Brandi A M, Barrande G, Lahlou N, Crumeyrolle M, Berthet M, Leblanc P, Peillon F, Li J Y
Unité INSERM 223, Faculté de Médecine Pitié-Salpêtrière, Paris, France.
Eur J Endocrinol. 1995 Feb;132(2):163-70. doi: 10.1530/eje.0.1320163.
The purpose of this study was to determine whether gonadotropin-releasing hormone (GnRH) may exert a direct action on human prolactinomas. On a series of 17 adenomas, we studied the effect of GnRH on the in vitro prolactin (PRL) secretion of dispersed and perifused cells of 10 cases and the [125I]GnRH agonist binding on frozen sections of three out of the adenomas studied in perifusion and on the membrane preparations of seven other cases. Two 20-min pulses of GnRH (10(-7) mol/l) stimulated the in vitro PRL secretion of three adenomas out of 10 (increase of 200, 444 and 205%, respectively, above basal levels). The GnRH receptors of three adenomas bound GnRH agonist (Des-Gly10-(D-Ala6)-GnRH ethylamide). The binding was specific, with a high affinity (Kd = 0.60, 0.48 and 0.40 nmol/l) similar to that of two human anterior pituitaries obtained post-mortem (Kd = 0.70 and 0.40 nmol/l). Indirect immunoperoxidase revealed that the majority of the cells (60-90%) in all the adenomas studied contained immunoreactive PRL. Four of them also contained cells immunoreactive to the alpha-subunit of the glycoprotein hormones. In none of the prolactinomas were cells immunoreactive to antiserum of anti-beta-luteinizing hormone, anti-beta-follicle-stimulating hormone or anti-beta-thyrotropin. All the prolactinomas that were responsive to GnRH in perifusion experiments and/or bound specifically to [125I]GnRH agonist were also immunoreactive for alpha-subunit. These results show that GnRH, via GnRH specific receptors, exerts a stimulation on in vitro PRL secretion in a subset of prolactinomas characterized by the presence of alpha-subunit.
本研究的目的是确定促性腺激素释放激素(GnRH)是否可能对人催乳素瘤发挥直接作用。在一系列17个腺瘤中,我们研究了GnRH对10例分散和灌流细胞的体外催乳素(PRL)分泌的影响,以及对灌流研究的3个腺瘤的冰冻切片和其他7例的膜制剂上[125I]GnRH激动剂的结合情况。两个20分钟的GnRH脉冲(10^(-7)mol/l)刺激了10个腺瘤中的3个腺瘤的体外PRL分泌(分别比基础水平增加200%、444%和205%)。3个腺瘤的GnRH受体结合了GnRH激动剂(去甘氨酸10-(D-丙氨酸6)-GnRH乙酰胺)。这种结合是特异性的,具有高亲和力(Kd = 0.60、0.48和0.40 nmol/l),与两个死后获得的人垂体前叶相似(Kd = 0.70和0.40 nmol/l)。间接免疫过氧化物酶显示,所有研究的腺瘤中的大多数细胞(60-90%)含有免疫反应性PRL。其中4个还含有对糖蛋白激素α亚基有免疫反应的细胞。在任何催乳素瘤中,均未发现对抗β-促黄体生成素、抗β-促卵泡生成素或抗β-促甲状腺激素抗血清有免疫反应的细胞。在灌流实验中对GnRH有反应和/或与[125I]GnRH激动剂特异性结合的所有催乳素瘤,对α亚基也有免疫反应。这些结果表明,GnRH通过GnRH特异性受体,对以α亚基存在为特征的一部分催乳素瘤的体外PRL分泌发挥刺激作用。