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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.

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。

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