Stavréus-Evers A, Parini P, Freyschuss B, Elger W, Reddersen G, Sahlin L, Eriksson H
Division for Reproductive Endocrinology L5:01, Department of Woman and Child Health, Karolinska Hospital, Karolinska Institutet, 171 76 Stockholm, Sweden.
J Steroid Biochem Mol Biol. 2001 Jul;78(1):83-8. doi: 10.1016/s0960-0760(01)00077-2.
The majority of data regarding biological effects of estrogens is based on studies in male rats or ovariectomized (Ovx) female rats. Therefore, in this study, the effects of estradiol treatment on the regulation of the hepatic estrogen receptor and the level of circulating angiotensinogen were examined in the intact female rat. The data were compared with that of the hypophysectomized (Hx) rat. Animals were treated with either low (physiological) or high (pharmacological) doses of estrogen. In intact rats, the hepatic estrogen receptor (ER) level increased with increasing doses of estrogen. This was in contrast to the Hx rats where growth hormone (GH) and dexametasone (Dex) in combination were the sole modulators of the estrogen receptor. The angiotensinogen level increased in normal rats after estrogen administration in a dose dependent manner, regardless of the mode of administration. The pure antiestrogen ICI 182 780 efficiently blocked the increase in circulating angiotensinogen. The conclusion is that in the normal female, estrogens are important modulators of the serum angiotensinogen level.
大多数关于雌激素生物学效应的数据基于对雄性大鼠或去卵巢(Ovx)雌性大鼠的研究。因此,在本研究中,在完整雌性大鼠中检测了雌二醇处理对肝脏雌激素受体调节和循环血管紧张素原水平的影响。将数据与垂体切除(Hx)大鼠的数据进行比较。动物接受低(生理)剂量或高(药理)剂量的雌激素治疗。在完整大鼠中,肝脏雌激素受体(ER)水平随雌激素剂量增加而升高。这与Hx大鼠相反,在Hx大鼠中,生长激素(GH)和地塞米松(Dex)联合是雌激素受体的唯一调节因子。无论给药方式如何,正常大鼠在给予雌激素后血管紧张素原水平呈剂量依赖性增加。纯抗雌激素ICI 182 780有效阻断循环血管紧张素原的增加。结论是,在正常雌性中,雌激素是血清血管紧张素原水平的重要调节因子。