The aim of the present study was to investigate the effect of omeprazole, a
n H+-K+-ATPase inhibitor, in myometrial smooth muscle strips from women und
ergoing elective caesarean section at term. Isolated myometrial strips take
n with informed consent were obtained from eight pregnant women undergoing
elective caesarean section at term (not in labour) and mounted in organ bat
hs for recording of isometric tension. We recorded the effect of increasing
concentrations of omeprazole on spontaneous and Ca2+-induced contractions
of myometrial smooth muscle and on contractions of myometrial smooth muscle
pretreated with indomethacin (3x10(-6) M) and L-NAME (3 x 10(-5) M). Omepr
azole (10(-4)-10(-3) M) decreased the amplitude and frequency of spontaneou
s contractions in a time- and concentration-dependent manner in all myometr
ial smooth muscle isolated from pregnant women. The decrease in amplitude o
f contractions in myometrial smooth muscle reached statistical significance
beginning from the concentration of 3 x 10(-4) M, Addition of indomethacin
(3 x 10(-6) M) and L-NAME (3x10(-5) M) in to the organ baths 30 min before
did not change relaxation responses to omeprazole. When 8 mM Ca2+-precontr
acted in Ca2+-free medium myometrial smooth muscle were exposed to increasi
ng concentrations of omeprazole (10(-5)-10(-3) M), omeprazole produced rela
xation responses in a time- and concentration-dependent manner, reaching st
atistical significance at 10(-4) M. These results show: (1) omeprazole time
- and concentration-dependently decreased spontaneous contractile activity
in myometrial smooth muscle isolated from pregnant women, (2) omeprazole-in
duced relaxations was not influenced by indomethacin and NG-nitro-L-arginin
e methyl ester (L-NAME), suggesting that it is not mediated by cyclooxygena
se products and nitric oxide, and (3) omeprazole brought about time- and co
ncentration-dependently relaxation of myometrial smooth muscle precontracte
d by 8 mM Ca2+ in Ca2+-free medium. This effect of omeprazole may be due to
blockade of the calcium channels. (C) 2001 Elsevier Science Inc. All right
s reserved.