Rm. Drummond et Rm. Wadsworth, CONTRACTION OF THE SHEEP MIDDLE CEREBRAL, PULMONARY AND CORONARY-ARTERIES INITIATED BY RELEASE OF INTRACELLULAR CALCIUM, Journal of autonomic pharmacology, 14(2), 1994, pp. 109-121
1 The aim of the study was to compare contraction initiated by intrace
llular Ca2+ release in the middle cerebral, coronary and pulmonary art
eries of the sheep. With all three arteries from the sheep, incubation
in Ca2+-free physiological salt solution (PSS) reduced agonist-induce
d contraction much more than occurred with the rabbit aorta. The intra
cellular Ca2+ store appeared to be of limited capacity, since contract
ion was transient in Ca2+-free conditions with most agonists. 2 In the
middle cerebral artery, contraction in Ca2+-free conditions was much
reduced if a previous contraction had been obtained (for 5-hydroxytryp
tamine, 5-HT, from 11 +/- 4 to 1 +/- 0.5% of control contraction in 2.
5 mM Ca2+, suggesting that the previous contraction had partly dischar
ged the intracellular Ca2+ store. Contraction was less affected in the
pulmonary artery and almost unaffected in the coronary artery (for 5-
HT, from 15 +/- 1 to 11 +/- 1%) by a previous contraction in Ca2+-free
conditions. 3 Rings prepared from small branches of the pulmonary and
coronary arteries were affected by Ca2+ deprivation in a similar mann
er to large diameter pulmonary and coronary artery rings. 4 In Ca2+-fr
ee PSS, contraction induced by prostaglandin E(2) was almost eliminate
d (3 +/- 1% of control contraction in 2.5 mM Ca2+, contractions induce
d by 5-HT and noradrenaline were reduced, and contraction induced by t
he thromboxane mimetic U46619 was least affected (up to 73 +/- 8%). 5
Increasing agonist concentration from EC(50) to the maximally effectiv
e concentration raised the percentage contraction remaining in the mid
dle cerebral artery (for noradrenaline from 7 +/- 2% to 12 +/- 3%) but
not in the pulmonary artery (for noradrenaline from 22 +/- 2% to 24 /- 6%). 6 The present study has revealed notable differences, in coupl
ing to intracellular Ca2+ release between the three vascular territori
es studied.