Effects of exogenous female sex-steroid hormones on lymphocyte beta(2)-adrenoceptors in normal females

被引:36
作者
Tan, KS
McFarlane, LC
Coutie, WJ
Lipworth, BJ
机构
[1] Department of Clinical Pharmacology, University of Dundee, Ninewells Hosp. and Medical School, Dundee
[2] Department of Clinical Pharmacology, University of Dundee, Ninewells Hosp. and Medical School
关键词
oestrogen; progesterone; beta(2)-adrenoceptors; lymphocyte; menstrual cycle;
D O I
10.1046/j.1365-2125.1996.3311.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have previously shown that lymphocyte beta(2)-adrenoceptors (AR) are under cyclical control of sex-steroid hormones with greater receptor density during the luteal phase of the menstrual cycle. It has also been postulated that abnormal cyclical regulation of beta(2)-AR might be a possible mechanism for premenstrual asthma. The effects of exogenous female sex-steroid hormones on lymphocyte beta(2)-AR function were studied in eight normal healthy females. They were evaluated at two successive menstrual cycles, during the follicular phase (day 1-6). They were randomized to receive single oral doses of either ethinyloestradiol 50 mu g or medroxyprogesterone 10 mg in a cross-over study. Lymphocyte beta(2)-AR parameters were evaluated at baseline (t(0)), 24 h (t(24)) and 72 h (t(72)) after ingestion. Baseline levels of progesterone and oestradiol were comparable on both cycles. Receptor density (beta(max)) increased significantly (P<0.01) from t(0) after progesterone but not oestradiol at t(24): a 1.39-fold geometric mean difference (95% CI 0.96-2.00) between t(24) vs t(0). Receptor affinity (K-d) and maximal cAMP response to isoprenaline (E(max)) were not altered by either treatment. These results show that exogenous progesterone but not oestradiol, given during the follicular phase, significantly increased beta(2)-AR. This, therefore, suggests that endogenous progesterone is probably responsible for previously observed increase in B-max during the luteal phase of the female menstrual cycle. These findings may suggest possible therapeutic strategies for modulation of beta(2)-AR in premenstrual asthma.
引用
收藏
页码:414 / 416
页数:3
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