Humanin Prevents Age-Related Cognitive Decline in Mice and is Associated with Improved Cognitive Age in Humans

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作者
Kelvin Yen
Junxiang Wan
Hemal H. Mehta
Brendan Miller
Amy Christensen
Morgan E. Levine
Matthew P. Salomon
Sebastian Brandhorst
Jialin Xiao
Su-Jeong Kim
Gerardo Navarrete
Daniel Campo
G. Jean Harry
Valter Longo
Christian J. Pike
Wendy J. Mack
Howard N. Hodis
Eileen M. Crimmins
Pinchas Cohen
机构
[1] University of Southern California,Leonard Davis School of Gerontology
[2] Yale School of Medicine,Department of Pathology
[3] John Wayne Cancer Institute at Providence Saint John’s Health Center,Department of Translational Molecular Medicine
[4] University of Southern California,Department of Molecular and Computational Biology
[5] National Institute of Environmental Health Sciences,Neurotoxicology Group, National Toxicology Program Laboratory
[6] Research Triangle Park,Departments of Medicine and Preventive Medicine
[7] University of Southern California Atherosclerosis Research Unit,undefined
[8] University of Southern California,undefined
来源
Scientific Reports | / 8卷
关键词
Cognitive Age; Cognitive Agents; Single Nucleotide Polymorphisms (SNP); Human Cell Culture Models; Barnes Maze Test;
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摘要
Advanced age is associated with a decline in cognitive function, likely caused by a combination of modifiable and non-modifiable factors such as genetics and lifestyle choices. Mounting evidence suggests that humanin and other mitochondrial derived peptides play a role in several age-related conditions including neurodegenerative disease. Here we demonstrate that humanin administration has neuroprotective effects in vitro in human cell culture models and is sufficient to improve cognition in vivo in aged mice. Furthermore, in a human cohort, using mitochondrial GWAS, we identified a specific SNP (rs2854128) in the humanin-coding region of the mitochondrial genome that is associated with a decrease in circulating humanin levels. In a large, independent cohort, consisting of a nationally-representative sample of older adults, we find that this SNP is associated with accelerated cognitive aging, supporting the concept that humanin is an important factor in cognitive aging.
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