Goodyer C G, Branchaud C L, Lefebvre Y
McGill University-Montreal Children's Hospital Research Institute, McGill Centre for the Study of Reproduction, Quebec, Canada.
J Clin Endocrinol Metab. 1993 May;76(5):1259-64. doi: 10.1210/jcem.76.5.8098715.
Using explant cultures of human anterior pituitary glands (9-19 weeks fetal age) and an acute (3-h) test protocol, we investigated fetal somatotrope responsiveness to human GH-releasing factor [hGRF-(1-44)] and somatostatin [SRIF-(1-14) and SRIF-(1-28)] as a function of age. Ontogenic data were analyzed using three age groups: 9-10, 12-13, and 15-19 weeks fetal age. Both daily (24-h) and acute test (3-h) basal GH secretion increases as a function of fetal age, with the greatest increase occurring after 12-13 weeks; however, the 3 h/24 h secretion ratio remains unchanged, at approximately 12%. GRF (0.1-10 nM) stimulates GH release in a dose-related fashion, regardless of fetal age; there is a significant increase in the response to both 1 nM (P < 0.05) and 10 nM (P < 0.01) GRF between 9-10 and 15-19 weeks fetal age and to 10 nM GRF (P < 0.05) between 12-13 and 15-19 weeks. Pretreatment of cultures (9-19 weeks) with 1 or 10 nM GRF for 24 h does not alter basal 3-h GH secretion, but significantly decreases subsequent responses to 1 or 10 nM GRF, respectively (P < 0.01). Pretreatment with 1 nM GRF does not alter a subsequent 3-h response to 10 nM GRF. SRIF-(1-14) (1-100 nM) causes a dose-related inhibition of basal GH secretion from as early as the ninth week of fetal life; there is a small age-related increase in the somatotrope response to 100 nM SRIF-(1-14) between 12-13 and 15-19 weeks fetal age (P < 0.05). In a group of 11- to 14-week-old fetal pituitaries, SRIF-(1-28) had a significantly (P < 0.05) greater inhibitory effect than SRIF-(1-14) at both 1 and 10 nM; the two peptides decreased basal GH secretion to a similar extent at 100 nM (52.8 +/- 4.0% of control value; P < 0.01). SRIF-(1-14) (10 and 100 nM) does not significantly alter 10 nM GRF-stimulated GH release from 9- to 10-week-old fetal pituitaries. However, by 12-13 weeks, 10 nM SRIF-(1-14) reduces GRF-stimulated GH secretion by 60% (P < 0.01), while 100 nM SRIF-(1-14) decreases it by 80% (P < 0.01); similar inhibitory effects are observed with 15- to 19-week-old fetal somatotropes.(ABSTRACT TRUNCATED AT 400 WORDS)
利用人垂体前叶外植体培养物(胎龄9 - 19周)和急性(3小时)试验方案,我们研究了胎儿生长激素细胞对人生长激素释放因子[hGRF-(1 - 44)]和生长抑素[SRIF-(1 - 14)和SRIF-(1 - 28)]的反应性随年龄的变化。使用三个年龄组分析个体发育数据:胎龄9 - 10周、12 - 13周和15 - 19周。每日(24小时)和急性试验(3小时)的基础生长激素分泌均随胎龄增加,在12 - 13周后增加最为显著;然而,3小时/24小时分泌比率保持不变,约为12%。生长激素释放因子(0.1 - 10 nM)以剂量相关方式刺激生长激素释放,与胎龄无关;在胎龄9 - 10周和15 - 19周之间,对1 nM(P < 0.05)和10 nM(P < 0.01)生长激素释放因子的反应显著增加,在12 - 13周和15 - 19周之间对10 nM生长激素释放因子的反应也显著增加(P < 0.05)。用1或10 nM生长激素释放因子对培养物(9 - 19周)预处理24小时不会改变基础3小时生长激素分泌,但分别显著降低随后对1或10 nM生长激素释放因子的反应(P < 0.01)。用1 nM生长激素释放因子预处理不会改变随后对10 nM生长激素释放因子的3小时反应。生长抑素-(1 - 14)(1 - 100 nM)从胎儿生命的第9周起就导致基础生长激素分泌呈剂量相关的抑制;在胎龄12 - 13周和15 - 19周之间,生长激素细胞对100 nM生长抑素-(1 - 14)的反应有与年龄相关的小幅增加(P < 0.05)。在一组11 - 14周龄的胎儿垂体中,在1 nM和10 nM时,生长抑素-(1 - 28)的抑制作用均显著大于生长抑素-(1 - 14)(P < 0.05);在100 nM时,两种肽将基础生长激素分泌降低到相似程度(对照值的52.8 +/- 4.0%;P < 0.01)。生长抑素-(1 - 14)(10和100 nM)不会显著改变10 nM生长激素释放因子刺激的9 - 10周龄胎儿垂体的生长激素释放。然而,到12 - 13周时,10 nM生长抑素-(1 - 14)将生长激素释放因子刺激的生长激素分泌降低60%(P < 0.01),而100 nM生长抑素-(1 - 14)将其降低80%(P < 0.01);在15 - 19周龄的胎儿生长激素细胞中也观察到类似的抑制作用。(摘要截选至400字)