University of Bristol: Discovery of novel brain fear mechanisms offers target for anxiety-reducing drugs

A new target in the brain which underpins the eliciting of anxiety and fear behaviours such as ‘freezing’ has been identified by neuroscientists. The University of Bristol researchers say the discovery of a key pathway in the brain, published in the journal eLife, offers a potential new drug target for treating anxiety and psychological disorders, which affect an estimated 264-million people worldwide.

Existing anxiety-reducing drugs are not always effective for all patients and often have unwanted side effects. Understanding the brain networks and mechanisms which underlie fear and anxiety may offer a new approach to developing better treatments for anxiety disorders.

Neuroscientists from Bristol’s School of Physiology, Pharmacology and Neuroscience, sought to investigate how the brain’s cerebellum, which is connected to many brain regions associated with survival networks, influences activity in another area of the brain called the periaqueductal grey (PAG). This PAG area lies at the hub of central networks that co-ordinate survival mechanisms including fear-evoked coping responses such as ‘freezing’.

To investigate this, researchers fitted animal models with electrodes to record activity within the brain’s PAG region and applied a conditioning task, whereby an auditory tone is paired with a small foot shock, eliciting the formation of a ‘fear memory’ and freezing, a behavioural index of fear. The team showed that within the brain’s PAG area, a subset of brain cells increased their responsiveness to the conditioned tone, consistent with encoding a fear memory.

However, when cerebellar output was altered during conditioning, the subsequent timing of fear-related neuronal activity in the PAG became less precise and the duration of fear-related freezing behaviour was increased confirming that cerebellar-periaqueductal grey interactions contribute to fear conditioning processes. The team showed that the manipulation of a direct cerebellar-PAG pathway, also caused impairments in fear conditioned freezing and ultrasonic vocalisations.

The study’s lead authors, Dr Charlotte Lawrenson and Dr Elena Paci, explain: “Until now, little was understood about how the cerebellum modulates neuronal activity in other brain regions, especially those related to fear and anxiety. Importantly, our results show that the cerebellum is part of the brain’s survival network that regulates fear memory processes at multiple timescales and in multiple ways; raising the possibility that dysfunctional interactions in the brain’s cerebellar-survival network may underlie fear-related disorders and comorbidities.”