Evidence map›Paper›PMID 24515302›Full record

ReviewMetabolic brain disease2015

Contributions of glycogen to astrocytic energetics during brain activation.

Gerald A Dienel, Nancy F Cruz

Open access · greenAbstract readReview
In one paragraph

Review in Metabolic brain disease, 2015. 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
5.2field-weighted citation impact, top 3% 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, 103 citations in OpenAlex.

  1. Glucose sparing by glycogenolysis (GSG) determines the relationship between brain metabolism and neurotransmission.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
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  19. The role of SLC transporters for brain health and disease.Cellular and molecular life sciences : CMLS · 2021
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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

2 authors at 1 institution in 1 country.

Gerald A DienelDepartment of Neurology, University of Arkansas for Medical Sciences, Slot 500, 4301 W. Markham St., Little Rock, AR, 72205, USA, gadienel@uams.edu.
Nancy F Cruz
University of Arkansas for Medical Sciences · US

Funding

FUNCTIONAL METABOLISM IN WORKING BRAINR01NS036728 · NINDS · UNIV OF ARKANSAS FOR MED SCIS · PI DIENEL, GERALD A. · 1999 to 2007
$1.8M
FUNCTIONAL METABOLIC ACTIVITY IN GLIA IN VIVOR01NS038230 · NINDS · UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK · PI DIENEL, GERALD A. · 2000 to 2003
$1.3M
Endoplasmic reticulum stress in diabetic brainR01DK081936 · NIDDK · UNIV OF ARKANSAS FOR MED SCIS · PI DIENEL, GERALD A. · 2009 to 2012
$1.3M
Functional activity in gliaR56NS038230 · NINDS · UNIV OF ARKANSAS FOR MED SCIS · PI DIENEL, GERALD A. · 2009 to 2009
$363k
NIDDK NIH HHS DK081936NIDDK NIH HHS R01 DK081936NINDS NIH HHS NS038230NINDS NIH HHS NS36728NINDS NIH HHS R01 NS036728NINDS NIH HHS R01 NS038230NINDS NIH HHS R56 NS038230
6 · The paper itself

Abstract

Glycogen is the major store of glucose in brain and is mainly in astrocytes. Brain glycogen levels in unstimulated, carefully-handled rats are 10-12 μmol/g, and assuming that astrocytes account for half the brain mass, astrocytic glycogen content is twice as high. Glycogen turnover is slow under basal conditions, but it is mobilized during activation. There is no net increase in incorporation of label from glucose during activation, whereas label release from pre-labeled glycogen exceeds net glycogen consumption, which increases during stronger stimuli. Because glycogen level is restored by non-oxidative metabolism, astrocytes can influence the global ratio of oxygen to glucose utilization. Compensatory increases in utilization of blood glucose during inhibition of glycogen phosphorylase are large and approximate glycogenolysis rates during sensory stimulation. In contrast, glycogenolysis rates during hypoglycemia are low due to continued glucose delivery and oxidation of endogenous substrates; rates that preserve neuronal function in the absence of glucose are also low, probably due to metabolite oxidation. Modeling studies predict that glycogenolysis maintains a high level of glucose-6-phosphate in astrocytes to maintain feedback inhibition of hexokinase, thereby diverting glucose for use by neurons. The fate of glycogen carbon in vivo is not known, but lactate efflux from brain best accounts for the major metabolic characteristics during activation of living brain. Substantial shuttling coupled with oxidation of glycogen-derived lactate is inconsistent with available evidence. Glycogen has important roles in astrocytic energetics, including glucose sparing, control of extracellular K(+) level, oxidative stress management, and memory consolidation; it is a multi-functional compound.

Indexed as

Energy MetabolismAnimalsArousalArtifactsAstrocytesBrainCarbonChemistry Techniques, AnalyticalGlucoseGlutamic AcidGlycogenGlycogenolysisHumansHypoglycemiaModels, NeurologicalNeuronsCarbonGlucoseGlutamic AcidGlycogenOxygenPotassium

Identifiers

PMID24515302
PMCPMC4130810
OpenAlexW2077168428

What OpenQuestion holds

Textmetadata
LicenceTDM
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.