TY - JOUR
T1 - A natriuretic peptides clearance receptor's agonist reduces pulmonary artery pressures and enhances cardiac performance in preclinical models
T2 - New hope for patients with pulmonary hypertension due to left ventricular heart failure
AU - Egom, Emmanuel Eroume
AU - Feridooni, Tiam
AU - Pharithi, Rebabonye B.
AU - Khan, Barkat
AU - Shiwani, Haaris A.
AU - Maher, Vincent
AU - El Hiani, Yassine
AU - Pasumarthi, Kishore B.S.
AU - Ribama, Hilaire A.
N1 - Funding Information:
This study was sponsored by ECTRS Lt (Dartmouth, Canada) and Bonsai Horizons Lt (Dublin, Ireland) (EEE), Grant-in-aid from the Heart and Stroke Foundation of Canada (KP); NSHRF studentship (TF).
Publisher Copyright:
© 2017 Elsevier Masson SAS
PY - 2017/9
Y1 - 2017/9
N2 - Background In patients with left ventricular heart failure (HF), the development of pulmonary hypertension (PH) is common and represents a strong predictor of death. Despite recent advances in the pathophysiological understanding there is as yet no prospect of cure of this deadly clinical entity and the majority of patients continue to progress to right ventricular failure and die. Furthermore, there is no single medical treatment currently approved for PH related to HF. There is, therefore an urgent unmet need to identify novel pharmacological agents that will prevent the progressive increased or reverse the elevated pulmonary arterial pressures while enhancing cardiac performance in HF. Method and results We here reported, for the first time, using a pressure-loop (P-V) conductance catheter system, that a specific natriuretic peptides clearance receptors’ agonist, the ring-deleted atrial natriuretic peptide analogue, cANF4-23 (cANF) reduces pulmonary artery pressures. Strikingly, the administration of the cANF in these mice decreased the RVSP by 50% (n = 5, F 25.687, DF 14, p < 0.001) and heart rate (HR) by 11% (n = 5, F 25.69, DF 14, p < 0.001) as well as enhancing cardiac performance including left ventricular contractility in mice. Most strikingly, mice lacking NPR-C were much more susceptible to develop HF, indicating that NPR-C is a critical protective receptor in the heart. Conclusion Natriuretic peptides clearance receptors’ agonists may, therefore represent a novel and attractive therapeutic strategy for PH related to HF, and ultimately improves the life expectancy and quality for millions of people around the planet.
AB - Background In patients with left ventricular heart failure (HF), the development of pulmonary hypertension (PH) is common and represents a strong predictor of death. Despite recent advances in the pathophysiological understanding there is as yet no prospect of cure of this deadly clinical entity and the majority of patients continue to progress to right ventricular failure and die. Furthermore, there is no single medical treatment currently approved for PH related to HF. There is, therefore an urgent unmet need to identify novel pharmacological agents that will prevent the progressive increased or reverse the elevated pulmonary arterial pressures while enhancing cardiac performance in HF. Method and results We here reported, for the first time, using a pressure-loop (P-V) conductance catheter system, that a specific natriuretic peptides clearance receptors’ agonist, the ring-deleted atrial natriuretic peptide analogue, cANF4-23 (cANF) reduces pulmonary artery pressures. Strikingly, the administration of the cANF in these mice decreased the RVSP by 50% (n = 5, F 25.687, DF 14, p < 0.001) and heart rate (HR) by 11% (n = 5, F 25.69, DF 14, p < 0.001) as well as enhancing cardiac performance including left ventricular contractility in mice. Most strikingly, mice lacking NPR-C were much more susceptible to develop HF, indicating that NPR-C is a critical protective receptor in the heart. Conclusion Natriuretic peptides clearance receptors’ agonists may, therefore represent a novel and attractive therapeutic strategy for PH related to HF, and ultimately improves the life expectancy and quality for millions of people around the planet.
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U2 - 10.1016/j.biopha.2017.07.027
DO - 10.1016/j.biopha.2017.07.027
M3 - Article
C2 - 28738523
AN - SCOPUS:85024867681
SN - 0753-3322
VL - 93
SP - 1144
EP - 1150
JO - Biomedicine and Pharmacotherapy
JF - Biomedicine and Pharmacotherapy
ER -