Rapid Mental Rejuvenation: Experimental Drug Reverses Age-Related Cognitive Decline Within Days – SciTechDaily

Posted: Published on December 7th, 2020

This post was added by Alex Diaz-Granados

Rapid mental rejuvenation in old mice suggests age-related losses may be broadly reversible.

Just a few doses of an experimental drug can reverse age-related declines in memory and mental flexibility in mice, according to a new study by UC San Francisco scientists. The drug, called ISRIB, has already been shown in laboratory studies to restore memory function months aftertraumatic brain injury (TBI), reverse cognitive impairments inDown Syndrome, preventnoise-related hearing loss, fightcertain types of prostate cancer, and evenenhance cognitionin healthy animals.

In the new study, published on December 1, 2020, in the open-access journal eLife, researchers showed rapid restoration of youthful cognitive abilities in aged mice, accompanied by a rejuvenation of brain and immune cells that could help explain improvements in brain function.

A cryo-electron microscope rendering of an ISRIB molecule. Credit: Adam Frost lab

ISRIBs extremely rapid effects show for the first time that a significant component of age-related cognitive losses may be caused by a kind of reversible physiological blockage rather than more permanent degradation, said Susanna Rosi, PhD, Lewis and Ruth Cozen Chair II and professor in the departments of Neurological Surgery and of Physical Therapy and Rehabilitation Science.

The data suggest that the aged brain has not permanently lost essential cognitive capacities, as was commonly assumed, but rather that these cognitive resources are still there but have been somehow blocked, trapped by a vicious cycle of cellular stress, added Peter Walter, PhD, a professor in the UCSF Department of Biochemistry and Biophysics and a Howard Hughes Medical Institute investigator. Our work with ISRIB demonstrates a way to break that cycle and restore cognitive abilities that had become walled off over time.

Walter has won numerous scientific awards, including the Breakthrough,LaskerandShawprizes, for his decades-long studies of cellular stress responses. ISRIB, discovered in 2013 in Walters lab, works by rebooting cells protein production machinery after it gets throttled by one of these stress responses a cellular quality control mechanism called the integrated stress response (ISR; ISRIB stands for ISR InhiBitor).

Peter Walter, PhD. Credit: Elisabeth Fall

The ISR normally detects problems with protein production in a cell a potential sign of viral infection or cancer-promoting gene mutations and responds by putting the brakes on cells protein-synthesis machinery.This safety mechanism is critical for weeding out misbehaving cells, but if stuck in the on position in a tissue like the brain, it can lead to serious problems, as cells lose the ability to perform their normal activities, Walter and colleagues have found.

In particular, recent animal studies by Walter and Rosi, made possible by early philanthropic support from The Rogers Family Foundation, have implicated chronic ISR activation in the persistent cognitive and behavioral deficits seen in patients after TBI, by showing that, in mice, brief ISRIB treatment can reboot the ISR and restore normal brain function almost overnight.

The cognitive deficits in TBI patients are often likened to premature aging, which led Rosi and Walter to wonder if the ISR could also underlie purely age-related cognitive decline. Aging is well known to compromise cellular protein production across the body, as lifes many insults pile up and stressors like chronic inflammation wear away at cells, potentially leading to widespread activation of the ISR.

Weve seen how ISRIB restores cognition in animals with traumatic brain injury, which in many ways is like a sped-up version of age-related cognitive decline, said Rosi, who is director of neurocognitive research in the UCSF Brain and Spinal Injury Center and a member of the UCSF Weill Institute for Neurosciences. It may seem like a crazy idea, but asking whether the drug could reverse symptoms of aging itself was just a logical next step.

In the new study, researchers led by Rosi lab postdoc Karen Krukowski, PhD, trained aged animals to escape from a watery maze by finding a hidden platform, a task that is typically hard for older animals to learn. But animals who received small daily doses of ISRIB during the three-day training process were able to accomplish the task as well as youthful mice, much better than animals of the same age who didnt receive the drug.

The researchers then tested how long this cognitive rejuvenation lasted and whether it could generalize to other cognitive skills. Several weeks after the initial ISRIB treatment, they trained the same mice to find their way out of a maze whose exit changed daily a test of mental flexibility for aged mice who, like humans, tend to get increasingly stuck in their ways.The mice who had received brief ISRIB treatment three weeks before still performed at youthful levels, while untreated mice continued to struggle.

Susanna Rosi, PhD. Credit: Susan Merrell

To understand how ISRIB might be improving brain function, the researchers studied the activity and anatomy of cells in the hippocampus, a brain region with a key role in learning and memory, just one day after giving animals a single dose of ISRIB. They found that common signatures of neuronal aging disappeared literally overnight: neurons electrical activity became more sprightly and responsive to stimulation, and cells showed more robust connectivity with cells around them while also showing an ability to form stable connections with one another usually only seen in younger mice.

