Growth hormone enhances the recovery of hypoglycemia via ventromedial hypothalamic neurons

FASEB J. 2019 Nov;33(11):11909-11924. doi: 10.1096/fj.201901315R. Epub 2019 Jul 31.

Abstract

Growth hormone (GH) is secreted during hypoglycemia, and GH-responsive neurons are found in brain areas containing glucose-sensing neurons that regulate the counter-regulatory response (CRR). However, whether GH modulates the CRR to hypoglycemia via specific neuronal populations is currently unknown. Mice carrying ablation of GH receptor (GHR) either in leptin receptor (LepR)- or steroidogenic factor-1 (SF1)-expressing cells were studied. We also investigated the importance of signal transducer and activator of transcription 5 (STAT5) signaling in SF1 cells for the CRR. GHR ablation in LepR cells led to impaired capacity to recover from insulin-induced hypoglycemia and to a blunted CRR caused by 2-deoxy-d-glucose (2DG) administration. GHR inactivation in SF1 cells, which include ventromedial hypothalamic neurons, also attenuated the CRR. The reduced CRR was prevented by parasympathetic blockers. Additionally, infusion of 2DG produced an abnormal hyperactivity of parasympathetic preganglionic neurons, whereas the 2DG-induced activation of anterior bed nucleus of the stria terminalis neurons was reduced in mice without GHR in SF1 cells. Mice carrying ablation of Stat5a/b genes in SF1 cells showed no defects in the CRR. In summary, GHR expression in SF1 cells is required for a normal CRR, and these effects are largely independent of STAT5 pathway.-Furigo, I. C., de Souza, G. O., Teixeira, P. D. S., Guadagnini, D., Frazão, R., List, E. O., Kopchick, J. J., Prada, P. O., Donato, J., Jr. Growth hormone enhances the recovery of hypoglycemia via ventromedial hypothalamic neurons.

Keywords: GH; autonomic nervous system; counter-regulatory response; cytokine; hypothalamus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Deoxyglucose / pharmacology
  • Growth Hormone / pharmacology*
  • Hypoglycemia / drug therapy*
  • Hypoglycemia / physiopathology
  • Hypothalamus / cytology
  • Hypothalamus / drug effects*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurons / physiology
  • Receptors, Leptin / genetics
  • Receptors, Leptin / metabolism
  • Receptors, Somatotropin / genetics
  • Receptors, Somatotropin / metabolism
  • Recovery of Function / drug effects*
  • STAT5 Transcription Factor / genetics
  • STAT5 Transcription Factor / metabolism
  • Signal Transduction / drug effects
  • Steroidogenic Factor 1 / genetics
  • Steroidogenic Factor 1 / metabolism

Substances

  • Receptors, Leptin
  • Receptors, Somatotropin
  • STAT5 Transcription Factor
  • Steroidogenic Factor 1
  • Growth Hormone
  • Deoxyglucose