Dopamine Neuron Activity Is Key To Conditioned Fear Extinction

When a feared outcome does not happen, activity in midbrain dopaminergic neurons is required to get rid of behavioral fear responses, researchers at the RIKEN Center for Brain Science have found. Their study study details the role of dopamine in ensuring that rats lose fear response in the prolonged absence of the stimulus.

Like animals, people develop conditioned responses, especially if strong negative emotions are involved. This fact was used beautifully in the movie Jaws as the simple musical theme frightened audiences, even when the shark was unseen.

Normally, fearful reactions will lessen over time as the conditioned stimulus (the music) is dissociated from the fearful experience (watching the movie). This is called fear extinction. When fear extinction does not happen normally, it can lead to anxiety disorders such as post-traumatic stress or phobias.

Fear Extinction Mechanisms

In order to understand how the brain regulates both the normal and pathological situations, the researchers performed a series of experiments in rats as they extinguished fearful associations. They reasoned that for fear extinction, an animal needs to recognize when an expected fearful event does not happen.

As dopamine neurons in some parts of the brain are known to be active when anticipated unpleasant events don’t happen, the team looked at dopamine neurons in a part of the brain called the ventral tegmental area (VTA).

Optogenetic inhibition of VTA-dopamine neurons during shock omission blocks extinction learning

Optogenetic inhibition of VTA-dopamine neurons during shock omission blocks extinction learning
Credit: Ray Luo et al, CC-BY

After conditioning rats to associate a specific sound with an aversive experience (a mild footshock), the team then began the extinction process. As expected, when the sound was played many times without the footshock, rats stopped behaving as if they were afraid of the sound.

However, when VTA dopamine neurons were silenced just after playing the sound — exactly when the rats expected their feet to be shocked — they could not unlearn the fear response. This showed that without VTA dopamine activity at that specific time, the mental link between the sound and the shock could not be removed.

Reward Vs. Fear Pathways

But what exactly does the VTA dopamine activity do?

This was not a simple question to answer because not all VTA dopamine neurons are connected to the same brain regions. Some are connected to brain regions known for their role in storing extinction memories, while others are connected areas related to reward learning.

Optogenetics allowed the team to block each of these pathways separately, and they found that they both affected fear extinction, but in opposite ways: blocking the reward pathway prevented fear extinction, while blocking the other pathway enhanced fear extinction.

VTA-dopamine neurons projecting to NAc mShell facilitate consolidation of extinction learning

VTA-dopamine neurons projecting to NAc mShell facilitate consolidation of extinction learning
Credit: Ray Luo et al, CC-BY

While the results are simple enough, obtaining them required technological effort. As team leader Joshua Johansen explained,

“This finding was possible because we were able to manipulate dopamine neurons based on their unique brain connectivity. We used both genetic and brain-circuit specific technologies coupled with techniques for manipulating neural electrical activity in anatomically and genetically defined cell populations.”

With this optogenetic setup, they were able to physically shine light into the brain and silence specific dopamine cell populations, which revealed their role in fear extinction.

Now that they have discovered two dopamine pathways that can regulate fear extinction in different ways, the team is working on ways to target these neurons with traditional pharmacology rather than optogenetics.

“Pharmacologically targeting the dopamine system will likely be an effective therapy for psychiatric conditions such as anxiety disorders when combined with clinically proven behavioral treatments such as exposure therapy. In order to provide effective, mechanism-based treatments for these conditions, future pre-clinical work will need to use molecular strategies that can separately target these distinct dopamine cell populations,”

said Johansen.

The work was supported by KAKENHI, the Strategic Research Program for Brain Sciences from the Ministry of Education, Culture, Sports, Science and Technology, and Kao Corporation.

Ray Luo, Akira Uematsu, Adam Weitemier, Luca Aquili, Jenny Koivumaa, Thomas J. McHugh & Joshua P. Johansen
A dopaminergic switch for fear to safety transitions
Nature Communications volume 9, Article number: 2483 (2018)

Top Image: RIKEN National Science Institute