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Monensin influences basal and human growth hormone-releasing hormone 44-induced release of stored and new rat growth hormone and prolactin

  • P. K. Farmer
    ,
  • J. M. Tyler
    ,
  • M. E. Stachura(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
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Open access

Abstract

When previous data suggested a growth hormone-releasing factor (GRF)-sensitive branch in intracellular hormone processing, the monensin-sensitive Golgi apparatus seemed a likely candidate. We examined monensin's effect on basal and GRF-stimulated release of newly synthesized and stored rat growth hormone (rGH) and rat prolactin (rPRL). 14C-Pre-labeled, perifused rat pituitary fragments were exposed to [3H]leucine in 0-10 fiM monensin; a pulse of 3 nM GRF assessed subsequent secretory responsivity. Monensin dose-dependently reduced basal release of stored [14C]rGH and [14C]rPRL. GRF timulated release of stored [14C]hormone was doubled after 0.03 μM and 0.1 μM monensin; higher concentrations diminished stored hormone release. Low concentrations of monensin accelerated basal (0.03 μM and 0.1 μM) and GRF-stimulated (0.03 μM) [3H]rGH and [3H]rPRL release without altering recovery; higher monensin concentrations (≥1 μM) reduced basal, and abolished GRF-stimulated, new hormone release and reduced total [3H]rGH and [3H]rPRL recovery. These data are consistent with a GRF-sensitive and monensin-influenced branch in intracellular hormone processing that regulates the fraction of new hormone exiting the cell without prior immersion in storage compartments.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 253-262 (10 pages)

Journal (Volume, Issue Number)

Molecular and Cellular Endocrinology (Volume 62, Issue 2)

Publication milestones

  • Published - 04/1989

Publication status

Published - 04/1989

ISSN

0303-7207

Publication IDs

  • Scopus: 0024507069
  • PubMed: 2501124

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Funding Details

Supported by the Medical Research Service of the Veterans Administration. We acknowledge with appreciation the excellent assistance of P. Kent, V. Phillips, and E. Shepard.