrine was nebulized in a dose which cause some direct lung vasorelaxation but which is still too low to provoke systemic vasodilatory effects. However, the results of an acute test of inhaled tolafentrine under general anesthesia may not reproduce the effects in an awake animal, but long term nebulization demonstrated strong anti-remodeling effects in the setting of MCT-induced PH.
Nevertheless, and notwithstanding the late initiation of the tolafentrine treatment, hemodynamics were dramatically improved after 2 weeks of inhalative tolafentrine treatment: RVSP values were markedly lower than those before onset of treatment, and cardiac index as well as total pulmonary resistance index were also fully normalized. Accordingly, the right heart hypertrophy was found to be largely decreased, as were the structural changes of the lung vasculature evoked by monocrotaline treatment. The increase in the medial thickness of the precapillary lung arteries was reversed, and the high percentage of fully muscularized peripheral pulmonary arteries decreased in response to tolafentrine inhalation. To our knowledge, this is the first time that combined selective PDE 3/4 inhibition (tolafentrine) has been shown to reverse established pulmonary hypertension both with respect to hemodynamics and the structural remodeling of the lung vasculature.
These findings suggest a potent anti-proliferative effect of combined selective PDE 3/4 inhibition in the lung vasculature, as has been suggested by preceding in vitro data. Selective and nonselective cAMP PDE inhibitors have been shown to elicit a concentration-dependent attenuation of mitogen-induced proliferation in rat and human PASMC predominantly via adenylyl cyclase and protein kinase A [30, 31]. Furthermore, PASMC receiving the combination of a PDE3 and a PDE4 inhibitor exhibited a significant additive or synergistic anti-mitogenic effect as compared to each PDE inhibitor used on its own.
Interestingly, an enhanced migratory capacity in response to PDGF was observed in PASMCs isolated form lungs of MCT treated rats as compared to matched control lungs. This is reminiscent of the reported higher migratory response of aortic SMCs derived from spontaneously hypertensive rats as compared to normotensive rats [31, 32]. Although the mechanisms responsible for the differential migratory responses of SMC are not known, increased collagenase activities might partly explain this phenomenon, since the destruction of extracellular matrix barriers is an important early step for SMC migration [33, 34]. Moreover, enhanced MAP kinase activities, such as extracellular signal-regulated kinase (ERK) and p38 kinase , might play a role in PDGF-induced vascular SMC migration, which is in line with the observation of increased ERK expression in the precapillary arteries of MCT-treated rats (data not shown).
The present study demonstrates for the first time that selective PDE 3/4 inhibition inhibits the migration of SMCs stimulated with PDGF in a concentration-dependent manner. The PDGF-BB-induced SMC migration was significantly inhibited by 0.05–0.3 μM tolafentrine. This is well in line with the study of T. Horio et al, who reported that adrenomedullin inhibits the migration of aortic SMCs in response to PDGF, probably through a cAMP-dependent process . Downstream effects of elevated cAMP levels, being relevant for the SMC migratory response, may include MAP kinase signaling and cytosolic Ca2+ regulation [37, 38].
In conclusion, we demonstrate for the first time that inhalation of a combined selective PDE3/4 inhibitor reverses pulmonary hypertension fully developed in response to monocrotaline in rats. This "reverse-remodeling" effect was true for hemodynamics, structural changes to the lung vascular wall, and key molecular pathways of matrix regulation. We provide evidence that inhibition of pulmonary artery SMC migration and MMP-based matrix regulation play a major role in the beneficial effect of inhaled tolafentrine in severe PAH. Reversal of structural lung vascular remodeling may apparently be achieved in pulmonary hypertension, at least in the experimental model of monocrotaline-induced PAH in rats.
This work was supported by the Deutsche Forschungsgemeinschaft (SFB 547), Project C6.
