Levy C, Mester J, Baulieu E E
J Endocrinol. 1981 Jul;90(1):1-7. doi: 10.1677/joe.0.0900001.
The oestradiol-induced increase of ornithine decarboxylase (ODC) activity in the 'withdrawn' chick oviduct was found to be inhibited by progesterone. In vitro (2 h at 37 degrees C), progesterone (1 mumol/l) abolished the effect of oestradiol (20 nmol/l), progesterone alone having no effect. In vivo, progesterone (3 mg/kg) inhibited approximately 70% of the augmentation of ODC activity induced in the oviduct within 2 to 6 h of treatment with oestradiol benzoate (1.5 mg/kg). Administration of progesterone alone in vivo caused an increase in the ODC activity, the maximum level measured after 6 h being similar to that obtained when the chicks were given both oestrogen and progesterone. In the rat uterus in vivo progesterone also inhibited the rise of ODC activity caused by oestradiol, approximately % inhibition being observed between 2 and 6 h after treatment. Progesterone alone had no effect on uterine ODC activity during this period.
已发现孕酮可抑制雌二醇诱导的“退缩”雏鸡输卵管中鸟氨酸脱羧酶(ODC)活性的增加。在体外(37℃下2小时),孕酮(1μmol/L)消除了雌二醇(20nmol/L)的作用,单独使用孕酮则无效果。在体内,孕酮(3mg/kg)在苯甲酸雌二醇(1.5mg/kg)处理2至6小时内,抑制了输卵管中诱导的ODC活性增加的约70%。单独在体内给予孕酮会导致ODC活性增加,6小时后测得的最高水平与同时给予雌激素和孕酮的雏鸡所获得的水平相似。在体内的大鼠子宫中,孕酮也抑制了由雌二醇引起的ODC活性升高,在处理后2至6小时之间观察到约%的抑制作用。在此期间,单独使用孕酮对子宫ODC活性没有影响。