Endothelium-derived mediators and hypoxic pulmonary vasoconstriction

P I Aaronson, T P Robertson, J P T Ward

    Research output: Contribution to journalLiterature reviewpeer-review

    95 Citations (Scopus)

    Abstract

    The vascular endothelium synthesises, metabolises or converts a multitude of vasoactive mediators, and plays a vital role in the regulation of pulmonary vascular resistance. Its role in hypoxic pulmonary vasoconstriction (HPV) is however controversial. Although HPV has been demonstrated in both pulmonary arteries where the endothelium has been removed and isolated pulmonary artery smooth muscle cells, many reports have shown either partial or complete dependence on an intact endothelium for sustained HPV (> similar to 20 min). However, despite many years of study no known endothelium-derived mediator has yet been unequivocally shown to be essential for HPV, although several may either facilitate the response or act as physiological brakes to limit the extent of HPV. In this article we review the evidence for and against the role of specific endothelium-derived mediators in HPV. We make the case for a facilitatory or permissive function of the endothelium, that in conjunction with a rise in smooth muscle intracellular Ca2+ initiated by a mechanism intrinsic to smooth muscle, allows the development of sustained HPV. In particular, we propose that in response to hypoxia the pulmonary vascular endothelium releases an as yet unidentified agent that causes Ca2+ sensitisation in the smooth muscle. (C) 2002 Elsevier Science B.V. All rights reserved.
    Original languageEnglish
    Pages (from-to)107 - 120
    Number of pages14
    JournalRESPIRATORY PHYSIOLOGY AND NEUROBIOLOGY
    Volume132
    Issue number1
    Publication statusPublished - 22 Aug 2002

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