Lh. Clapp et al., CA2-ACTIVATED CL- CURRENTS IN PULMONARY ARTERIAL MYOCYTES(), American journal of physiology. Heart and circulatory physiology, 39(5), 1996, pp. 1577-1584
Currents from smooth muscle cells isolated from the pulmonary arterial
tree of the rat were recorded under voltage clamp using the whole cel
l configuration of the patch-clamp technique. Rapid increases in cytos
olic free calcium evoked by flash photolysis of Nitr-5 activated a cur
rent that, following ion substitution and pharmacological experiments,
proved to be carried by Cl-. This current [I-Cl(Ca)] was evoked indep
endently of photolytic by-products and, although smaller, was still ac
tivated in the absence of pipette ATP. Experiments revealed that I-CI(
Ca) was evoked in 80% of the cells isolated from the main pulmonary ar
tery but only in 43% of the cells isolated from small vessels (200-400
mu m ID). Application of caffeine also resulted in activation of I-Cl
(Ca), although the response current magnitude was larger in the main p
ulmonary artery. Photolysis of Nitr-5 still activated I-Cl(Ca) in the
presence of caffeine, suggesting that Ca2+ release is not a prerequisi
te for activation of I-Cl(Ca). These results represent the first elect
rophysiological recordings of Cl- currents from small pulmonary arteri
al vessels and indicate that their Ca2+ regulation and/or distribution
may be different throughout the pulmonary circulation.