Scientists discover the neurons that rewrite traumatic memories

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It is estimated that almost a third of all people will suffer from fear- or stress-related disorders at one point in their lives.
It is estimated that almost a third of all people will suffer from fear- or stress-related disorders at one point in their lives.
It is estimated that about one-third of all people will suffer from fear or stress-related disorders at some point in their lives. The memory of some traumatic experiences can have long-standing effects on a person’s life leading to post-traumatic stress disorder and other mental health issues, that can ruin a person’s life.
Now for the first time, in neuroscience research, neuroscientists at EPFL have located the cells that help reprogram long-lasting memories of traumatic experiences towards safety, a study that was published in Science.
Now, a new study shows – at the cellular level – how therapy can treat even long-term memories of trauma. “Our findings shed, for the first time, light onto the processes that underlie the successful treatment of traumatic memories,” says EPFL Professor Johannes Gräff, whose lab carried out the study.

Scientists still don’t understand exactly how neurons store memories in general. Especially for those scientists working in the field of traumatic memories, the long-debated question has always been whether a person dealing with traumatic memories attenuates*  their fear by suppressing the original memory trace of the fear or rewrites their original fear trace, thereby moving towards safety. Although they don’t exclude suppression, the findings from this study show for the first time the importance of rewriting in treating traumatic memories.

Research in this area focuses on understanding the brain’s capacity to reduce traumatic memories, but surprisingly few studies have investigated treatment options for attenuating long-lasting trauma (aka “remote fear”) in animal models.

*lessens their intensity

Study results

Cross section of the mouse hippocampus - a brain region involved in learningand memory - indicating in green cells that are active when mice recall a 1month old traumatic memory, and in red cells that are active when miceunderwent an extinction training, which resembles exposure therapy in humans. Copyright: EPFL / Gräff Group
Cross section of the mouse hippocampus – a brain region involved in learning and memory – indicating in green cells that are active when mice recall a 1month old traumatic memory, and in red cells that are active when mice underwent an extinction training, which resembles exposure therapy in humans. Copyright: EPFL / Gräff Group

The EPFL scientists found that remote fear attenuation in the brain is connected to the activity of the same group of neurons that are also involved in storing these memories. Working with mice, the scientists have located these neurons in the brain’s dentate gyrus, an area of the hippocampus that is involved in the encoding, recall, and the reduction of fear.

The mice used in the study are genetically modified to carry a “reporter” gene that produces an identifiable and measurable signal, e.g. a fluorescent protein, following neuronal activity. Using a fear-training exercise that produces long-lasting traumatic memories, the scientists first identified the subpopulation of neurons in the dentate gyrus that are involved in storing long-term traumatic memories.

The mice then underwent fear-reducing training, which resembles exposure-based therapy in humans – the most efficient form of trauma therapy in humans today. Surprisingly, when the researchers looked again into the brain of the mice, some of the neurons active at recalling the traumatic memories were still active when the animals no longer showed fear. Importantly, the less the mice were scared, the more cells became reactivated. This was the first hint that the same population of neurons may be involved in storing and attenuating traumatic memories.

The researchers then reduced the excitability of the recall neurons during the exposure therapy and found that the mice showed poorer fear reduction compared to controls. But when they reduced the excitability of other neurons in the dentate gyrus, there was no such effect, showing that the recall neurons in the dentate gyrus are crucial for fear attenuation.

Finally, when the researchers enhanced the excitability of these recall neurons during the therapeutic intervention, they found that the mice showed an improved fear reduction. Thus, they concluded that attenuating remote fear memories depends on the continued activity of the neurons they identified in the dentate gyrus.

Source: EPFL