Evidence map›Paper›PMID 40862774›Full record

ArticleCells2025

N-Lactoyl Phenylalanine Disrupts Insulin Signaling, Induces Inflammation, and Impairs Mitochondrial Respiration in Cell Models.

Laila Hedaya, Khaled Naja, Shamma Almuraikhy, Najeha Anwardeen, Asma A Elashi, Maha Al-Asmakh, Susu M Zughaier, Meritxell Espino-Guarch, Osama Y Aldirbashi, Gavin P Davey and 1 more

Abstract read
In one paragraph

Article in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

11 authors.

Laila HedayaBiomedical Research Center, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0001-5136-9746
Khaled NajaBiomedical Research Center, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0001-9259-3082
Shamma AlmuraikhyBiomedical Research Center, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0003-4572-9738
Najeha AnwardeenBiomedical Research Center, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0002-7263-4905
Asma A ElashiBiomedical Research Center, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0002-6927-5622
Maha Al-AsmakhDepartment of Biomedical Sciences, College of Health Sciences, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.
Susu M ZughaierCollege of Medicine, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0001-7487-8770
Meritxell Espino-GuarchLaboratory of Immunoregulation, Translational Medicine, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0002-7211-3229
Osama Y AldirbashiDepartment of Lab Medicine & Pathology, Hamad Medical Corporation, Doha P.O. Box 3050, Qatar.
Gavin P DaveySchool of Biochemistry and Immunology, Trinity College Dublin, D02 PN40 Dublin, Ireland.ORCID 0000-0002-8667-8781
Mohamed A ElrayessBiomedical Research Center, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.ORCID 0000-0003-3803-4604

Funding

Qatar National Research Fund ARG01-0420-230007
6 · The paper itself

Abstract

N-lactoyl amino acids (Lac-AAs) are key players that regulate appetite and body weight. The most prominent and well-studied member is N-lactoyl phenylalanine (Lac-Phe), which can be induced by food intake, exercise and metformin treatment. However, its broader metabolic impact remains insufficiently characterized. This study investigates the effects of Lac-Phe on insulin signaling, inflammation, and mitochondrial respiration using HepG2 and differentiated C2C12 cell models, as well as isolated rat brain mitochondria and synaptosomes. Our results demonstrate that Lac-Phe significantly impairs insulin-stimulated phosphorylation of key proteins in the insulin signaling pathway, particularly in skeletal muscle cells, indicating disrupted insulin signaling. Additionally, Lac-Phe exposure increases the secretion of pro-inflammatory cytokines in C2C12 skeletal muscle cells and markedly impairs mitochondrial respiration in HepG2 liver cells and rat brain-derived synaptosomes, but not in isolated mitochondria. These findings highlight potential adverse metabolic effects of Lac-Phe, especially when administered at high concentrations, and underscore the necessity of conducting a comprehensive risk assessment and dose optimization before considering Lac-Phe or related Lac-AAs as therapeutic agents. Our work provides important insights into the molecular liabilities associated with Lac-Phe and calls for further studies to balance its therapeutic promise against possible metabolic risks.

Indexed as

InflammationInsulinMitochondriaPhenylalanineSignal TransductionAnimalsBrainCell RespirationHep G2 CellsHumansMaleMiceModels, BiologicalRatsSynaptosomesInsulinPhenylalaninecytokinesinsulin signalingmitochondrial respirationN-lactoyl phenylalanine

Identifiers

PMID40862774
PMCPMC12384308

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.