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Centre de Medecine Nucleaire, Unite de Soins Hospital Neuro-Cardiologique, 69003 Lyon, France
Service de Radioanalyse Hospital Neuro-Cardiologique, 69003 Lyon, France
Department de Pharmacologie Clinique Hospital Neuro-Cardiologique, 69003 Lyon, France
Service Pharmaceutique Hospital Neuro-Cardiologique, 69003 Lyon, France
Inserm U34 Hopital Debrousse, 69005 Lyon, France
Inserm U45 Hopital Edouard Herriot, 69374 Lyon, France
Department of Pediatrics University of North Carolina, Chapel Hill, North Carolina 27514
Address requests for reprints to: Genevieve Sassolas, Centre de Medecine Nucleaire, Hopital Neuro-Cardiologique, 59 Boulevard Pinel, 69394 Lyon Cedex 3, France.
Synthetic human pancreatic tumor GH-releasing hormone (hpGRH l-44-NH2) was given by iv bolus injection to 10 normal men at doses of 75, 150, 300, and 600 µg. At all doses the plasma GH responses were similar in an individual subject. Among subjects, however, the responses were significantly different, with peak GH concentrations ranging between 9.0 µg/liter and 54.9 µg/liter. The GH released in response to GRH was bioactive in the Nb2 lymphoma cell multiplication assay. The circulating GH 30 and 60 min after GRH was detected in 3 molecular forms corresponding to little, big, and big-big GH. These forms averaged 50%, 30%, and 20% of the total immunoreactive GH, respectively. The mean rise of plasma somatomedin-C, from 1.86 U/ml to 2.21 U/ml 24 h after GRH, was not statistically significant. A small but statistically significant GRH dose-dependent rise in plasma PRL (mean PRL concentrations 10 min after 600 fig GRH, 11.13 µg/liter occurred consistently after GRH injection. The evidence that the GH released by GRH is bioactive supports the potential use of GRH for therapeutic applications.
* This work was supported by Fondation pour la Recherche Medicale Francaise, by SANOFI, and by USPHS Grant AM-01022.
Received December 13, 1983.
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