Calcium activated adenylyl cyclase AC8 but not AC1 is required for prolonged behavioral anxiety

Mol Brain. 2016 May 27;9(1):60. doi: 10.1186/s13041-016-0239-x.

Abstract

Background: Anxiety disorder is a state of mental discomfort while acute anxiety induces an enhancement of vigilance/arousal or increased anxious responses. Most of the previous studies investigated basic mechanisms for acute anxiety, while less information is available for prolonged or repetitive anxiety.

Results: In the present study, we wanted to examine possible molecular mechanisms for behavioral anxiety after repeated exposures. Performing a paradigm of five sessions of the elevated plus-maze (EPM), we show that the repeated exposure to the EPM induces a long-lasting anxiety causing a gradual increase of anxiolytic activity, which is maintained for at least 21 days. Genetic deletion of AC8 (adenylyl cyclase 8) but not AC1 abolished long-lasting anxiety.

Conclusions: Our results suggest that calcium-stimulated AC8 is required to sustain the long-lasting anxiety caused by repeated EPM testing, and we can identify in AC8 a novel target for treating anxiety-related mood disorders.

Keywords: Adenylyl cyclase 8; Anterior cingulate cortex; Anxiety; Elevated plus-maze; Memory; N-Methyl-D-aspartate; Retest.

MeSH terms

  • Adenylyl Cyclases / metabolism*
  • Animals
  • Anxiety / enzymology*
  • Anxiety / physiopathology
  • Behavior, Animal*
  • Calcium / pharmacology*
  • Calcium Channels, L-Type / metabolism
  • Male
  • Maze Learning / drug effects
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Naloxone / pharmacology
  • Receptors, N-Methyl-D-Aspartate / metabolism

Substances

  • Calcium Channels, L-Type
  • Receptors, N-Methyl-D-Aspartate
  • Naloxone
  • Adenylyl Cyclases
  • adenylyl cyclase 1
  • adenylyl cyclase 8
  • Calcium

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