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雌激素和孕激素对绝经后子宫内膜生物化学及形态学的影响。

Effects of estrogens and progestins on the biochemistry and morphology of the postmenopausal endometrium.

作者信息

Whitehead M I, Townsend P T, Pryse-Davies J, Ryder T A, King R J

出版信息

N Engl J Med. 1981 Dec 31;305(27):1599-605. doi: 10.1056/NEJM198112313052701.

Abstract

To study the effects of exogenous estrogens on the postmenopausal endometrium, and to determine the time course and minimum dosage of added progestins necessary to oppose estrogen stimulation, we obtained endometrial specimens from symptomatic postmenopausal women being treated with various preparations of estrogens and progestins. Morphologic changes were assessed with light and electron microscopy, and biochemical effects through measurement of DNA synthesis, estradiol and progesterone receptors, and isocitric and estradiol dehydrogenase activity. For comparison, identical studies were carried out on specimens from premenopausal women in the proliferative and secretory phases of their cycle. All the estrogens exerted stimulatory effects in the postmenopausal specimens that were comparable to those observed in the premenopausal proliferative-phase specimens. Estropipate, subcutaneous estradiol, and conjugated estrogens had some hyperphysiologic effects. Maximal progestational effects occurred in the postmenopausal specimens only after norethindrone was administered for six days, and a constant level of activity equal to that in premenopausal secretory-phase specimens was then observed until the 10th day of exposure. Similar maximal effects occurred after six days of treatment with D/L-norgestrel (150 and 5 mg daily [10 mg daily produced less complete changes]). We conclude that many estrogen preparations subject the endometrium to a potent stimulus. Norethindrone and norgestrel are protective because they counteract the proliferative effects of estrogens, but the currently recommended daily dosages of these progestins can be greatly reduced without loss of response.

摘要

为研究外源性雌激素对绝经后子宫内膜的影响,并确定对抗雌激素刺激所需添加孕激素的时间进程和最小剂量,我们从正在接受各种雌激素和孕激素制剂治疗的有症状绝经后妇女身上获取了子宫内膜标本。通过光学显微镜和电子显微镜评估形态学变化,并通过测量DNA合成、雌二醇和孕激素受体以及异柠檬酸和雌二醇脱氢酶活性来评估生化效应。为作比较,对处于月经周期增殖期和分泌期的绝经前妇女的标本进行了相同的研究。所有雌激素在绝经后标本中均产生了与绝经前增殖期标本中观察到的刺激作用相当的效果。炔雌醇、皮下注射雌二醇和结合雌激素有一些超生理效应。仅在炔诺酮给药六天后,绝经后标本中才出现最大孕激素效应,随后在暴露的第10天观察到与绝经前分泌期标本相当的恒定活性水平。用消旋炔诺酮治疗六天后也出现了类似的最大效应(每日150和5毫克[每日10毫克产生的变化不太完全])。我们得出结论,许多雌激素制剂会对子宫内膜产生强烈刺激。炔诺酮和炔诺孕酮具有保护作用,因为它们能抵消雌激素的增殖作用,但目前推荐的这些孕激素的每日剂量可以大幅降低而不影响反应。

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