Abstract

The past decade has seen several critical advances in our understanding of hypothalamic–pituitary–adrenal (HPA) axis regulation. Homeostatic physiological circuits need to integrate multiple internal and external stimuli and provide a dynamic output appropriate for the response parameters of their target tissues. The HPA axis is an example of such a homeostatic system. Recent studies have shown that circadian rhythmicity of the major output of this system—the adrenal glucocorticoid hormones corticosterone in rodent and predominately cortisol in man—comprises varying amplitude pulses that exist due to a subhypothalamic pulse generator. Oscillating endogenous glucocorticoid signals interact with regulatory systems within individual parts of the axis including the adrenal gland itself, where a regulatory network can further modify the pulsatile release of hormone. The HPA axis output is in the form of a dynamic oscillating glucocorticoid signal that needs to be decoded at the cellular level. If the pulsatile signal is abolished by the administration of a long-acting synthetic glucocorticoid, the resulting disruption in physiological regulation has the potential to negatively impact many glucocorticoid-dependent bodily systems. Even subtle alterations to the dynamics of the system, during chronic stress or certain disease states, can potentially result in changes in functional output of multiple cells and tissues throughout the body, altering metabolic processes, behavior, affective state, and cognitive function in susceptible individuals. The recent development of a novel chronotherapy, which can deliver both circadian and ultradian patterns, provides great promise for patients on glucocorticoid treatment.

Highlights

  • The past decade has seen several critical advances in our understanding of hypothalamic–pituitary–adrenal (HPA) axis regulation

  • Pulsatile glucocorticoid production arises due to a subhypothalamic pulse generator and is the intrinsic property of the feed-forward feedback interplay between the pituitary and adrenal glands

  • Long-standing models of glucocorticoid receptor (GR) and mineralocorticoid receptor (MR) working in collaboration and in opposition have retained their validity for the most part, with recent evidence for a role of MR in increasing GR transactivation potential during pulsatile glucocorticoid treatment, via a tethering mechanism

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Summary

Essential points

Pulsatile glucocorticoid production arises due to a subhypothalamic pulse generator and is the intrinsic property of the feed-forward feedback interplay between the pituitary and adrenal glands. It is a multisystem axis that utilizes feed-forward and feedback loops to regulate glucocorticoid hormone levels within the physiological range appropriate for system homeostasis This is an equilibrium control system we have called continuous dynamic equilibration [1]. These cells project to the capillaries of the median eminence, where they secrete corticotropin-releasing hormone (CRH) (and AVP) directly into the portal system and thence pituitary corticotrophs to regulate adrenocorticotropin (ACTH) secretion. This travels in the systemic circulation to reach the zona fasciculata of the adrenal cortex to activate the synthesis and subsequent release of glucocorticoid hormones [7]

Dynamics Within the HPA Axis in Health
Lightman et al ACTH and Cortisol Secretion in Disease
Glucocorticoids ACTH
Decoding the Glucocorticoid Oscillating Signal at the Cellular Level
Peripheral circulating CORT
Altered HPA Dynamics in Disease
Treatment with Synthetic Glucocorticoids
Findings
Pharmacological Modulation of the Psychiatric

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