Chobanian A, Brecher P I, Lille R D, Wotiz H H
J Lipid Res. 1968 Nov;9(6):701-6.
The metabolism of labeled sex hormones was examined in human, canine, and rat aortas. Isolated arterial tissue converted estrone to estradiol, estradiol to estrone, and estrone sulfate to estrone and estradiol. The arterial wall also appeared to metabolize testosterone to androstenedione and an unidentified, relatively nonpolar derivative. Both estrogens and testosterone appeared to enter the arterial wall rapidly. No competition in arterial uptake between the two hormones was apparent. No specific arterial binding of estradiol could be demonstrated. The concentration of estradiol-(3)H in the canine aorta exceeded that in the plasma 1-6 hr after estradiol-(3)H administration. The uptake and disappearance of estradiol-(3)H in the aorta generally resembled the patterns observed in body tissues other than the adrenal gland and uterus. The uptake of estradiol-(3)H was greatest in the adrenal gland while its retention was maximum in the uterus.
在人类、犬类和大鼠的主动脉中研究了标记性激素的代谢情况。离体动脉组织可将雌酮转化为雌二醇,将雌二醇转化为雌酮,并将硫酸雌酮转化为雌酮和雌二醇。动脉壁似乎还能将睾酮代谢为雄烯二酮和一种未鉴定的、相对非极性的衍生物。雌激素和睾酮似乎都能迅速进入动脉壁。两种激素在动脉摄取方面未表现出竞争。未证实雌二醇有特异性的动脉结合。给予³H-雌二醇后1 - 6小时,犬主动脉中³H-雌二醇的浓度超过血浆中的浓度。主动脉中³H-雌二醇的摄取和消失模式总体上与肾上腺和子宫以外的身体组织中观察到的模式相似。³H-雌二醇在肾上腺中的摄取最大,而在子宫中的潴留最大。