- D'Alonzo GE, Barst RJ, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, Fishman AP, Goldring RM, Groves BM, Kernis JT: Survival in patients with primary pulmonary hypertension. Results from a national prospective registry. Ann Intern Med 1991, 115:343–349.View ArticlePubMedGoogle Scholar
- Archer S, Rich S: Primary pulmonary hypertension: a vascular biology and translational research "Work in progress". Circulation 2000, 102:2781–2791.View ArticlePubMedGoogle Scholar
- Bendeck MP, Zempo N, Clowes AW, Galardy RE, Reidy MA: Smooth muscle cell migration and matrix metalloproteinase expression after arterial injury in the rat. Circ Res 1994, 75:539–545.View ArticlePubMedGoogle Scholar
- Strauss BH, Robinson R, Batchelor WB, Chisholm RJ, Ravi G, Natarajan MK, Logan RA, Mehta SR, Levy DE, Ezrin AM, Keeley FW: In vivo collagen turnover following experimental balloon angioplasty injury and the role of matrix metalloproteinases. Circ Res 1996, 79:541–550.View ArticlePubMedGoogle Scholar
- Frisdal E, Gest V, Vieillard-Baron A, Levame M, Lepetit H, Eddahibi S, Lafuma C, Harf A, Adnot S, Dortho MP: Gelatinase expression in pulmonary arteries during experimental pulmonary hypertension. Eur Respir J 2001, 18:838–845.View ArticlePubMedGoogle Scholar
- Qin Y, Zhou A, Ben X, Shen J, Liang Y, Li F: All-trans retinoic acid in pulmonary vascular structural remodeling in rats with pulmonary hypertension induced by monocrotaline. Chin Med J (Engl) 2001, 114:462–465.Google Scholar
- Cowan KN, Heilbut A, Humpl T, Lam C, Ito S, Rabinovitch M: Complete reversal of fatal pulmonary hypertension in rats by a serine elastase inhibitor. Nat Med 2000, 6:698–702.View ArticlePubMedGoogle Scholar
- Zaidi SH, You XM, Ciura S, Husain M, Rabinovitch M: Overexpression of the serine elastase inhibitor elafin protects transgenic mice from hypoxic pulmonary hypertension. Circulation 2002, 105:516–521.View ArticlePubMedGoogle Scholar
- Giannelli G, Iannone F, Marinosci F, Lapadula G, Antonaci S: The effect of bosentan on matrix metalloproteinase-9 levels in patients with systemic sclerosis-induced pulmonary hypertension. Curr Med Res Opin 2005, 21:327–332.View ArticlePubMedGoogle Scholar
- Schermuly RT, Kreisselmeier KP, Ghofrani HA, Yilmaz H, Butrous G, Ermert L, Ermert M, Weissmann N, Rose F, Guenther A, Walmrath D, Seeger W, Grimminger F: Chronic sildenafil treatment inhibits monocrotaline-induced pulmonary hypertension in rats. Am J Respir Crit Care Med 2004, 169:39–45.View ArticlePubMedGoogle Scholar
- Schermuly RT, Kreisselmeier KP, Ghofrani HA, Samidurai A, Pullamsetti S, Weissmann N, Schudt C, Ermert L, Seeger W, Grimminger F: Antiremodeling effects of iloprost and the dual-selective phosphodiesterase 3/4 inhibitor tolafentrine in chronic experimental pulmonary hypertension. Circ Res 2004, 94:1101–1108.View ArticlePubMedGoogle Scholar
- Beavo JA: Cyclic nucleotide phosphodiesterases: functional implications of multiple isoforms. Physiol Rev 1995, 75:725–748.PubMedGoogle Scholar
- Manganiello VC, Murata T, Taira M, Belfrage P, Degerman E: Diversity in cyclic nucleotide phosphodiesterase isoenzyme families. Arch Biochem Biophys 1995, 322:1–13.View ArticlePubMedGoogle Scholar
- Ghofrani HA, Pepke-Zaba J, Barbera JA, Channick R, Keogh AM, Gomez-Sanchez MA, Kneussl M, Grimminger F: Nitric oxide pathway and phosphodiesterase inhibitors in pulmonary arterial hypertension. J Am Coll Cardiol 2004, 43:68S-72S.View ArticlePubMedGoogle Scholar
- Ghofrani HA, Pepke-Zaba J, Barbera JA, Channick R, Keogh AM, Gomez-Sanchez MA, Kneussl M, Grimminger F: Nitric oxide pathway and phosphodiesterase inhibitors in pulmonary arterial hypertension. J Am Coll Cardiol 2004, 43:68S-72S.View ArticlePubMedGoogle Scholar
