| Literature DB >> 28877458 |
John C Newman1, Anthony J Covarrubias2, Minghao Zhao3, Xinxing Yu4, Philipp Gut5, Che-Ping Ng2, Yu Huang6, Saptarsi Haldar6, Eric Verdin7.
Abstract
Ketogenic diets recapitulate certain metabolic aspects of dietary restriction such as reliance on fatty acid metabolism and production of ketone bodies. We investigated whether an isoprotein ketogenic diet (KD) might, like dietary restriction, affect longevity and healthspan in C57BL/6 male mice. We find that Cyclic KD, KD alternated weekly with the Control diet to prevent obesity, reduces midlife mortality but does not affect maximum lifespan. A non-ketogenic high-fat diet (HF) fed similarly may have an intermediate effect on mortality. Cyclic KD improves memory performance in old age, while modestly improving composite healthspan measures. Gene expression analysis identifies downregulation of insulin, protein synthesis, and fatty acid synthesis pathways as mechanisms common to KD and HF. However, upregulation of PPARα target genes is unique to KD, consistent across tissues, and preserved in old age. In all, we show that a non-obesogenic ketogenic diet improves survival, memory, and healthspan in aging mice. Published by Elsevier Inc.Entities:
Keywords: beta-hydroxybutyrate; healthspan; ketogenic diet; longevity
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Year: 2017 PMID: 28877458 PMCID: PMC5605815 DOI: 10.1016/j.cmet.2017.08.004
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287