• 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

抗雄激素(氧雄龙)对实验性诱导犬前列腺增生影响的研究。II. 内分泌学分析。

Study of the effect of an anti-androgen (oxendolone) on experimentally induced canine prostatic hyperplasia. II. Endocrinological analysis.

作者信息

Okada K, Oishi K, Yoshida O, Sudo K, Kawase M, Nakayama R

机构信息

Department of Urology, Faculty of Medicine, Kyoto University, Japan.

出版信息

Urol Res. 1988;16(2):73-8. doi: 10.1007/BF00261959.

DOI:10.1007/BF00261959
PMID:2453093
Abstract

The results of hormonal investigation of effects of an antiandrogen, Oxendolone (OXD), alone or in combination with medroxyprogesterone acetate (MPA), on experimentally induced canine BPH are reported. Seventeen beagle dogs were divided into 5 groups: 2 castrate controls for Group 0, 3 BPH controls for Group 1 which received 3 alpha-androstanediol (3 alpha-A) and estradiol (E2) for one year, and 12 dogs consisting of 3 groups which received 3 alpha-A and E2 for 6 months followed by testosterone propionate (TP) and E2 for another 6 months. The last 3 groups were treated with either 200 mg/week of OXD (Group 3) or OXD + 30 mg/week of MPA (Group 4), and otherwise untreated with these hormones (Group 2, T-E controls). On the blood hormone analysis, both T and 5 alpha-dihydrotestosterone (DHT) were generally lowered in the T-E administered groups (Group 2, 3 and 4) compared to those in Group 1. While MPA significantly decreased these androgen levels, OXD did not influence at all. The concentrations of E2 were similar. Although T content in the prostate did not differ significantly within the experimental groups, DHT was the highest in Group 1 and the lowest in Group 4 and was nearly the same level to Group 0. MPA reduced tissue DHT content but OXD did not. In the receptor assay study, nuclear androgen receptor (AR) content in Group 3 and 4 was significantly lower than that in Group 1. No obvious decrease in nuclear AR content could be seen among the other groups.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了抗雄激素奥生多龙(OXD)单独或与醋酸甲羟孕酮(MPA)联合使用对实验诱导的犬良性前列腺增生(BPH)影响的激素研究结果。17只比格犬分为5组:0组为2只去势对照犬,1组为3只BPH对照犬,接受3α-雄甾二醇(3α-A)和雌二醇(E2)治疗1年,另外12只犬分为3组,先接受3α-A和E2治疗6个月,随后接受丙酸睾酮(TP)和E2治疗6个月。最后3组分别用200mg/周的OXD(3组)或OXD + 30mg/周的MPA(4组)治疗,否则不接受这些激素治疗(2组,T-E对照)。血液激素分析显示,与1组相比,T-E给药组(2、3和4组)的T和5α-双氢睾酮(DHT)普遍降低。虽然MPA显著降低了这些雄激素水平,但OXD没有任何影响。E2的浓度相似。虽然前列腺中的T含量在实验组之间没有显著差异,但DHT在1组中最高,在4组中最低,与0组水平相近。MPA降低了组织DHT含量,但OXD没有。在受体测定研究中,3组和4组的核雄激素受体(AR)含量显著低于1组。其他组之间未观察到核AR含量明显下降。(摘要截短至250字)

