The effects of brefeldin A, a putative specific agent that disassemble
s the Golgi apparatus were assessed on the contractility of de-endothe
lised rat aorta. Brefeldin A inhibited, either as pre-or as post-treat
ment, the contractions elicited by K+ (75 mM) or phenylephrine (10 mu
M), being significantly more potent upon the latter. The thapsigargin
(1 mu M)-induced rat aorta contraction was less sensitive to brefeldin
A inhibition. Pre-treatment with brefeldin A (30-100 mu M) did not af
fect phenylephrine-induced transient contractions in Ca2+-free medium,
but strongly inhibited the phenylephrine-induced sustained contractio
ns upon re-admission of Ca2+ to the medium. Brefeldin A was unable to
prevent Ca2+ stores refilling. We concluded that brefeldin A inhibits
Ca2+ entry but not the pathways activated after Ca2+ stores depletion
or the pathways responsible for replenishment of these stores in rat a
orta, presumably by disassembling the Golgi apparatus network. (C) 199
7 Elsevier Science B.V.