{"title":"Effect of capsaicin on membrane currents in cultured vascular smooth muscle cells of rat aorta","authors":"Yi-Ching Lo , Sheng-Nan Wu , Jiunn-Ren Wu , Ing-Jun Chen","doi":"10.1016/0926-6917(95)90039-X","DOIUrl":null,"url":null,"abstract":"<div><p>The application of capsaicin (1 μM) produced a minor relaxant effect in endothelium-denuded rat aortae. However, capsaicin caused a greater relaxation of blood vessels precontracted with high K<sup>+</sup> or phenylephrine. The effects of capsaicin on the ionic currents were also examined in A7r5 vascular smooth muscle cells. The tight-seal whole-cell voltage clamp technique was used. Capsaicin inhibited the Ba<sup>2+</sup> inward current (I<sub>Ba</sub>) through the voltage-dependent L-type Ca<sup>2+</sup> channel in a concentration-dependent fashion, whereas calcitonin gene-related peptide and phenylephrine produced a minor increase in I<sub>Ba</sub>. Capsaicin did not alter the overall shape of current-voltage relationship of I<sub>Ba</sub>. However, capsaicin (3 μM) shifted the quasi-steady-state inactivation curve of I<sub>Ba</sub> to more negative membrane potential by about 5 mV. These effects of capsaicin on I<sub>Ba</sub> were reversible. In addition, capsaicin had inhibitory effects on voltage dependent K<sup>+</sup> currents. These results suggest that inhibition of the voltage-dependent L-type Ca<sup>2+</sup> channel is involved in the capsaicin-induced relaxation of the vascular smooth muscle, whereas capsaicin-induced inhibition of voltage-dependent K<sup>+</sup> channels might produced an increase in cell excitability.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"292 3","pages":"Pages 321-328"},"PeriodicalIF":0.0000,"publicationDate":"1995-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)90039-X","citationCount":"23","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/092669179590039X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 23
Abstract
The application of capsaicin (1 μM) produced a minor relaxant effect in endothelium-denuded rat aortae. However, capsaicin caused a greater relaxation of blood vessels precontracted with high K+ or phenylephrine. The effects of capsaicin on the ionic currents were also examined in A7r5 vascular smooth muscle cells. The tight-seal whole-cell voltage clamp technique was used. Capsaicin inhibited the Ba2+ inward current (IBa) through the voltage-dependent L-type Ca2+ channel in a concentration-dependent fashion, whereas calcitonin gene-related peptide and phenylephrine produced a minor increase in IBa. Capsaicin did not alter the overall shape of current-voltage relationship of IBa. However, capsaicin (3 μM) shifted the quasi-steady-state inactivation curve of IBa to more negative membrane potential by about 5 mV. These effects of capsaicin on IBa were reversible. In addition, capsaicin had inhibitory effects on voltage dependent K+ currents. These results suggest that inhibition of the voltage-dependent L-type Ca2+ channel is involved in the capsaicin-induced relaxation of the vascular smooth muscle, whereas capsaicin-induced inhibition of voltage-dependent K+ channels might produced an increase in cell excitability.