Evidence map›Paper›PMID 31000957›Full record

ArticleAnnals of neurosciences2018

Role of DNA Methylation in Hypobaric Hypoxia-Induced Neurodegeneration and Spatial Memory Impairment.

Rahul Kumar, Vishal Jain, Neetu Kushwah, Aastha Dheer, Kamla Prasad Mishra, Dipti Prasad, Shashi Bala Singh

Open access · bronzeAbstract read
In one paragraph

Article in Annals of neurosciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. The Chromatin-Oxygen Sensor GeneInternational journal of molecular sciences · 2022
    Article
  10. Review
  11. Article
  12. Andrographolide: Regulating the Master Regulator NF-κB.Indian journal of clinical biochemistry : IJCB · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. 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

7 authors at 2 institutions in 1 country.

Rahul KumarNeurobiology Division, Defence Institute of Physiology and Allied Science (DIAPS), DRDO, New Delhi, India.
Vishal JainNeurophysiology Division, Defence Institute of Physiology and Allied Science (DIAPS), DRDO, New Delhi, India.
Neetu KushwahNeurobiology Division, Defence Institute of Physiology and Allied Science (DIAPS), DRDO, New Delhi, India.
Aastha DheerNeurobiology Division, Defence Institute of Physiology and Allied Science (DIAPS), DRDO, New Delhi, India.
Kamla Prasad MishraDirectorate General Life Sciences, Defence research Development Organisation (DRDO), Government of India, DRDO Bhawan, Rajaji Marg, New Delhi, India.
Dipti PrasadNeurobiology Division, Defence Institute of Physiology and Allied Science (DIAPS), DRDO, New Delhi, India.
Shashi Bala SinghDirectorate General Life Sciences, Defence research Development Organisation (DRDO), Government of India, DRDO Bhawan, Rajaji Marg, New Delhi, India.
Defence Institute of Physiology and Allied Sciences · INGovernment of India · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypobaric hypoxia (HH) is a major stress factor that is associated with physiological, biochemical, molecular and genomic alterations. Brain is the organ that reacts sensitively to oxygen deprivation, which leads to oxidative stress and cognitive function impairment. Our previous studies have reported that downregulation of brain derived neurotrophic factor (BDNF) leads to neurodegeneration and memory impairment. The aim of the present study was to investigate the effect of HH exposure on DNA methylation and its regulation in BDNF expression, neurodegeneration and spatial memory impairment. For this purpose, Sprague Dawley rats were exposed to HH at a simulated altitude of 25,000 feet for 14 days. Real-time polymerase chain reaction was used for transcriptional expression of DNA Methyltransferases (DNMTs) including DNMT1, DNMT3a and -DNMT3b, and immunoblotting was used for the translational expression of DNMT1, DNMT3a, DNMT3b, Methyl CpG binding protein 2 (MeCP2), pMeCP2 and BDNF in rat hippocampus. Additionally, neuronal morphology alteration and neurodegeneration in CA1 region of hippocampus were investigated though Cresyl violet (CV) staining and Fluoro-Jade C staining respectively. Results obtained suggested that HH exposure increased the expression of DNMT1 DNMT3b at the mRNA as well as protein level, whereas no significant change was observed in the level of DNMT3a. Furthermore, the level of pMeCP2 and BDNF were significantly decreased; however, the expression level of MeCP2 was significantly increased. The CV and Fluoro-Jade C-positive cells were significantly enhanced in the CA1 region of hippocampus in the HH exposed group as compared to unexposed rats. Thus, the present study concluded that HH decreases neuronal activation by the upregulation of DNA methylation and MeCP2 and decreased the expression of pMeCP2, which result in the downregulation of BDNF. The decreased BDNF expression is associated with neuronal loss and spatial memory impairment. This study highlights that DNMT inhibition could be an important therapeutic target for neurodegenerative diseases.

Indexed as

Brain-derived neurotrophic factorDNA methyltransferaseHypobaric hypoxiaMethyl CpG binding protein 2Neurodegeneration

Identifiers

PMID31000957
PMCPMC6470337
OpenAlexW2820111490

What OpenQuestion holds

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Registered trials

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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.