Evidence map›Paper›PMID 30612333›Full record

ReviewMolecular neurobiology2019

The Role of Ceramide and Sphingosine-1-Phosphate in Alzheimer's Disease and Other Neurodegenerative Disorders.

Kinga Czubowicz, Henryk Jęśko, Przemysław Wencel, Walter J Lukiw, Robert P Strosznajder

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 161 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 2 pooled it
11.0field-weighted citation impact, top 1% 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

161 citing papers in PubMed, 2 syntheses or guidelines pooled it, 278 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Circular RNAEnvironment & health (Washington, D.C.) · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

101 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Kinga CzubowiczLaboratory of Preclinical Research and Environmental Agents, Department of Neurosurgery, M. Mossakowski Medical Research Centre, Polish Academy of Sciences, 5 Pawinskiego St., PL-02106, Warsaw, Poland.
Henryk JęśkoDepartment of Cellular Signalling, Mossakowski Medical Research Centre, Polish Academy of Sciences, 5 Pawinskiego St., PL-02106, Warsaw, Poland.
Przemysław WencelLaboratory of Preclinical Research and Environmental Agents, Department of Neurosurgery, M. Mossakowski Medical Research Centre, Polish Academy of Sciences, 5 Pawinskiego St., PL-02106, Warsaw, Poland.
Walter J LukiwLSU Neuroscience Center and Departments of Neurology and Ophthalmology, Louisiana State University School of Medicine, New Orleans, LA, 70112, USA.
Robert P StrosznajderLaboratory of Preclinical Research and Environmental Agents, Department of Neurosurgery, M. Mossakowski Medical Research Centre, Polish Academy of Sciences, 5 Pawinskiego St., PL-02106, Warsaw, Poland. rstrosznajder@imdik.pan.pl.ORCID http://orcid.org/0000-0002-1922-0295
Mossakowski Medical Research Institute, Polish Academy of Sciences · PLLouisiana State University Health Sciences Center New Orleans · US

Funding

Instytut Medycyny Doswiadczalnej i Klinicznej im. M. Mossakowskiego, Polskiej Akademii Nauk T. No 7Narodowym Centrum Nauki 2013/11/N/NZ4/02233National Institutes of Health NIA AG038834
6 · The paper itself

Abstract

Bioactive sphingolipids-ceramide, sphingosine, and their respective 1-phosphates (C1P and S1P)-are signaling molecules serving as intracellular second messengers. Moreover, S1P acts through G protein-coupled receptors in the plasma membrane. Accumulating evidence points to sphingolipids' engagement in brain aging and in neurodegenerative disorders such as Alzheimer's, Parkinson's, and Huntington's diseases and amyotrophic lateral sclerosis. Metabolic alterations observed in the course of neurodegeneration favor ceramide-dependent pro-apoptotic signaling, while the levels of the neuroprotective S1P are reduced. These trends are observed early in the diseases' development, suggesting causal relationship. Mechanistic evidence has shown links between altered ceramide/S1P rheostat and the production, secretion, and aggregation of amyloid β/α-synuclein as well as signaling pathways of critical importance for the pathomechanism of protein conformation diseases. Sphingolipids influence multiple aspects of Akt/protein kinase B signaling, a pathway that regulates metabolism, stress response, and Bcl-2 family proteins. The cross-talk between sphingolipids and transcription factors including NF-κB, FOXOs, and AP-1 may be also important for immune regulation and cell survival/death. Sphingolipids regulate exosomes and other secretion mechanisms that can contribute to either the spread of neurotoxic proteins between brain cells, or their clearance. Recent discoveries also suggest the importance of intracellular and exosomal pools of small regulatory RNAs in the creation of disturbed signaling environment in the diseased brain. The identified interactions of bioactive sphingolipids urge for their evaluation as potential therapeutic targets. Moreover, the early disturbances in sphingolipid metabolism may deliver easily accessible biomarkers of neurodegenerative disorders.

Indexed as

Alzheimer DiseaseAnimalsCeramidesHumansLysophospholipidsMicroRNAsNerve DegenerationSignal TransductionSphingosineCeramidesLysophospholipidsMicroRNAsSphingosinesphingosine 1-phosphateAlzheimer’s diseaseCeramideHuntington’s diseasemicroRNAParkinson’s diseaseSphingosine-1-phosphate

Identifiers

PMID30612333
PMCPMC6614129
OpenAlexW2906835093

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.