Di Paolo T, Falardeau P
Biochem Biophys Res Commun. 1984 Aug 30;123(1):312-6. doi: 10.1016/0006-291x(84)90414-5.
We have investigated dopamine (DA) receptors in estradiol-induced PRL-secreting pituitary tumors and intact pituitary tissue. Female rats were injected at 3-week intervals with 2 mg estradiol valerate (EV) or with diluent. After 21 weeks, adenomatous changes in the pituitary gland of EV-treated rats were seen and plasma PRL concentrations reached 2 micrograms/ml. Bromocriptine (2.5 mg/kg) was then administered for 1 month to half of the control rats and half of the rats bearing tumors. Anterior pituitary weight was increased in EV-treated rats compared to controls while the affinity and the density of DA receptors as assessed by [3H]spiperone binding remained unchanged. Bromocriptine (CB-154) induced a 70% decrease in the density of DA receptors without any change in affinity both in normal pituitaries and in tumors. Concurrently, the elevated plasma concentrations of PRL in the tumor bearing rats were decreased to control values following the CB-154 treatment. Our data suggest that rats with primary estrogen-induced PRL secreting tumors have normal pituitary DA receptors.
我们研究了雌二醇诱导的泌乳素分泌型垂体肿瘤及完整垂体组织中的多巴胺(DA)受体。雌性大鼠每隔3周注射2mg戊酸雌二醇(EV)或稀释剂。21周后,观察到经EV处理的大鼠垂体出现腺瘤样改变,血浆泌乳素浓度达到2微克/毫升。然后给一半的对照大鼠和一半的荷瘤大鼠连续1个月给予溴隐亭(2.5mg/kg)。与对照组相比,经EV处理的大鼠垂体前叶重量增加,而通过[3H]螺哌隆结合评估的DA受体亲和力和密度保持不变。溴隐亭(CB-154)使正常垂体和肿瘤中DA受体密度降低70%,而亲和力无任何变化。同时,CB-154治疗后,荷瘤大鼠血浆中升高的泌乳素浓度降至对照值。我们的数据表明,原发性雌激素诱导的泌乳素分泌型肿瘤大鼠的垂体DA受体正常。