Inhibition of voltage-gated K+ currents by endothelin-1 in human pulmonary arterial myocytes

Larissa A. Shimoda, J. T. Sylvester, Gregory M. Booth, Tenille H. Shimoda, Sonya Meeker, Bradley J. Undem, James S. K. Sham
2001 American Journal of Physiology - Lung cellular and Molecular Physiology  
Inhibition of voltage-gated K ϩ currents by endothelin-1 in human pulmonary arterial myocytes. Am J Physiol Lung Cell Mol Physiol 281: L1115-L1122, 2001.-Recent studies demonstrate that endothelin-1 (ET-1) constricts human pulmonary arteries (PA). In this study, we examined possible mechanisms by which ET-1 might constrict human PA. In smooth muscle cells freshly isolated from these arteries, whole cell patch-clamp techniques were used to examine voltage-gated K ϩ (KV) currents. K V currents
more » ... e isolated by addition of 100 nM charybdotoxin and were identified by current characteristics and inhibition by 4-aminopyridine (10 mM). ET-1 (10 Ϫ8 M) caused significant inhibition of KV current. Staurosporine (1 nM), a protein kinase C (PKC) inhibitor, abolished the effect of ET-1. Rings of human intrapulmonary arteries (0.8-2 mm OD) were suspended in tissue baths for isometric tension recording. ET-1-induced contraction was maximal at 10 Ϫ8 M, equal to that induced by K V channel inhibition with 4-aminopyridine, and attenuated by PKC inhibitors. These data suggest that ET-1 constricts human PA, possibly because of myocyte depolarization via PKC-dependent inhibition of KV. Our results are consistent with data we reported previously in the rat, suggesting similar mechanisms may be operative in both species. lung; protein kinase C; vascular smooth muscle; pulmonary arterial smooth muscle cells
doi:10.1152/ajplung.2001.281.5.l1115 pmid:11597902 fatcat:eocckj7dkndxbgafqtjf6hqf7i