Evidence map›Paper›PMID 25252946›Full record

ArticleAmerican journal of physiology. Cell physiology2014

Functional mitochondrial analysis in acute brain sections from adult rats reveals mitochondrial dysfunction in a rat model of migraine.

Nathan T Fried, Cynthia Moffat, Erin L Seifert, Michael L Oshinsky

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

41 citing papers in PubMed, 51 citations in OpenAlex.

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  9. Tracing the path of disruption:CNS neuroscience & therapeutics · 2024
    Review
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  14. Characterizing region-specific glucose metabolic profile of the rodent brain using Seahorse XFe96 analyzer.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    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

4 authors at 1 institution in 1 country.

Nathan T FriedThomas Jefferson University, Department of Neurology, Philadelphia, Pennsylvania;
Cynthia MoffatThomas Jefferson University, Department of Pathology, Anatomy and Cell Biology, Philadelphia, Pennsylvania.
Erin L SeifertThomas Jefferson University, Department of Pathology, Anatomy and Cell Biology, Philadelphia, Pennsylvania.
Michael L OshinskyThomas Jefferson University, Department of Neurology, Philadelphia, Pennsylvania; Michael.Oshinsky@jefferson.edu.
Thomas Jefferson University · US

Funding

Alcohol Tissue InjuryT32AA007463 · NIAAA · THOMAS JEFFERSON UNIVERSITY · PI HOEK, JOANNES B, VADIGEPALLI, RAJANIKANTH · 1985 to 2021
$9.1M
Progression of Headache Associated with Recurrent Dural Inflammation (PI: MichaelR01NS061571 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI OSHINSKY, MICHAEL L. · 2007 to 2011
$1.6M
Mentoring Junior Investigators in Alcohol ResearchK05AA017261 · NIAAA · THOMAS JEFFERSON UNIVERSITY · PI HOEK, JOANNES B · 2008 to 2012
$1.1M
NIAAA NIH HHS K05-AA017261NIAAA NIH HHS T32 AA007463NINDS NIH HHS R01-NS061571
6 · The paper itself

Abstract

Mitochondrial dysfunction has been implicated in many neurological disorders that only develop or are much more severe in adults, yet no methodology exists that allows for medium-throughput functional mitochondrial analysis of brain sections from adult animals. We developed a technique for quantifying mitochondrial respiration in acutely isolated adult rat brain sections with the Seahorse XF Analyzer. Evaluating a range of conditions made quantifying mitochondrial function from acutely derived adult brain sections from the cortex, cerebellum, and trigeminal nucleus caudalis possible. Optimization of this technique demonstrated that the ideal section size was 1 mm wide. We found that sectioning brains at physiological temperatures was necessary for consistent metabolic analysis of trigeminal nucleus caudalis sections. Oxygen consumption in these sections was highly coupled to ATP synthesis, had robust spare respiratory capacities, and had limited nonmitochondrial respiration, all indicative of healthy tissue. We demonstrate the effectiveness of this technique by identifying a decreased spare respiratory capacity in the trigeminal nucleus caudalis of a rat model of chronic migraine, a neurological disorder that has been associated with mitochondrial dysfunction. This technique allows for 24 acutely isolated sections from multiple brain regions of a single adult rat to be analyzed simultaneously with four sequential drug treatments, greatly advancing the ability to study mitochondrial physiology in adult neurological disorders.

Indexed as

AnimalsBrainEnergy MetabolismMigraine DisordersMitochondriaOxygen ConsumptionRatsTemperatureadult brain sectionsbrain energy metabolismmitochondrianeurological disordersneuron-glial interactions

Identifiers

PMID25252946
PMCPMC4254950
OpenAlexW2316934182

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.