Effect of an oxytocin receptor antagonist and rho kinase inhibitor on the [Ca++]i sensitivity of human myometrium.

OBJECTIVE

The purpose of this study was to assess the possible mechanism and effect of oxytocin receptor on the sensitization of the contractile proteins to [Ca(++)](i).

STUDY

DESIGN

Myometrial strips were prepared from biopsy specimens that had been taken at term (37-40 weeks of gestation) cesarean delivery from 22 women, before the onset of labor. Simultaneous measurements of [Ca(++)](i) and tension were performed on spontaneously contracting strips. The effects of a specific oxytocin receptor antagonist, L371,257, and a rho kinase inhibitor, Y-27632, on the [Ca(++)](i) and tension transients were determined.

RESULTS

Application of L371,257 (90 nmol/L) to spontaneously contracting muscle strips reduced peak tension to 43%+/-12% of its original value without affecting peak [Ca(++)](i) (105%+/-15%). More tension is developed at each [Ca(++)](i) during the falling phase, relative to the rising phase of each spontaneous contraction; this asymmetric [Ca(++)](i)-tension relationship was abolished by L371,257. The subsequent application of oxytocin (3 micromol/L) reversed the effects of the antagonist on tension. An inhibitor of rho kinase (Y-27632) caused a concentration-dependent inhibition of spontaneous contractions without affecting the underlying Ca(++) signals. The addition of oxytocin (1 nmol/L) to spontaneously active myometrium increased both the duration of the Ca(++) signal and the sensitivity of the contractile machinery to [Ca(++)](i); only the latter effect was prevented by Y-27632.

CONCLUSION

Oxytocin independently regulates the duration of the periodic Ca(++) signals and the sensitivity of the contractile machinery to Ca(++). The latter is likely to be mediated by rho kinase, which is essential for the effective coupling of increases in [Ca(++)](i) to tension.