• 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

单剂量他莫昔芬对成年去卵巢大鼠的生物学活性。

The biological activity of a single dose of tamoxifen in the adult ovariectomized rat.

作者信息

Bowman S P, Jones C A, Leake A, Morris I D

出版信息

Br J Pharmacol. 1983 Apr;78(4):617-22. doi: 10.1111/j.1476-5381.1983.tb09411.x.

DOI:10.1111/j.1476-5381.1983.tb09411.x
PMID:6405831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2044754/
Abstract

1 The peripheral and central activities of tamoxifen were studied in the ovariectomized adult rat, up to 16 d after a single dose of 7.0 or 0.7 mg/kg. 2 Food consumption and body weight were decreased; only food consumption returned to control values after 16 d. 3 The weights of the uterus and of the uterine luminal fluid were increased for up to 8 d. 4 Serum follicle-stimulating hormone (FSH) concentrations decreased, but only significantly 1 and 8 d after 7.0 mg tamoxifen/kg. Serum luteinizing hormone (LH) and prolactin concentrations were elevated for up to 4 d. 5 Lordosis behaviour was absent throughout the period studied. 6 Within 3 d of administration, tamoxifen partially antagonized the oestrogen-induced changes in uterine luminal fluid, prolactin and LH secretion and lordosis behaviour. 7 Tamoxifen did not alter oestrogen-induced changes in uterine weight, food consumption and body weight. 8 The experiments demonstrate that tamoxifen is active for up to 16 d after a single intraperitoneal dose; oestrogen agonist, partial agonist and antagonist activities were demonstrated. The duration and type of activity depends upon the dose of tamoxifen and the target tissue response examined.

摘要
  1. 在成年去卵巢大鼠中研究了他莫昔芬的外周和中枢活性,单次给予7.0或0.7mg/kg剂量后长达16天。2. 食物摄入量和体重下降;仅食物摄入量在16天后恢复到对照值。3. 子宫和子宫腔液的重量增加,持续长达8天。4. 血清促卵泡激素(FSH)浓度降低,但仅在给予7.0mg/kg他莫昔芬后1天和8天显著降低。血清促黄体生成素(LH)和催乳素浓度升高,持续长达4天。5. 在整个研究期间均未出现脊柱前凸行为。6. 在给药后3天内,他莫昔芬部分拮抗了雌激素诱导的子宫腔液、催乳素和LH分泌以及脊柱前凸行为的变化。7. 他莫昔芬未改变雌激素诱导的子宫重量、食物摄入量和体重变化。8. 实验表明,单次腹腔注射剂量后,他莫昔芬的活性可持续长达16天;表现出雌激素激动剂、部分激动剂和拮抗剂活性。活性的持续时间和类型取决于他莫昔芬的剂量和所检测的靶组织反应。

相似文献

1
The biological activity of a single dose of tamoxifen in the adult ovariectomized rat.单剂量他莫昔芬对成年去卵巢大鼠的生物学活性。
Br J Pharmacol. 1983 Apr;78(4):617-22. doi: 10.1111/j.1476-5381.1983.tb09411.x.
2
Time-related effects of en-clomiphene upon central and peripheral oestrogen target tissues and cytoplasmic receptors.恩杂鲁胺对中枢和外周雌激素靶组织及细胞质受体的时间相关效应。
J Endocrinol. 1981 Apr;89(1):117-28. doi: 10.1677/joe.0.0890117.
3
Agonist and antagonist activity of en-clomiphene upon oestrogen-mediated events in the uterus, pituitary gland and brain of the rat.
J Endocrinol. 1981 Mar;88(3):367-74. doi: 10.1677/joe.0.0880367.
4
Effect of gonadotropin-releasing hormone antagonists on serum follicle-stimulating hormone and luteinizing hormone under conditions of singular follicle-stimulating hormone secretion.促性腺激素释放激素拮抗剂在单一促卵泡激素分泌条件下对血清促卵泡激素和促黄体生成素的影响。
Biol Reprod. 1985 Mar;32(2):391-8. doi: 10.1095/biolreprod32.2.391.
5
Serum FSH, LH, and prolactin in adult ovariectomized mice bearing silastic implants of estradiol: responses to social cues.
Biol Reprod. 1976 Sep;15(2):147-52. doi: 10.1095/biolreprod15.2.147.
6
Action of luteinizing hormone-releasing factor (lrf) in the initiation of lordosis behavior in the estrone-primed ovariectomized female rat.促黄体生成素释放因子(LRF)对雌激素预处理的去卵巢雌性大鼠弓背行为起始的作用。
Neuroendocrinology. 1975;17(4):309-18. doi: 10.1159/000122369.
7
Effects of tamoxifen on serum prolactin levels, pituitary immunoreactive prolactin cells and uterine growth in estradiol-treated ovariectomized rats.他莫昔芬对经雌二醇处理的去卵巢大鼠血清催乳素水平、垂体免疫反应性催乳素细胞及子宫生长的影响。
Horm Metab Res. 1996 Apr;28(4):171-6. doi: 10.1055/s-2007-979154.
8
Effects of starvation in rats on serum levels of follicle stimulating hormone, luteinizing hormone, thyrotropin, growth hormone and prolactin; response to LH-releasing hormone and thyrotropin-releasing hormone.饥饿对大鼠血清促卵泡激素、黄体生成素、促甲状腺激素、生长激素和催乳素水平的影响;对促黄体激素释放激素和促甲状腺激素释放激素的反应。
Endocrinology. 1977 Feb;100(2):580-7. doi: 10.1210/endo-100-2-580.
9
Effect of pentobarbital on serum levels of LH, FSH and prolactin in long-term ovariectomized rats.
Neuroendocrinology. 1978;27(5-6):239-46. doi: 10.1159/000122816.
10
Plasma and pituitary gonadotropins and prolactin after hysterectomy and treatment with uterine extracts in female rats. A kinetic study.
Exp Clin Endocrinol. 1988 Dec;92(2):137-44. doi: 10.1055/s-0029-1210794.

