TY - JOUR
T1 - Properties of large-conductance K+ channels in human myometrium during pregnancy and labour
AU - Khan, R. N.
AU - Smith, S. K.
AU - Morrison, J. J.
AU - Ashford, M. L.J.
PY - 1993
Y1 - 1993
N2 - The conversion of the electrically silent pregnant uterus to highly excitable at term represents a dramatic physiological event which is poorly understood. Here we provide the first description, from single-channel recordings, of a large conductance (212 pS) calcium-activated potassium channel (BK(Ca)) in human pregnant myometrium which, in labour tissue, is either absent or has been considerably altered in its physiological and pharmacological properties. In the latter, the K+ channels have an identical conductance (221 pS) and K+ selectivity to BK(Ca) channels but exhibit no Ca2+ or voltage sensitivity. We have termed these BK channels. Furthermore, the activity of the BK(Ca) channel from pregnant tissue is inhibited by internal application of Ba2+ but not tetraethylammonium (TEA), whereas the activity of the BK channel is sensitive to internal TEA but not Ba2+. The role of the BK(Ca) channel may be to suppress myometrial activity during gestation whereas BK channel activity may be important in providing a Ca2+- independent K+ conductance which would allow cytoplasmic Ca2+ levels to rise without activating a counteracting Ca2+-dependent outward current, normally provided by the BK(Ca) channels which, by its very nature, would tend to oppose depolarization. The findings suggest that K+ channels may have an important role in determining the functional activity of the myometrium.
AB - The conversion of the electrically silent pregnant uterus to highly excitable at term represents a dramatic physiological event which is poorly understood. Here we provide the first description, from single-channel recordings, of a large conductance (212 pS) calcium-activated potassium channel (BK(Ca)) in human pregnant myometrium which, in labour tissue, is either absent or has been considerably altered in its physiological and pharmacological properties. In the latter, the K+ channels have an identical conductance (221 pS) and K+ selectivity to BK(Ca) channels but exhibit no Ca2+ or voltage sensitivity. We have termed these BK channels. Furthermore, the activity of the BK(Ca) channel from pregnant tissue is inhibited by internal application of Ba2+ but not tetraethylammonium (TEA), whereas the activity of the BK channel is sensitive to internal TEA but not Ba2+. The role of the BK(Ca) channel may be to suppress myometrial activity during gestation whereas BK channel activity may be important in providing a Ca2+- independent K+ conductance which would allow cytoplasmic Ca2+ levels to rise without activating a counteracting Ca2+-dependent outward current, normally provided by the BK(Ca) channels which, by its very nature, would tend to oppose depolarization. The findings suggest that K+ channels may have an important role in determining the functional activity of the myometrium.
UR - https://www.scopus.com/pages/publications/0027406230
U2 - 10.1098/rspb.1993.0002
DO - 10.1098/rspb.1993.0002
M3 - Article
AN - SCOPUS:0027406230
SN - 0962-8452
VL - 251
SP - 9
EP - 15
JO - Proceedings of the Royal Society B: Biological Sciences
JF - Proceedings of the Royal Society B: Biological Sciences
IS - 1330
ER -