5-HT(1A) receptor and apoptosis contribute to interferon-α-induced "depressive-like" behavior in mice

Neurosci Lett. 2012 Apr 18;514(2):173-8. doi: 10.1016/j.neulet.2012.02.087. Epub 2012 Mar 5.

Abstract

Interferon-α (IFN-α)-induced "depressive-like" behavior is a major limitation for the treatment of hepatitis C virus (HCV), especially for patients with psychiatric disorders. Recently, serotonin 1A (5-HT(1A)) receptor and cellular apoptosis are involved in mechanism(s) contributing to depression. To gain insight into this mechanism(s), we used C57BL/6J mice to examine the impact of IFN-α on the modulation of 5-HT(1A) receptor and cellular apoptosis and their relationship. Our results showed that repeated administration of IFN-α (6 MIU/kg, s.c.) induced "depressive-like" behavior of mice in the forced swim test, tail suspension test and sucrose preference test. Besides, the depressive mice exhibited a notable downregulation of 5-HT(1A) receptor and upregulation of cleaved caspase-3 and Bax/Bcl-2 ratio. These changes could be blocked by the 5-HT(1A) receptor agonist 8-OH-DPAT (0.5 mg/kg, i.p., 30 min before IFN-α administration), but not by the standard antidepressant imipramine (10 mg/kg, i.p., 30 min before IFN-α administration) although both of them could ameliorate the depressive-like behavior of mice. These findings indicated that repeated injection with IFN-α provoked "depressive-like" behavior through cellular apoptosis, which could be ameliorated by the activation of 5-HT(1A) receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology
  • Apoptosis / physiology*
  • Behavior, Animal / drug effects*
  • Behavior, Animal / physiology
  • Depression / chemically induced
  • Depression / metabolism*
  • Hindlimb Suspension
  • Imipramine / pharmacology
  • Interferon-alpha / pharmacology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Motor Activity / drug effects
  • Motor Activity / physiology
  • Receptor, Serotonin, 5-HT1A / metabolism*

Substances

  • Antidepressive Agents
  • Interferon-alpha
  • Receptor, Serotonin, 5-HT1A
  • Imipramine