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达那唑对子宫细胞质和细胞核雌激素结合能力的影响。

Influence of danazol on cytoplasmic and nuclear estrogen binding capacity in the uterus.

作者信息

Sanfilippo J S, Teichman J, Melvin J R, Wittliff J L

出版信息

Am J Obstet Gynecol. 1983 Oct 15;147(4):364-8. doi: 10.1016/s0002-9378(16)32226-8.

DOI:10.1016/s0002-9378(16)32226-8
PMID:6684884
Abstract

Sprague-Dawley rats with estrous cycles were exposed to danazol (Danocrine) at a single dose of 10 mg/kg for either 6 or 24 hours, or daily until a pattern of no cycles (6 days) was noted on vaginal smears. The animals were individually housed and exposed to a 14-hour light/10-hour dark environment. Prior to drug administration, daily vaginal smears were obtained to ensure cycle normalcy. After the appropriate exposure to medication, the animals were killed, the uterine horns were removed, and determination was made of cytoplasmic and nuclear estrogen receptors. The animals in the control group (6 and 24 hours, and daily injected) received vehicle only (mineral oil). The influence of danazol on sex-steroid receptor levels appeared to be related to the phase of the estrous cycle at the time of sacrifice. At both 6 and 24 hours of exposure to danazol, there was a slight decrease in specific estrogen binding capacity of cytosols, with no alteration in the levels of nuclear receptors in the uteri of rats with cycles. In the groups with no cycles, there was an increase in cytosolic estrogen binding capacity at 1 and 6 days of danazol treatment, with a slight decrease in nuclear receptor binding when compared with treated rats with cycles. Statistical evaluation revealed a significant difference in cytosolic estrogen binding capacity between the series with cycles and the series without cycles (p less than 0.01). This study provides further information in regard to danazol action on cytosol and nuclear receptors correlated with phase of the estrous cycle.

摘要

将处于发情周期的斯普拉格-道利大鼠以10毫克/千克的单次剂量给予达那唑(达那唑胶囊),持续6小时或24小时,或每日给药,直至阴道涂片显示无周期(6天)的模式。动物单独饲养,置于14小时光照/10小时黑暗的环境中。在给药前,每日采集阴道涂片以确保周期正常。在适当接触药物后,处死动物,取出子宫角,并测定细胞质和细胞核雌激素受体。对照组的动物(6小时、24小时和每日注射组)仅接受赋形剂(矿物油)。达那唑对性类固醇受体水平的影响似乎与处死时的发情周期阶段有关。在接触达那唑6小时和24小时时,细胞质中特异性雌激素结合能力略有下降,有周期的大鼠子宫中核受体水平无变化。在无周期的组中,达那唑治疗1天和6天时细胞质雌激素结合能力增加,与有周期的治疗大鼠相比,核受体结合略有下降。统计学评估显示,有周期组和无周期组之间细胞质雌激素结合能力存在显著差异(p小于0.01)。本研究提供了关于达那唑对与发情周期阶段相关的细胞质和核受体作用的进一步信息。

相似文献

1
Influence of danazol on cytoplasmic and nuclear estrogen binding capacity in the uterus.达那唑对子宫细胞质和细胞核雌激素结合能力的影响。
Am J Obstet Gynecol. 1983 Oct 15;147(4):364-8. doi: 10.1016/s0002-9378(16)32226-8.
2
Cytoplasmic and nuclear estrogen binding capacity in the rat uterus during treatment with danazol and testosterone.达那唑和睾酮治疗期间大鼠子宫的细胞质和细胞核雌激素结合能力
Eur J Obstet Gynecol Reprod Biol. 1986 Apr;21(4):245-52. doi: 10.1016/0028-2243(86)90024-9.
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Evaluation of danazol influence upon the uterus using scanning electron microscopic morphometric and biochemical analyses.使用扫描电子显微镜形态计量学和生化分析评估达那唑对子宫的影响。
Surg Gynecol Obstet. 1985 May;160(5):421-8.
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Progestin-like effects of danazol on rabbit uterus.达那唑对兔子宫的孕激素样作用。
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5
Increased accumulation of estrogen receptors in pituitary nuclei of danazol treated rats.达那唑治疗的大鼠垂体核中雌激素受体的积累增加。
Biol Reprod. 1979 Aug;21(1):27-32. doi: 10.1095/biolreprod21.1.27.
6
Competitive inhibition by danazol of oestradiol binding to rabbit and ovine uterine oestradiol receptor.达那唑对雌二醇与兔和绵羊子宫雌二醇受体结合的竞争性抑制作用。
J Steroid Biochem. 1980 Nov;13(11):1325-9. doi: 10.1016/0022-4731(80)90093-x.
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Studies on the mechanism of action of danazol and gestrinone (R2323) in the rat: evidence for a masked estrogen component.
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Danazol suppression of luteinizing hormone in the rat: evidence for mediation by both androgen and estrogen receptors.达那唑对大鼠促黄体生成素的抑制作用:雄激素和雌激素受体介导的证据
Proc Soc Exp Biol Med. 1990 May;194(1):54-7. doi: 10.3181/00379727-194-43054.
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Danazol binding and translocation of steroid receptors.达那唑与类固醇受体的结合及转位
Am J Obstet Gynecol. 1980 Feb 15;136(4):426-9. doi: 10.1016/0002-9378(80)90665-1.
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Estrogenic and antiestrogenic effects of danazol administration in studies of estradiol receptor binding.在雌二醇受体结合研究中,达那唑给药的雌激素和抗雌激素作用。
Am J Obstet Gynecol. 1981 May 1;140(1):62-9. doi: 10.1016/0002-9378(81)90258-1.