Evidence map›Paper›PMID 30535784›Full record

ReviewMolecular biology reports2019

Cytosolic lipid excess-induced mitochondrial dysfunction is the cause or effect of high fat diet-induced skeletal muscle insulin resistance: a molecular insight.

Baishali Alok Jana, Pavan Kumar Chintamaneni, Praveen Thaggikuppe Krishnamurthy, Ashish Wadhwani, Suresh Kumar Mohankumar

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Myokines and mitochondrial function in cardiometabolic diseases.Journal of physiology and biochemistry · 2026
    Review
  3. Review
  4. Observational
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Energy metabolism in health and diseases.Signal transduction and targeted therapy · 2025
    Review
  12. Article
  13. Article
  14. Review
  15. Prospects of potential adipokines as therapeutic agents in obesity-linked atherogenic dyslipidemia and insulin resistance.The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

5 authors at 1 institution in 1 country.

Baishali Alok Jana *Department of Pharmaceutical Biotechnology, JSS College of Pharmacy (A Constituent College of JSS Academy of Higher Education & Research, Mysuru, Karnataka, India), Ootacamund, Tamil Nadu, 643001, India.
Pavan Kumar Chintamaneni *Department of Pharmacology, JSS College of Pharmacy (A Constituent College of JSS Academy of Higher Education & Research, Mysuru, Karnataka, India), Ootacamund, Tamil Nadu, 643001, India.
Praveen Thaggikuppe KrishnamurthyDepartment of Pharmacology, JSS College of Pharmacy (A Constituent College of JSS Academy of Higher Education & Research, Mysuru, Karnataka, India), Ootacamund, Tamil Nadu, 643001, India.
Ashish WadhwaniDepartment of Pharmaceutical Biotechnology, JSS College of Pharmacy (A Constituent College of JSS Academy of Higher Education & Research, Mysuru, Karnataka, India), Ootacamund, Tamil Nadu, 643001, India.
Suresh Kumar MohankumarDepartment of Pharmacognosy & Phytopharmacy, TIFAC CORE in Herbal Drugs, JSS College of Pharmacy (A Constituent College of JSS Academy of Higher Education & Research, Mysuru, Karnataka, India), P.B. 20, Rocklands, Ootacamund, Tamil Nadu, 643001, India. suresh.jsscpo@jssuni.edu.in.
JSS Academy of Higher Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria play a central role in the energy homeostasis in eukaryotic cells by generating ATP via oxidative metabolism of nutrients. Excess lipid accumulation and impairments in mitochondrial function have been considered as putative mechanisms for the pathogenesis of skeletal muscle insulin resistance. Accumulation of lipids in tissues occurs due to either excessive fatty acid uptake, decreased fatty acid utilization or both. Consequently, elevated levels cytosolic lipid metabolites, triglycerides, diacylglycerol and ceramides have been demonstrated to adversely affect glucose homeostasis. Several recent studies indicate that reduced insulin-stimulated ATP synthesis and reduced expression of mitochondrial enzymes and PPAR-γ coactivator, in high fat feeding (lipid overload) are associated with insulin resistance. Despite the fact, few notable studies suggest mitochondrial dysfunction is prevalent in type 2 diabetes mellitus; it is still not clear whether the defects in mitochondrial function are the cause of insulin resistance or the consequential effects of insulin resistance itself. Thus, there is a growing interest in understanding the intricacies of mitochondrial function and its association with cytosolic lipid excess. This review therefore critically examines the molecular cascades linking cytosolic lipid excess and mitochondrial dysfunction in the pathogenesis of high fat diet-induced insulin resistance in skeletal muscle. The sequential processes following the excess intake of high fat diet in skeletal muscle includes, accumulation of cytosolic fatty acids, increased production of reactive oxygen species, mutations and ageing, and decreased mitochondrial biogenesis. The consequent mitochondrial dysfunction is then leading to decreased β-oxidation, respiratory functions and glycolysis and increased glucolipotoxicity. These events collectively induce the insulin resistance in skeletal muscle.

Indexed as

Diet, High-FatInsulin ResistanceAnimalsCytosolHumansLipidsMitochondriaMuscle, SkeletalLipidsCytosolic lipidsHigh fat dietInsulin resistanceMitochondriaType 2 diabetes mellitus

Identifiers

PMID30535784
OpenAlexW2905127295

What OpenQuestion holds

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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.