Exercise-Induced Muscle Factor Promotes Memory

Running releases an enzyme that is associated with memory function in mice and humans.  

By | June 23, 2016

New brain cells (green) are induced by exerciseHENRIETTE VAN PRAAG AND LINDA KITABAYASHIWorking out is good for the brain. Now, a team of scientists from the U.S. and Germany has a clearer idea why. A protein called cathepsin B, produced and secreted by muscle during exercise, is required for exercise-induced memory improvement and brain cell production in mice, the scientists reported in Cell Metabolism today (June 23). They also showed that levels of cathepsin B are positively correlated with fitness and memory in humans.

“This is a super exciting area. Exercise has so many health benefits, yet we know so little about many of these effects at a molecular level,” said biologist David James of the University of Sydney who did not participate in the work.

“This paper provides a convincing mechanism that involves running-induced increases in a particular protein—cathepsin B—that appears to promote neurogenesis by enhancing expression of a growth factor—BDNF—in the brain,” added neuroscientist Paul Frankland of the University of Toronto who also was not involved in the study. “This is a long chain of events, from exercise to muscle to brain to cognition,” he said, “but the authors do a great job at demonstrating each of the links.”

Running has been shown in animals to have a variety of effects on the brain, including enhanced memory function and increased production of new brain cells (neurogenesis). In humans, a correlation between exercise and memory function has also been observed. But how muscle activity might be mechanistically linked to memory has been somewhat of a mystery.

To hunt for mucle-produced factors called myokines that might modulate brain function, Henriette van Praag of the National Institute on Aging and colleagues treated rat muscle cells in culture with the drug AICAR—“an exercise mimetic,” explained van Praag, meaning it boosts the cells’ metabolic activities. Among the proteins upregulated in the treated cells was a secreted factor, small enough to traverse the blood-brain barrier, that had previously been shown to be upregulated in muscle during exercise: cathepsin B.

In mice that exercised for two to four weeks, plasma levels of cathepsin B were significantly increased, van Praag’s team found. And the animals showed improved memory as well as increased neurogenesis in their hippocampi—a brain region involved in learning and memory. Mice that were genetically engineered to lack cathepsin B, on the other hand, did not show these exercise-related effects.

The team also showed that cathepsin B treatment of murine adult hippocampal progenitor cells in culture induced the expression of two key nerve growth factors—brain-derived neurotrophic factor (BDNF) and doublecortin—which may explain how the myokine induces neurogenesis.

In rhesus monkeys and humans, four months of treadmill training increased blood levels of cathepsin B, the team showed, and this increase was correlated with improved memory recall in the human study participants.

Intriguingly, while some earlier studies have reported cathepsin B to have neuroprotective effects, a number of others have suggested that cathepsin B is involved in neuronal cell death during brain injury and the onset of Alzheimer’s disease. Others have reported high levels of cathepsin B in various cancers.

With that in mind, “the observation that [cathepsin B] might encode benefits of exercise in the brain is almost counter-intuitive,” said James.

If the link between cathepsin B and improved memory can be confirmed in humans, however, then “pharmacological targeting of cathespin b might be used to enhance cognition,” suggested Frankland.

Exercise itself might also provide such cognitive benefit, of course, but “a lot of people who are at risk of Alzheimer’s disease are not very mobile, or they have cardiovascular problems that prevent them from exercising,” explained study coauthor Emrah Düzel of the German Center for Neurodegenerative Diseases and of University Madeburg. “So identifying peripheral factors that you could substitute without having the need to actually exercise would be important.”

H.Y. Moon et al., “Running-induced systemic cathepsin B secretion is associated with memory function,” Cell Metabolism, doi:10.1016/j.cmet.2016.05.025, 2016.

 

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Comments

Avatar of: kpetrak

kpetrak

Posts: 14

June 24, 2016

Very interesting. I wonder what information could be gathered by comparing e.g., the incidence of Alzheimers in top-athletes population (e.g., long-distance runners) versus a "couch-potato" control...

Avatar of: mightythor

mightythor

Posts: 83

June 25, 2016

kpetrak -- a good question.  Carefully controlled studies suggest that regular exercise can slow the development of Alzheimer's disease in at-risk populations, although it cannot reverse the symptoms.  Elucidating mechanisms is trickier.  The suggestion here that cathepsin B may induce nerve growth factor expression and also trigger neuronal cell death, perhaps under different circumstances, is particularly intriguing. 

Avatar of: Bmeister

Bmeister

Posts: 1

Replied to a comment from kpetrak made on June 24, 2016

June 30, 2016

this is pretty easy to answer: mouse models with the APP-swedisch mutation and presenilin mutants will not develop amyloids and will not suffer from neurodegeneration, if you place a running wheel/treadmill into their cages. I think this was published a couple of years ago by the Selkoe lab, without drawing the right conclusions from this (striking) result. I.e. excercise (and exploration, you can get a similar result from giving the mice something to play with) works better than any known medication!

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