This article reviews the contribution of ion channels to membrane potential
, the ion channels expressed in myometrium, and the effect of ion channel a
ctivity on the control of myometrial intracellular free calcium. Plasma mem
branes constitute barriers to permeability that establish concentration gra
dients of ions inside versus outside the cell. Na+, Ca2+, and Cl- are norma
lly in higher concentration gradients of ions inside whereas K+ is higher i
nside. In myometrium, Ca2+ entry into cells mediated myometrial membrane po
tential changes and serves as the internal signal for contraction. K+ efflu
x is thought to promote repolarization after an action potential and to par
ticipate in setting the resting membrane potential. Ions cross the cell mem
brane through channels that have different regulated properties and selecti
vities. Ion movement has been measured by a number of techniques, including
radiolabeled ion flux, use of intracellular indicators,a nd patch-clamp me
thodology. A number of myometrial Ca2+ channels have been described, includ
ing voltage-regulated L-type channels and Ca2+ entry in response to intrace
llular Ca2+ store depletion. Fast Na+ channels may contribute to cation ent
ry late in pregnancy. K+ channels in myometrium include Ca2+-activated chan
nels, a delayed rectifier, and an inward rectifier. A Ca2+-activated Cl- ch
annel is also present in myometrium. In addition to being regulated by Ca2, the activity of a number of these channels can be regulated by uterine co
ntractants and relaxants. regulation of ion channel activity can affect int
racellular free Ca2+ concentrations in the myometrium. Therefore, control o
f ion channel activity represents one of several approaches for controlling
myometrial contractile activity. Copyright (C) 2000 by the Society for Gyn
ecologic Investigation.