Summary: Researchers report on how sleep deprivation affects the ability to form new memories.
Source: Univeristy of Michigan.
Scientists have known that a lack of sleep can interfere with the ability to learn and make memories. Now, a group of University of Michigan researchers have found how sleep deprivation affects memory-making in the brain.
Previously, researchers knew that depriving mice of sleep after the mice performed a task resulted in the mice forgetting aspects of that task. But researchers weren’t sure what function of the hippocampus—two seahorse-shaped structures located in the temporal lobe of the brain where many long-term memories are made—was kept from doing its job.
Now, U-M researchers have found that interfering with sleep-associated oscillations—or the rhythmic firing of neurons—in one subsection of the hippocampus is likely the culprit. Their results are published in Nature Communications.
To test the role of oscillations in memory formation, the researchers, led by graduate student Nicolette Ognjanovski, recorded the baseline hippocampal activity of a group of mice. They placed mice into a new environment, let them explore, gave them a mild foot shock, then put them back into their home cages to rest and sleep normally.
“If you return the mouse to that same structure a day or even a couple months later, they will have this very stereotyped fear response, which is that they freeze,” said Sara Aton, an assistant professor in the Department of Molecular, Cellular and Developmental Biology and senior author of the paper. “But if you sleep-deprive an animal for a few hours after that context-shock pairing, the mouse won’t remember it the next day.”
The researchers found that in normally sleeping mice, sleep-associated oscillations in a subsection of the hippocampus called CA1 were more robust after learning. They then took a new group of mice, recorded their baseline hippocampal activity and had them complete the same task. The researchers also gave these mice a drug to inhibit a small population of inhibitory neurons in CA1 that express parvalbumin.
The researchers didn’t change the sleep behavior of the animal—they slept normally. But turning off the activity of parvalbumin-expressing neurons disrupted the rhythmic firing of surrounding CA1 neurons while those animals were asleep. Suppressing the parvalbumin-expressing cells appeared to completely wipe out the normal learning-associated increase in oscillations in that section of the mouse’s hippocampus.
“There’s an old theorem called Hebb’s Law, which is, ‘Fire together, wire together,'” Aton said. “If you can get two neurons to fire with great regularity in close proximity to each other, it’s very likely you’re going to affect the strength of connections between them.”
When the neurons were kept from firing together regularly and rhythmically, the mice forgot there was any fearful association with their task.
“The dominant oscillatory activity, which is so critical for learning, is controlled by a very small number of the total cell population in the hippocampus,” said Ognjanovski, also a first author of the study. “This changes the narrative of what we understand about how networks work. The oscillations that parvalbumin cells control are linked to global network changes, or stability. Memories aren’t stored in single cells, but distributed through the network.”
The researchers also compared the stability of the neurons’ connections between the control group and the group whose sleep oscillations were disrupted. They found that not only were the connections stronger in the control group after their learning trial, but that those neuronal connections were also stronger. These changes were blocked when sleep-associated hippocampal oscillations were experimentally disrupted.
“It seems like this population of neurons that is generating rhythms in the brain during sleep is providing some informational content for reinforcing memories,” Aton said. “The rhythm itself seems to be the most critical part, and possibly why you need to have sleep in order to form these memories.”
Next, the researchers plan to test whether restoring hippocampal oscillations (mimicking the effects of sleep in CA1) is sufficient for promoting normal memory formation when mice are sleep-deprived.
About this memory research article
Funding: The research was funded by the RIKEN Brain Science Institute, the Howard Hughes Medical Institute, and the JPB Foundation.
Source: Morgan Sherburne – Univeristy of Michigan Image Source: NeuroscienceNews.com image is adapted from the University of Michigan news release. Original Research: Full open access research for “Parvalbumin-expressing interneurons coordinate hippocampal network dynamics required for memory consolidation” by Nicolette Ognjanovski, Samantha Schaeffer, Jiaxing Wu, Sima Mofakham, Daniel Maruyama, Michal Zochowski & Sara J. Aton in Nature Communications. Published online April 6 2017 doi:10.1038/ncomms15039
Cite This NeuroscienceNews.com Article
[cbtabs][cbtab title=”MLA”]Univeristy of Michigan “Sleep on It: Researchers Find What Makes Memories Tick.” NeuroscienceNews. NeuroscienceNews, 7 April 2017. <https://neurosciencenews.com/sleep-memory-6361/>.[/cbtab][cbtab title=”APA”]Univeristy of Michigan (2017, April 7). Sleep on It: Researchers Find What Makes Memories Tick. NeuroscienceNew. Retrieved April 7, 2017 from https://neurosciencenews.com/sleep-memory-6361/[/cbtab][cbtab title=”Chicago”]Univeristy of Michigan “Sleep on It: Researchers Find What Makes Memories Tick.” https://neurosciencenews.com/sleep-memory-6361/ (accessed April 7, 2017).[/cbtab][/cbtabs]
Parvalbumin-expressing interneurons coordinate hippocampal network dynamics required for memory consolidation
Activity in hippocampal area CA1 is essential for consolidating episodic memories, but it is unclear how CA1 activity patterns drive memory formation. We find that in the hours following single-trial contextual fear conditioning (CFC), fast-spiking interneurons (which typically express parvalbumin (PV)) show greater firing coherence with CA1 network oscillations. Post-CFC inhibition of PV+ interneurons blocks fear memory consolidation. This effect is associated with loss of two network changes associated with normal consolidation: (1) augmented sleep-associated delta (0.5–4 Hz), theta (4–12 Hz) and ripple (150–250 Hz) oscillations; and (2) stabilization of CA1 neurons’ functional connectivity patterns. Rhythmic activation of PV+ interneurons increases CA1 network coherence and leads to a sustained increase in the strength and stability of functional connections between neurons. Our results suggest that immediately following learning, PV+ interneurons drive CA1 oscillations and reactivation of CA1 ensembles, which directly promotes network plasticity and long-term memory formation.
“Parvalbumin-expressing interneurons coordinate hippocampal network dynamics required for memory consolidation” by Nicolette Ognjanovski, Samantha Schaeffer, Jiaxing Wu, Sima Mofakham, Daniel Maruyama, Michal Zochowski & Sara J. Aton in Nature Communications. Published online April 6 2017 doi:10.1038/ncomms15039