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- W1998332595 endingPage "114" @default.
- W1998332595 startingPage "81" @default.
- W1998332595 abstract "Pulmonary arterial hypertension (PAH) is a hemodynamic abnormality that ultimately results in mortality due to right heart failure. Although the clinical manifestations of primary and secondary PAH are diverse, medial hypertrophy and arterial vasoconstriction are key components in the vascular remodeling leading to PAH. Abnormalities in the homeostasis of intracellular Ca(2+), transmembrane flux of ions, and membrane potential may play significant roles in the processes leading to pulmonary vascular remodeling. Decreased activity of K(+) channels causes membrane depolarization, leading to Ca(2+) influx. The elevated cytoplasmic Ca(2+) is a major trigger for pulmonary vasoconstriction and an important stimulus for vascular smooth muscle proliferation. Dysfunctional K(+) channels have also been linked to inhibition of apoptosis and contribute further to the medial hypertrophy. This review focuses on the relative role of K(+) and Ca(2+) ions and channels in human pulmonary artery smooth muscle cells in the development of PAH." @default.
- W1998332595 created "2016-06-24" @default.
- W1998332595 creator A5034938550 @default.
- W1998332595 creator A5064320372 @default.
- W1998332595 creator A5071225484 @default.
- W1998332595 date "2002-09-01" @default.
- W1998332595 modified "2023-09-29" @default.
- W1998332595 title "Ion channels in pulmonary arterial hypertension" @default.
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