Estrogen, like other steroids, is now believed to possess rapid membra
ne effects independent of the classical gene activation pathway of ste
roid action. The presence of membrane estrogen receptors has been demo
nstrated in different cell types, but not yet in vascular tissue. In v
ivo, estrogen administration rapidly promotes acetylcholine-induced va
sodilation of the coronary and peripheral vascular beds of postmenopau
sal women. Estrogen also causes relaxation of precontracted isolated a
rterial segments and perfused organ preparations, within minutes of ad
ministration of the hormone. These rapid vasomotor effects of estrogen
may be related to blockade of the cell membrane voltage-dependent cal
cium channels, resulting in inhibition of extracellular Ca2+ mobilizat
ion and flux. Recently, estradiol has been shown to rapidly affect cyc
lic nucleotide turnover in vascular segments, smooth muscle, and epith
elial cell cultures, suggesting the possibility of a ''cross-talk'' be
tween membrane-mediated events and nuclear receptor activation.