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We are analyzing https://link.springer.com/article/10.1007/s00360-025-01616-1.

Title:
The cold truth: torpor as a confound in studies of caloric restriction | Journal of Comparative Physiology B
Description:
Calorie restriction has been shown to dramatically extend lifespan in a range of species. Beyond longevity, calorie restriction is also reported to improve cognitive function, ameliorate neurodegeneration and peripheral nerve damage, reduce cancer incidence, and is commonly used to increase motivation in studies of behaviour. The mouse has been the most common species for these experiments and whilst efforts are ongoing to demonstrate the benefits of calorie restriction in humans, the evidence in mice is most compelling. Many mechanisms have been proposed for the beneficial effects of calorie restriction, but we note that one potentially important factor has seldom been considered: namely that mice readily enter torpor in response to food restriction. Torpor is a remarkable protective physiological state characterized by profound reductions in body temperature, oxygen consumption, heart rate, and activity. In this review, we describe the dietary protocols used to study the effects of calorie restriction and present the case that mice in these studies are highly likely to have entered torpor. We discuss the extent to which torpor might influence or mediate the measured outcomes. We highlight that induction of torpor is an important confound that is rarely, if at all, considered in calorie restriction research and make recommendations for the design and conduct of future studies.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Education
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Content Management System {๐Ÿ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {๐Ÿ“ˆ}

What is the average monthly size of link.springer.com audience?

๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

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Keywords {๐Ÿ”}

torpor, pubmed, restriction, article, google, scholar, mice, calorie, cas, central, fasting, studies, temperature, caloric, dietary, effects, mouse, daily, data, food, day, lifespan, protocols, feeding, longevity, function, reduced, period, physiol, mitchell, aging, sci, weight, improved, httpsdoiorgs, research, cognitive, experiments, enter, body, fig, periods, induce, restricted, likelihood, health, benefits, response, metabolic, disease,

Topics {โœ’๏ธ}

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Questions {โ“}

  • Bouma HR, Carey HV, Kroese FG (2010) Hibernation: the immune system at rest?
  • Cava E, Fontana L (2013) Will calorie restriction work in humans?
  • Could torpor be a confounding factor in studies of dietary restriction?
  • Hence, the question arises: does torpor continue over prolonged periods of calorie restriction?

