Evidence map›Paper›PMID 37904726›Full record

ReviewCNS neuroscience & therapeutics2024

Neuroprotective effects of gemfibrozil in neurological disorders: Focus on inflammation and molecular mechanisms.

Mehraveh Sadeghi Ivraghi, Mohammad Yasin Zamanian, Reena Gupta, Harun Achmad, Hashem O Alsaab, Ahmed Hjazi, Rosario Mireya Romero-Parra, Enas R Alwaily, Beneen M Hussien, Elham Hakimizadeh

Open access · goldAbstract readReview
In one paragraph

Review in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  12. Neurotrophic Effects ofInternational journal of molecular sciences · 2024
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  16. Special Issue "Neurogenetics in Neurology".International journal of molecular sciences · 2024
    Article
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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

10 authors at 10 institutions in 6 countries.

Mehraveh Sadeghi IvraghiSchool of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
Mohammad Yasin ZamanianNeurophysiology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.ORCID 0000-0003-0944-0320
Reena GuptaInstitute of Pharmaceutical Research, GLA University, Mathura, India.
Harun AchmadDepartment of Pediatric Dentistry, Faculty of Dentistry, Hasanuddin University, Makassar, Indonesia.
Hashem O AlsaabPharmaceutics and Pharmaceutical Technology, Taif University, Taif, Saudi Arabia.
Ahmed HjaziDepartment of Medical Laboratory Sciences, College of Applied Medical Sciences, Prince Sattam bin Abdulaziz University, Al-Kharj, Saudi Arabia.
Rosario Mireya Romero-ParraUniversidad Continental, Lima, Peru.
Enas R AlwailyMicrobiology Research Group, College of Pharmacy, Al-Ayen University, Thi-Qar, Iraq.
Beneen M HussienMedical Laboratory Technology Department, College of Medical Technology, The Islamic University, Najaf, Iraq.
Elham HakimizadehPhysiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
GLA University · INHamedan University of Medical Sciences · IRHasanuddin University · IDIraqi University · IQPrince Sattam Bin Abdulaziz University · SAQazvin University of Medical Sciences · IRRafsanjan University of Medical Sciences · IRTaif University · SAThi Qar University · IQUniversidad Continental · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGemfibrozil (Gem) is a drug that has been shown to activate PPAR-α, a nuclear receptor that plays a key role in regulating lipid metabolism. Gem is used to lower the levels of triglycerides and reduce the risk of coronary heart disease in patients. Experimental studies in vitro and in vivo have shown that Gem can prevent or slow the progression of neurological disorders (NDs), including cerebral ischemia (CI), Alzheimer's disease (AD), Parkinson's disease (PD), and multiple sclerosis (MS). Neuroinflammation is known to play a significant role in these disorders.

methodThe literature review for this study was conducted by searching Scopus, Science Direct, PubMed, and Google Scholar databases.

resultThe results of this study show that Gem has neuroprotective effects through several cellular and molecular mechanisms such as: (1) Gem has the ability to upregulate pro-survival factors (PGC-1α and TFAM), promoting the survival and function of mitochondria in the brain, (2) Gem strongly inhibits the activation of NF-κB, AP-1, and C/EBPβ in cytokine-stimulated astroglial cells, which are known to increase the expression of iNOS and the production of NO in response to proinflammatory cytokines, (3) Gem protects dopamine neurons in the MPTP mouse model of PD by increasing the expression of PPARα, which in turn stimulates the production of GDNF in astrocytes, (4) Gem reduces amyloid plaque pathology, reduces the activity of glial cells, and improves memory, (5) Gem increases myelin genes expression (MBP and CNPase) via PPAR-β, and (6) Gem increases hippocampal BDNF to counteract depression.

conclusionAccording to the study, Gem was investigated for its potential therapeutic effect in NDs. Further research is needed to fully understand the therapeutic potential of Gem in NDs.

Indexed as

Neuroprotective AgentsParkinson DiseaseAnimalsCytokinesGemfibrozilHumansInflammationMicePPAR alphaCytokinesGemfibrozilNeuroprotective AgentsPPAR alphagemfibrozilneuroinflammationneurological disordersneuroprotectivePPAR-α

Identifiers

PMID37904726
PMCPMC10916451
OpenAlexW4388033365

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.