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Carbon monoxide: a novel pulmonary artery vasodilator in neonatal llamas of the Andean altiplano

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2008
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Herrera Videla, Emilio
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Carbon monoxide: a novel pulmonary artery vasodilator in neonatal llamas of the Andean altiplano
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Author
  • Herrera Videla, Emilio;
  • Reyes, Roberto V.;
  • Giussani, Dino A.;
  • Riquelme González, Raquel;
  • Sanhueza Reinoso, Emilia;
  • Ebensperger Darrouy, Germán;
  • Casanello, Paola;
  • Méndez, Natalia;
  • Ebensperger, Renato;
  • Sepúlveda Kattan, Esteban;
  • Pulgar, Víctor M.;
  • Cabello, Gertrudis;
  • Blanco, Carlos E.;
  • Hanson, Mark A.;
  • Parer, Julian T.;
  • Llanos Mansilla, Jorge;
Abstract
Aims To study the nitric oxide (NO) and carbon monoxide roles in the regulation of the pulmonary circulation in lowland and highland newborn sheep and llamas. Methods and results We used neonatal sheep (Ovis aries) and llamas (Lama glama) whose gestation and delivery took place at low (580 m) or high (3600 m) altitude. In vivo, we measured the cardiopulmonary function basally and with a NO synthase (NOS) blockade and calculated the production of carbon monoxide by the lung. In vitro, we determined NOS and soluble guanylate cyclase (sGC) expression, NOS activity, and haemoxygenase (HO) expression in the lung. Pulmonary arterial pressure was elevated at high altitude in sheep but not in llamas. Sheep at high altitude relative to sea level had significantly greater total lung NOS activity and eNOS protein, but reduced sGC and HO expression and carbon monoxide production. In contrast, llamas showed no difference in NO function between altitudes, but a pronounced increase in pulmonary carbon monoxide production and HO expression at high altitude. Conclusions In the llama, enhanced pulmonary carbon monoxide, rather than NO, protects against pulmonary hypertension in the newborn period at high altitude. This shift in pulmonary dilator strategy from NO to carbon monoxide has not been previously described, and it may give insight into new treatments for excessive pulmonary vasoconstriction.
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This work was funded by the Fondo Nacional de Ciencia y Tecnologı´a (FONDECYT), Chile, Grant 1050479 and The Wellcome Trust Collaborative Research Initiative (CRIG), UK, Grant 072256. E.A.H. was a Fellow of Programa de Mejoramiento de la Calidad y la Equidad de la Educacio´n Superior (MECESUP), Chile, Grant UCh0115 and Beca Universidad de Chile, Grant PG/54/2005 (PhD programme).
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URI: https://repositorio.uchile.cl/handle/2250/128461
DOI: doi:10.1093/cvr/cvm013
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Cardiovascular Research (2008) 77, 197–201
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