Literature DB >> 9396467

Ca2+ release from intracellular stores is an initial step in hypoxic pulmonary vasoconstriction of rat pulmonary artery resistance vessels.

C H Gelband1, H Gelband.   

Abstract

BACKGROUND: A reduction in oxygen tension in the lungs is believed to inhibit a voltage-dependent K+ (Kv) current, which is thought to result in membrane depolarization leading to hypoxic pulmonary vasoconstriction (HPV). However, the direct mechanism by which hypoxia inhibits Kv current is not understood. METHODS AND
RESULTS: Experiments were performed on rat pulmonary artery resistance vessels and single smooth muscle cells isolated from these vessels to examine the role of Ca2+ release from intracellular stores in initiating HPV. In contractile experiments, hypoxic challenge of endothelium-denuded rat pulmonary artery resistance vessels caused either a sustained or transient contraction in Ca2+-containing or Ca2+-free solution, respectively (n=44 vessels from 11 animals). When the ring segments were treated with either thapsigargin (5 micromol/L), ryanodine (5 micromol/L), or cyclopiazonic acid (5 micromol/L) in Ca2+-containing or Ca2+-free solution, a significant increase in pulmonary arterial tone was observed (n=44 vessels from 11 animals). Subsequent hypoxic challenge in the presence of each agent produced no further increase in tone (n=44 vessels from 11 animals). In isolated pulmonary resistance artery cells loaded with fura 2, hypoxic challenge, thapsigargin, ryanodine, and cyclopiazonic acid resulted in a significant increase in [Ca2+]i (n=18 cells from 6 animals) and depolarization of the resting membrane potential (n=22 cells from 6 animals). However, with prior application of thapsigargin, ryanodine, or cyclopiazonic acid, a hypoxic challenge produced no further change in [Ca2+]i (n=18 from 6 animals) or membrane potential (n=22 from 6 animals). Finally, application of an anti-Kv1.5 antibody increased [Ca2+]i and caused membrane depolarization. Subsequent hypoxic challenge resulted in a further increase in [Ca2+]i with no effect on membrane potential (n=16 cells from 4 animals).
CONCLUSIONS: In rat pulmonary artery resistance vessels, an initial event in HPV is a release of Ca2+ from intracellular stores. This rise in [Ca2+]i causes inhibition of voltage-dependent K+ channels (possibly Kv1.5), membrane depolarization, and an increase in pulmonary artery tone.

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Year:  1997        PMID: 9396467     DOI: 10.1161/01.cir.96.10.3647

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  15 in total

1.  Voltage-independent calcium entry in hypoxic pulmonary vasoconstriction of intrapulmonary arteries of the rat.

Authors:  T P Robertson; D Hague; P I Aaronson; J P Ward
Journal:  J Physiol       Date:  2000-06-15       Impact factor: 5.182

2.  Functional ion channels in human pulmonary artery smooth muscle cells: Voltage-dependent cation channels.

Authors:  Amy L Firth; Carmelle V Remillard; Oleksandr Platoshyn; Ivana Fantozzi; Eun A Ko; Jason X-J Yuan
Journal:  Pulm Circ       Date:  2011-01-01       Impact factor: 3.017

Review 3.  Hypoxia. 4. Hypoxia and ion channel function.

Authors:  Larissa A Shimoda; Jan Polak
Journal:  Am J Physiol Cell Physiol       Date:  2010-12-22       Impact factor: 4.249

4.  Divergent roles of glycolysis and the mitochondrial electron transport chain in hypoxic pulmonary vasoconstriction of the rat: identity of the hypoxic sensor.

Authors:  R M Leach; H M Hill; V A Snetkov; T P Robertson; J P Ward
Journal:  J Physiol       Date:  2001-10-01       Impact factor: 5.182

5.  Hypoxia reduces KCa channel activity by inducing Ca2+ spark uncoupling in cerebral artery smooth muscle cells.

Authors:  Guiling Zhao; Adebowale Adebiyi; Qi Xi; Jonathan H Jaggar
Journal:  Am J Physiol Cell Physiol       Date:  2007-02-21       Impact factor: 4.249

Review 6.  ROS-dependent signaling mechanisms for hypoxic Ca(2+) responses in pulmonary artery myocytes.

Authors:  Yong-Xiao Wang; Yun-Min Zheng
Journal:  Antioxid Redox Signal       Date:  2010-03-01       Impact factor: 8.401

7.  Heterogeneous gene expression and functional activity of ryanodine receptors in resistance and conduit pulmonary as well as mesenteric artery smooth muscle cells.

Authors:  Yun-Min Zheng; Qing-Song Wang; Qing-Hua Liu; Rakesh Rathore; Vishal Yadav; Yong-Xiao Wang
Journal:  J Vasc Res       Date:  2008-04-23       Impact factor: 1.934

8.  PLCγ1-PKCε-IP3R1 signaling plays an important role in hypoxia-induced calcium response in pulmonary artery smooth muscle cells.

Authors:  Vishal R Yadav; Tengyao Song; Lin Mei; Leroy Joseph; Yun-Min Zheng; Yong-Xiao Wang
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-02-01       Impact factor: 5.464

9.  Ca2+ responses of pulmonary arterial myocytes to acute hypoxia require release from ryanodine and inositol trisphosphate receptors in sarcoplasmic reticulum.

Authors:  Jian Wang; Larissa A Shimoda; J T Sylvester
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2012-05-11       Impact factor: 5.464

Review 10.  Hypoxic pulmonary vasoconstriction.

Authors:  J T Sylvester; Larissa A Shimoda; Philip I Aaronson; Jeremy P T Ward
Journal:  Physiol Rev       Date:  2012-01       Impact factor: 46.500

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