引用本文的文献

1
Stress facilitates classical conditioning in males, but impairs classical conditioning in females through activational effects of ovarian hormones.压力促进雄性的经典条件反射,但通过卵巢激素的激活作用损害雌性的经典条件反射。
Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):4066-71. doi: 10.1073/pnas.95.7.4066.

本文引用的文献

1
Effect of antiestrogens on pituitary prolactin production in normal and pituitary tumor-bearing rats.
Neuroendocrinology. 1980 Jun;30(6):389-95. doi: 10.1159/000123032.
2
Uterine bioassay of tamoxifen, trioxifene and a new estrogen antagonist (LY117018) in rats and mice.他莫昔芬、三苯氧胺及一种新型雌激素拮抗剂(LY117018)在大鼠和小鼠中的子宫生物测定
Life Sci. 1980 Apr 28;26(17):1453-8. doi: 10.1016/0024-3205(80)90049-1.
3
Hypothalamic, pituitary and uterine cytoplasmic and nuclear oestrogen receptors and their relationship to the serum concentration of tamoxifen and its metabolite, 4-hydroxytamoxifen, in the ovariectomized rat.去卵巢大鼠下丘脑、垂体及子宫的细胞质和细胞核雌激素受体及其与他莫昔芬及其代谢产物4-羟基他莫昔芬血清浓度的关系。
J Endocrinol. 1982 Aug;94(2):167-75. doi: 10.1677/joe.0.0940167.
4
Biological activity and steroid receptor interactions of cyclofenil with the oestrogen target tissues of the brain, pituitary gland and uterus of the rat.
J Reprod Fertil. 1982 Jul;65(2):355-66. doi: 10.1530/jrf.0.0650355.
5
Estrogens and breast cancer.
Clin Obstet Gynecol. 1981 Mar;24(1):301-22. doi: 10.1097/00003081-198103000-00025.
6
Agonist and antagonist activity of en-clomiphene upon oestrogen-mediated events in the uterus, pituitary gland and brain of the rat.
J Endocrinol. 1981 Mar;88(3):367-74. doi: 10.1677/joe.0.0880367.
7
Role of estrogens in ovulation: A study using the estrogen-antagonist, I.C.I. 46,474.
Endocrinology. 1970 Sep;87(3):542-51. doi: 10.1210/endo-87-3-542.
8
Studies on the mechanism of action of the nonsteroidal antioestrogen tamoxifen (I.C.I. 46,474) in the rat.关于非甾体抗雌激素他莫昔芬(I.C.I. 46,474)在大鼠体内作用机制的研究。
Mol Cell Endocrinol. 1977 Apr;7(2):177-92. doi: 10.1016/0303-7207(77)90066-1.
9
The effect of synthetic anti-oestrogens on the growth and biochemistry of rat mammary tumours.
Eur J Cancer (1965). 1975 Aug;11(8):571-9. doi: 10.1016/0014-2964(75)90129-2.
10
Tamoxifen as an anti-tumour agent: role of oestradiol and prolactin.
J Endocrinol. 1976 Feb;68(02):305-11. doi: 10.1677/joe.0.0680305.