Ca(2+)‐activated Cl‐ and K+ channels and their modulation by endothelin‐1 in rat pulmonary arterial smooth muscle cells

KJ Salter*, JL Turner, S. Albarwani, LH Clapp, RZ Kozlowski

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةArticleمراجعة النظراء

33 اقتباسات (Scopus)


Using the patch‐clamp recording technique, we observed that endothelin‐1 (ET‐1; 0.8‐16 nM) enhanced a voltage‐activated outward current (Iout) and induced periodic oscillations of inward current in smooth muscle cells isolated from small pulmonary arteries (200‐400 microns in diameter). Anion substitution experiments revealed that the ET‐1‐induced inward current was carried by Cl‐ ions. Application of bosentan (10 microM; and ETA and ETB receptor antagonist) and FR 139317 (1‐10 microM; a selective ETA receptor antagonist) prevented initiation of inward currents or enhancement of Iout by ET‐1. The ETB receptor agonist tetra‐Ala‐endothelin‐1 (1‐20 nM) failed to evoke these responses. Caffeine (10 mM) induced a single transient inward current and prevented any further activation of inward current, or enhancement of Iout, by subsequent application of 16 nM ET‐1, suggesting that these currents were mediated by Ca2+ release from internal stores. Rapid intracellular release of Ca2+ by photolysis of nitr‐5 activated an inward Cl‐ current and increased the magnitude of Iout. These results demonstrate the existence of Ca(2+)‐activated Cl‐ and K+ channels in pulmonary arterial smooth muscle. The physiological role of these channels is at present uncertain, although their activation may be involved in the contractile responses of pulmonary arterial smooth muscle to ET‐1.

اللغة الأصليةEnglish
الصفحات (من إلى)815-824
عدد الصفحات10
دوريةExperimental Physiology
مستوى الصوت80
رقم الإصدار5
المعرِّفات الرقمية للأشياء
حالة النشرPublished - سبتمبر 1 1995

ASJC Scopus subject areas

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