Cited by 16Growth Hormone and Insulin-like Growth FactorsHypothalamic control of reproductive hormonesPituitary Gland Disorders and Treatments

Regulation of pituitary growth hormone-secretagogue and growth hormone-releasing hormone receptor RNA expression in young Dwarf rats

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HORIKAWA, REIKO, TACHIBANA, TOSHAKI, KATSUMATA, NORIYUKI, ISHIKAWA, HIROSHI, TANAKA, TOSHIAKI·2000·Endocrine Journal

Abstract

Growth hormone-secretagogue receptor (GHSR) RNA is known to be expressed in the hypothalamus and pituitary. Since endogenous GH secretagogue (GHS) is still unknown, the physiological role of GHS and GHSR in growth is not well understood. In this study, we have determined the effects of growth hormone in GH-releasing hormone receptor (GHRHR) and GHSR RNA expression in spontaneous Dwarf rats (SDRs) which are deficient in GH secretion, with or without GH replacement. Twenty-five-day-old SDRs received daily s.c. injection of human GH (40 microg/kg BW x 2/day) or control solution for two weeks. On day 40, the rats were sacrificed by decapitation and the pituitaries were immediately removed and quickly frozen. Total RNA was extracted from the pituitary, and mRNA coding GHSR was detected and semi-quantitated by competitive RT-PCR. Pituitaries from control SDRs showed strong GHSR RNA expression and the expression level was 5 to 10 times higher in females than in males. When GH was replaced, GHSR RNA expression greatly decreased. Pituitary GHRHR RNA expression, determined by RNase Protection Assay, was similar in male and female control animals; and was also greatly reduced in rats treated with GH when compared to the control. These results suggest that the expression of both GHSR and GHRHR is regulated by growth hormone, presumably via changes in hypothalamic GHRH and/or endogenous GHS. The apparent sexual dimorphism in GHSR indicates different regulatory effects of sex steroid in young growing SDRs.

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Crossref · 10.1507/endocrj.47.supplmarch_s53

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  • E2 may upregulate receptor-dependent actions of GHRP.

    “Laboratory data are consistent with a unifying notion that E 2 may upregulate receptor-dependent actions of GHRP.”

    From Determinants of dual secretagogue drive of burst-like growth hormone secretion in premenopausal women studied under a selective estradiol clamp (2005) · cites this paper as [54]

    The Abstract and RNA analysis section report substantially higher pituitary GHSR RNA in female than male dwarf rats and suggest sex-steroid regulation. They do not test E2 or show that it upregulates receptor-dependent responses to GHRP; the measured outcome was receptor RNA expression, not GHRP action. (LLM, conf=0.78)

    Experimental — accuracy not yet measured
  • Gene transcripts encoding the pituitary GHRP receptor are 2- to 10-fold more abundant in the adult female than male rodent pituitary.

    “gene transcripts encoding the pituitary GHRP receptor are 2to 10-fold more abundant in the adult female than male rodent pituitary”

    From Determinants of dual secretagogue drive of burst-like growth hormone secretion in premenopausal women studied under a selective estradiol clamp (2005) · cites this paper as [54]

    The RNA analysis reports about tenfold higher pituitary GHSR RNA in female than male spontaneous dwarf rats; the study examined young rats at day 40, not adults. The Discussion also reports that GHSR expression became higher in males in normal rats at day 45. The source therefore does not support the claim’s generalization to adult rodents or its 2-to-10-fold range. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • E2 induces transcription of the human GHRP receptor gene in vitro.

    “and E 2 induces transcription of the human GHRP receptor gene in vitro (23,54,55).”

    From Determinants of dual secretagogue drive of burst-like growth hormone secretion in premenopausal women studied under a selective estradiol clamp (2005) · cites this paper as [54]

    The Abstract and RNA analysis discuss GHSR RNA expression in dwarf-rat pituitaries, including differences between males and females and suppression after GH treatment. A search for E2 or estradiol-induced transcription of the human GHRP receptor gene in vitro found no passage addressing that claim; the rat findings do not establish or contradict it. Page numbers were not available in our copy. (LLM, conf=0.75)

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Authors
HORIKAWA, R., TACHIBANA, T., KATSUMATA, N., ISHIKAWA, H., & TANAKA, T.
Affiliations
  • Endocrine Research Laboratoy, National Children';s Medical Research Center
  • Jikei University School of Medicine (JP)
Venue
Endocrine Journal
Published
2000
Volume
47
Issue
SupplMarch
Pages
S53-S56
ISSN
  • 0918-8959 (ISSN-L)
  • 1348-4540
OpenAlex
W2134884098
Cited by
16
References
6
Citations by year
2025: 1 · 2018: 1 · 2012: 2
FWCI
0.50
Type
journal article
Language
en
Open access
Locations
  • Endocrine Journal (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
  • Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
Keywords
growth hormone secretagogue receptor, growth hormone-releasing hormone receptor, pituitary gland, dwarf rats, growth hormone replacement therapy, growth hormone regulation, sex differences, gene expression regulation
MeSH terms
Animals, Animals, Newborn, Dwarfism, Female, Humans, Injections, Subcutaneous, Male, Pituitary Gland, Rats, Mutant Strains, Receptors, Cell Surface, RNA, Messenger, Sex Characteristics, Receptors, Neuropeptide, Receptors, Pituitary Hormone-Regulating Hormone, Human Growth Hormone, Receptors, G-Protein-Coupled, Rats, Receptors, Ghrelin

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