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September 14, 2021
Hormone links exercise with cognitive benefits
At a Glance
- Researchers found that irisin, an exercise-induced hormone, improves cognitive performance in mice.
- The hormone, which is identical in people, could potentially be used to treat cognitive disorders such as Alzheimer鈥檚 disease.
Exercise may benefit brain health and improve cognitive performance during aging. It鈥檚 also associated with reduced Alzheimer鈥檚 disease risk and cognitive decline. But the mechanisms responsible aren鈥檛 well understood. Factors secreted into the bloodstream may play a role. If so, these factors would be promising leads for developing treatments for cognitive disorders.
Past studies found that exercise induces production of FNDC5, a protein found on the surfaces of certain cells. FNDC5 can activate neuroprotective genes in the hippocampus, the brain region in charge of memory formation. The outer part of FNDC5 can be cleaved off to form a hormone called irisin, which is released into the bloodstream. A team of researchers, led by Dr. Christiane Wrann at Massachusetts General Hospital and Harvard Medical School, investigated whether irisin is responsible for mediating the cognitive benefits of exercise.
The study was supported in part by several NIH institutes (see below). Results appeared in Nature Metabolism on August 20, 2021.
First, the researchers deleted the gene encoding FNDC5 in mice, thereby removing irisin. They then compared the effects of exercise on cognitive performance in these 鈥渒nockout鈥 mice and in control mice. Some mice had an exercise wheel to run on, while others did not.
Control mice who could freely exercise showed improved cognitive performance over those that could not. But in the knockout mice, exercise made no difference in cognitive performance. The knockout mice also showed greater cognitive decline with age than control mice.
Next, the researchers delivered irisin directly into the mice鈥檚 brains. Doing so improved cognitive performance in both knockout and control mice.聽聽
The team examined the neurons in the knockout mice in a part of the hippocampus. They found that newly born neurons in this area had abnormal activation patterns, structure, and gene activity.
The researchers then tested the therapeutic potential of irisin in mouse models of Alzheimer鈥檚 disease. They delivered the gene for irisin into the mice, which led to irisin production in the liver. The blood of these mice, in turn, contained elevated irisin levels. Two months after treatment, the researchers tested the mice鈥檚 cognitive performance. The irisin-treated mice performed better on the tests than untreated mice. Treated mice also showed signs of reduced neuroinflammation鈥攁 process related to neurodegenerative diseases鈥攊n the hippocampus. In addition, the researchers found that irisin could cross the blood-brain barrier to act on the brain.
These results suggest that exercise may improve cognitive performance by increasing irisin levels. 鈥淭his is particularly important inasmuch as irisin, a small natural peptide, would be much easier to develop into a therapeutic than the much larger membrane-bound protein FNDC5,鈥 Wrann says.
Irisin is identical in mice and people. Its blood levels in people have also been shown to rise with endurance exercise. It could thus potentially help to treat a variety of cognitive disorders. Wrann adds, 鈥渟ince irisin does not specifically target amyloid plaques, but rather neuroinflammation directly, we鈥檙e optimistic it could have beneficial effects on neurodegenerative diseases beyond just Alzheimer鈥檚.鈥
鈥攂y Brian Doctrow, Ph.D.
Related Links
- Exercise-Induced Protein May Reverse Age-Related Cognitive Decline
- Exercise and New Nerve Cell Growth in Alzheimer鈥檚 Disease
- Shivering Triggers Brown Fat to Produce Heat and Burn Calories
- Moderate Exercise May Improve Memory in Older Adults
References: Islam MR, Valaris S, Young MF, Haley EB, Luo R, Bond SF, Mazuera S, Kitchen RR, Caldarone BJ, Bettio LEB, Christie BR, Schmider AB, Soberman RJ, Besnard A, Jedrychowski MP, Kim H, Tu H, Kim E, Choi SH, Tanzi RE, Spiegelman BM, Wrann CD. Nat Metab. 2021 Aug;3(8):1058-1070. doi: 10.1038/s42255-021-00438-z. Epub 2021 Aug 20. PMID:聽34417591
Funding: NIH鈥檚 最新麻豆视频 Institute of Neurological Disorders and Stroke (NINDS), 最新麻豆视频 Institute on Aging (NIA), 最新麻豆视频 Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), 最新麻豆视频 Cancer Institute (NCI), and 最新麻豆视频 Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Cure Alzheimer鈥檚 Fund; Alzheimer鈥檚 Association; Massachusetts General Hospital鈥檚 McCance Center for Brain Health, Claflin Distinguished Scholar Award, and Molecular Imaging Core; Harvard NeuroDiscovery Center; Hassenfeld Child Health Innovation Institute; Harvard Brain Science Initiative; Michael Smith Foundation for Health Research (MSFHR); FRAXA Research Foundation; Fragile X Research Foundation of Canada (FXRFC); Natural Sciences and Engineering Research Council of Canada (NSERC); Canadian Institutes of Health Research (CIHR); The JPB Foundation