F. Morishita et al., ROLE OF THE SODIUM-CALCIUM EXCHANGE MECHANISM AND THE EFFECT OF MAGNESIUM ON SODIUM-FREE AND HIGH-POTASSIUM CONTRACTURES IN PREGNANT HUMAN MYOMETRIUM, American journal of obstetrics and gynecology, 172(1), 1995, pp. 186-195
OBJECTIVE: Periodic uterine relaxation in labor relieves the fetus fro
m hypoxia related to sustained contractions. A reduction in intracellu
lar calcium is essential for relaxation. Therefore we aimed to clarify
the extrusion mechanisms of intracellular calcium ions in pregnant hu
man myometrium. STUDY DESIGN: Isometric contraction of small muscle bu
ndles obtained from human myometrium at term was recorded. High-potass
ium and sodium-free solutions could induce stable contractures that re
vealed initial phasic contractions followed by tonic contractions. The
effects of external calcium, external magnesium, nifedipine, and calc
ium adenosine triphosphatase inhibitors on both contractures were then
examined. RESULTS: Because maximum tonic contraction was induced by 4
8 mmol/L potassium, this concentration was used. Both contractures dep
ended on external calcium concentrations. Nifedipine, 10(-7) mol/L inh
ibited both initial phasic contractions and the tonic phase of the hig
h-potassium contracture; however, it could not suppress the tonic phas
e of the sodium-free contracture. Calcium adenosine triphosphatase inh
ibitors, cyclopiazonic acid and lauryl sulfate, potentiated the tensio
ns of tonic phases in both contractures; the effect of lauryl sulfate
was stronger than that of cyclopiazonic acid. When external magnesium
was gradually increased (from 0 to 9.6 mmol/L), both phasic contractio
ns and the tonic phase of the high-potassium contracture transiently i
ncreased, followed by a reduction of tension, whereas the tonic phase
of the sodium-free contracture was markedly inhibited by magnesium in
a dose-dependent manner. CONCLUSION: The presence of the sodium-calciu
m exchange mechanism and the specific inhibitory effect of magnesium w
ere indicated in human myometrium during pregnancy. These mechanisms m
ight prevent the long tonic contractions, to protect the fetus from hy
poxia during pregnancy and parturition.