Literature DB >> 23604914

AgingDB: A database for oxidative stress and calorie restriction in the study of aging.

Dae Ui Park1, Chul Hong Kim, Seong Eui Hong, Byung Pal Yu, Hae Young Chung.   

Abstract

Aging can be characterized in all living organisms as the inevitable biological changes that occur with advancing age. The aging process is time-dependent and leads to functional declines and increased incidences of disease. The underlying pathphysiologic processes of aging may best be explained using several interacting biological processes: genomic activity, oxidative stress, and age-related disease processes, all of which modify the rate and progression of aging. In this report, we describe a database, termed AgingDB, used to retrieve information on the biomolecules known to be modulated during the aging process and by the life-prolonging action of caloric restriction (CR). To enhance the usefulness of AgingDB, we include data collected from studies of CR's anti-oxidative action on gene expression, oxidative stress, and many chronic age-related diseases. We organized AgingDB into two sections A) apoptosis and the various mitochondrial biomolecules that play a role in aging; B) nuclear transcription factors known to be_sensitive to oxidative environment. AgingDB features an imagemap of biomolecular signal pathways and visualized information that includes protein-protein interactions of biomolecules. Authorized users can submit a new biomolecule or edit an existing biomolecule to reflect latest developments. By making available the most update information through AgingDB, we expect to assist researchers who are exploring the molecular basis of age-related changes modified by the life-prolonging action of CR. For the reader's convenience and accessibility, AgingDB is freely available at http://agingdb.bio.pusan.ac.kr/.

Year:  2003        PMID: 23604914      PMCID: PMC3456816          DOI: 10.1007/s11357-003-0002-y

Source DB:  PubMed          Journal:  J Am Aging Assoc        ISSN: 2152-4041


  13 in total

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Authors:  Matt Kaeberlein; Beatrice Jegalian; Mitch McVey
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Journal:  J Mol Biol       Date:  2001-03-30       Impact factor: 5.469

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Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

6.  Database resources of the National Center for Biotechnology Information: 2002 update.

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Journal:  Nucleic Acids Res       Date:  2002-01-01       Impact factor: 16.971

7.  Gene expression profile of the aging process in rat liver: normalizing effects of growth hormone replacement.

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Journal:  Mol Endocrinol       Date:  2001-02

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Journal:  Physiol Rev       Date:  1993-01       Impact factor: 37.312

9.  Age-associated decline in ascorbic acid concentration, recycling, and biosynthesis in rat hepatocytes--reversal with (R)-alpha-lipoic acid supplementation.

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Journal:  FASEB J       Date:  1998-09       Impact factor: 5.191

10.  Gene expression profile of aging and its retardation by caloric restriction.

Authors:  C K Lee; R G Klopp; R Weindruch; T A Prolla
Journal:  Science       Date:  1999-08-27       Impact factor: 47.728

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