Central growth hormone action regulates metabolism during pregnancy

Am J Physiol Endocrinol Metab. 2019 Nov 1;317(5):E925-E940. doi: 10.1152/ajpendo.00229.2019. Epub 2019 Sep 3.

Abstract

The maternal organism undergoes numerous metabolic adaptations to become prepared for the demands associated with the coming offspring. These metabolic adaptations involve changes induced by several hormones that act at multiple levels, ultimately influencing energy and glucose homeostasis during pregnancy and lactation. Previous studies have shown that central growth hormone (GH) action modulates glucose and energy homeostasis. However, whether central GH action regulates metabolism during pregnancy and lactation is still unknown. In the present study, we generated mice carrying ablation of GH receptor (GHR) in agouti-related protein (AgRP)-expressing neurons, in leptin receptor (LepR)-expressing cells or in the entire brain to investigate the role played by central GH action during pregnancy and lactation. AgRP-specific GHR ablation led to minor metabolic changes during pregnancy and lactation. However, while brain-specific GHR ablation reduced food intake and body adiposity during gestation, LepR GHR knockout (KO) mice exhibited increased leptin responsiveness in the ventromedial nucleus of the hypothalamus during late pregnancy, although their offspring showed reduced growth rate. Additionally, both Brain GHR KO and LepR GHR KO mice had lower glucose tolerance and glucose-stimulated insulin secretion during pregnancy, despite presenting increased insulin sensitivity, compared with control pregnant animals. Our findings revealed that during pregnancy central GH action regulates food intake, fat retention, as well as the sensitivity to insulin and leptin in a cell-specific manner. Together, the results suggest that GH acts in concert with other "gestational hormones" to prepare the maternal organism for the metabolic demands of the offspring.

Keywords: food intake; gestation; glucose homeostasis; hypothalamus; leptin resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity / genetics
  • Animals
  • Brain Chemistry / genetics
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Eating
  • Female
  • Glucose Intolerance / genetics
  • Glucose Intolerance / metabolism
  • Growth Hormone / physiology*
  • Insulin Resistance / genetics
  • Leptin / metabolism
  • Mice
  • Mice, Knockout
  • Neurons / metabolism
  • Pregnancy
  • Pregnancy, Animal / metabolism*
  • Receptors, Leptin / metabolism

Substances

  • Carrier Proteins
  • Leptin
  • Receptors, Leptin
  • Growth Hormone
  • somatotropin-binding protein