• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Enzymatic sulfation of steroids. XVI. Very rapid effects of steroid hormones on hepatic cortisol sulfation in intact male rats.

作者信息

Singer S S, Moshtaghie A

出版信息

Biochim Biophys Acta. 1981 Nov 23;666(2):212-5. doi: 10.1016/0005-2760(81)90109-0.

DOI:10.1016/0005-2760(81)90109-0
PMID:6946837
Abstract

Hepatic glucocorticoid sulfotransferase activity in male rats was elevated approximately 200, 100 or 60%, respectively, by administration of 0.20 mg estradiol, 1.0 mg testosterone or 12 mg progesterone daily for 2 days. Administration of 3.0 mg corticosterone daily, for 2 days, was without effect. All observed hormone effects were due to elevation of the concentration of sulfotransferase III, the glucocorticoid-preferring steroid sulfotransferase of rat liver. The response of the enzyme activity to the estrogen was blocked by puromycin or actinomycin D. The relationship between these studies and general endocrine control of sulfotransferase production is discussed.

摘要

相似文献

1
Enzymatic sulfation of steroids. XVI. Very rapid effects of steroid hormones on hepatic cortisol sulfation in intact male rats.
Biochim Biophys Acta. 1981 Nov 23;666(2):212-5. doi: 10.1016/0005-2760(81)90109-0.
2
Enzymatic sulfation of steroids. II. The sulfation of corticosterone by the glucocorticoid sulfotransferases of rat liver cytosol.
Biochim Biophys Acta. 1978 Feb 13;539(1):19-30. doi: 10.1016/0304-4165(78)90117-4.
3
Enzymatic sulfation of steroids. X. Pharmacological progesterone effects on rat liver glucocorticoid sulfotransferases and brief study of short-term effects of hormonal steroids on the enzymes.
Biochem Pharmacol. 1980 Dec 1;29(23):3181-8. doi: 10.1016/0006-2952(80)90583-3.
4
Enzymatic sulfation of steroids. XVIII. study of the specific estradiol-17 beta sulfotransferase of rat liver cytosol, that converts the estrogen to its 3-sulfate, and some elements of the endocrine control of its production.类固醇的酶促硫酸化。十八。大鼠肝细胞溶胶中特异性雌二醇-17β硫酸转移酶的研究,该酶将雌激素转化为其3-硫酸盐,以及其产生的内分泌控制的一些要素。
Can J Biochem Cell Biol. 1983 Jan;61(1):15-22. doi: 10.1139/o83-003.
5
Enzymatic sulfation of steroids: II. The control of the hepatic cortisol sulfotransferase activity and of the individual hepatic steroid sulfotransferases of rats by gonads and gonadal hormones.类固醇的酶促硫酸化作用:II. 性腺和性腺激素对大鼠肝脏皮质醇硫酸转移酶活性及各肝脏类固醇硫酸转移酶的调控
Endocrinology. 1976 Nov;99(5):1346-52. doi: 10.1210/endo-99-5-1346.
6
Enzymatic sulfation of steroids: I. The enzymatic basis for the sex difference in cortisol sulfation by rat liver preparations.类固醇的酶促硫酸化:I. 大鼠肝脏制剂中皮质醇硫酸化性别差异的酶学基础。
Endocrinology. 1976 Apr;98(4):963-74. doi: 10.1210/endo-98-4-963.
7
Enzymatic sulfation of steroids. XV. Studies differentiating between rat liver androgen, estrogen, bile acid, glucocorticoid and phenol sulfotransferases.类固醇的酶促硫酸化。十五。区分大鼠肝脏雄激素、雌激素、胆汁酸、糖皮质激素和酚硫酸转移酶的研究。
Biochim Biophys Acta. 1982 Jan 4;700(1):110-7. doi: 10.1016/0167-4838(82)90298-9.
8
Enzymatic sulfation of steroids. XIX. Cortisol sulfotransferase activity, glucocorticoid sulfotransferases, and tyrosine aminotransferase induction in chicken, gerbil, and hamster liver.
Can J Biochem Cell Biol. 1985 Jan;63(1):23-32. doi: 10.1139/o85-004.
9
Enzymatic sulfation of steroids. XI. The extensive purification and some properties of hepatic sulfotransferase III from female rats.
Can J Biochem. 1980 Aug;58(8):660-6. doi: 10.1139/o80-092.
10
Enzymatic sulfation of steroids--XX. Effects of ten drugs on the hepatic glucocorticoid sulfotransferase activity of rats in vitro and in vivo.类固醇的酶促硫酸化——XX. 十种药物对大鼠肝糖皮质激素硫酸转移酶活性的体内外影响
Biochem Pharmacol. 1984 Nov 1;33(21):3485-90. doi: 10.1016/0006-2952(84)90124-2.