{"title":"Modulation of Substance P-Induced K+ Current in Coronary Endothelium","authors":"N. R. Sharma, M. Davis","doi":"10.3109/10623329609024695","DOIUrl":null,"url":null,"abstract":"Substance P (SP) activates an outward K+ current, membrane hyperpolarization and increases cytosolic Ca2+ ([Ca2+],) in porcine coronary artery endothelial cells (PCAECs). We tested the importance of Ca2+, CAMP, cGMP, arachidonic acid and G protein-linked pathways in modulating whole-cell K+ currents activated by SP. Current or membrane potential and [Ca2+], were measured simultaneously in single cells in response to SP (10 nM), using the perforated patch technique and fura-2 microfluorimetry. Partial block of Kcachannels by D-tubocurarine resulted in a significant reduction in SP-induced membrane hyperpolarization and the plateau phase of the cell [Ca2+]i response. In PCAECs preloaded with BAPTA, SP failed to elevate [Ca2+]i or activate outward current. In Ca2+-free bath solution, SP induced transient elevations in [Ca2+]i and outward current. With SP still present, addition of 1 mM Ca2+ to the bath after [Ca2+]i returned to resting levels elevated [Ca2+]i and elicited outward current. Acute application o...","PeriodicalId":11588,"journal":{"name":"Endothelium-journal of Endothelial Cell Research","volume":"29 1","pages":"189-197"},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endothelium-journal of Endothelial Cell Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10623329609024695","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Substance P (SP) activates an outward K+ current, membrane hyperpolarization and increases cytosolic Ca2+ ([Ca2+],) in porcine coronary artery endothelial cells (PCAECs). We tested the importance of Ca2+, CAMP, cGMP, arachidonic acid and G protein-linked pathways in modulating whole-cell K+ currents activated by SP. Current or membrane potential and [Ca2+], were measured simultaneously in single cells in response to SP (10 nM), using the perforated patch technique and fura-2 microfluorimetry. Partial block of Kcachannels by D-tubocurarine resulted in a significant reduction in SP-induced membrane hyperpolarization and the plateau phase of the cell [Ca2+]i response. In PCAECs preloaded with BAPTA, SP failed to elevate [Ca2+]i or activate outward current. In Ca2+-free bath solution, SP induced transient elevations in [Ca2+]i and outward current. With SP still present, addition of 1 mM Ca2+ to the bath after [Ca2+]i returned to resting levels elevated [Ca2+]i and elicited outward current. Acute application o...