- Schermuly RT, Roehl A, Weissmann N, Ghofrani HA, Schudt C, Tenor H, Grimminger F, Seeger W, Walmrath D: Subthreshold doses of specific phosphodiesterase type 3 and 4 inhibitors enhance the pulmonary vasodilatory response to nebulized prostacyclin with improvement in gas exchange. J Pharmacol Exp Ther 2000, 292:512–520.PubMedGoogle Scholar
- Schermuly RT, Krupnik E, Tenor H, Schudt C, Weissmann N, Rose F, Grimminger F, Seeger W, Walmrath D, Ghofrani HA: Coaerosolization of phosphodiesterase inhibitors markedly enhances the pulmonary vasodilatory response to inhaled iloprost in experimental pulmonary hypertension. Maintenance of lung selectivity. Am J Respir Crit Care Med 2001, 164:1694–1700.View ArticlePubMedGoogle Scholar
- Ghofrani HA, Rose F, Schermuly RT, Olschewski H, Wiedemann R, Weissmann N, Schudt C, Tenor H, Seeger W, Grimminger F: Amplification of the pulmonary vasodilatory response to inhaled iloprost by subthreshold phosphodiesterase types 3 and 4 inhibition in severe pulmonary hypertension. Crit Care Med 2002, 30:2489–2492.View ArticlePubMedGoogle Scholar
- Huxtable RJ: Activation and pulmonary toxicity of pyrrolizidine alkaloids. Pharmacol Ther 1990, 47:371–389.View ArticlePubMedGoogle Scholar
- Rosenberg HC, Rabinovitch M: Endothelial injury and vascular reactivity in monocrotaline pulmonary hypertension. Am J Physiol 1988, 255:H1484-H1491.PubMedGoogle Scholar
- Kato S, Sugimura H, Kishiro I, Machida M, Suzuki H, Kaneko N: Suppressive effect of pulmonary hypertension and leukocyte activation by inhaled prostaglandin E1 in rats with monocrotaline-induced pulmonary hypertension. Exp Lung Res 2002, 28:265–273.View ArticlePubMedGoogle Scholar
- Nagaya N, Okumura H, Uematsu M, Shimizu W, Ono F, Shirai M, Mori H, Miyatake K, Kangawa K: Repeated inhalation of adrenomedullin ameliorates pulmonary hypertension and survival in monocrotaline rats. Am J Physiol Heart Circ Physiol 2003, 285:H2125-H2131.View ArticlePubMedGoogle Scholar
- Schermuly RT, Yilmaz H, Ghofrani HA, Woyda K, Pullamsetti S, Schulz A, Gessler T, Dumitrascu R, Weissmann N, Grimminger F, Seeger W: Inhaled Iloprost Reverses Vascular Remodeling in Chronic Experimental Pulmonary Hypertension. Am J Respir Crit Care Med 2005, 172:358–363.View ArticlePubMedGoogle Scholar
- Schermuly R, Schmehl T, Gunther A, Grimminger F, Seeger W, Walmrath D: Ultrasonic nebulization for efficient delivery of surfactant in a model of acute lung injury. Impact on gas exchange. Am J Respir Crit Care Med 1997, 156:445–453.View ArticlePubMedGoogle Scholar
- Schermuly RT, Ghofrani HA, Enke B, Weissmann N, Grimminger F, Seeger W, Schudt C, Walmrath D: Low-dose systemic phosphodiesterase inhibitors amplify the pulmonary vasodilatory response to inhaled prostacyclin in experimental pulmonary hypertension. Am J Respir Crit Care Med 1999, 160:1500–1506.View ArticlePubMedGoogle Scholar
- Fink L, Seeger W, Ermert L, Hanze J, Stahl U, Grimminger F, Kummer W, Bohle RM: Real-time quantitative RT-PCR after laser-assisted cell picking. Nat Med 1998, 4:1329–1333.View ArticlePubMedGoogle Scholar
- Irani C, Goncharova EA, Hunter DS, Walker CL, Panettieri RA, Krymskaya VP: Phosphatidylinositol 3-kinase but not tuberin is required for PDGF-induced cell migration. Am J Physiol Lung Cell Mol Physiol 2002, 282:L854-L862.View ArticlePubMedGoogle Scholar
- Olschewski H, Olschewski A, Rose F, Schermuly R, Schutte H, Weissmann N, Seeger W, Grimminger F: Physiologic basis for the treatment of pulmonary hypertension. J Lab Clin Med 2001, 138:287–297.View ArticlePubMedGoogle Scholar
- Olschewski H, Rose F, Grunig E, Ghofrani HA, Walmrath D, Schulz R, Schermuly R, Grimminger F, Seeger W: Cellular pathophysiology and therapy of pulmonary hypertension. J Lab Clin Med 2001, 138:367–377.View ArticlePubMedGoogle Scholar
