| Literature DB >> 25976661 |
Juewon Kim1, Young-Gyu Kang2, Jee-young Lee3, Dong-hwa Choi4, Young-uk Cho5, Jae-Min Shin3, Jun Seong Park2, John Hwan Lee2, Wan Gi Kim6, Dae Bang Seo6, Tae Ryong Lee7, Yusei Miyamoto8, Kyoung Tai No9.
Abstract
Dehydroabietic acid (DAA) is a naturally occurring diterpene resin acid of confers, such as pinus species (P. densiflora, P. sylvestris) and grand fir (Abies grandis), and it induces various biological actions including antimicrobial, antiulcer, and cardiovascular activities. The cellular targets that mediate these actions are largely unknown yet. In this report, we suggest that DAA is an anti-aging reagent. DAA has lifespan extension effects in Caenorhabditis elegans, prevents lipofuscin accumulation, and prevents collagen secretion in human dermal fibroblasts. We found that these anti-aging effects are primarily mediated by SIRT1 activation. Lifespan extension effects by DAA were ameliorated in sir-2.1 mutants and SIRT1 protein expression was increased, resulting in the deacetylation of SIRT1 target protein PGC-1α. Moreover, DAA binds directly to the SIRT1 protein independent of the SIRT1 substrate NAD(+) levels. Through a molecular docking study, we also propose a binding model for DAA-SIRT1. Taken together, our results demonstrate that the anti-aging effects are the first identified biological property of DAA and that the direct activation of SIRT1 enzymatic activity suggests the potential use of this natural diterpene, or related compounds, in age-related diseases or as a preventive reagent against the aging process.Entities:
Keywords: Binding model; Dehydroabietic acid; Longevity; Phytochemical; SIRT1
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Year: 2015 PMID: 25976661 DOI: 10.1016/j.mce.2015.05.006
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102