相似文献

1
Study of the effect of an anti-androgen (oxendolone) on experimentally induced canine prostatic hyperplasia. II. Endocrinological analysis.抗雄激素(氧雄龙)对实验性诱导犬前列腺增生影响的研究。II. 内分泌学分析。
Urol Res. 1988;16(2):73-8. doi: 10.1007/BF00261959.
2
Study of the effect of an anti-androgen (oxendolone) on experimentally induced canine prostatic hyperplasia. I. Morphological analysis.抗雄激素(氧雄龙)对实验性诱导的犬前列腺增生影响的研究。I. 形态学分析。
Urol Res. 1988;16(2):67-72. doi: 10.1007/BF00261958.
3
Effects of a new steroidal aromatase inhibitor, TZA-2237, and/or chlormadinone acetate on hormone-induced and spontaneous canine benign prostatic hyperplasia.新型甾体芳香化酶抑制剂TZA - 2237和/或醋酸氯地孕酮对激素诱导型和自发性犬良性前列腺增生的影响。
Eur J Endocrinol. 2000 Oct;143(4):543-54. doi: 10.1530/eje.0.1430543.
4
Effects of the new steroidal antiandrogen TZP-4238 on hormone-induced canine prostatic hyperplasia.新型甾体类抗雄激素TZP-4238对激素诱导的犬前列腺增生的影响。
Prostate. 1992;21(4):315-29. doi: 10.1002/pros.2990210408.
5
Androgen- and estrogen-receptor content in spontaneous and experimentally induced canine prostatic hyperplasia.自发性及实验性诱导犬前列腺增生中的雄激素和雌激素受体含量
J Clin Invest. 1980 May;65(5):1051-9. doi: 10.1172/JCI109757.
6
Three-month treatment with a long-acting gonadotropin-releasing hormone agonist of patients with benign prostatic hyperplasia: effects on tissue androgen concentration, 5 alpha-reductase activity and androgen receptor content.长效促性腺激素释放激素激动剂对良性前列腺增生患者进行三个月治疗:对组织雄激素浓度、5α-还原酶活性及雄激素受体含量的影响
J Clin Endocrinol Metab. 1989 Feb;68(2):461-8. doi: 10.1210/jcem-68-2-461.
7
The effects of diethylstilbestrol and medroxyprogesterone acetate on kinetics and production of testosterone and dihydrotestosterone in patients with prostatic carcinoma.己烯雌酚和醋酸甲羟孕酮对前列腺癌患者睾酮和双氢睾酮动力学及生成的影响。
J Clin Endocrinol Metab. 1976 Dec;43(6):1226-33. doi: 10.1210/jcem-43-6-1226.
8
Androgen and prostatic stroma.雄激素与前列腺基质。
Asian J Androl. 2003 Mar;5(1):19-26.
9
Androgen receptor content of nafoxidine treated experimentally induced canine prostatic hyperplasia.萘福昔定治疗实验性诱导犬前列腺增生的雄激素受体含量
Clin Invest Med. 1985;8(1):29-34.
10
Serum levels of follicle stimulating hormone, luteinizing hormone, prolactin, testosterone, 5 alpha-dihydrotestosterone, 5 alpha-androstane-3 alpha, 17 beta-diol, 5 alpha-androstane-3 beta, 17 beta-diol, and 17 beta-estradiol from male beagles with spontaneous or induced benign prostatic hyperplasia.来自患有自发性或诱发性良性前列腺增生的雄性比格犬的血清促卵泡激素、促黄体生成素、催乳素、睾酮、5α-二氢睾酮、5α-雄烷-3α,17β-二醇、5α-雄烷-3β,17β-二醇和17β-雌二醇水平。
Invest Urol. 1981 Nov;19(3):142-7.

引用本文的文献

1
A Rationalized Approach to Design and Discover Novel Non-steroidal Derivatives through Computational Aid for the Treatment of Prostate Cancer.通过计算辅助设计和发现新型非甾体衍生物治疗前列腺癌的合理化方法。
Curr Comput Aided Drug Des. 2024;20(5):575-589. doi: 10.2174/1573409919666230626113346.

本文引用的文献

1
The Etiology of Benign Prostatic Hypertrophy.良性前列腺增生的病因
Bull N Y Acad Med. 1947 Dec;23(12):696-704.
2
Studies on the canine prostate gland. I. Factors influencing its size and weight.犬前列腺研究。I. 影响其大小和重量的因素。
J Comp Pathol. 1962 Jul;72:321-31. doi: 10.1016/s0368-1742(62)80037-x.
3
5alpha-reduction of an anti-androgen TSAA-291, 16beta-ethyl-17beta-hydroxy-4-estren-3-one, by nuclear 5alpha-reductase in rat prostates.抗雄激素TSAA-291(16β-乙基-17β-羟基-4-雌烯-3-酮)在大鼠前列腺中被核5α-还原酶进行5α-还原反应。
Steroids. 1981 Jul;38(1):55-71. doi: 10.1016/0039-128x(81)90021-0.
4
Radioimmunoassay for serum levels of an anti-androgen TSAA-291 (Oxendolone) in rats.大鼠血清抗雄激素TSAA - 291(奥生多龙)水平的放射免疫测定
J Pharmacobiodyn. 1984 Jun;7(6):378-84. doi: 10.1248/bpb1978.7.378.
5
Specific interaction of radioactive anti-androgen TSAA-291 with androgen receptor in rat prostates.
Acta Endocrinol (Copenh). 1982 Jul;100(3):473-80. doi: 10.1530/acta.0.1000473.
6
Changes in the activities of microsomal enzymes involved in hepatic steroid metabolism in the rat after administration of androgenic, estrogenic, progestational, anabolic and catatoxic steroids.给予雄性激素、雌激素、孕激素、同化激素和抗毒激素后大鼠肝脏中参与类固醇代谢的微粒体酶活性的变化。
Biochem Pharmacol. 1984 Apr 15;33(8):1235-41. doi: 10.1016/0006-2952(84)90175-8.
7
Estrogen receptors in human prostate: evidence for multiple binding sites.
J Clin Endocrinol Metab. 1983 Jul;57(1):166-76. doi: 10.1210/jcem-57-1-166.
8
A simple, rapid, and sensitive DNA assay procedure.一种简单、快速且灵敏的DNA检测程序。
Anal Biochem. 1980 Mar 1;102(2):344-52. doi: 10.1016/0003-2697(80)90165-7.
9
Androgen- and estrogen-receptor content in spontaneous and experimentally induced canine prostatic hyperplasia.自发性及实验性诱导犬前列腺增生中的雄激素和雌激素受体含量
J Clin Invest. 1980 May;65(5):1051-9. doi: 10.1172/JCI109757.
10
[Radioimmunoassay of sex steroid hormones. 4. Radioimmunoassay of testosterone].[性甾体激素的放射免疫测定。4. 睾酮的放射免疫测定]
Horumon To Rinsho. 1973 Aug;21(8):867-73.