Evidence map›Paper›PMID 33364448›Full record

ArticleBiochemistry and biophysics reports2021

Acetoacetate enhancement of glucose mediated DNA glycation.

M Bagherzadeh-Yazdi, M Bohlooli, M Khajeh, F Ghamari, M Ghaffari-Moghaddam, N Poormolaie, A Khatibi, P Hasanein, N Sheibani

Open access · goldAbstract read
In one paragraph

Article in Biochemistry and biophysics reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 8 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

9 authors at 4 institutions in 2 countries.

M Bagherzadeh-YazdiDepartment of Biology, University of Zabol, Zabol, Iran.
M BohlooliDepartment of Biology, University of Zabol, Zabol, Iran.
M KhajehDepartment of Chemistry, University of Zabol, Zabol, Iran.
F GhamariDepartment of Biology, Payame Noor University, Ghazvin, Iran.
M Ghaffari-MoghaddamDepartment of Chemistry, University of Zabol, Zabol, Iran.
N PoormolaieDepartment of Chemistry, University of Zabol, Zabol, Iran.
A KhatibiDepartment of Biotechnology, Alzahra University, Tehran, Iran.
P HasaneinDepartment of Biology, University of Zabol, Zabol, Iran.
N SheibaniDepartments of Ophthalmology and Visual Sciences, Cell and Regenerative Biology, and Biomedical Engineering, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Zabol University · IRAlzahra University · IRPayame Noor University · IRUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acetoacetate (AA) is a ketone body, which generates reactive oxygen species (ROS). ROS production is impacted by the formation of covalent bonds between amino groups of biomacromolecules and reducing sugars (glycation). Glycation can damage DNA by causing strand breaks, mutations, and changes in gene expression. DNA damage could contribute to the pathogenesis of various diseases, including neurological disorders, complications of diabetes, and aging. Here we studied the enhancement of glucose-mediated DNA glycation by AA for the first time. The effect of AA on the structural changes, Amadori and advanced glycation end products (AGEs) formation of DNA incubated with glucose for 4 weeks were investigated using various techniques. These included UV-Vis, circular dichroism (CD) and fluorescence spectroscopy, and agarose gel electrophoresis. The results of UV-Vis and fluorescence spectroscopy confirmed that AA increased the DNA-AGE formation. The NBT test showed that AA also increased Amadori product formation of glycated DNA. Based on the CD and agarose gel electrophoresis results, the structural changes of glycated DNA was increased in the presence of AA. The chemiluminescence results indicated that AA increased ROS formation. Thus AA has an activator role in DNA glycation, which could enhance the adverse effects of glycation under high glucose conditions.

Indexed as

AA, AcetoacetateAcetoacetateAdvanced glycation end productsAGEs, Advanced glycation end productsAmadori productsCD, Circular DichroismDNA, Deoxyribonucleic AcidGlycated DNAKetone bodyNBT, Nitro blue Tetrazolium

Identifiers

PMID33364448
PMCPMC7750490
OpenAlexW3112246157

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.