Abstract
Spontaneous inward and outward currents were studied with perforated patch recording in freshly dispersed rabbit pulmonary artery smooth muscle cells. With physiological potassium concentrations, spontaneous outward and inward currents were recorded at negative membrane potentials. Ion substitution experiments revealed that the outward and inward currents were respectively potassium and chloride conductance increases. Both conductances were abolished by bath application of caffeine (2-10 mM), which releases calcium from internal stores. The rise time and half-decay time of spontaneous potassium currents were both about 25 ms. The spontaneous chloride current has a rise time of 30 ms and decayed exponentially with a time constant (tau) of 70 ms at -50 mV. The tau value was increased by depolarization and increased e-fold for a change of 99 mV in membrane potential. In every cell examined when the spontaneous currents occurred as biphasic events, typically between -20 mV and -40 mV, outward currents preceded inward currents in over 90% of these events whereas the inward current always preceded the outward current in caffeine- and noradrenaline-evoked responses. An explanation for these data is that there may be localization of some chloride channels with respect to the caffeine-sensitive calcium store.
MeSH Terms
Animals
Caffeine/pharmacology
Calcium/physiology
Chloride Channels/drug effects,metabolism
Female
In Vitro Techniques
Ion Channel Gating/drug effects,physiology
Ion Channels/drug effects,metabolism
Male
Membrane Potentials/drug effects,physiology
Muscle, Smooth, Vascular/cytology,drug effects,metabolism
Norepinephrine/pharmacology
Potassium/physiology
Pulmonary Artery/cytology,drug effects,metabolism
Rabbits
Chemicals
Chloride Channels
Ion Channels
Caffeine
Potassium
Calcium
Norepinephrine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hogg R C
Department of Pharmacology and Clinical Pharmacology, St. George's Hospital Medical School, London, UK.
Wang Q
Helliwell R M
Large W A
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