EFFECT OF GROWTH HORMONE-RELEASING FACTOR (1–44)NH2 ADMINISTRATION ON SOMATOTROPIN IN PIGS

1990 ◽  
Vol 70 (3) ◽  
pp. 785-793 ◽  
Author(s):  
J. L. JOHNSON ◽  
M. T. COFFEY ◽  
K. L. ESBENSHADE ◽  
B. R. SCHRICKER

Two experiments were conducted to examine the dose response and optimum pattern of subcutaneous (s.c.) administration of human growth hormone-releasing factor [hGRF (1–44)NH2]on serum somatotropin (ST) in barrows. In exp. 1, 10 barrows (79.9 ± 3.3 kg) were used in a replicated 5 × 5 Latin square and blood samples were collected for 300 min from a single injection of hGRF. Injecting 0, 1, 10, 40 or 100 μg hGRF kg−1 resulted in dose related increase (P < 0.01) in peak concentrations of pST (3.93, 4.41, 10.61, 16.01 and 23.56 ng mL−1), and area under the ST response curve (AUC) (565.4, 546.2, 757.5, 1048.0 and 1314.0 ng min mL−1, respectively). The 40 μg kg−1 dose resulted in a higher (P < 0.05) peak pST and AUC than 0 or 1 μg hGRF kg−1. Peak concentration and AUC were greater (P < 0.05) for the 100 μg hGRF kg−1 dose compared with the 0, 1 and 10 μg hGRF kg−1 doses, but there was no difference between the 40 and 100 μg kg−1 doses. In exp. 2, eight barrows (85.4 ± 8.0 kg) were used in a replicated 4 × 4 Latin square to examine the relationship between pattern of hGRF administration and serum ST. Blood samples were collected −15, 0 and 15 min from initiation of administration and then hourly for 24 h. Treatments were designed to deliver 160 μg hGRF kg−1 every 24 h and were administered as 40 μg kg−1 injected four times daily, 80 μg kg−1 injected twice daily or by continuous s.c. infusion. There was no difference (P > 0.10) between treatments for peak ST concentration, AUC or area above the ST baseline. These data indicated a dose response to s.c. hGRF injections and ST in barrows. Further, ST response was not altered by the pattern of s.c. administration when barrows received 160 μg hGRF kg−1 daily by either 4 or 2 discrete injections or by continuous infusion. Key words: Swine, somatotropin, growth hormone-releasing factor

1983 ◽  
Vol 61 (24) ◽  
pp. 1249-1253 ◽  
Author(s):  
M. Losa ◽  
G. K. Stalla ◽  
O. A. M�ller ◽  
K. Werder

1987 ◽  
Vol 253 (5) ◽  
pp. E508-E514
Author(s):  
J. Weiss ◽  
M. J. Cronin ◽  
M. O. Thorner

Growth hormone (GH) is secreted as pulses in vivo. To understand the signals governing this periodicity, we have established a perifusion-based model of pulsatile GH release. Male rat anterior pituitaries were dispersed and perifused with pulses of human growth hormone-releasing factor-(1--40) (GHRF), with or without a continuous or discontinuous somatostatin tonus. An experiment was composed of a 1-h base-line collection followed by four 3-h cycles; each contained single or paired 10-min infusion(s) of 3 nM GHRF. In testing the impact of somatostatin, the protocol was identical except that 0.3 nM somatostatin was added 30 min into the base-line period and then was either continued throughout the study or withdrawn during the periods of GHRF infusion. GH base lines with somatostatin were lower than vehicle base lines (P less than 0.05). GHRF pulses generated consistent peaks of GH release between 200 and 300 ng. min-1. (10(7) cells)-1, and these peaks were not altered by continuous somatostatin. In contrast, withdrawal of somatostatin during GHRF administration elicited markedly higher GH peaks (P less than 0.05) and more total GH release (P less than 0.05). This response could not be accounted for by the additive effects of GHRF and somatostatin withdrawal.


2009 ◽  
Vol 39 (4) ◽  
pp. 364-374 ◽  
Author(s):  
JACOB BONGERS ◽  
EDGAR P. HEIMER ◽  
THEODORE LAMBROS ◽  
YU-CHING E. PAN ◽  
ROBERT M. CAMPBELL ◽  
...  

2007 ◽  
Vol 100 (1) ◽  
pp. 49-58 ◽  
Author(s):  
Eckhardt S. Ferdinandi ◽  
Paul Brazeau ◽  
Kim High ◽  
Bryan Procter ◽  
Stephen Fennell ◽  
...  

Nature ◽  
1985 ◽  
Vol 315 (6018) ◽  
pp. 413-416 ◽  
Author(s):  
Robert E. Hammer ◽  
Ralph L. Brinster ◽  
Michael G. Rosenfeld ◽  
Ronald M. Evans ◽  
Kelly E. Mayo

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