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Pulmonary artery hypertension: pertinent vasomotorial cytokines

Shi-Min Yuan

Department of Cardiothoracic Surgery, The First Hospital of Putian, Teaching Hospital, Fujian Medical University, Putian 351100, Fujian Province,People’s Republic of China

* Corresponding Author: Shi-Min Yuan, email

European Cytokine Network 2017, 28(1), 1-7. https://doi.org/10.1684/ecn.2016.0386

Abstract

Pulmonary artery hypertension is a syndrome that shows similar clinical and pathophysiological features characterized by elevated pulmonary arterial pressure and resistance. There have been a series of hypotheses trying to describe the development of pulmonary artery hypertension; however, none of them perfectly explains its pathogenesis. To highlight the pathogenesis, novel vasomotorial cytokines including hypoxia-inducible factor-1α endothelin-1, urotensin II, Krüppel-like factor 4, calcitonin gene-related peptide, angiopoietins and serotonin closely related to pulmonary artery hypertension are discussed. The development of the new agents relating to these cytokines may improve the relevant treatment strategies.

Keywords

cytokines, pathogenesis, pulmonary hypertension

Cite This Article

APA Style
Yuan, S. (2017). Pulmonary artery hypertension: pertinent vasomotorial cytokines. European Cytokine Network, 28(1), 1–7. https://doi.org/10.1684/ecn.2016.0386
Vancouver Style
Yuan S. Pulmonary artery hypertension: pertinent vasomotorial cytokines. Eur Cytokine Network. 2017;28(1):1–7. https://doi.org/10.1684/ecn.2016.0386
IEEE Style
S. Yuan, “Pulmonary artery hypertension: pertinent vasomotorial cytokines,” Eur. Cytokine Network, vol. 28, no. 1, pp. 1–7, 2017. https://doi.org/10.1684/ecn.2016.0386



cc Copyright © 2017 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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