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Fasting and prolonged food restriction differentially affect GH secretion independently of GH receptor signaling in AgRP neurons.
de Sousa, Maria E; Gusmao, Daniela O; Dos Santos, Willian O; Moriya, Henrique T; de Lima, Felipe F; List, Edward O; Kopchick, John J; Donato, Jose.
Affiliation
  • de Sousa ME; Department of Physiology and Biophysics, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, 05508-000, Brazil.
  • Gusmao DO; Department of Physiology and Biophysics, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, 05508-000, Brazil.
  • Dos Santos WO; Department of Physiology and Biophysics, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, 05508-000, Brazil.
  • Moriya HT; Biomedical Engineering Laboratory, Escola Politecnica, Universidade de Sao Paulo, Sao Paulo, 05508-010, Brazil.
  • de Lima FF; Biomedical Engineering Laboratory, Escola Politecnica, Universidade de Sao Paulo, Sao Paulo, 05508-010, Brazil.
  • List EO; Edison Biotechnology Institute and Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, 45701, USA.
  • Kopchick JJ; Edison Biotechnology Institute and Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, 45701, USA.
  • Donato J; Department of Physiology and Biophysics, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, 05508-000, Brazil.
J Neuroendocrinol ; : e13254, 2023 Mar 12.
Article de En | MEDLINE | ID: mdl-36964750
ABSTRACT
Growth hormone (GH) receptor (GHR) is abundantly expressed in neurons that co-release the agouti-related protein (AgRP) and neuropeptide Y (NPY) in the arcuate nucleus of the hypothalamus (ARH). Since ARHAgRP/NPY neurons regulate several hypothalamic-pituitary-endocrine axes, this neuronal population possibly modulates GH secretion via a negative feedback loop, particularly during food restriction, when ARHAgRP/NPY neurons are highly active. The present study aims to determine the importance of GHR signaling in ARHAgRP/NPY neurons on the pattern of GH secretion in fed and food-deprived male mice. Additionally, we compared the effect of two distinct situations of food deprivation 16 h of fasting or four days of food restriction (40% of usual food intake). Overnight fasting strongly suppressed both basal and pulsatile GH secretion. Animals lacking GHR in ARHAgRP/NPY neurons (AgRP∆GHR mice) did not exhibit differences in GH secretion either in the fed or fasted state, compared to control mice. In contrast, four days of food restriction increased GH pulse frequency, basal GH secretion, and pulse irregularity/complexity (measured by sample entropy), whereas pulsatile GH secretion was not affected in both control and AgRP∆GHR mice. Hypothalamic Ghrh mRNA levels were unaffected by fasting or food restriction, but Sst expression increased in acutely fasted mice, but decreased after prolonged food restriction in both control and AgRP∆GHR mice. Our findings indicate that short-term fasting and prolonged food restriction differentially affect the pattern of GH secretion, independently of GHR signaling in ARHAgRP/NPY neurons.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Neuroendocrinol Sujet du journal: ENDOCRINOLOGIA / NEUROLOGIA Année: 2023 Type de document: Article Pays d'affiliation: Brésil

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Neuroendocrinol Sujet du journal: ENDOCRINOLOGIA / NEUROLOGIA Année: 2023 Type de document: Article Pays d'affiliation: Brésil