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:The cold truth: torpor as a confound in studies of caloric restriction
         description:Calorie restriction has been shown to dramatically extend lifespan in a range of species. Beyond longevity, calorie restriction is also reported to improve cognitive function, ameliorate neurodegeneration and peripheral nerve damage, reduce cancer incidence, and is commonly used to increase motivation in studies of behaviour. The mouse has been the most common species for these experiments and whilst efforts are ongoing to demonstrate the benefits of calorie restriction in humans, the evidence in mice is most compelling. Many mechanisms have been proposed for the beneficial effects of calorie restriction, but we note that one potentially important factor has seldom been considered: namely that mice readily enter torpor in response to food restriction. Torpor is a remarkable protective physiological state characterized by profound reductions in body temperature, oxygen consumption, heart rate, and activity. In this review, we describe the dietary protocols used to study the effects of calorie restriction and present the case that mice in these studies are highly likely to have entered torpor. We discuss the extent to which torpor might influence or mediate the measured outcomes. We highlight that induction of torpor is an important confound that is rarely, if at all, considered in calorie restriction research and make recommendations for the design and conduct of future studies.
         datePublished:2025-06-09T00:00:00Z
         dateModified:2025-06-09T00:00:00Z
         pageStart:1
         pageEnd:14
         license:http://creativecommons.org/licenses/by/4.0/
         sameAs:https://doi.org/10.1007/s00360-025-01616-1
         keywords:
            Calorie restriction
            Fasting
            Torpor
            Longevity
            Health
            Diet
            Animal Physiology
            Biomedicine
            general
            Human Physiology
            Zoology
            Biochemistry
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            name:Journal of Comparative Physiology B
            issn:
               1432-136X
               0174-1578
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            name:Springer Berlin Heidelberg
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               name:William S. R. Wheatley
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                     name:University of Bristol
                     address:
                        name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
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                     address:
                        name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
                        type:PostalAddress
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                        name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
                        type:PostalAddress
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                     name:University of Bristol
                     address:
                        name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
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ScholarlyArticle:
      headline:The cold truth: torpor as a confound in studies of caloric restriction
      description:Calorie restriction has been shown to dramatically extend lifespan in a range of species. Beyond longevity, calorie restriction is also reported to improve cognitive function, ameliorate neurodegeneration and peripheral nerve damage, reduce cancer incidence, and is commonly used to increase motivation in studies of behaviour. The mouse has been the most common species for these experiments and whilst efforts are ongoing to demonstrate the benefits of calorie restriction in humans, the evidence in mice is most compelling. Many mechanisms have been proposed for the beneficial effects of calorie restriction, but we note that one potentially important factor has seldom been considered: namely that mice readily enter torpor in response to food restriction. Torpor is a remarkable protective physiological state characterized by profound reductions in body temperature, oxygen consumption, heart rate, and activity. In this review, we describe the dietary protocols used to study the effects of calorie restriction and present the case that mice in these studies are highly likely to have entered torpor. We discuss the extent to which torpor might influence or mediate the measured outcomes. We highlight that induction of torpor is an important confound that is rarely, if at all, considered in calorie restriction research and make recommendations for the design and conduct of future studies.
      datePublished:2025-06-09T00:00:00Z
      dateModified:2025-06-09T00:00:00Z
      pageStart:1
      pageEnd:14
      license:http://creativecommons.org/licenses/by/4.0/
      sameAs:https://doi.org/10.1007/s00360-025-01616-1
      keywords:
         Calorie restriction
         Fasting
         Torpor
         Longevity
         Health
         Diet
         Animal Physiology
         Biomedicine
         general
         Human Physiology
         Zoology
         Biochemistry
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs00360-025-01616-1/MediaObjects/360_2025_1616_Fig1_HTML.png
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs00360-025-01616-1/MediaObjects/360_2025_1616_Fig2_HTML.png
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs00360-025-01616-1/MediaObjects/360_2025_1616_Fig3_HTML.png
      isPartOf:
         name:Journal of Comparative Physiology B
         issn:
            1432-136X
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            Periodical
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         name:Springer Berlin Heidelberg
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
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      author:
            name:William S. R. Wheatley
            url:http://orcid.org/0009-0003-8042-7222
            affiliation:
                  name:University of Bristol
                  address:
                     name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
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            email:[email protected]
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                  address:
                     name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
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            name:Ludovico Taddei
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                  name:University of Bristol
                  address:
                     name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
                     type:PostalAddress
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            name:Timna Hitrec
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                     name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
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                     name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
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         name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
         type:PostalAddress
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         name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
         type:PostalAddress
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         name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
         type:PostalAddress
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      address:
         name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
         type:PostalAddress
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      address:
         name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
         type:PostalAddress
      name:University of Bristol
      address:
         name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
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      url:http://orcid.org/0009-0003-8042-7222
      affiliation:
            name:University of Bristol
            address:
               name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
               type:PostalAddress
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      name:Christopher J. Marshall
      affiliation:
            name:University of Bristol
            address:
               name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
               type:PostalAddress
            type:Organization
      name:Ludovico Taddei
      affiliation:
            name:University of Bristol
            address:
               name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
               type:PostalAddress
            type:Organization
            name:University of Bologna
            address:
               name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
               type:PostalAddress
            type:Organization
      name:Timna Hitrec
      affiliation:
            name:University of Bristol
            address:
               name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
               type:PostalAddress
            type:Organization
            name:University of Bologna
            address:
               name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
               type:PostalAddress
            type:Organization
      name:Anthony E. Pickering
      affiliation:
            name:University of Bristol
            address:
               name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
               type:PostalAddress
            type:Organization
      name:Michael T. Ambler
      affiliation:
            name:University of Bristol
            address:
               name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
               type:PostalAddress
            type:Organization
PostalAddress:
      name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
      name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
      name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
      name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
      name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
      name:Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy
      name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
      name:School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK

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