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K(V)7 channels are involved in hypoxia-induced vasodilatation of porcine coronary arteries

Hedegaard, E. R. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark
Nielsen, B. D. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark.; Dept Rheumatol, Aarhus Univ Hosp, Aarhus, Denmark
Kun, A. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark
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Hughes, A. D. (author)
Fac Med, Natl Heart & Lung Inst, Univ London Imperial Coll Sci Technol & Med, London, England
Kroigaard, C. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark
Mogensen, S. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark
Matchkov, V. V. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark
Fröbert, Ole, 1964- (author)
Region Örebro län,Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, University of Aarhus, Aarhus, Denmark; Department of Cardiology, Örebro University Hospital, Örebro, Sweden
Simonsen, U. (author)
Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark
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Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark Dept Biomed Pulm & Cardiovasc Pharmacol, Univ Aarhus, Aarhus, Denmark; Dept Rheumatol, Aarhus Univ Hosp, Aarhus, Denmark (creator_code:org_t)
2013-12-10
2014
English.
In: British Journal of Pharmacology. - : Wiley-Blackwell. - 0007-1188 .- 1476-5381. ; 171:1, s. 69-82
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background and PurposeHypoxia causes vasodilatation of coronary arteries, but the underlying mechanisms are poorly understood. We hypothesized that hypoxia reduces intracellular Ca2+ concentration ([Ca2+](i)) by opening of K channels and release of H2S. Experimental ApproachPorcine coronary arteries without endothelium were mounted for measurement of isometric tension and [Ca2+](i), and the expression of voltage-gated K channels K(V)7 channels (encoded by KCNQ genes) and large-conductance calcium-activated K channels (K(Ca)1.1) was examined. Voltage clamp assessed the role of K(V)7 channels in hypoxia. Key ResultsGradual reduction of oxygen concentration from 95 to 1% dilated the precontracted coronary arteries and this was associated with reduced [Ca2+](i) in PGF(2) (10M)-contracted arteries whereas no fall in [Ca2+](i) was observed in 30mM K-contracted arteries. Blockers of ATP-sensitive voltage-gated potassium channels and K(Ca)1.1 inhibited hypoxia-induced dilatation in PGF(2)-contracted arteries; this inhibition was more marked in the presence of the K(v)7 channel blockers, XE991 and linopirdine, while a K(V)7.1 blocker, failed to change hypoxic vasodilatation. XE991 also inhibited H2S- and adenosine-induced vasodilatation. PCR revealed the expression of K(V)7.1, K(V)7.4, K(V)7.5 and K(Ca)1.1 channels, and K(Ca)1.1, K(V)7.4 and K(V)7.5 were also identified by immunoblotting. Voltage clamp studies showed the XE991-sensitive current was more marked in hypoxic conditions. ConclusionThe K(V)7.4 and K(V)7.5 channels, which we identified in the coronary arteries, appear to have a major role in hypoxia-induced vasodilatation. The voltage clamp results further support the involvement of K(V)7 channels in this vasodilatation. Activation of these K(V)7 channels may be induced by H2S and adenosine.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

potassium channels
K(V)7
H2S
adenosine
hypoxia
calcium
coronary
vasodilatation

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