Short CommunicationInsular muscarinic signaling regulates anxiety-like behaviors in rats on the elevated plus-maze

- Insular microinjection and rat elevated plus-maze are the main methods.
- Insular mAChR activation by nonselective and M1-, M4-selective agonists down-regulate anxiety-like behaviors.
- Insular mAChR inhibition by nonselective and M1-, M4-selective antagonists up-regulate anxiety-like behaviors.

Anxiety is one of the most prevalent neuropsychiatric disorders, and little is known about its pathogenesis. In order to investigate the neural mechanisms of this mental disorder, we used rat behavior in the elevated plus-maze as an animal model of anxiety and the insular cortex (insula) as a brain target. The microinjection of non-selective and selective M1 and M4 muscarinic acetylcholine receptor (mAChR) agonists or antagonists was used to explore whether the insular muscarinic receptor and its subtypes regulate levels of anxiety. The results showed that both non-selective and selective M1 and M4 mAChR agonists increased the time spent on exploring in the open arms, whereas antagonists decreased exploration. Our results indicate that activation of insular mAChRs could produce anxiolytic effects, whereas inhibition of insular mAChRs could increase anxiety. We concluded that the insular muscarinic system plays a role in the modulation of anxiety, and dysfunction of mAChR signaling may be involved in the mechanism of anxiogenesis.