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

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 conditi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Scientific reports 2018-09, Vol.8 (1), p.14212-10, Article 14212
Hauptverfasser: Yen, Kelvin, Wan, Junxiang, Mehta, Hemal H., Miller, Brendan, Christensen, Amy, Levine, Morgan E., Salomon, Matthew P., Brandhorst, Sebastian, Xiao, Jialin, Kim, Su-Jeong, Navarrete, Gerardo, Campo, Daniel, Harry, G. Jean, Longo, Valter, Pike, Christian J., Mack, Wendy J., Hodis, Howard N., Crimmins, Eileen M., Cohen, Pinchas
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-018-32616-7