Evidence map›Paper›PMID 16179343›Full record

ArticleThe Journal of biological chemistry2005

Physiological and pathological changes in glucose regulate brain Akt and glycogen synthase kinase-3.

Buffie Clodfelder-Miller, Patrizia De Sarno, Anna A Zmijewska, Ling Song, Richard S Jope

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

55 citing papers in PubMed, 121 citations in OpenAlex.

  1. Article
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  8. New Insights into the Regulation of mTOR Signaling via CaInternational journal of molecular sciences · 2023
    Review
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  19. Review
  20. Novel Roles for the Insulin-Regulated Glucose Transporter-4 in Hippocampally Dependent Memory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
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.

Buffie Clodfelder-MillerDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, Alabama 35294-0017, USA.
Patrizia De Sarno
Anna A Zmijewska
Ling Song
Richard S Jope
University of Alabama at Birmingham · US

Funding

LITHIUM EFFECTS ON CHOLINERGIC ACTIVITYR01MH038752 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI JOPE, RICHARD S. · 1985 to 2015
$4.4M
NEURONAL SIGNALING--OXIDANTS AND ALZHEIMERS DISEASER01NS037768 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JOPE, RICHARD S · 1999 to 2007
$1.8M
GSK3beta: Signaling and apoptosisR01AG021045 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JOPE, RICHARD S · 2003 to 2007
$1.2M
NIA NIH HHS AG021045NIA NIH HHS R01 AG021045NIMH NIH HHS R01 MH038752NINDS NIH HHS NS37768NINDS NIH HHS R01 NS037768
6 · The paper itself

Abstract

Insulin regulates the phosphorylation and activities of Akt and glycogen synthase kinase-3 (GSK3) in peripheral tissues, but in the brain it is less clear how this signaling pathway is regulated in vivo and whether it is affected by diabetes. We found that Akt and GSK3 are sensitive to glucose, because fasting decreased and glucose administration increased by severalfold the phosphorylation of Akt and GSK3 in the cerebral cortex and hippocampus of non-diabetic mice. Brain Akt and GSK3 phosphorylation also increased after streptozotocin administration (3 days), which increased blood glucose and depleted blood insulin, indicating regulation by glucose availability even with deficient insulin. Changes in Akt and GSK3 phosphorylation and activities in epididymal fat were opposite to those of brain after streptozotocin treatment. Streptozotocin-induced hyperglycemia and increased brain Akt and GSK3 phosphorylation were reversed by lowering blood glucose with insulin administration. Long term hyperglycemia also increased brain Akt and GSK3 phosphorylation, both 4 weeks after streptozotocin and in db/db insulin-resistant mice. Thus, the Akt-GSK3 signaling pathway is regulated in mouse brain in vivo in response to physiological and pathological changes in insulin and glucose.

Indexed as

Adipose TissueAnimalsBlood GlucoseBody WeightBrainCerebral CortexEnzyme-Linked Immunosorbent AssayEpididymisFood DeprivationGlucoseGlycogen Synthase Kinase 3HippocampusImmunoblottingImmunoprecipitationInsulinMaleBlood GlucoseGlucoseGlycogen Synthase Kinase 3InsulinProto-Oncogene Proteins c-aktStreptozocin

Identifiers

PMID16179343
PMCPMC1361688
OpenAlexW1970945779

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.