Papavasiliou S S, Zmeili S, Herbon L, Duncan-Weldon J, Marshall J C, Landefeld T D
Endocrinology. 1986 Aug;119(2):691-8. doi: 10.1210/endo-119-2-691.
In this study we examined the changes in alpha and LH beta mRNAs in anterior pituitaries of male and female rats after castration. mRNA concentrations were measured by an optimized RNA dot blot hybridization assay. Rat alpha and LH beta cDNAs were nick-translated to specific activities of 2-5 X 10(8) cpm/micrograms and were used as hybridization probes. The total RNA per assay, RNA per dot, and saturating amounts of probe were optimized. The intra- and interassay coefficients of variation were 5% and 28%, respectively. Both alpha and LH beta mRNA concentrations increased after castration, but marked differences were observed in the kinetics of responses in male and female rats. In males, alpha and LH beta mRNAs were increased by 24 h postcastration (by 25% and 38%, respectively), and 4- to 5-fold increases over intact controls were evident by 18 days. Alpha mRNA rose rapidly and had doubled by 2 days, whereas LH beta mRNA concentrations showed a similar increase by 6-7 days postcastration. The slower rise in LH beta mRNA was associated with a transient decline in serum and pituitary LH concentrations between 2 and 6 days after castration. In female rats, alpha mRNA increased more slowly. Alpha concentrations had doubled by 10 days, while a similar increase in LH beta mRNA occurred 7 days after castration. Thereafter, both subunit mRNAs continued to rise, and by day 20 alpha mRNA was increased 5-fold and LH beta mRNA 16-fold over values in intact females. Serum and pituitary LH concentrations rose gradually, and both were increased by 7-10 days after castration. The increase in serum and pituitary LH followed a time course similar to that of the progressive rise in LH beta mRNA concentrations. These data show that an increase in steady state LH subunit mRNA concentrations is one of the mechanisms involved in increased gonadotropin biosynthesis and secretion after castration. The kinetics of LH subunit mRNA and LH secretory responses are different in male and female rats and suggest that the concentration of LH beta mRNA may be a limiting factor in LH secretion.
在本研究中,我们检测了阉割后雄性和雌性大鼠垂体前叶中α亚基和促黄体生成素β亚基(LHβ)mRNA的变化。通过优化的RNA斑点印迹杂交试验测定mRNA浓度。将大鼠α亚基和LHβ亚基的cDNA缺口平移至比活为2 - 5×10⁸ cpm/μg,并用作杂交探针。对每次试验的总RNA、每个斑点的RNA以及探针的饱和量进行了优化。试验内和试验间的变异系数分别为5%和28%。阉割后α亚基和LHβ亚基的mRNA浓度均升高,但雄性和雌性大鼠在反应动力学上存在显著差异。在雄性大鼠中,阉割后24小时α亚基和LHβ亚基的mRNA分别增加了25%和38%,到18天时比完整对照增加了4至5倍。α亚基mRNA迅速上升,在2天时增加了一倍,而LHβ亚基mRNA浓度在阉割后6至7天出现类似增加。LHβ亚基mRNA上升较慢与阉割后2至6天血清和垂体LH浓度的短暂下降有关。在雌性大鼠中,α亚基mRNA增加较慢。α亚基浓度在10天时增加了一倍,而LHβ亚基mRNA在阉割后7天出现类似增加。此后,两个亚基的mRNA持续上升,到第20天时,α亚基mRNA比完整雌性大鼠的值增加了5倍,LHβ亚基mRNA增加了16倍。血清和垂体LH浓度逐渐上升,阉割后7至10天均增加。血清和垂体LH的增加与LHβ亚基mRNA浓度的逐渐上升具有相似的时间进程。这些数据表明,稳态LH亚基mRNA浓度的增加是阉割后促性腺激素生物合成和分泌增加所涉及的机制之一。LH亚基mRNA的动力学和LH分泌反应在雄性和雌性大鼠中不同,提示LHβ亚基mRNA的浓度可能是LH分泌的限制因素。