Cella S G, Locatelli V, Broccia M L, Menegola E, Giavini E, De Gennaro Colonna V, Torsello A, Wehrenberg W B, Müller E E
Department of Pharmacology, Chemotherapy and Toxicology, University of Milan, Italy.
J Endocrinol. 1994 Jan;140(1):111-7. doi: 10.1677/joe.0.1400111.
We have studied the effects of intra-amniotic administration of an anti-GH-releasing hormone serum (GHRH-Ab) on day 16 of fetal life in the rat, when the ontogenetic development of the GHRH neuronal system occurs. Control animals received normal rabbit serum. Following delivery, body weight was monitored for the next 30 days as an index of somatic growth, and the following indices of somatotrophic function were determined: plasma and pituitary GH, pituitary GH mRNA, hypothalamic GHRH and somatostatin mRNA, and the in vivo GH responsiveness to GHRH. At birth, GHRH-Ab-treated rats had a body weight that was equivalent to that of control rats but, starting from postnatal day 6 up to day 30, they had a significantly reduced body weight. Pituitary weight, the absolute pituitary GH content and GH mRNA levels were lower in experimental compared with control rats, while pituitary GH concentrations were similar in the two groups, thus implying that there was a defect, not only in GH synthesis, but also in GH release. In agreement with this theory, basal GH levels and GHRH-stimulated GH secretion were reduced in GHRH-Ab-treated rats but, in contrast, hypothalamic regulation of GH secretion appeared to be working in these rats as they were still able to respond to the low plasma GH by increasing GHRH and decreasing somatostatin mRNA levels. These findings indicate that deprivation of GHRH during fetal life induces long-lasting changes of growth rate and somatotrophic function.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了在大鼠胎儿期第16天羊膜腔内注射抗生长激素释放激素血清(GHRH-Ab)的影响,此时GHRH神经元系统正处于个体发生发育阶段。对照动物注射正常兔血清。分娩后,监测接下来30天的体重作为躯体生长指标,并测定以下生长激素功能指标:血浆和垂体生长激素、垂体生长激素mRNA、下丘脑GHRH和生长抑素mRNA,以及生长激素对GHRH的体内反应性。出生时,接受GHRH-Ab处理的大鼠体重与对照大鼠相当,但从出生后第6天到第30天,它们的体重显著降低。与对照大鼠相比,实验大鼠的垂体重量、垂体生长激素绝对含量和生长激素mRNA水平较低,而两组的垂体生长激素浓度相似,这意味着不仅生长激素合成存在缺陷,生长激素释放也存在缺陷。与此理论一致,接受GHRH-Ab处理的大鼠基础生长激素水平和GHRH刺激的生长激素分泌减少,但相反,这些大鼠的生长激素分泌下丘脑调节似乎仍在起作用,因为它们仍能通过增加GHRH和降低生长抑素mRNA水平来对低血浆生长激素做出反应。这些发现表明,胎儿期缺乏GHRH会导致生长速率和生长激素功能的长期变化。(摘要截断于250字)