Sandrini M, Vergoni A V, Bertolini A
Istituto di Farmacologia, Università di Modena, Italy.
J Endocrinol Invest. 1993 Oct;16(9):679-81. doi: 10.1007/BF03348909.
In intact adult male rats an inhibitor of aromatase and an inhibitor of 5 alpha-reductase did not change the characteristics of [3H]imipramine binding sites in cerebral cortex, hypothalamus, and hippocampus. Testosterone, estradiol and dihydrotestosterone prevented the effect of castration on the number of [3H]imipramine binding sites, but had no effect in non-castrated animals. These data suggest that testosterone and its major metabolites, estradiol and dihydrotestosterone, are equally effective with regard to imipramine binding sites.
在成年雄性大鼠中,芳香化酶抑制剂和5α-还原酶抑制剂不会改变大脑皮层、下丘脑和海马体中[3H]丙咪嗪结合位点的特征。睾酮、雌二醇和双氢睾酮可防止去势对[3H]丙咪嗪结合位点数量的影响,但对未去势动物无效。这些数据表明,睾酮及其主要代谢产物雌二醇和双氢睾酮对丙咪嗪结合位点的作用同样有效。