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We are analyzing https://link.springer.com/article/10.1186/1471-213x-8-49.

Title:
Age- and calorie-independent life span extension from dietary restriction by bacterial deprivation in Caenorhabditis elegans | BMC Developmental Biology
Description:
Background Dietary restriction (DR) increases life span and delays age-associated disease in many organisms. The mechanism by which DR enhances longevity is not well understood. Results Using bacterial food deprivation as a means of DR in C. elegans, we show that transient DR confers long-term benefits including stress resistance and increased longevity. Consistent with studies in the fruit fly and in mice, we demonstrate that DR also enhances survival when initiated late in life. DR by bacterial food deprivation significantly increases life span in worms when initiated as late as 24 days of adulthood, an age at which greater than 50% of the cohort have died. These survival benefits are, at least partially, independent of food consumption, as control fed animals are no longer consuming bacterial food at this advanced age. Animals separated from the bacterial lawn by a barrier of solid agar have a life span intermediate between control fed and food restricted animals. Thus, we find that life span extension from bacterial deprivation can be partially suppressed by a diffusible component of the bacterial food source, suggesting a calorie-independent mechanism for life span extension by dietary restriction. Conclusion Based on these findings, we propose that dietary restriction by bacterial deprivation increases longevity in C. elegans by a combination of reduced food consumption and decreased food sensing.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
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Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {πŸ“ˆ}

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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How Does Link.springer.com Make Money? {πŸ’Έ}

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Keywords {πŸ”}

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Topics {βœ’οΈ}

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WebPage:
      mainEntity:
         headline:Age- and calorie-independent life span extension from dietary restriction by bacterial deprivation in Caenorhabditis elegans
         description:Dietary restriction (DR) increases life span and delays age-associated disease in many organisms. The mechanism by which DR enhances longevity is not well understood. Using bacterial food deprivation as a means of DR in C. elegans, we show that transient DR confers long-term benefits including stress resistance and increased longevity. Consistent with studies in the fruit fly and in mice, we demonstrate that DR also enhances survival when initiated late in life. DR by bacterial food deprivation significantly increases life span in worms when initiated as late as 24 days of adulthood, an age at which greater than 50% of the cohort have died. These survival benefits are, at least partially, independent of food consumption, as control fed animals are no longer consuming bacterial food at this advanced age. Animals separated from the bacterial lawn by a barrier of solid agar have a life span intermediate between control fed and food restricted animals. Thus, we find that life span extension from bacterial deprivation can be partially suppressed by a diffusible component of the bacterial food source, suggesting a calorie-independent mechanism for life span extension by dietary restriction. Based on these findings, we propose that dietary restriction by bacterial deprivation increases longevity in C. elegans by a combination of reduced food consumption and decreased food sensing.
         datePublished:2008-05-05T00:00:00Z
         dateModified:2008-05-05T00:00:00Z
         pageStart:1
         pageEnd:13
         license:http://creativecommons.org/licenses/by/2.0
         sameAs:https://doi.org/10.1186/1471-213X-8-49
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            Life Span
            Dietary Restriction
            Life Span Extension
            Increase Life Span
            Nematode Growth Medium
            Developmental Biology
            Animal Models
            Life Sciences
            general
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               name:Matt Kaeberlein
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      headline:Age- and calorie-independent life span extension from dietary restriction by bacterial deprivation in Caenorhabditis elegans
      description:Dietary restriction (DR) increases life span and delays age-associated disease in many organisms. The mechanism by which DR enhances longevity is not well understood. Using bacterial food deprivation as a means of DR in C. elegans, we show that transient DR confers long-term benefits including stress resistance and increased longevity. Consistent with studies in the fruit fly and in mice, we demonstrate that DR also enhances survival when initiated late in life. DR by bacterial food deprivation significantly increases life span in worms when initiated as late as 24 days of adulthood, an age at which greater than 50% of the cohort have died. These survival benefits are, at least partially, independent of food consumption, as control fed animals are no longer consuming bacterial food at this advanced age. Animals separated from the bacterial lawn by a barrier of solid agar have a life span intermediate between control fed and food restricted animals. Thus, we find that life span extension from bacterial deprivation can be partially suppressed by a diffusible component of the bacterial food source, suggesting a calorie-independent mechanism for life span extension by dietary restriction. Based on these findings, we propose that dietary restriction by bacterial deprivation increases longevity in C. elegans by a combination of reduced food consumption and decreased food sensing.
      datePublished:2008-05-05T00:00:00Z
      dateModified:2008-05-05T00:00:00Z
      pageStart:1
      pageEnd:13
      license:http://creativecommons.org/licenses/by/2.0
      sameAs:https://doi.org/10.1186/1471-213X-8-49
      keywords:
         Life Span
         Dietary Restriction
         Life Span Extension
         Increase Life Span
         Nematode Growth Medium
         Developmental Biology
         Animal Models
         Life Sciences
         general
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         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2F1471-213X-8-49/MediaObjects/12861_2007_Article_333_Fig1_HTML.jpg
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                  name:University of Washington
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                     type:PostalAddress
                  type:Organization
            type:Person
            name:Brian K Kennedy
            affiliation:
                  name:University of Washington
                  address:
                     name:Department of Biochemistry, University of Washington, Seattle, USA
                     type:PostalAddress
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            type:Person
            name:Matt Kaeberlein
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                  address:
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      name:University of Washington
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         type:PostalAddress
      name:University of Washington
      address:
         name:Department of Biochemistry, University of Washington, Seattle, USA
         type:PostalAddress
      name:University of Washington
      address:
         name:Department of Biochemistry, University of Washington, Seattle, USA
         type:PostalAddress
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      name:Erica D Smith
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            name:University of Washington
            address:
               name:Department of Pathology, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
            name:University of Washington
            address:
               name:Department of Biochemistry, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Tammi L Kaeberlein
      affiliation:
            name:University of Washington
            address:
               name:Department of Pathology, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      name:Brynn T Lydum
      affiliation:
            name:University of Washington
            address:
               name:Department of Pathology, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      name:Jennifer Sager
      affiliation:
            name:University of Washington
            address:
               name:Department of Pathology, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      name:K Linnea Welton
      affiliation:
            name:University of Washington
            address:
               name:Department of Biochemistry, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      name:Brian K Kennedy
      affiliation:
            name:University of Washington
            address:
               name:Department of Biochemistry, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      name:Matt Kaeberlein
      affiliation:
            name:University of Washington
            address:
               name:Department of Pathology, University of Washington, Seattle, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Pathology, University of Washington, Seattle, USA
      name:Department of Biochemistry, University of Washington, Seattle, USA
      name:Department of Pathology, University of Washington, Seattle, USA
      name:Department of Pathology, University of Washington, Seattle, USA
      name:Department of Pathology, University of Washington, Seattle, USA
      name:Department of Biochemistry, University of Washington, Seattle, USA
      name:Department of Biochemistry, University of Washington, Seattle, USA
      name:Department of Pathology, University of Washington, Seattle, USA

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