Evidence map›Paper›PMID 41193613›Full record

ArticleScientific reports2025

Skeletal muscle insulin resistance in prediabetes: a lipidomic perspective on diacylglycerols, ceramides, and phospholipids.

Irena Markova, Martina Hüttl, Jakub Šťastný, Iveta Zapletalova, Petr Kačer, Vladimír Hönig, Tereza Kacerova, Hana Malinska

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Toll Like Receptor 4: A Potential Link Between Obesity and Metabolic Diseases.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026
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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

8 authors.

Irena MarkovaCentre for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic. irma@ikem.cz.
Martina HüttlCentre for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Jakub ŠťastnýFaculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences, Prague, Czech Republic.
Iveta ZapletalovaDepartment of Pharmacology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic.
Petr KačerFaculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences, Prague, Czech Republic.
Vladimír HönigFaculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences, Prague, Czech Republic.
Tereza KacerovaFaculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences, Prague, Czech Republic.
Hana MalinskaCentre for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Funding

CZ-OPENSCREEN LM2023052EATRIS-CZ LM2023053Ministry of Health of the Czech Republic IKEM, IN 00023001Palacky University, Olomouc IGA_LF_2025_009
6 · The paper itself

Abstract

Lipid metabolism disorders, accompanied by the accumulation of lipids, are believed to contribute to skeletal muscle insulin resistance development. These alterations may attenuate insulin signaling and glucose uptake and utilization. However, the specific roles of individual lipids remain incompletely understood. The study examined the relationship between skeletal muscle lipid composition and insulin resistance in a non-obese prediabetic hereditary hypertriglyceridemic (HHTg) rats. Male HHTg rats aged 4 and 12 months, exhibiting insulin resistance, and dyslipidaemia were used in this study. Skeletal muscle lipidomic profiles were analyzed using tandem mass spectrometry. Compared to age-matched Wistar controls, HHTg rats exhibited increased serum triglycerides, elevated NEFA and impaired glucose tolerance. Impaired muscle insulin sensitivity in HHTg rats was associated with the accumulation of triglycerides and 1,3-diacylglycerols, and most notably with an increase in specific ceramide species (18:0, 22:0, 24:0, 24:1) in both 4- and 12-month-old animals. Elevated mRNA expression of Degs1, a key enzyme in ceramide biosynthesis, may underlie the observed ceramide accumulation. Lipidomic profiling revealed decreases in membrane phospholipids, including phosphatidylethanolamine (PE 41:2), lysophosphatidylcholine (LPC 22:6), and lysophosphatidylethanolamine (LPE 20:0). In HHTg prediabetic model, skeletal muscle insulin resistance develops independently of obesity and prior to diabetes onset, driven by the accumulation of lipotoxic diacylglycerols and ceramides, alongside a reduction in specific phospholipids and lysophospholipids. Impaired fatty acid oxidation and enhanced ceramide biosynthesis contribute to ectopic lipid deposition, with ceramides exerting a more pronounced effect on insulin signaling. Strain-specific alterations in lipid metabolism are more significant than age-related alterations.

Indexed as

CeramidesDiglyceridesInsulin ResistanceLipidomicsMuscle, SkeletalPhospholipidsPrediabetic StateAnimalsLipid MetabolismMaleRatsRats, WistarTriglyceridesCeramidesDiglyceridesPhospholipidsTriglyceridesCeramidesDiacylglycerolsInsulin sensitivityLipidomicsPhospholipidsSkeletal muscle

Identifiers

PMID41193613
PMCPMC12589396

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.