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Pulmonary hypertension. Normal pulmonary vascular bed high-flow low-pressure capacity to dilate and recruit unused vasculature in order to accommodate increases in blood flow normal resting 14 mmHg Pulmonary hypertension
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Pulmonary hypertension • Normal pulmonary vascular bed • high-flow • low-pressure • capacity to dilate and recruit unused vasculaturein order to accommodate increases in blood flow • normal resting 14 mmHg • Pulmonaryhypertension • capacity to dilate is lost resulting in elevated pulmonary artery pressure • pulmonary hypertension 25 mmHg rest
Pulmonary hypertension - pathology • Pulmonary arterial hypertrophy • VSM proliferation • luminal narrowing • intimal hyperplasia in small vessels • thrombotic lesions • intrapulmonary venular fibrosis • Hydrostatic oedema
Pulmonary Hypertension • primary pulmonary hypertension (PPH) • Familial or idiopathic • Very rare • secondary PH • COPD, emphysema, pulmonary fibrosis, immune diseases, preterm birth • Not clear if mechanisms common
Pulmonary vessel hyperplasia in PHDu et al. (2003) NEJM 348:500
Mechanisms of pulmonary hypertension • Decreased endogenous vasodilator activity • eNOS reduced in PA of PPH • decreased PGI2excretion • Impaired K+ channel activity • Increased vasoconstrictor activities • plasma & tissue ET-1 raised in PH • Increased platelet derived activities • 5-HT • TxA2
K+ channel abnormalities in Primary PH (PPH)Archer & Rich (2000) Circulation 102:2782 • Decreased Kv1.5 in PPH • Impaired K+ current in PPH SPH – secondary PH Donor and NPH - normals
5-HT in pulmonary hypertensionMacLean (1999) TIPS 20:490 Blood vessel alveolar lumen
TxA2 and 5-HT in pulmonary hypertensionMacLean (1999) TIPS 20:490 PH TP TP 5-HT1 Arterial contraction Arterial contraction 5HT1 agonist TP – TxA2 receptor TP agonist
Mechanisms of PHArcher & Rich (2000) Circulation 102:2782 Genotype, triggers
Angiopoietin-1 • 70 kDa angiogenic factor essential for lungvascular development • Recruits muscle cells to endothelial tubes, creating arterioles • Produced by smooth-muscle cells and pericytes • Ang-1 k/o die in utero • little arterialdevelopment in the lungs and other organs • Ang-1 minimally detectablein normal human lung after development
Angiopoietin-1 levels correlate with PVRin pulmonary hypertensionDu et al. (2003) NEJM 348:500 Ang-1 mRNA protein
Signalling mechanisms in PH Some PPH : • Mutations in Bone morphogenetic protein receptor (BMPR) • IS BMPR INVOLVED IN OTHER FORMS OF PH?
Angiopoietin decreases BMPR expressionin cultured pulmonary artery endothelial cellsDu et al. (2003) NEJM 348:500 + Ang-1 controls
Signalling molecules in PH Du et al. (2003) NEJM 348:500 PH control Ang-1 – only in PH Ang-2 – little change TIE-2 – little change BMPR – absent in PH
Signalling - summary • BMPR suppressive in PH • Mutation associated with PH • Angiopoetin-1 implicated as causal in pulmonary hypertension • Induces tissue growth and remodelling • Expressed in PH • Suppresses BMPR expression
Pulmonary hypertension therapies • Vasodilators • Ca2+ channel blockers nifedipine, diltiazem • Less than 30% useful response - reduction in PA pressure without reducing cardiac output • continuous i.v. PGI2 • improvement in severe PPH • antiplatelet effects? • Antiproliferative? • Tolerance • inhaled iloprost (stable PGI2 analog) • inhaled NO
Inhaled Iloprost for Severe Pulmonary Hypertension Olschewski et al. (2002) NEJM 347, 322
Inhaled NO in neonatal PH (full term)Tworetsky et al. (2001) Lancet 357, 118 PaO2 kPa • Improved oxygenation in premature neonates • No increased survival PAP/SAP Dose ppm
Inhaled ethyl nitrite gas for persistent pulmonary hypertension of the newborn Moya et al. (2002) Lancet; 360:141 Changes in postductal oxygen saturation during dose escalation of o-nitrosoethanol gas, maintenance, and shut off
Sildenafil Lowers Pulmonary Vascular Resistance in neonatalpigs Shekerdemian et al. (2000) AJRCCM 165, 1098-1102 drug 30 25 20 15 control meconium Mean PA pressure (mmHg) nitric oxide sildenafil 0 60 120 180 240 Time (min)
Change in 6-min walking distance Endothelin antagonists - Bosentan improves exercise tolerance in severe PHChannick et al. (2001) Lancet 358, 1119
Simvastatin attenuates pulmonary artery neointimal formationNishimura et al. (2002) AJRCCM 166,1403-1408 • Normal rat intra-acinar artery • 50% narrowing 4 weeks after injury • C +D Injury plus simvastatin
Simvastatin prevents the development of pulmonary arterial hypertensionNishimura et al. (2002) AJRCCM 166,1403-1408 PMV – pneumonectomy, monocrotaline plus vehicle PMS – injury plus Statin Numbers indicate treatment days after injury
Decrease in eNOS mRNA and its restoration by simvastatinNishimura et al. (2002) AJRCCM 166,1403-1408 PMV – Injury + vehicle control PMS – injury plus Statin
Mechanisms of PHArcher & Rich (2000) Circulation 102:2782 Genotype, triggers