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Vol. 282, Issue 1, 256-261, 1997
Facultad de Ciencias Biológicas, Universidad de
Concepción, Chile
Ethodin has been used to induce labor through a mechanism that does not
involve the estrogen-preparatory process being postulated as necessary
for ensuring the events in a normal labor. The cellular mechanisms
involved in that process are unknown. We used an isolated organ bath
preparation for mouse uterine horns and a primary culture of mouse
myometrial smooth muscle cells to analyze the cellular mechanisms
involved in the contractile action of this drug in the myometrium.
Ethodin at a concentration of 10 µM and Compound 48/80 (1 µg/ml)
evoked contractions of uterine horns in an isolated organ bath
preparation. Uterine contractile responses showed a transient increase
in contractile tension that lasted 2 to 3 min. Tachyphylaxis was
observed after four or five successive stimuli, which consisted in
additions and washings of the drug at an interval of 10 min. The
primary smooth muscle mouse myometrium cells contained a high
proportion of relaxed cells that varied widely in length (5-160 µm).
Cell lengths decreased in response to the application of serotonin (10 µM) and oxytocin (0.1 µM) but were not affected after the addition
of ethodin (10 µM). However, the cells contracted after a purified
fraction of mast cells that had been degranulated by the action of the
drug ethodin, which was added to the culture medium. These results
provide some evidence related to the mechanism of myometrial
contractile action of ethodin and support the hypothesis that mast
cells may be involved in the regulation of myometrium contractility.