- Wharton J, Davie N, Upton PD, Yacoub MH, Polak JM, Morrell NW: Prostacyclin analogues differentially inhibit growth of distal and proximal human pulmonary artery smooth muscle cells. Circulation 2000, 102:3130–3136.View ArticlePubMedGoogle Scholar
- Phillips PG, Long L, Wilkins MR, Morrell NW: cAMP phosphodiesterase inhibitors potentiate effects of prostacyclin analogs in hypoxic pulmonary vascular remodeling. Am J Physiol Lung Cell Mol Physiol 2005, 288:L103-L115.View ArticlePubMedGoogle Scholar
- Hsieh CC, Lau Y: Migration of vascular smooth muscle cells is enhanced in cultures derived from spontaneously hypertensive rat. Pflugers Arch 1998, 435:286–292.View ArticlePubMedGoogle Scholar
- Pauly RR, Passaniti A, Bilato C, Monticone R, Cheng L, Papadopoulos N, Gluzband YA, Smith L, Weinstein C, Lakatta EG: Migration of cultured vascular smooth muscle cells through a basement membrane barrier requires type IV collagenase activity and is inhibited by cellular differentiation. Circ Res 1994, 75:41–54.View ArticlePubMedGoogle Scholar
- Johnson JL, van Eys GJ, Angelini GD, George SJ: Injury induces dedifferentiation of smooth muscle cells and increased matrix-degrading metalloproteinase activity in human saphenous vein. Arterioscler Thromb Vasc Biol 2001, 21:1146–1151.View ArticlePubMedGoogle Scholar
- Yang GY, Yao JS, Huey M, Hashimoto T, Young WL: Participation of PI3K and ERK1/2 pathways are required for human brain vascular smooth muscle cell migration. Neurochem Int 2004, 44:441–446.View ArticlePubMedGoogle Scholar
- Horio T, Kohno M, Kano H, Ikeda M, Yasunari K, Yokokawa K, Minami M, Takeda T: Adrenomedullin as a novel antimigration factor of vascular smooth muscle cells. Circ Res 1995, 77:660–664.View ArticlePubMedGoogle Scholar
- Graves LM, Bornfeldt KE, Raines EW, Potts BC, Macdonald SG, Ross R, Krebs EG: Protein kinase A antagonizes platelet-derived growth factor-induced signaling by mitogen-activated protein kinase in human arterial smooth muscle cells. Proc Natl Acad Sci U S A 1993, 90:10300–10304.View ArticlePubMedPubMed CentralGoogle Scholar
- Bornfeldt KE, Raines EW, Nakano T, Graves LM, Krebs EG, Ross R: Insulin-like growth factor-I and platelet-derived growth factor-BB induce directed migration of human arterial smooth muscle cells via signaling pathways that are distinct from those of proliferation. J Clin Invest 1994, 93:1266–1274.View ArticlePubMedPubMed CentralGoogle Scholar
- Rabinovitch M: Investigational approaches to pulmonary hypertension. Toxicol Pathol 1991, 19:458–469.View ArticlePubMedGoogle Scholar
- Tozzi CA, Poiani GJ, Harangozo AM, Boyd CD, Riley DJ: Pressure-induced connective tissue synthesis in pulmonary artery segments is dependent on intact endothelium. J Clin Invest 1989, 84:1005–1012.View ArticlePubMedPubMed CentralGoogle Scholar
- McCawley LJ, Li S, Benavidez M, Halbleib J, Wattenberg EV, Hudson LG: Elevation of intracellular cAMP inhibits growth factor-mediated matrix metalloproteinase-9 induction and keratinocyte migration. Mol Pharmacol 2000, 58:145–151.PubMedGoogle Scholar
- Peracchia F, Tamburro A, Prontera C, Mariani B, Rotilio D: cAMP involvement in the expression of MMP-2 and MT-MMP1 metalloproteinases in human endothelial cells. Arterioscler Thromb Vasc Biol 1997, 17:3185–3190.View ArticlePubMedGoogle Scholar
- Takahashi N, Tetsuka T, Uranishi H, Okamoto T: Inhibition of the NF-kappaB transcriptional activity by protein kinase A. Eur J Biochem 2002, 269:4559–4565.View ArticlePubMedGoogle Scholar
- Yoshimura S, Morishita R, Hayashi K, Yamamoto K, Nakagami H, Kaneda Y, Sakai N, Ogihara T: Inhibition of intimal hyperplasia after balloon injury in rat carotid artery model using cis-element 'decoy' of nuclear factor-kappaB binding site as a novel molecular strategy. Gene Ther 2001, 8:1635–1642.View ArticlePubMedGoogle Scholar
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 (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.