Evidence map›Paper›PMID 23874783›Full record

ArticlePloS one2013

Distinct pools of non-glycolytic substrates differentiate brain regions and prime region-specific responses of mitochondria.

Do Yup Lee, Zhiyin Xun, Virginia Platt, Helen Budworth, Christie A Canaria, Cynthia T McMurray

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 26 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

6 authors at 3 institutions in 2 countries.

Do Yup LeeLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA.
Zhiyin Xun
Virginia Platt
Helen Budworth
Christie A Canaria
Cynthia T McMurray
Lawrence Berkeley National Laboratory · USBuck Institute for Research on Aging · USKookmin University · KR

Funding

Transcription-Coupled & Replication-Associated Excision RepairP01CA092584 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI John A. Tainer · 2001 to 2026
$89.6M
Training in Basic Research on Aging and Age-Related DiseaseT32AG000266 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI Lisa M Ellerby · 1998 to 2026
$13.8M
TRAFFICKING DEFECTS IN HUNTINGTONS DISEASER01NS040738 · NINDS · MAYO CLINIC ROCHESTER · PI MCMURRAY, CYNTHIA THERESE · 2001 to 2009
$3.4M
Mismatch Repair and DNA expansionR01GM066359 · NIGMS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI MCMURRAY, CYNTHIA THERESE · 2004 to 2011
$2.9M
Metabolic markers for mitochondrial functionR01ES020766 · NIEHS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI MCMURRAY, CYNTHIA THERESE · 2011 to 2015
$2.3M
Age of Onset and Huntingtons DiseaseR01NS062384 · NINDS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI MCMURRAY, CYNTHIA THERESE · 2009 to 2010
$1.3M
MT Function and Dysfunction in Single Neurons in VivoRC1NS069177 · NINDS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI MCMURRAY, CYNTHIA THERESE, NORTHEN, TRENT R. · 2009 to 2010
$1.0M
NCI NIH HHS CA092584NCI NIH HHS P01 CA092584NIA NIH HHS T32 AG000266NIEHS NIH HHS R01 ES020766NIGMS NIH HHS GM066359NIGMS NIH HHS R01 GM066359NINDS NIH HHS NS062384NINDS NIH HHS NS069177NINDS NIH HHS NS40738NINDS NIH HHS R01 NS040738NINDS NIH HHS R01 NS062384NINDS NIH HHS RC1 NS069177
6 · The paper itself

Abstract

Many hereditary diseases are characterized by region-specific toxicity, despite the fact that disease-linked proteins are generally ubiquitously expressed. The underlying basis of the region-specific vulnerability remains enigmatic. Here, we evaluate the fundamental features of mitochondrial and glucose metabolism in synaptosomes from four brain regions in basal and stressed states. Although the brain has an absolute need for glucose in vivo, we find that synaptosomes prefer to respire on non-glycolytic substrates, even when glucose is present. Moreover, glucose is metabolized differently in each brain region, resulting in region-specific "signature" pools of non-glycolytic substrates. The use of non-glycolytic resources increases and dominates during energy crisis, and triggers a marked region-specific metabolic response. We envision that disease-linked proteins confer stress on all relevant brain cells, but region-specific susceptibility stems from metabolism of non-glycolytic substrates, which limits how and to what extent neurons respond to the stress.

Indexed as

AnimalsBrainGlucoseGlycolysisMiceMice, Inbred C57BLMitochondriaSubstrate SpecificitySynaptosomesGlucose

Identifiers

PMID23874783
PMCPMC3714274
OpenAlexW2073549379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.