A new model for the HPA axis explains dysregulation of stress hormones on the timescale of weeks

Mol Syst Biol. 2020 Jul;16(7):e9510. doi: 10.15252/msb.20209510.

Abstract

Stress activates a complex network of hormones known as the hypothalamic-pituitary-adrenal (HPA) axis. The HPA axis is dysregulated in chronic stress and psychiatric disorders, but the origin of this dysregulation is unclear and cannot be explained by current HPA models. To address this, we developed a mathematical model for the HPA axis that incorporates changes in the total functional mass of the HPA hormone-secreting glands. The mass changes are caused by HPA hormones which act as growth factors for the glands in the axis. We find that the HPA axis shows the property of dynamical compensation, where gland masses adjust over weeks to buffer variation in physiological parameters. These mass changes explain the experimental findings on dysregulation of cortisol and ACTH dynamics in alcoholism, anorexia, and postpartum. Dysregulation occurs for a wide range of parameters and is exacerbated by impaired glucocorticoid receptor (GR) feedback, providing an explanation for the implication of GR in mood disorders. These findings suggest that gland-mass dynamics may play an important role in the pathophysiology of stress-related disorders.

Keywords: dynamical compensation; endocrine circuits; exact adaptation; mathematical models of disease; systems medicine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenocorticotropic Hormone / metabolism*
  • Alcoholism / metabolism
  • Animals
  • Anorexia / metabolism
  • Endocrine Glands / growth & development*
  • Endocrine Glands / metabolism
  • Feedback, Physiological
  • Humans
  • Hydrocortisone / metabolism*
  • Hypothalamo-Hypophyseal System / metabolism*
  • Hypothalamo-Hypophyseal System / physiopathology
  • Models, Theoretical
  • Mood Disorders / metabolism*
  • Pituitary-Adrenal System / metabolism*
  • Pituitary-Adrenal System / physiopathology
  • Postpartum Period / metabolism
  • Receptors, Glucocorticoid / metabolism
  • Software
  • Stress, Physiological*

Substances

  • Receptors, Glucocorticoid
  • Adrenocorticotropic Hormone
  • Hydrocortisone