When you’re born, your brain is set up with all the physical abilities it needs to do everything it will ever do during your lifetime. But that’s not quite enough. Your brain needs experiences to shape it, building and reinforcing connections that give rise to memories and knowledge. This is true for learning how to ride a bike, memorizing state capitals, and even learning how to be afraid. Scientists have long thought they understood the neuroscientific root of aversive learning — the connection between a sensory stimulus and the brain’s perception of a threat. New research is changing this commonly accepted picture of the brain, though, potentially rewriting neuroscience textbooks.
In a study published Monday in the journal Nature Neuroscience, a team of scientists performed a series of experiments on mice to explore how the brain responds to uncomfortable feelings to build and reinforce aversive learning processes in the brain. Their specific focus was on the amygdalae, two small brain structures that are involved in learning and memory. Whereas scientist have long understood that the lateral amygdala was primarily responsible for aversive learning, this study shows that the central amygdala may actually be the seat of this process. These findings could change the way we treat psychological conditions like post-traumatic stress disorder (PTSD).
To probe the neuroscience of fear, a team of scientists led by Bo Li at Cold Spring Harbor Laboratory in New York devised experiments that allowed them to observe mice’s central and lateral amygdalae immediately after a negative sensory experience — a minor shock to the foot. The scientists observed that the mice’s response to the negative feeling originates in the central amygdala and is then registered in the lateral amygdala. In further experiments, scientists inhibited a set of neurons in the central amygdala — PKC-delta (protein kinase C-delta), named for the protein they express. When these mice received the foot shock, lateral amygdala activity was much weaker than before. This reinforces the revised view that PKC-delta neurons are a crucial part of conveying information about uncomfortable sensory experiences from the central amygdala to the lateral amygdala.
“If the conventional view was correct, you should see normal levels of activity in the lateral amygdala — where the activity supposedly begins. But this wasn’t the case,” said Li in a statement.
In one particularly strange experiment, the scientists actually implanted aversive memories that had never happened in the mice’s brains. They did this with a laser that activated PKC-delta neurons in the hopes of creating a false memory of an uncomfortable event.
“This causes no pain to the mice, but they don’t like it — it makes them feel uncomfortable, just as getting a mild shock makes them uncomfortable. It’s the kind of stimulation that leads to an aversive memory, the kind you learn from,” said Li in the statement.
The mice were given the neural stimulation in a cage with two chambers, and when given the option to wander around the cage, they avoided the chamber in which they had received the laser stimulation. This suggests that activating the PKC-delta neurons had indeed created a false memory and that these aversive memories are controlled to some degree by the PKC-delta neurons in the central amygdala.
The researchers call these neurons “fear-on” cells, and they hope that their research will help scientists better understand how patients with PTSD can have fear memories triggered by unrelated stimuli so they can be treated more effectively.
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