Unveiling the brain mechanism behind memory consolidation in sleep

Neuroscientists have established in recent decades the idea that some of each day's experiences are converted by the brain into permanent memories during sleep the same night. Now, a new study proposes a mechanism that determines which memories are tagged as important enough to linger in the brain until sleep makes them permanent.

Led by researchers at NYU Grossman School of Medicine, the new study revolves around brain cells called neurons that "fire"—bring about swings in the balance of their positive and negative charges—to transmit electrical signals that encode memories. Large groups of neurons in a brain region called the hippocampus fire together in rhythmic cycles, creating sequences of signals within milliseconds of each other that can encode complex information.

Called "sharp wave-ripples," these "shouts" to the rest of the brain represent the near-simultaneous firing of 15 percent of hippocampal neurons, and are named for the shape they take when their activity is captured by electrodes and recorded on a graph.

While past studies had linked ripples with memory formation during sleep, the new study, published online March 28 in the journal Science, found that daytime events followed immediately by 5 to 20 sharp wave-ripples are replayed more during sleep and so consolidated into permanent memories. Events followed by very few or no sharp wave-ripples failed to form lasting memories.

Our study finds that sharp wave-ripples are the physiological mechanism used by the brain to 'decide' what to keep and what to discard."

György Buzsáki, MD, PhD, senior study author, the Biggs Professor of Neuroscience in the Department of Neuroscience and Physiology at NYU Langone Health

Walk and pause

The new study is based on a known pattern: humans and other mammals experience the world for a few moments, then pause, then experience a little more, then pause again. After we pay attention to something, say the study authors, brain computation often switches into an "idle" reassessment mode. Such momentary pauses occur throughout the day, but the longest idling periods occur during sleep.

Dr. Buzsáki and colleagues had previously established that no sharp wave-ripples occur as we actively explore sensory information or move, but only during the idle pauses before or after. The current study found that sharp wave-ripples represent the natural tagging mechanism during such pauses after waking experiences, with the tagged neuronal patterns reactivated during post-task sleep.

Importantly, sharp wave-ripples are known to be made up of the firing of hippocampal "place cells" in a specific order that encodes, for instance, every room we enter and every section of a maze entered by a mouse. For memories that are remembered, those same cells fire at high speed, as we sleep, "playing back the recorded event thousands of times per night," as the study authors put it. The process strengthens the connections between the cells involved.

For the current study, successive maze runs by study mice were tracked via electrodes by populations of hippocampal cells that constantly changed over time, despite recording very similar experiences. This revealed for the first time the maze runs during which ripples occurred during waking pauses and then were replayed during sleep.

Sharp wave-ripples were typically recorded when a mouse paused to enjoy a sugary treat after each maze run. The consumption of the reward, say the authors, prepared the brain to switch from an exploratory to an idle pattern, so that sharp wave-ripples could occur.

Using dual-sided silicon probes, the research team was able to record up to 500 neurons simultaneously in the hippocampi of animals during maze runs. This in turn created a challenge, because data becomes exceedingly complex the more neurons are independently recorded. To gain an intuitive understanding of the data, visualize neuronal activity, and form hypotheses, the team successfully reduced the number of dimensions in the data, which is in some ways like converting a 3D into a flat one, without losing the data's integrity.

"We worked to take the external world out of the equation, and looked at the mechanisms by which the mammalian brain innately and subconsciously tags some memories to become permanent," said first author Wannan (Winnie) Yang, PhD, a graduate student in the Buzsáki Lab. "Why such a system evolved is still a mystery, but future research may reveal devices or therapies that can adjust sharp wave-ripples to improve memory, or even lessen recall of traumatic events."

Along with Dr. Buzsáki and Dr. Yang, study authors from NYU Langone's Neuroscience Institute were Roman Huszár and Thomas Hainmueller. Kirill Kiselev, of NYU's Center for Neural Science, was also an author, as was Chen Sun of Mila, the Quebec Artificial Intelligence Institute, in Montréal. The work was supported by National Institutes of Health grants R01MH122391 and U19NS107616.