Evidence map›Paper›PMID 28539831›Full record

ArticleInternational journal of biological sciences2017

Aldehyde Dehydrogenases 1A2 Expression and Distribution are Potentially Associated with Neuron Death in Spinal Cord of Tg(SOD1*G93A)1Gur Mice.

Huiting Liang, Chengsi Wu, Youqing Deng, Lei Zhu, Jie Zhang, Weiming Gan, Chunyan Tang, Renshi Xu

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. A new perspective on HIV: effects of HIV on brain-heart axis.Frontiers in cardiovascular medicine · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    Article
  14. Article
  15. 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

8 authors at 2 institutions in 1 country.

Huiting LiangDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Chengsi WuDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Youqing DengDepartment of Neurology, Third Affiliated Hospital of Nanchang University, Nanchang 330008, Jiangxi, China.
Lei ZhuDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Jie ZhangDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Weiming GanDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Chunyan TangDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Renshi XuDepartment of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
First Affiliated Hospital of Nanchang University · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pathogenesis of amyotrophic lateral sclerosis (ALS) has not been unclear yet, it might be associated with the abnormal expression and distribution of certain proteins. Aldehyde dehydrogenases 1A2 (ALDH1A2) was thought to be one of potential candidates. Therefore, in this study we observed and analyzed the alteration of the expression and distribution of ALDH1A2 in the spinal cord of wild-type (WT) and Tg(SOD1*G93A)1Gur mice. We compared the expression and distribution of ALDH1A2 in the different segments, anatomic regions and neural cells of spinal cord at the different stages of WT and Tg(SOD1*G93A)1Gur mice applied the methods of fluorescent immunohistochemistry and western blot. Results revealed that ALDH1A2 extensively expressed and distributed in the spinal cord of adult WT and Tg(SOD1*G93A)1Gur mice. The expression and distribution of ALDH1A2 in the white matter including the anterior, posterior and lateral funiculus were more than that in the gray matter including the central canal, the anterior and dorsal horn. ALDH1A2 majorly expressed and distributed in the astrocyte, microglial, oligodendrocyte and neuron cells. The ALDH1A2 expression significantly decreased and redistributed in some anatomic regions of spinal cord at the onset and progression stages of Tg(SOD1*G93A)1Gur mice. The expression decrease of ALDH1A2 followed with the increase of neuron cells death. This study suggested that the alteration of expression and distribution of ALDH1A2 was potentially associated with the pathogenesis of ALS.

Indexed as

Aldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAmyotrophic Lateral SclerosisAnimalsDisease Models, AnimalDisease ProgressionImmunohistochemistryMiceMice, Inbred C57BLMice, TransgenicMotor NeuronsRetinal DehydrogenaseSpinal CordSuperoxide DismutaseSuperoxide Dismutase-1Aldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAldh1a2 protein, mouseRetinal DehydrogenaseSuperoxide DismutaseSuperoxide Dismutase-1aldehyde dehydrogenases 1A2Amyotrophic lateral sclerosisglial cellneuronpathogenesis.

Identifiers

PMID28539831
PMCPMC5441175
OpenAlexW2610829879

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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.