Evidence map›Paper›PMID 26700733›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2016

Circadian clocks govern calorie restriction-mediated life span extension through BMAL1- and IGF-1-dependent mechanisms.

Sonal A Patel, Amol Chaudhari, Richa Gupta, Nikkhil Velingkaar, Roman V Kondratov

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sonal A PatelDepartment of Biological, Geological, and Environmental Sciences, and Center for Gene Regulation in Health and Diseases, Cleveland State University, Cleveland, Ohio, USA.
Amol ChaudhariDepartment of Biological, Geological, and Environmental Sciences, and Center for Gene Regulation in Health and Diseases, Cleveland State University, Cleveland, Ohio, USA.
Richa GuptaDepartment of Biological, Geological, and Environmental Sciences, and Center for Gene Regulation in Health and Diseases, Cleveland State University, Cleveland, Ohio, USA.
Nikkhil VelingkaarDepartment of Biological, Geological, and Environmental Sciences, and Center for Gene Regulation in Health and Diseases, Cleveland State University, Cleveland, Ohio, USA.
Roman V KondratovDepartment of Biological, Geological, and Environmental Sciences, and Center for Gene Regulation in Health and Diseases, Cleveland State University, Cleveland, Ohio, USA r.kondratov@csuohio.edu.
Cleveland State University · US

Funding

Diversity Supplement for Circadian Clock and Dietary RestrictionR01AG039547 · NIA · CLEVELAND STATE UNIVERSITY · PI Roman V Kondratov · 2011 to 2026
$5.5M
Nikon A1RSI Confocal MicroscopeS10OD010381 · OD · CLEVELAND STATE UNIVERSITY · PI BARIK, SAILEN · 2012 to 2012
$591k
NIA NIH HHS 1R01AG039547NIA NIH HHS R01 AG039547NIH HHS S10 OD010381
6 · The paper itself

Abstract

Calorie restriction (CR) increases longevity in many species by unknown mechanisms. The circadian clock was proposed as a potential mediator of CR. Deficiency of the core component of the circadian clock-transcriptional factor BMAL1 (brain and muscle ARNT [aryl hydrocarbon receptor nuclear translocator]-like protein 1)-results in accelerated aging. Here we investigated the role of BMAL1 in mechanisms of CR. The 30% CR diet increased the life span of wild-type (WT) mice by 20% compared to mice on anad libitum(AL) diet but failed to increase life span ofBmal1(-/-)mice. BMAL1 deficiency impaired CR-mediated changes in the plasma levels of IGF-1 and insulin. We detected a statistically significantly reduction of IGF-1 in CRvs.AL by 50 to 70% in WT mice at several daily time points tested, while inBmal1(-/-)the reduction was not significant. Insulin levels in WT were reduced by 5 to 9%, whileBmal1(-/-)induced it by 10 to 35% at all time points tested. CR up-regulated the daily average expression ofBmal1(by 150%) and its downstream target genesPeriods(by 470% forPer1and by 130% forPer2). We propose that BMAL1 is an important mediator of CR, and activation of BMAL1 might link CR mechanisms with biologic clocks.-Patel, S. A., Chaudhari, A., Gupta, R., Velingkaar, N., Kondratov, R. V. Circadian clocks govern calorie restriction-mediated life span extension through BMAL1- and IGF-1-dependent mechanisms.

Indexed as

Life ExpectancyAnimalsARNTL Transcription FactorsBlood GlucoseBlotting, WesternBody WeightCaloric RestrictionCircadian ClocksFemaleInsulinInsulin-Like Growth Factor ILongevityMaleMice, Inbred C57BLMice, KnockoutMotor ActivityARNTL Transcription FactorsBlood GlucoseBmal1 protein, mouseInsulinInsulin-Like Growth Factor Iagingfood anticipationgene expressionglucoseinsulintranscription

Identifiers

PMID26700733
PMCPMC4799504
OpenAlexW2261939670

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.