Lawson D M, Sensui N, Gala R R
Life Sci. 1984 Jan 30;34(5):455-9. doi: 10.1016/0024-3205(84)90500-9.
Mature female Sprague-Dawley (SD) and Long-Evans (LE) rats were ovariectomized (OVX), fitted with indwelling atrial catheters and given a single sc injection of either 25 or 100 micrograms polyestradiol phosphate (PEP); seven days later blood samples were withdrawn at two hour intervals from 1100 to 2100 hours to detect the presence of an afternoon surge of prolactin (PRL). Other groups of OVX rats of both strains also treated with PEP and catheterized as above were sampled before and at 2, 5, 10 and 30 min after iv administration of 1 microgram synthetic thyrotropin releasing hormone (TRH). Pituitary (AP) and uterine weights were determined following sacrifice one day after TRH treatment. Separate groups of OVX rats of both strains treated with 100 micrograms PEP were decapitated 7 days later and each AP was removed and homogenized. The AP homogenates and plasma samples were assayed for PRL by radioimmunoassay. Rats of both strains had afternoon PRL surges and in both strains the magnitude and/or duration of the surges were enhanced by the higher dose of PEP. However, within each PEP dose LE rats released significantly more PRL during the surge than did SD rats. Rats of both strains also released PRL in response to TRH and this response was enhanced in both strains by the higher of the two doses of PEP. However, there were no differences between the strains at 25 micrograms PEP and at 100 micrograms PEP SD rats released significantly more PRL to TRH than did LE rats. Pituitary weight and PRL concentration were not different between the strains at either dose of PEP but LE rats had significantly heavier uteri at both doses of PEP compared to SD rats. These data not only show that strain differences exist in estrogen-induced or mediated PRL release in the rat but also indicate that the differences are not uniform. This latter observation suggests that the estrogen-induced mechanisms examined in this study are for the most part independent of each other.
将成年雌性斯普拉格 - 道利(SD)大鼠和朗 - 伊文斯(LE)大鼠进行卵巢切除(OVX),植入心房留置导管,并皮下注射25微克或100微克的聚磷酸雌二醇(PEP);7天后,在11:00至21:00每隔2小时采集血样,以检测下午催乳素(PRL)激增的情况。两组OVX大鼠均用PEP处理并按上述方法插管,在静脉注射1微克合成促甲状腺激素释放激素(TRH)之前以及之后2、5、10和30分钟进行采样。在TRH处理一天后处死大鼠,测定垂体(AP)和子宫重量。两组接受100微克PEP处理的OVX大鼠在7天后断头,取出每个AP并匀浆。通过放射免疫测定法测定AP匀浆和血浆样品中的PRL。两种品系的大鼠下午都有PRL激增,并且两种品系中较高剂量的PEP均增强了激增的幅度和/或持续时间。然而,在每个PEP剂量组中,LE大鼠在激增期间释放的PRL明显多于SD大鼠。两种品系的大鼠对TRH也有PRL释放反应,并且两种品系中较高剂量的PEP均增强了这种反应。然而,在25微克PEP剂量组中两种品系之间没有差异,在100微克PEP剂量组中,SD大鼠对TRH释放的PRL明显多于LE大鼠。在两种PEP剂量下,两种品系之间的垂体重量和PRL浓度没有差异,但与SD大鼠相比,两种PEP剂量下LE大鼠的子宫明显更重。这些数据不仅表明大鼠在雌激素诱导或介导的PRL释放中存在品系差异,还表明这些差异并不一致。后一观察结果表明,本研究中检测的雌激素诱导机制在很大程度上是相互独立的。