Evidence map›Paper›PMID 36769295›Full record

ArticleInternational journal of molecular sciences2023

Gemfibrozil-Induced Intracellular Triglyceride Increase in SH-SY5Y, HEK and Calu-3 Cells.

Cornel Manuel Bachmann, Daniel Janitschke, Anna Andrea Lauer, Tobias Erhardt, Tobias Hartmann, Marcus Otto Walter Grimm, Heike Sabine Grimm

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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. 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

7 authors.

Cornel Manuel BachmannExperimental Neurology, Saarland University, 66421 Homburg, Germany.
Daniel JanitschkeExperimental Neurology, Saarland University, 66421 Homburg, Germany.ORCID 0000-0001-8966-0184
Anna Andrea LauerExperimental Neurology, Saarland University, 66421 Homburg, Germany.ORCID 0000-0002-8327-452X
Tobias ErhardtPhysical Therapy, Campus Karlsruhe, SRH University of Applied Health Sciences, 76185 Karlsruhe, Germany.
Tobias HartmannExperimental Neurology, Saarland University, 66421 Homburg, Germany.ORCID 0000-0001-7481-6430
Marcus Otto Walter GrimmExperimental Neurology, Saarland University, 66421 Homburg, Germany.ORCID 0000-0002-4160-6506
Heike Sabine GrimmExperimental Neurology, Saarland University, 66421 Homburg, Germany.

Funding

EURO-FINGERS 01ED2003European Commission under the frame-work programme of the European Union, LipiDiDiet 211696the EU Joint Programme - Neurodegenerative Disease Research (JPND) and BMBF grants MIND-AD 01ED1509
6 · The paper itself

Abstract

Gemfibrozil is a drug that has been used for over 40 years to lower triglycerides in blood. As a ligand for peroxisome proliferative-activated receptor-alpha (PPARα), which is expressed in many tissues, it induces the transcription of numerous genes for carbohydrate and lipid-metabolism. However, nothing is known about how intracellular lipid-homeostasis and, in particular, triglycerides are affected. As triglycerides are stored in lipid-droplets, which are known to be associated with many diseases, such as Alzheimer's disease, cancer, fatty liver disease and type-2 diabetes, treatment with gemfibrozil could adversely affect these diseases. To address the question whether gemfibrozil also affects intracellular lipid-levels, SH-SY5Y, HEK and Calu-3 cells, representing three different metabolically active organs (brain, lung and kidney), were incubated with gemfibrozil and subsequently analyzed semi-quantitatively by mass-spectrometry. Importantly, all cells showed a strong increase in intracellular triglycerides (SH-SY5Y: 170.3%; HEK: 272.1%; Calu-3: 448.1%), suggesting that the decreased triglyceride-levels might be due to an enhanced cellular uptake. Besides the common intracellular triglyceride increase, a cell-line specific alteration in acylcarnitines are found, suggesting that especially in neuronal cell lines gemfibrozil increases the transport of fatty acids to mitochondria and therefore increases the turnover of fatty acids for the benefit of additional energy supply, which could be important in diseases, such as Alzheimer's disease.

Indexed as

Alzheimer DiseaseNeuroblastomaFatty AcidsGemfibrozilHumansHypolipidemic AgentsTriglyceridesFatty AcidsGemfibrozilHypolipidemic AgentsTriglyceridesAlzheimer’s diseasecarnitinesgemfibrozillipid dropletslipidomicslung diseaseslyso-phosphatidylcholinephosphatidylcholineplasmalogensrenal diseasestriglycerides

Identifiers

PMID36769295
PMCPMC9917468

What Socratic 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 Socratic graph.