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Metabolic clearance and plasma disappearance rates of human pancreatic tumor growth hormone releasing factor in man.
L A Frohman, J L Thominet, C B Webb, M L Vance, H Uderman, J Rivier, W Vale, M O Thorner
L A Frohman, J L Thominet, C B Webb, M L Vance, H Uderman, J Rivier, W Vale, M O Thorner
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Research Article

Metabolic clearance and plasma disappearance rates of human pancreatic tumor growth hormone releasing factor in man.

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Abstract

The metabolic clearance rate (MCR) and plasma disappearance rate (t1/2) of human pancreatic tumor growth hormone releasing factor [hpGRF(1-40)] was determined in normal adult male subjects by single injection and constant infusion techniques. Single injections of 1, 3.3, and 10 micrograms/kg hpGRF(1-40) were administered intravenously, plasma immunoreactive (IR) GRF levels were measured during the subsequent 180 min, and biexponential curve analysis was performed. Graded, dose-constant infusions of hpGRF(1-40) at rates of 1, 3.3, 10, and 33 ng/kg per min were administered and the MCR was calculated from measurement of steady state plasma IR-GRF levels at each infusion rate. The postinfusion disappearance rate was determined by linear regression analysis of plasma IR-GRF levels during the 120-min period after cessation of the infusion. The calculated MCR during the single injection study was 194 +/- 17.5 liters/m2 per d and was not significantly different from the calculated value during the constant infusion study (202 +/- 16 liters/m2 per d). The disappearance rate during the single injection study was subdivided into two linear phases: an initial equilibration phase (7.6 +/- 1.2 min) and a subsequent elimination phase (51.8 +/- 5.4 min). The latter was similar to the linear disappearance rate observed (41.3 +/- 3.0 min) after cessation of the constant infusion. The chromatographic and biologic characteristics of plasma IR-GRF, 30 min after injection, were similar to those of synthetic hpGRF(1-40). The results have been discussed in relation to the MCR of other hypothalamic hormones and have been used to extrapolate secretion rates of GRF in patients with ectopic GRF production.

Authors

L A Frohman, J L Thominet, C B Webb, M L Vance, H Uderman, J Rivier, W Vale, M O Thorner

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ISSN: 0021-9738 (print), 1558-8238 (online)

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