Evidence map›Paper›PMID 25356430›Full record

ArticleAnnals of clinical and translational neurology2014

Brain diabetic neurodegeneration segregates with low intrinsic aerobic capacity.

Joungil Choi, Krish Chandrasekaran, Tyler G Demarest, Tibor Kristian, Su Xu, Kadambari Vijaykumar, Kevin Geoffrey Dsouza, Nathan R Qi, Paul J Yarowsky, Rao Gallipoli and 4 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

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  10. NADInternational journal of molecular sciences · 2022
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  15. From Metabolic Syndrome to Neurological Diseases: Role of Autophagy.Frontiers in cell and developmental biology · 2021
    Review
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  17. Article
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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

14 authors at 3 institutions in 1 country.

Joungil ChoiDepartment of Neurology, University of Maryland Baltimore, Maryland, 21201 ; Veterans Affairs Medical Center Baltimore, Maryland, 21201.
Krish ChandrasekaranDepartment of Neurology, University of Maryland Baltimore, Maryland, 21201 ; Veterans Affairs Medical Center Baltimore, Maryland, 21201.
Tyler G DemarestDepartment of Anesthesiology, University of Maryland Baltimore, Maryland, 21201.
Tibor KristianVeterans Affairs Medical Center Baltimore, Maryland, 21201 ; Department of Anesthesiology, University of Maryland Baltimore, Maryland, 21201.
Su XuDepartment of Radiology, University of Maryland Baltimore, Maryland, 21201.
Kadambari VijaykumarDepartment of Neurology, University of Maryland Baltimore, Maryland, 21201 ; Veterans Affairs Medical Center Baltimore, Maryland, 21201.
Kevin Geoffrey DsouzaDepartment of Neurology, University of Maryland Baltimore, Maryland, 21201 ; Veterans Affairs Medical Center Baltimore, Maryland, 21201.
Nathan R QiDepartment of Internal Medicine, University of Michigan Ann Arbor, Michigan, 48109.
Paul J YarowskyDepartment of Pharmacology, University of Maryland Baltimore, Maryland, 21201.
Rao GallipoliDepartment of Radiology, University of Maryland Baltimore, Maryland, 21201.
Lauren G KochDepartment of Anesthesiology, University of Michigan Ann Arbor, Michigan, 48109.
Gary M FiskumDepartment of Anesthesiology, University of Maryland Baltimore, Maryland, 21201.
Steven L BrittonDepartment of Anesthesiology, University of Michigan Ann Arbor, Michigan, 48109.
James W RussellDepartment of Neurology, University of Maryland Baltimore, Maryland, 21201 ; Veterans Affairs Medical Center Baltimore, Maryland, 21201.
University of Maryland, Baltimore · USVeterans Health Administration · USUniversity of Michigan–Ann Arbor · US

Funding

PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILLIAM H HERMAN · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joyce Lee · 2010 to 2026
$20.3M
Research BaseP30DK072488 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI MITCHELL, BRAXTON D, TAYLOR, SIMEON I. · 2005 to 2019
$17.3M
SYTEMS AND INTEGRATIVE BIOLOGYT32GM008322 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOW, MALCOLM JAMES · 1990 to 2020
$5.7M
RESOURCE FOR RAT GENETIC MODELS OF AEROBIC CAPACITYR24RR017718 · NCRR · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI BRITTON, STEVEN LOYAL · 2003 to 2011
$4.0M
HIGH-FIELD ANIMAL MRI: PEDIATRIC HEAD INJURY, PAINS10RR019935 · NCRR · UNIVERSITY OF MARYLAND BALTIMORE · PI GULLAPALLI, RAO P · 2005 to 2005
$2.0M
Biology of Aerobic Capacity and Insulin ResistanceR01DK077200 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURANT, CHARLES F · 2008 to 2012
$1.5M
SIRT1 Overexpression in Cellular Mitochondrial Metabolism and FunctionR21RR024888 · NCRR · UNIVERSITY OF MARYLAND BALTIMORE · PI RUSSELL, JAMES W · 2008 to 2009
$413k
Improving Autonomic Function and Balance in Diabetic NeuropathyI01RX001030 · VA · BALTIMORE VA MEDICAL CENTER · PI RUSSELL, JAMES W · 2015 to 2017
–
Nudix hydrolases and mitochondrial dynamics in acute neurodegenerative diseaseI01BX000917 · VA · BALTIMORE VA MEDICAL CENTER · PI KRISTIAN, TIBOR · 2011 to 2019
–
BLRD VA I01 BX000917NCRR NIH HHS R21 RR024888NCRR NIH HHS R24 RR017718NCRR NIH HHS S10 RR019935NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK072488NIDDK NIH HHS P30 DK089503NIDDK NIH HHS P60 DK020572NIDDK NIH HHS R01 DK077200NIGMS NIH HHS T32 GM008322RRD VA I01 RX001030
6 · The paper itself

Abstract

objectivesDiabetes leads to cognitive impairment and is associated with age-related neurodegenerative diseases including Alzheimer's disease (AD). Thus, understanding diabetes-induced alterations in brain function is important for developing early interventions for neurodegeneration. Low-capacity runner (LCR) rats are obese and manifest metabolic risk factors resembling human "impaired glucose tolerance" or metabolic syndrome. We examined hippocampal function in aged LCR rats compared to their high-capacity runner (HCR) rat counterparts.

methodsHippocampal function was examined using proton magnetic resonance spectroscopy and imaging, unbiased stereology analysis, and a Y maze. Changes in the mitochondrial respiratory chain function and levels of hyperphosphorylated tau and mitochondrial transcriptional regulators were examined.

resultsThe levels of glutamate, myo-inositol, taurine, and choline-containing compounds were significantly increased in the aged LCR rats. We observed a significant loss of hippocampal neurons and impaired cognitive function in aged LCR rats. Respiratory chain function and activity were significantly decreased in the aged LCR rats. Hyperphosphorylated tau was accumulated within mitochondria and peroxisome proliferator-activated receptor-gamma coactivator 1α, the NAD(+)-dependent protein deacetylase sirtuin 1, and mitochondrial transcription factor A were downregulated in the aged LCR rat hippocampus.

interpretationThese data provide evidence of a neurodegenerative process in the hippocampus of aged LCR rats, consistent with those seen in aged-related dementing illnesses such as AD in humans. The metabolic and mitochondrial abnormalities observed in LCR rat hippocampus are similar to well-described mechanisms that lead to diabetic neuropathy and may provide an important link between cognitive and metabolic dysfunction.

Identifiers

PMID25356430
PMCPMC4184561
OpenAlexW2162473817

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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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.