Chronic growth hormone (GH) hypersecretion induces reciprocal and reversible changes in mRNA levels from hypothalamic GH-releasing hormone and somatostatin …

J Bertherat, J Timsit, MT Bluet-Pajot… - The Journal of …, 1993 - Am Soc Clin Investig
J Bertherat, J Timsit, MT Bluet-Pajot, JJ Mercadier, D Gourdji, C Kordon, J Epelbaum
The Journal of clinical investigation, 1993Am Soc Clin Investig
Effects of growth hormone (GH) hypersecretion on somatostatin-(SRIH) and GH-releasing
hormone (GHRH) were studied by in situ hybridization and receptor autoradiography in rats
bearing a GH-secreting tumor. 6 and 18 wk after tumor induction, animals displayed a sharp
increase in body weight and GH plasma levels; pituitary GH content was reduced by 47 and
55%, while that of prolactin and thyrotropin was unchanged. At 18 wk, hypothalamic GHRH
and SRIH levels had fallen by 84 and 52%, respectively. In parallel, the density of GHRH …
Effects of growth hormone (GH) hypersecretion on somatostatin-(SRIH) and GH-releasing hormone (GHRH) were studied by in situ hybridization and receptor autoradiography in rats bearing a GH-secreting tumor. 6 and 18 wk after tumor induction, animals displayed a sharp increase in body weight and GH plasma levels; pituitary GH content was reduced by 47 and 55%, while that of prolactin and thyrotropin was unchanged. At 18 wk, hypothalamic GHRH and SRIH levels had fallen by 84 and 52%, respectively. In parallel, the density of GHRH mRNA per arcuate neuron was reduced by 52 and 50% at 6 and 18 wk, while SRIH mRNA levels increased by 71 and 83% in the periventricular nucleus (with no alteration in the hilus of the dentate gyrus). The numbers of GHRH- and SRIH-synthetizing neurons in the hypothalamus were not altered in GH-hypersecreting rats. Resection of the tumor restored hypothalamic GHRH and SRIH mRNAs to control levels. GH hypersecretion did not modify 125I-SRIH binding sites on GHRH neurons. Thus, chronic GH hypersecretion affects the expression of the genes encoding for GHRH and SRIH. The effect is long lasting, not desensitizable and reversible.
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The Journal of Clinical Investigation