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他莫昔芬和ICI 182,780与去卵巢-甲状腺切除大鼠甲状腺激素的相互作用。

Tamoxifen and ICI 182,780 interactions with thyroid hormone in the ovariectomized-thyroidectomized rat.

作者信息

Dipippo V A, Powers C A

机构信息

Department of Pharmacology, New York Medical College, Valhalla 10595, USA.

出版信息

J Pharmacol Exp Ther. 1997 Apr;281(1):142-8.

PMID:9103491
Abstract

Studies of estradiol and tamoxifen actions to modulate the actions of thyroid hormone (triiodothyronine, T3) in the rat have shown that a subset of estrogen responses require T3 for expression. Also, tamoxifen acts as a partial agonist in estrogen responses that are T3 independent, but acts as a full estrogen agonist in T3-dependent responses. This study examined whether the differing behavior of tamoxifen (a triphenylethylene antiestrogen) in T3-independent and T3-dependent estrogen responses would be shared with ICI 182,780, a steroidal antiestrogen. An ovariectomized-thyroidectomized rat model was used. Drug vehicle, tamoxifen alone (0.4 mg/kg), ICI 182,780 alone (2 mg/kg) or tamoxifen plus ICI 182,780 were given for 3 weeks to ovariectomized-thyroidectomized rats with or without T3 replacement (10 microg/kg). T3-independent estrogen responses measured were the induction of uterine growth and induction of pituitary growth hormone (GH) in the absence of T3. T3-dependent estrogen responses measured were antagonism of T3-evoked increases in pituitary GH, body weight, tibia length and hepatic malic enzyme, and increases in serum triglycerides. Tamoxifen acted as a partial agonist in T3-independent estrogen responses, whereas ICI 182,780 acted as a potent pure antagonist in such responses; it lacked agonist efficacy and totally blocked tamoxifen effects. In T3-dependent estrogen responses, tamoxifen acted as a full estrogen agonist. ICI 182,780 acted as a weak agonist in some T3-dependent responses and lacked agonist efficacy in others. Moreover, ICI 182,780 had poor efficacy in blocking tamoxifen actions in T3-dependent responses. The results indicate that ICI 182,780, like tamoxifen, displays a duality in its pharmacological behavior which pivots on the T3 dependence of the estrogen response.

摘要

关于雌二醇和他莫昔芬对大鼠甲状腺激素(三碘甲状腺原氨酸,T3)作用的调节研究表明,雌激素反应的一个亚群需要T3来表达。此外,他莫昔芬在不依赖T3的雌激素反应中作为部分激动剂起作用,但在依赖T3的反应中作为完全雌激素激动剂起作用。本研究考察了甾体类抗雌激素ICI 182,780是否会与他莫昔芬(一种三苯乙烯类抗雌激素)在不依赖T3和依赖T3的雌激素反应中表现出不同的行为。使用了卵巢切除 - 甲状腺切除的大鼠模型。将药物载体、单独的他莫昔芬(0.4mg/kg)、单独的ICI 182,780(2mg/kg)或他莫昔芬加ICI 182,780给予卵巢切除 - 甲状腺切除的大鼠,持续3周,这些大鼠有或没有T3替代(10μg/kg)。所测量的不依赖T3的雌激素反应是在没有T3的情况下子宫生长的诱导和垂体生长激素(GH)的诱导。所测量的依赖T3的雌激素反应是对T3引起的垂体GH、体重、胫骨长度和肝苹果酸酶增加的拮抗作用,以及血清甘油三酯的增加。他莫昔芬在不依赖T3的雌激素反应中作为部分激动剂起作用,而ICI 182,780在这种反应中作为强效纯拮抗剂起作用;它缺乏激动剂效力并完全阻断他莫昔芬的作用。在依赖T3的雌激素反应中,他莫昔芬作为完全雌激素激动剂起作用。ICI 182,780在一些依赖T3的反应中作为弱激动剂起作用,而在其他反应中缺乏激动剂效力。此外,ICI 182,780在阻断依赖T3的反应中他莫昔芬的作用方面效力不佳。结果表明,ICI 182,780与他莫昔芬一样,在其药理学行为上表现出二元性,这种二元性取决于雌激素反应对T3的依赖性。

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