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Effects of lemakalim on changes in Ca2+ concentration and mechanical activity induced by noradrenaline in the rabbit mesenteric artery.
- Source :
-
British journal of pharmacology [Br J Pharmacol] 1991 Sep; Vol. 104 (1), pp. 227-33. - Publication Year :
- 1991
-
Abstract
- 1. Effects of (-)-cromakalim (lemakalim) on tension and Ca2+ mobilization induced by noradrenaline (NA) were investigated by measuring intracellular Ca2+ concentration ([Ca2+]i) isometric tension and production of inositol-1,4,5-trisphosphate (IP3) in smooth muscle strips of the rabbit mesenteric artery. 2. In thin smooth muscle strips, 10 microM NA produced a large phasic, followed by a small tonic increase in [Ca2+]i, which correlated well with the evoked phasic and tonic contractions, respectively. Lemakalim (0.1-10 microM) lowered the resting [Ca2+]i without a decrease in the resting tension, and also inhibited the increased [Ca2+]i and tension induced by 10 microM NA, all in a concentration-dependent manner. Glibenclamide (1 microM) inhibited these actions of lemakalim. 3. In Ca(2+)-free solution containing 2 mM EGTA, NA (10 microM) transiently increased [Ca2+]i, tension and synthesis of IP3. Lemakalim (over 0.01 microM) inhibited these actions of NA in Ca(2+)-free solution containing 5.9 mM K+, but not in Ca(2+)-free solution containing 128 mM K+. These actions of lemakalim were prevented by glibenclamide (1 microM). Lemakalim (1 microM) did not modify the increases in [Ca2+]i and tension induced by 10 mM caffeine. 4. In beta-escin-skinned strips, 10 microM NA increased [Ca2+]i in Ca(2+)-free solution containing 50 microM EGTA, 3 microM guanosine triphosphate (GTP) and 2 microM Fura 2 after the storage sites were loaded by application of 0.3 microM Ca2+ for 2 min, suggesting that Ca2+ is released from intracellular storage sites following activation of the alpha-adrenoceptor. Lemakalim (1 microM) did not inhibit the Ca2+ release from storage sites induced by NA. 5. We conclude that lemakalim inhibits NA-induced Ca2 + release due to inhibition of NA-induced 'P3 production in a manner dependent on the membrane potential and causes inhibition of the phasic contraction induced by NA.
- Subjects :
- Animals
Benzopyrans antagonists & inhibitors
Calcium physiology
Cromakalim
Escin pharmacology
In Vitro Techniques
Inositol 1,4,5-Trisphosphate biosynthesis
Isometric Contraction drug effects
Male
Membrane Potentials drug effects
Mesenteric Arteries drug effects
Mesenteric Arteries metabolism
Muscle Contraction drug effects
Muscle, Smooth, Vascular metabolism
Myelin Sheath physiology
Neuromuscular Depolarizing Agents pharmacology
Norepinephrine pharmacology
Pyrroles antagonists & inhibitors
Rabbits
Benzopyrans pharmacology
Calcium metabolism
Muscle, Smooth, Vascular drug effects
Norepinephrine antagonists & inhibitors
Pyrroles pharmacology
Vasodilator Agents pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0007-1188
- Volume :
- 104
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- British journal of pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 1786512
- Full Text :
- https://doi.org/10.1111/j.1476-5381.1991.tb12411.x