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妊娠末期及用RU 486引产的大鼠子宫中β2 -肾上腺素能受体反应

Beta 2-adrenoceptor response in the rat uterus at the end of gestation and after induction of labor with RU 486.

作者信息

el Alj A, Breuiller M, Jolivet A, Ferre F, Germain G

机构信息

INSERM U262, Physiologie et physiopathologie de la reproduction, Maternité Baudelocque, Paris, France.

出版信息

Can J Physiol Pharmacol. 1989 Sep;67(9):1051-7. doi: 10.1139/y89-166.

DOI:10.1139/y89-166
PMID:2557147
Abstract

To study the relationship between the progesterone environment and beta-adrenoceptors in the myometrium, rats were treated with the antiprogestin RU 486 (10 mg per rat) at 08:30 h on day 21 of gestation. Under these conditions, more than 60% of animals delivered within 24 h after this treatment, while none of the control animals delivered within the same time period. beta-Adrenoceptors were identified using the radiolabeled antagonist (-)-[125I] iodocyanopindolol. The density (Bmax approximately 33-45 fmol/mg protein) and the affinity (KD approximately 0.105-0.106 nM) were not changed (during the late stages of gestation) in RU 486 treated rats compared with control rats. These results were correlated with the relaxation of longitudinal and circular strips of myometrium placed in high KC1 medium and exposed to beta-adrenoceptor agonists. The adrenoceptors implicated in the relaxation of myometrial strips were mainly of the beta 2-subtype. There was no difference in their affinity between control and RU 486 treated rats. Mean pA2 values were 8.46 for propranolol and 8.27 for ICI 118-551 against salbutamol. Altogether these results indicate in the rat that the blockade of the action of progesterone at its receptor site by RU 486 did not modify either the affinity or the sensitivity of beta 2-adrenoceptors in the myometrium, although it induced parturition.

摘要

为研究孕酮环境与子宫肌层β - 肾上腺素能受体之间的关系,在妊娠第21天的08:30给大鼠注射抗孕激素RU 486(每只大鼠10毫克)。在这些条件下,超过60%的动物在该处理后24小时内分娩,而同期对照动物均未分娩。使用放射性标记拮抗剂( - ) - [125I]碘氰吲哚洛尔鉴定β - 肾上腺素能受体。与对照大鼠相比,RU 486处理的大鼠(在妊娠后期)的受体密度(Bmax约为33 - 45 fmol/mg蛋白)和亲和力(KD约为0.105 - 0.106 nM)没有变化。这些结果与置于高钾培养基中并暴露于β - 肾上腺素能受体激动剂的子宫肌层纵行和环行条带的松弛相关。参与子宫肌层条带松弛的肾上腺素能受体主要是β2亚型。对照大鼠和RU 486处理的大鼠之间它们的亲和力没有差异。普萘洛尔对沙丁胺醇的平均pA2值为8.46,ICI 118 - 551对沙丁胺醇的平均pA2值为8.27。总之,这些结果表明在大鼠中,RU 486在其受体位点阻断孕酮的作用,虽然诱导了分娩,但并未改变子宫肌层β2 - 肾上腺素能受体的亲和力或敏感性。

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