The role of galanin and its receptor in the feedback regulation of growth hormone secretion
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Date
Authors
Clifton, Donald K.
Steiner, Robert A.
Grafstein-Dunn, Ellen
Chan, Yvonne Y.
Burton, Kimberly A.
Delemarre-van de Waal, Henriette A.
Journal Title
Journal ISSN
Volume Title
Publisher
Endocrine Society
Abstract
GH controls its own secretion through a mechanism involving short-loop
feedback regulation of the synthesis and release of GH-releasing hormone
(GHRH). GHRH neurons coexpress the peptide galanin, but the functional
significance of this coexpression is unknown. In this study, we tested the
hypotheses that 1) galanin gene expression in GHRH neurons is regulated by
GH and 2) somatostatin (SS) or GHRH neurons are a target for the action of
galanin in the hypothalamus. First, we compared levels of galanin
messenger RNA (mRNA) in GHRH neurons between normal male rats and Lewis
dwarf rats, which have markedly reduced blood levels of GH. The brains of
normal and dwarf animals were processed for detection of galanin mRNA and
GHRH mRNA by double-label in situ hybridization. We observed that Lewis
dwarf rats had significantly reduced levels of galanin mRNA in their GHRH
neurons (P < 0.05). Next, we tested the hypothesis that GH regulates
galanin gene expression in GHRH neurons by experimentally altering
circulating levels of GH. Three groups of adult male rats were used: 1)
intact rats (n = 7); 2) hypophysectomized (hypox) rats (n = 7); and 3)
hypox rats treated with 1.5 mg of rat GH (rGH) over a 3-day period (n =
6). At the end of the treatment period, the animals were killed, and their
brains were collected and processed for double-label in situ hybridization
for GHRH mRNA and galanin mRNA. The signal level of galanin mRNA in GHRH
neurons was reduced in hypox animals to less than 10% of that in intact
controls (P < 0.0001); whereas, the levels of galanin mRNA signal in GHRH
neurons did not differ significantly between the groups of intact and
rGH-treated hypox rats. Finally, to determine whether SS or GHRH neurons
are targets for galanin, we used double-label in situ hybridization to
determine whether either of these populations of neurons express galanin
receptor mRNA. A subset of SS neurons in the PeN appeared to express the
galanin receptor mRNA, whereas few, if any, GHRH neurons appeared to do
so. We conclude that galanin, like its cotransmitter GHRH, is a target for
GH action, and we infer that galanin may play a role in the feedback
control of GH secretion by exerting a direct effect on SS neurons.
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Citation
Endocrinology. 1996 Dec;137(12):5303-10
