Evidence map›Paper›PMID 33867932›Full record

ArticleFrontiers in molecular neuroscience2021

Severe Spinal Cord Injury in Rats Induces Chronic Changes in the Spinal Cord and Cerebral Cortex Metabolism, Adjusted by Thiamine That Improves Locomotor Performance.

Alexandra Boyko, Polina Tsepkova, Vasily Aleshin, Artem Artiukhov, Garik Mkrtchyan, Alexander Ksenofontov, Lyudmila Baratova, Sergey Ryabov, Anastasia Graf, Victoria Bunik

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 28 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

10 authors at 4 institutions in 1 country.

Alexandra BoykoFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.
Polina TsepkovaFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.
Vasily AleshinFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.
Artem ArtiukhovFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.
Garik MkrtchyanFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.
Alexander KsenofontovBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia.
Lyudmila BaratovaBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia.
Sergey RyabovRussian Cardiology Research-and-Production Complex, Ministry of Health of the Russian Federation, Moscow, Russia.
Anastasia GrafFaculty of Biology, Lomonosov Moscow State University, Moscow, Russia.
Victoria BunikFaculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.
Lomonosov Moscow State University · RUMinistry of Health of the Russian Federation · RUMoscow Institute of Physics and Technology · RUSechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our study aims at developing knowledge-based strategies minimizing chronic changes in the brain after severe spinal cord injury (SCI). The SCI-induced long-term metabolic alterations and their reactivity to treatments shortly after the injury are characterized in rats. Eight weeks after severe SCI, significant mitochondrial lesions outside the injured area are demonstrated in the spinal cord and cerebral cortex. Among the six tested enzymes essential for the TCA cycle and amino acid metabolism, mitochondrial 2-oxoglutarate dehydrogenase complex (OGDHC) is the most affected one. SCI downregulates this complex by 90% in the spinal cord and 30% in the cerebral cortex. This is associated with the tissue-specific changes in other enzymes of the OGDHC network. Single administrations of a pro-activator (thiamine, or vitamin B1, 1.2 mmol/kg) or a synthetic pro-inhibitor (triethyl glutaryl phosphonate, TEGP, 0.02 mmol/kg) of OGDHC within 15-20 h after SCI are tested as protective strategies. The biochemical and physiological assessments 8 weeks after SCI reveal that thiamine, but not TEGP, alleviates the SCI-induced perturbations in the rat brain metabolism, accompanied by the decreased expression of (acetyl)p53, increased expression of sirtuin 5 and an 18% improvement in the locomotor recovery. Treatment of the non-operated rats with the OGDHC pro-inhibitor TEGP increases the p53 acetylation in the brain, approaching the brain metabolic profiles to those after SCI. Our data testify to an important contribution of the OGDHC regulation to the chronic consequences of SCI and their control by p53 and sirtuin 5.

Indexed as

2-oxoglutarate dehydrogenaseamino acids metabolismcerebral cortexp53phosphonate analog of 2-oxo acidsirtuin 5spinal cord injurythiamine

Identifiers

PMID33867932
PMCPMC8044794
OpenAlexW3149306048

What Socratic 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 Socratic graph.