Evidence map›Paper›PMID 33710529›Full record

ArticleMetabolic brain disease2021

Acetyl-L-carnitine confers neuroprotection against lipopolysaccharide (LPS) -induced neuroinflammation by targeting TLR4/NFκB, autophagy, inflammation and oxidative stress.

Nida Jamali-Raeufy, Fahimeh Alizadeh, Zhila Mehrabi, Soraya Mehrabi, Mina Goudarzi

Erratum issuedAbstract read
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In one paragraph

Article in Metabolic brain disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Acetylcarnitine in cerebrospinal fluid and blood as a protective factor for neuromyelitis optica spectrum disorders: a mendelian randomization study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  4. Review
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  6. From Stress to Synapse: The Neuronal Atrophy Pathway to Mood Dysregulation.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Autophagy markers, cognitive deficits and depressive symptoms in Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2024
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Mechanisms of TLR4-Mediated Autophagy and Nitroxidative Stress.Frontiers in cellular and infection microbiology · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Nida Jamali-RaeufyDepartment of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. jamali_nida@yahoo.com.ORCID http://orcid.org/0000-0003-2416-0335
Fahimeh AlizadehDepartment of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Zhila MehrabiDepartment of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Soraya MehrabiDepartment of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mina GoudarziDepartment of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Iran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acetyl-L-carnitine has been shown to exert neuroprotection against neurodegenerative diseases. The present study was performed to evaluate neuroprotection effects of acetyl-L-carnitine against lipopolysaccharide (LPS) -induced neuroinflammation and clarify possible mechanisms. A single dose (500 µg/kg) of LPS was intraperitoneally injected to rats to induce model. The animals were intraperitoneally treated with different doses of acetyl-L-carnitine (30, 60, and 100) for 6 days. Y-maze task, single-trial passive avoidance and novel object recognition tests were used to evaluate memory impairments. ELISA assay was used to evaluate the expression of TLR4/NFκB, autophagic and oxidative stress markers. Our result showed that intraperitoneal injection of LPS resulted in initiation of neuroinflammation by activation of TLR4/NFκB, suppression of autophagic markers such as LC3 II/ LC3 I ratio and becline-1, and excessive production of ROS and MDA. Intraperitoneal administration of acetyl-L-carnitine contributed to neuroprotection against LPS -induced neuroinflammation by suppression of TLR4/NFκB pathway, restoring activity of autophagy and inhibition of oxidative stress. Collectively, our findings show that acetyl-L-carnitine attenuated LPS-induced neuroinflammation by targeting TLR4/NFκB pathway, autophagy and oxidative stress.

Indexed as

LipopolysaccharidesAcetylcarnitineAnimalsAnti-Inflammatory AgentsAutophagyBeclin-1Injections, IntraperitonealMaleMicrotubule-Associated ProteinsNeuroinflammatory DiseasesNeuroprotective AgentsNF-kappa BOxidative StressPsychomotor PerformanceRatsRats, WistarAcetylcarnitineAnti-Inflammatory AgentsAnxa3 protein, ratBeclin-1Becn1 protein, ratLipopolysaccharidesMicrotubule-Associated ProteinsNeuroprotective AgentsNF-kappa BTlr4 protein, ratToll-Like Receptor 4Acetyl-L-carnitineAutophagy and oxidative stressLipopolysaccharide (LPS) -induced neuroinflammationTLR4/NFκB pathway

Identifiers

PMID33710529
OpenAlexW3134883036

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.