Central serotonin transporter levels are associated with stress hormone response and anxiety

Psychopharmacology (Berl). 2011 Feb;213(2-3):563-72. doi: 10.1007/s00213-010-1903-y. Epub 2010 Jun 29.

Abstract

Rationale: Negative mood states are characterized by both stress hormone dysregulation and serotonergic dysfunction, reflected by altered thalamic serotonin transporter (5-HTT) levels. However, so far, no study examined the individual association between cortisol response and cerebral in vivo 5-HTT levels in patients suffering from negative mood states.

Objective: The objective of this cross-sectional study was to assess the interrelation of cortisol response, thalamic 5-HTT levels, and anxiety in healthy subjects and two previously published samples of patients with unipolar major depression (UMD) and obsessive-compulsive disorder (OCD), controlling for age, gender, 5-HTT genotype, smoking, and seasonality.

Methods: Regional 5-HTT levels and cortisol response to dexamethasone-corticotropin (Dex-CRH) challenge were assessed in consecutive samples of medication-free patients suffering from UMD (N = 10) and OCD (N = 10), and 20 healthy volunteers. The intervention used was combined Dex-CRH test and [(11)C]DASB positron emission tomography. The main outcome measures were: 5-HTT binding potential (BP(ND)) in a predefined thalamic ROI, cortisol response defined as the maximum cortisol increase in the combined Dex-CRH-test, and state of anxiety from the state-trait-anxiety inventory.

Results: Reduced thalamic 5-HTT BP(ND) was associated with increased cortisol response (r = -0.35, p < 0.05; in patients: r = -0.53, p < 0.01) and with increased state anxiety (r = -0.46, p < 0.01), surviving correction for age, gender, 5-HTT genotype, smoking, and seasonality (p < 0.05). The 5-HTT genotype, on the contrary, was not significantly associated with cortisol response (p = 0.19) or negative mood (p = 0.23).

Conclusion: The association between stress hormone response, thalamic 5-HTT levels, and anxiety in patients suffering from negative mood states suggests an interaction between two major mechanisms implicated in negative mood states in humans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenocorticotropic Hormone / pharmacology
  • Adult
  • Anxiety Disorders / physiopathology*
  • Case-Control Studies
  • Cross-Sectional Studies
  • Depressive Disorder, Major / physiopathology*
  • Dexamethasone / pharmacology
  • Female
  • Humans
  • Hydrocortisone / metabolism
  • Male
  • Middle Aged
  • Obsessive-Compulsive Disorder / physiopathology*
  • Positron-Emission Tomography / methods
  • Serotonin Plasma Membrane Transport Proteins / metabolism*
  • Thalamus / metabolism

Substances

  • Serotonin Plasma Membrane Transport Proteins
  • Dexamethasone
  • Adrenocorticotropic Hormone
  • Hydrocortisone