Evidence map›Paper›PMID 40938478›Full record

ReviewMolecular biology reports2025

Comprehensive review on alcohol-induced protein modifications in hepatic mitochondrial membranes and their functional implications.

Kuruvalli Gouthami, P C Nagajyothi, Deepika Shekhawat, Ayantika Santra, Subhasish Maity, Venkata Prasad Surtineni, Selvam Arjunan, Vaddi Damodara Reddy, Jaesool Shim

Abstract readReview
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In one paragraph

Review in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Kuruvalli Gouthami *Department of Biochemistry, REVA University, Rukmini Knowledge Park, Kattigenahalli, Yelahanka, Bangalore, 560064, Karnataka, India.
P C Nagajyothi *Department of Biochemistry, REVA University, Rukmini Knowledge Park, Kattigenahalli, Yelahanka, Bangalore, 560064, Karnataka, India.
Deepika ShekhawatDepartment of Biochemistry, REVA University, Rukmini Knowledge Park, Kattigenahalli, Yelahanka, Bangalore, 560064, Karnataka, India.
Ayantika SantraDepartment of Biochemistry, REVA University, Rukmini Knowledge Park, Kattigenahalli, Yelahanka, Bangalore, 560064, Karnataka, India.
Subhasish MaityDepartment of Biochemistry, REVA University, Rukmini Knowledge Park, Kattigenahalli, Yelahanka, Bangalore, 560064, Karnataka, India.
Venkata Prasad SurtineniDR Biosciences, Research and Development Unit, Bettahalasuru, Bangalore, 562157, India.
Selvam ArjunanLerner Research Institute, Department of Cardiovascular and Metabolic Sciences, Cleveland Clinic, Cleveland, OH, 44195, USA.
Vaddi Damodara ReddyDepartment of Biochemistry, REVA University, Rukmini Knowledge Park, Kattigenahalli, Yelahanka, Bangalore, 560064, Karnataka, India. reddidamodar@gmail.com.
Jaesool ShimSchool of Mechanical Engineering, Yeungnam University, Gyeongsan, 38541, Republic of Korea. jshim@ynu.ac.kr.

Funding

National Research Foundation of Korea (NRF) grants 2023-00280665
6 · The paper itself

Abstract

Chronic alcohol consumption induces significant structural and functional impairments in hepatic mitochondria, primarily mediated through increased production of reactive oxygen and nitrogen species (ROS/RNS), leading to oxidative and nitrosative damage. The mitochondrial electron transport chain (ETC), especially complexes I, II, IV, and V, is a major target of such damage, resulting in diminished catalytic activities as demonstrated by decreased NADH dehydrogenase and cytochrome c oxidase activities in ethanol-fed rat models. Notably, succinate dehydrogenase (complex II) remains largely unaffected, consistent with prior studies. Peroxynitrite-mediated nitration of critical subunits further compromises ETC function, impairing oxidative phosphorylation and ATP synthesis. Ethanol-induced mitochondrial dysfunction also involves altered mitochondrial protein synthesis due to inhibited translation of mitochondrial-encoded polypeptides, disruption of nuclear-mitochondrial cross-talk, and increased proteolytic degradation of respiratory chain proteins. Additionally, ethanol exposure reduces cytochrome content, especially cytochrome a a3, exacerbating impaired electron transfer and respiratory capacity. Membrane transport processes are disrupted, as evidenced by altered Na⁺/K⁺-ATPase activity and compromised membrane fluidity, further impacting cellular homeostasis. Oxidative modifications to mitochondrial protein thiols, elevated protein carbonylation, and increased protein acetylation, particularly mediated by Sirt3 dysregulation, contribute to mitochondrial dysfunction. These post-translational modifications (PTMs) alter enzyme activity, protein stability, and mitochondrial signalling pathways. Cumulatively, these biochemical and molecular alterations compromise mitochondrial membrane polarization, β-oxidation, and ATP production, contributing to alcoholic liver disease pathogenesis. Our review elucidates multiple mechanistic facets of alcohol-induced mitochondrial injury, emphasizing the critical role of oxidative/nitrosative stress and PTMs in mitochondrial and hepatic cellular dysfunction.

Indexed as

EthanolMitochondria, LiverMitochondrial MembranesProtein Processing, Post-TranslationalAnimalsHumansLiverMitochondrial ProteinsOxidative PhosphorylationOxidative StressRatsReactive Nitrogen SpeciesReactive Oxygen SpeciesEthanolMitochondrial ProteinsReactive Nitrogen SpeciesReactive Oxygen SpeciesALDCytochrome cElectron transport chainNADH dehydrogenaseΒ-oxidation

Identifiers

What OpenQuestion holds

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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.