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Lifespan-extending effects of royal jelly and its related substances on the nematode Caenorhabditis elegans.
- Source :
-
PloS one [PLoS One] 2011; Vol. 6 (8), pp. e23527. Date of Electronic Publication: 2011 Aug 09. - Publication Year :
- 2011
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Abstract
- Background: One of the most important challenges in the study of aging is to discover compounds with longevity-promoting activities and to unravel their underlying mechanisms. Royal jelly (RJ) has been reported to possess diverse beneficial properties. Furthermore, protease-treated RJ (pRJ) has additional pharmacological activities. Exactly how RJ and pRJ exert these effects and which of their components are responsible for these effects are largely unknown. The evolutionarily conserved mechanisms that control longevity have been indicated. The purpose of the present study was to determine whether RJ and its related substances exert a lifespan-extending function in the nematode Caenorhabditis elegans and to gain insights into the active agents in RJ and their mechanism of action.<br />Principal Findings: We found that both RJ and pRJ extended the lifespan of C. elegans. The lifespan-extending activity of pRJ was enhanced by Octadecyl-silica column chromatography (pRJ-Fraction 5). pRJ-Fr.5 increased the animals' lifespan in part by acting through the FOXO transcription factor DAF-16, the activation of which is known to promote longevity in C. elegans by reducing insulin/IGF-1 signaling (IIS). pRJ-Fr.5 reduced the expression of ins-9, one of the insulin-like peptide genes. Moreover, pRJ-Fr.5 and reduced IIS shared some common features in terms of their effects on gene expression, such as the up-regulation of dod-3 and the down-regulation of dod-19, dao-4 and fkb-4. 10-Hydroxy-2-decenoic acid (10-HDA), which was present at high concentrations in pRJ-Fr.5, increased lifespan independently of DAF-16 activity.<br />Conclusions/significance: These results demonstrate that RJ and its related substances extend lifespan in C. elegans, suggesting that RJ may contain longevity-promoting factors. Further analysis and characterization of the lifespan-extending agents in RJ and pRJ may broaden our understanding of the gene network involved in longevity regulation in diverse species and may lead to the development of nutraceutical interventions in the aging process.
- Subjects :
- Active Transport, Cell Nucleus drug effects
Aging genetics
Aging physiology
Animals
Bees chemistry
Caenorhabditis elegans genetics
Caenorhabditis elegans physiology
Caenorhabditis elegans Proteins genetics
Caenorhabditis elegans Proteins metabolism
Cell Nucleus metabolism
Chromatography methods
Dose-Response Relationship, Drug
Fatty Acids chemistry
Fatty Acids metabolism
Fatty Acids, Monounsaturated pharmacology
Forkhead Transcription Factors
Gene Expression Profiling
Gene Expression Regulation drug effects
Green Fluorescent Proteins genetics
Green Fluorescent Proteins metabolism
Longevity genetics
Longevity physiology
Mutation
Oligonucleotide Array Sequence Analysis
Peptide Hydrolases metabolism
Promoter Regions, Genetic genetics
Reverse Transcriptase Polymerase Chain Reaction
Transcription Factors genetics
Transcription Factors metabolism
Aging drug effects
Caenorhabditis elegans drug effects
Fatty Acids pharmacology
Longevity drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 6
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 21858156
- Full Text :
- https://doi.org/10.1371/journal.pone.0023527