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DOI 10.1016/s0301-2115(02)00415-3

Медицинская библиотека · European journal of obstetrics, gynecology, and reproductive biology · 2003

Sex hormone effects in non-pregnant rat and human myometrium.

Vedernikov Yuri P, Hartke James R, de Long Mitchell A, Saade George R, Garfield Robert E

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Аннотация

OBJECTIVE

To study effects of sex hormones on spontaneous contractility and on the effects of depolarizing agent potassium chloride (KCl), M-cholinoceptor and prostaglandin receptor agonists on non-pregnant rat and human uterine tissues.

STUDY

DESIGN

Uterine rings from ovariectomized rats treated with sex hormones or placebo, and uterine strips from premenopausal and postmenopausal women were equilibrated in Krebs buffer (t=37 degrees C, pH approximately 7.4) for isometric tension recordings. Spontaneous contractile activity and contractions in response to KCl, eicosanoids, and acetylcholine were compared.

RESULTS

In tissues from ovariectomized rats, spontaneous contractility was increased, while KCl-induced contractions were decreased. Treatment with 17beta-estradiol, but not progesterone, inhibited spontaneous contractions, but potentiated KCl evoked contractions. Treatment with 17beta-estradiol did not influence responses to prostanoids in ovariectomized rats, while treatment with both sex hormones restored decreased the responses. Spontaneous contractility and responses to KCl were less in uterine tissues from postmenopausal versus premenopausal women. Hormone replacement therapy partly restored the responses to KCl, prostanoids, and acetylcholine.

CONCLUSIONS

Ovarian steroids modulate spontaneous contractile activity, responses to depolarization, prostanoids and M-cholinoceptor activation in non-pregnant rat and human uterine tissues in vitro.

Для цитирования: Vedernikov Yuri P, Hartke James R, de Long Mitchell A, Saade George R, Garfield Robert E. Sex hormone effects in non-pregnant rat and human myometrium.. European journal of obstetrics, gynecology, and reproductive biology. 2003. DOI: 10.1016/s0301-2115(02)00415-3.

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