Pk10453, a nonselective platelet-derived growth factor receptor inhibitor, prevents the progression of pulmonary arterial hypertension

Venkatrao Medarametla, Stephen Festin, Chuluunbaatar Sugarragchaa, Alexander Eng, Amir Naqwi, Timothy Wiedmann, Lawrence S. Zisman

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

The platelet-derived growth factor (PDGF) signaling pathway has been found to be activated in human pulmonary arterial hypertension (PAH) and in animal models of the disease. Our study tested the hypothesis that a novel, nonselective inhaled PDGF receptor inhibitor, PK10453, would decrease pulmonary hypertension both in the rat monocrotaline (MCT) model and the rat MCT plus pneumonectomy (MCT+PN) model of PAH. PK10453, delivered by inhalation for 4 (D4)- and 8 (D8)-minute exposures 3 times a day for 2 weeks, decreased right ventricular systolic pressure (RVSP) in both the rat MCT and rat MCT+PN models: RVSP was 80.4±2.6 mmHg in the vehicle MCT group (n=6), 44.4±5.8 mmHg in the D4 MCT group (n=6), and 37.1±4.5 mmHg in the D8 MCT group (n=5; P < 0.001 vs. vehicle); RVSP was 75.7±7.1 mmHg in the vehicle MCT+PN group (n=9), 40.4±2.7 mmHg in the D4 MCT+PN group (n=10), and 43.0±3.0 mmHg in the D8 MCT+PN group (n=8; P < 0.001). In the rat MCT+PN model, continuous telemetry monitoring of pulmonary artery pressures also demonstrated that PK10453 prevented the progression of PAH. Imatinib given by inhalation was equally effective in the MCT model but was not effective in the MCT+PN model. Immunohistochemistry demonstrated increased activation of the PDGF β receptor compared to the PDGFα receptor in neointimal and perivascular lesions found in the MCT+PN model. We show that imatinib is selective for the PDGF α receptor, whereas PK10453 has a lower half-maximal inhibitor concentration (IC50) for inhibition of kinase activity of both the PDGF α and PDGFβ receptors compared to imatinib. In conclusion, PK10453, when delivered by inhalation, significantly decreased the progression of PAH in the rat MCT and MCT+PN models. Nonselective inhibition of both the PDGF α and PDGF β r ceptors may have a therapeutic advantage over selective PDGF α receptor inhibition in PAH.

Original languageEnglish (US)
Pages (from-to)82-102
Number of pages21
JournalPulmonary Circulation
Volume4
Issue number1
DOIs
StatePublished - Mar 1 2014

Keywords

  • Kinase inhibitors
  • Platelet-derived growth factor (PDGF)
  • Pulmonary arterial hypertension

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