Evidence map›Paper›PMID 30136168›Full record

ArticleJournal of bioenergetics and biomembranes2018

Mitochondrial NADH redox potential impacts the reactive oxygen species production of reverse Electron transfer through complex I.

Hervé Dubouchaud, Ludivine Walter, Michel Rigoulet, Cécile Batandier

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In one paragraph

Article in Journal of bioenergetics and biomembranes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

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  20. Modelling mitochondrial ROS production by the respiratory chain.Cellular and molecular life sciences : CMLS · 2020
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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

4 authors.

Hervé DubouchaudUniversité Grenoble Alpes, INSERM, LBFA, Grenoble, France.
Ludivine WalterLaboratoire de Biologie et Modélisation de la Cellule, ENS, CNRS, UMR 5239, F-69364, Lyon, France.
Michel RigouletInstitut de Biochimie et de Génétique de la cellule du CNRS, UMR 5095, Bordeaux, France.
Cécile BatandierUniversité Grenoble Alpes, INSERM, LBFA, Grenoble, France. Cecile.Batandier@univ-grenoble-alpes.fr.ORCID 0000-0003-1173-458X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is substantial evidence that Reactive Oxygen Species (ROS) play a major part in cell functioning. Although their harmfulness through oxidative stress is well documented, their role in signaling and sensing as an oxidative signal still needs to be investigated. In most cells, the mitochondrial Electron Transport Chain (ETC) is the primary source of ROS. The production of ROS by reverse electron transfer through complex I has been demonstrated both in an experimental context but also in many pathophysiological situations. Therefore, understanding the mechanisms that regulate this ROS production is of great interest to control its harmful effects. We used nigericin, Pi and valinomycin as tools to modulate the pH gradient (∆pH) and the membrane potential (∆Ψ) of the protonmotive force (∆p) in liver and muscle mitochondria to accurately determine how these parameters control the ROS production. We show that a high ∆Ψ is the "sine qua none" condition for ROS production from the reverse electron transfer (RET) through the complex I. However, a high ∆Ψ is not the only condition governing ROS production. Indeed, using tools that modulate the mitochondrial NADH level, we also demonstrate that ROS production is directly related to the mitochondrial redox potential when the membrane potential is almost stable.

Indexed as

AnimalsElectron Transport Complex IHumansMitochondria, HeartNADRatsRats, WistarReactive Oxygen SpeciesElectron Transport Complex INADReactive Oxygen SpeciesComplex IMitochondriaNADH redox potentialReverse electron transferROS

Identifiers

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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.