MECHANISMS IN ENDOCRINOLOGY: Lessons from growth hormone receptor gene-disrupted mice: are there benefits of endocrine defects?

Eur J Endocrinol. 2018 May;178(5):R155-R181. doi: 10.1530/EJE-18-0018. Epub 2018 Feb 19.

Abstract

Growth hormone (GH) is produced primarily by anterior pituitary somatotroph cells. Numerous acute human (h) GH treatment and long-term follow-up studies and extensive use of animal models of GH action have shaped the body of GH research over the past 70 years. Work on the GH receptor (R)-knockout (GHRKO) mice and results of studies on GH-resistant Laron Syndrome (LS) patients have helped define many physiological actions of GH including those dealing with metabolism, obesity, cancer, diabetes, cognition and aging/longevity. In this review, we have discussed several issues dealing with these biological effects of GH and attempt to answer the question of whether decreased GH action may be beneficial.

Publication types

  • Review

MeSH terms

  • Animals
  • Endocrine System Diseases / genetics*
  • Endocrine System Diseases / physiopathology*
  • Endocrine System Diseases / psychology
  • Growth Hormone / physiology*
  • Human Growth Hormone / physiology*
  • Humans
  • Laron Syndrome / genetics
  • Laron Syndrome / physiopathology
  • Longevity
  • Mice
  • Mice, Knockout / genetics*
  • Receptors, Somatotropin / genetics*

Substances

  • Receptors, Somatotropin
  • Human Growth Hormone
  • Growth Hormone