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激素注射对犬前列腺中雌激素、雄激素和孕激素胞质受体水平的影响。

Effect of hormone injections on levels of cytosolic receptors for estrogen, androgen and progesterone in dog prostate.

作者信息

Frenette G, Dube J Y, Tremblay R R

出版信息

J Steroid Biochem. 1982 Sep;17(3):271-6. doi: 10.1016/0022-4731(82)90199-6.

Abstract

We have studied the effects of estradiol injections on cytosolic estrogen, androgen and progesterone receptor levels in order to understand the role of this steroid in the induction of prostatic hyperplasia in the dog. Adult mongrel dogs were castrated and were then given injections of estradiol (0.25, 0.8 or 2.5 mg) dissolved in olive oil containing 5% benzyl alcohol on days 0, 2, 5 and 7 after castration. Steroid receptor levels were determined by Scatchard analysis using charcoal assay one day after the last injection. All three receptors were increased maximally with the 0.8 mg dosage when compared with castrated controls. Estradiol binding increased from 89 +/- 10 (mean +/- SEM) to 361 +/- 37 fmol per mg prot., androgen binding from 47 +/- 5 to 123 +/- 11 fmol per mg prot. and progesterone binding from 26 +/- 3 to 211 +/- 36 fmol per mg prot. The small dose of estradiol. (0.25 mg) produced a significant (P less than 0.05) increase of the progesterone receptor levels from 25 +/- 3 to 48 +/- 14 fmol/mg prot. Substitution of estradiol by 5 alpha-androstan-3 beta,17 beta-diol (2.5 or 25 mg) resulted in receptor levels similar to castrated animals. However treatment with 5 alpha-androstan-3 alpha,17 beta-diol (25 mg) alone or in combination with estradiol (0.25 mg) increased significantly the androgen receptor while it decreased the estrogen receptor. These results show that the administration of estradiol at doses used to induce experimental prostate hyperplasia produce measurable effects in the prostate and suggest that the estradiol receptor may be implicated in this phenomenon.

摘要

我们研究了雌二醇注射对胞质雌激素、雄激素和孕激素受体水平的影响,以了解这种类固醇在犬前列腺增生诱导中的作用。成年杂种犬被阉割,然后在阉割后的第0、2、5和7天,注射溶解于含5%苯甲醇的橄榄油中的雌二醇(0.25、0.8或2.5毫克)。在最后一次注射后一天,通过使用活性炭分析法的Scatchard分析来测定类固醇受体水平。与阉割对照组相比,所有三种受体在0.8毫克剂量时增加到最大值。雌二醇结合量从每毫克蛋白89±10(平均值±标准误)增加到361±37飞摩尔,雄激素结合量从每毫克蛋白47±5增加到123±11飞摩尔,孕激素结合量从每毫克蛋白26±3增加到211±36飞摩尔。小剂量的雌二醇(0.25毫克)使孕激素受体水平从25±3显著(P<0.05)增加到48±14飞摩尔/毫克蛋白。用5α-雄甾烷-3β,17β-二醇(2.5或25毫克)替代雌二醇导致受体水平与阉割动物相似。然而,单独用5α-雄甾烷-3α,17β-二醇(25毫克)或与雌二醇(0.25毫克)联合治疗显著增加了雄激素受体,同时降低了雌激素受体。这些结果表明,用于诱导实验性前列腺增生的剂量的雌二醇给药在前列腺中产生了可测量的影响,并表明雌二醇受体可能与这一现象有关。

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