Evidence map›Paper›PMID 30538807›Full record

ArticleOxidative medicine and cellular longevity2018

ALDH2 Activity Reduces Mitochondrial Oxygen Reserve Capacity in Endothelial Cells and Induces Senescence Properties.

G Nannelli, E Terzuoli, V Giorgio, S Donnini, P Lupetti, A Giachetti, P Bernardi, M Ziche

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  3. Correlation BetweenCardiovascular therapeutics · 2026
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  4. Review
  5. DownregulatedCells · 2025
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  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Trimethylamine oxide induces pyroptosis of vascular endothelial cells through ALDH2/ROS/NLRP3/GSDMD pathway.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2022
    Article
  16. Aging related impairment of brain microvascular bioenergetics involves oxidative phosphorylation and glycolytic pathways.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Article
  17. Review
  18. Review
  19. Article
  20. 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.

G NannelliDepartment of Life Sciences, University of Siena, Siena, Italy.
E TerzuoliDepartment of Life Sciences, University of Siena, Siena, Italy.
V GiorgioDepartment of Biomedical Sciences, University of Padua, Padua, Italy.ORCID 0000-0002-4229-3054
S DonniniDepartment of Life Sciences, University of Siena, Siena, Italy.ORCID 0000-0001-6617-1644
P LupettiDepartment of Life Sciences, University of Siena, Siena, Italy.
A GiachettiDepartment of Life Sciences, University of Siena, Siena, Italy.
P BernardiDepartment of Biomedical Sciences, University of Padua, Padua, Italy.
M ZicheDepartment of Life Sciences, University of Siena, Siena, Italy.ORCID 0000-0002-9564-214X
University of Siena · ITUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial cells (ECs) are dynamic cells that turn from growth into senescence, the latter being associated with cellular dysfunction, altered metabolism, and age-related cardiovascular diseases. Aldehyde dehydrogenase 2 (ALDH2) is a mitochondrial enzyme metabolizing acetaldehyde and other toxic aldehydes, such as 4-hydroxynonenal (4-HNE). In conditions in which lipid peroxidation products and reactive oxygen species (ROS) are accumulated, ECs become dysfunctional and significantly contribute to the progression of vascular-dependent diseases. The aim of the present study has been to investigate whether inhibition of ALDH2 alters endothelial functions together with the impairment of bioenergetic functions, accelerating the acquisition of a senescent phenotype. HUVECs transfected with siRNA targeting ALDH2 or treated with daidzin, an ALDH2 inhibitor, were used in this study. We observed an alteration in cell morphology associated with endothelial dysfunctions. Loss of ALDH2 reduced cell proliferation and migration and increased paracellular permeability. To assess bioenergetic function in intact ECs, extracellular flux analysis was carried out to establish oxygen consumption rates (OCR). We observed a decrease in mitochondrial respiration and reserve capacity that coincided with SA-

Indexed as

Aldehyde Dehydrogenase, MitochondrialCell RespirationCellular SenescenceHumansHuman Umbilical Vein Endothelial CellsMitochondriaAldehyde Dehydrogenase, MitochondrialALDH2 protein, human

Identifiers

PMID30538807
PMCPMC6261243
OpenAlexW2900743432

What OpenQuestion 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 OpenQuestion graph.