Fregly M J
Pharmacol Biochem Behav. 1980 Jan;12(1):131-6. doi: 10.1016/0091-3057(80)90427-x.
Female rats treated with estradiol benzoate for 23 weeks at doses of 25 and 44 microgram/kg/day had an attenuated drinking response to peripheral administration of graded doses of angiotensin I and angiotensin II. No significant difference between the responses of the two estrogen-treated groups was observed, suggesting that maximal attenuation had been attained with the lower dose. Angiotensin II (50, 100 and 200 microgram/kg, IP) increased urine output and urinary sodium excretion rate in a graded fashion with increasing doses in both control and estrogen-treated rats. However, the latter had a somewhat greater response. Administration of angiotensin I (50, 100 and 200 microgram/kg, SC) had a similar, but less consistent, effect on urine output and urinary sodium excretion rate in both control and estrogen-treated groups. The attenuated drinking response of estrogen-treated rats to angiotensin I and angiotensin II suggests either that administered angiotensin failed to gain access to the brain or that central receptors mediating thirst are less sensitive in estrogen-treated rats. The present studies fail to distinguish between these possibilities.
用剂量为25和44微克/千克/天的苯甲酸雌二醇对雌性大鼠进行23周的处理后,这些大鼠对外周给予不同剂量的血管紧张素I和血管紧张素II的饮水反应减弱。未观察到两个雌激素处理组的反应之间存在显著差异,这表明较低剂量已达到最大减弱效果。血管紧张素II(50、100和200微克/千克,腹腔注射)在对照大鼠和雌激素处理的大鼠中均随着剂量增加而以分级方式增加尿量和尿钠排泄率。然而,后者的反应稍大一些。血管紧张素I(50、100和200微克/千克,皮下注射)对对照大鼠组和雌激素处理组的尿量和尿钠排泄率有类似但不太一致的影响。雌激素处理的大鼠对血管紧张素I和血管紧张素II的饮水反应减弱表明,要么给予的血管紧张素无法进入大脑,要么介导口渴的中枢受体在雌激素处理的大鼠中不太敏感。目前的研究未能区分这些可能性。