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  4. Perinatal hypoxia triggers alterations in K+ channels of adult pulmonary artery smooth muscle cells.
 
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Titre

Perinatal hypoxia triggers alterations in K+ channels of adult pulmonary artery smooth muscle cells.

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
American Journal of Physiology - Lung Cellular and Molecular Physiology  
Auteur(s)
Marino, M.
Auteure/Auteur
Bény, J.L.
Auteure/Auteur
Peyter, A.C.
Auteure/Auteur
Bychkov, R.
Auteure/Auteur
Diaceri, G.
Auteure/Auteur
Tolsa, J.F.
Auteure/Auteur
Liens vers les personnes
Peyter, Anne-Christine  
Tolsa, Jean-François  
Liens vers les unités
Néonatologie  
ISSN
1040-0605
Statut éditorial
Publié
Date de publication
2007-08
Volume
293
Numéro
5
Première page
L1171
Dernière page/numéro d’article
1182
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article
Résumé
Adverse events during the perinatal period, like hypoxia, have been associated with adult diseases. In pulmonary vessels, K(+) channels play an important role in the regulation of vascular tone. In the fetus, Ca(2+)-activated K(+) channels (K(Ca)) are predominant, whereas from birth voltage-gated K(+) channels (K(V)) prevail in the adult. We postulated that perinatal hypoxia could alter this maturational shift and influence regulation of pulmonary vascular tone in relation to K(+) channels in adulthood. We evaluated the effects of perinatal hypoxia on K(V) and K(Ca) channels in the adult main pulmonary artery (PA) using a murine model. Electrophysiological measurements showed a greater outward current in PA smooth muscle cells of mice born in hypoxia than in controls. In controls, only K(V) channels contributed to this current, whereas in mice born in hypoxia both K(V) and K(Ca) channels were implicated. K(V) channel activity was even higher in mice born in hypoxia than in controls. Therefore, perinatal hypoxia results in increased K(Ca) and K(V) channel activity in adult PA. Moreover, PA of adults born in hypoxia displayed higher large-conductance K(Ca) alpha-subunit and K(V)1.5 alpha-subunit protein expression than controls. Interestingly, relaxation induced by nitric oxide (NO) donors [S-nitroso-N-acetyl-D,l-penicillamine, 2-(N,N-diethylamino)-diazenolate-2-oxide] in isolated PA of control mice was not mediated by K(Ca) channels and only slightly by K(V) channels, whereas following perinatal hypoxia both K(Ca) and K(V) channels contributed to this relaxation. Thus perinatal hypoxia results in altered expression and activity of different K(+) channels in the adult main PA, which could contribute to modifications of pulmonary vasoreactivity.
Sujets

Animals

Anoxia/metabolism

Blotting, Western

Female

Mice

Mice, Inbred C57BL

Muscle, Smooth, Vascu...

Nitric Oxide Donors/p...

Potassium Channels/me...

Pulmonary Artery/cyto...

Vasodilation

PID Serval
serval:BIB_520D1B33E6B2
DOI
10.1152/ajplung.00126.2007
PMID
17720874
WOS
000250870700011
Permalien
https://iris.unil.ch/handle/iris/48261
Date de création
2008-01-25T12:18:02.919Z
Date de création dans IRIS
2025-05-20T14:36:45Z
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