Edery M, Barnova A, Drosdowsky M, Guggiari M, Vives C, Rudali G
Biomed Pharmacother. 1985;39(6):326-30.
This study compares the relative biological potencies of a known antiestrogen tamoxifen to two triarylethylene compounds which have been shown previously to be potent inhibitors of rodent mammary tumorigenesis. Based on a) uterotrophic and anti-uterotrophic tests, b) indexes of cellularity, and c) protein content, these studies indicate that the trans, as well as the cis, isomers of bromotriphenylethylene are partial estrogen antagonists with no estrogenic effects in rat uteri and partial agonists in mouse uteri, whereas tamoxifen shows partial antiestrogenic/estrogenic effects in rats and is fully estrogenic in mice.
本研究比较了一种已知的抗雌激素药物他莫昔芬与两种三芳基乙烯化合物的相对生物学活性,这两种化合物先前已被证明是啮齿动物乳腺肿瘤发生的有效抑制剂。基于a)子宫营养和抗子宫营养试验、b)细胞计数指标以及c)蛋白质含量,这些研究表明,溴三苯乙烯的反式和顺式异构体在大鼠子宫中是部分雌激素拮抗剂,无雌激素作用,在小鼠子宫中是部分激动剂,而他莫昔芬在大鼠中表现出部分抗雌激素/雌激素作用,在小鼠中是完全雌激素作用。