The researchers are continuing to study exactly how the ISR disrupts cognition in aging and other conditions and to understand how long ISRIBs cognitive benefits may last. Among other puzzles raised by the new findings is the discovery that ISRIB also alters the function of the immune systems T cells, which also are prone to age-related dysfunction. The findings suggest another path by which the drug could be improving cognition in aged animals, and could have implications for diseases from Alzheimers to diabetes that have been linked to heightened inflammation caused by an aging immune system.

This was very exciting to me because we know that aging has a profound and persistent effect on T cells and that these changes can affect brain function in the hippocampus, said Rosi. At the moment, this is just an interesting observation, but it gives us a very exciting set of biological puzzles to solve.

Rosi and Walter were introduced by neuroscientist Regis Kelly, PhD, executive director of the University of Californias QB3 biotech innovation hub, following Walters 2013 study showing that the drug seemed to instantly enhance cognitive abilities in healthy mice. To Rosi, the results from that study implied some walled-off cognitive potential in the brain that the molecule was somehow unlocking, and she wondered if this extra cognitive boost might benefit patients with neurological damage from traumatic brain injury.

The labs joined forces to study the question in mice, and were astounded by what they found. ISRIB didnt just make up for some of the cognitive deficits in mice with traumatic brain injury it erased them. This had never been seen before, Rosi said. The mantra in the field was that brain damage is permanent irreversible. How could a single treatment with a small molecule make them disappear overnight?

Further studies demonstrated that neurons throughout the brains of animals with traumatic brain injury are thoroughly jammed up by the ISR. Using ISRIB to release those brakes lets brain cells immediately get back to their normal business. More recently, studies in animals with very mild repetitive brain injury akin to pro athletes who experience many mild concussions over many years showed that ISRIB could reverseincreased risk-taking behavior associated with damage to self-control circuits in the frontal cortex.

Added to this, Karens new results in aging mice are just amazing. Its not often that you find a drug candidate that shows so much potential and promise, Walter added. This project also shows the power of the UCSF community Susanna and I didnt know each other and were living in different worlds until Regis Kelly brought us together, making this powerful connection that neither of us had realized before.

Amazing breakthroughs like this need more than the brilliance and experimental skills of Susanna and Peter, said Kelly. They also need donors like the Rogers Family Foundation willing to bridge the gap between great basic research and products that could be highly beneficial to society.

ISRIB has been licensed by Calico, a South San Francisco, Calif. company exploring the biology of aging, and the idea of targeting the ISR to treat disease has been picked up by many other pharmaceutical companies, Walter says.

One might think that interfering with the ISR, a critical cellular safety mechanism, would be sure to have serious side effects, but so far in all their studies, the researchers have observed none. This is likely due to two factors, Walter says. First, it takes just a few doses of ISRIB to reset unhealthy, chronic ISR activationback to a healthier state, after which it can still respond normally to problems in individual cells. Second, ISRIB has virtually no effect when applied to cells actively employing the ISR in its most powerful form against an aggressive viral infection, for example.

Naturally, both of these factors make the molecule much less likely to have negative side effects and more attractive as a potential therapeutic. It almost seems too good to be true, but with ISRIB we seem to have hit a sweet spot for manipulating the ISR with an ideal therapeutic window, Walter said.

Reference: Small molecule cognitive enhancer reverses age-related memory decline in mice by Karen Krukowski, Amber Nolan, Elma S Frias, Morgane Boone, Gonzalo Ureta, Katherine Grue, Maria-Serena Paladini, Edward Elizarraras, Luz Delgado, Sebastian Bernales, Peter Walter and Susanna Rosi, 1 December 2020, eLife. DOI: 10.7554/eLife.62048

Authors: Other authors on the study were Amber Nolan, Elma S. Frias, Morgane Boone, Katherine Grue, Maria-Serena Paladini, and Edward Elizarraras of UCSF; and Gonzalo Ureta, Luz Delgado and Sebastian Bernales of Fundacin Ciencia & Vida in Santiago, Chile. Bernales is also an employee of Praxis Biotech, LLC.

Funding: The study was supported by continued generous support of the Rogers Family Foundation, as well as the UCSF Weill Innovation Award, the U.S. National Institutes of Health (NIH R01AG056770), National Institute on Aging (NIA F32AG054126); National Center for Advancing Translational Sciences (NCATS TL1 TR001871); ANID Project AFB 170004; National Institute of Neurological Disorders and Stroke (NINDS K08NS114170) and the Howard Hughes Medical Institute (HHMI).

Disclosures: Gonzalo Ureta works at Fundacion Ciencia & Vida and receives partial funding from Praxis Biotech. Sebastian Bernales is an employee of Praxis Biotech. Peter Walter is an inventor on U.S. Patent 9708247 held by the Regents of the University of California that describes ISRIB and its analogs. Rights to the invention have been licensed by UCSF to Calico.

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