Evidence map›Paper›PMID 40085305›Full record

ArticleJournal of molecular neuroscience : MN2025

Effect of Fatty Acyl Composition for Lysophosphatidylinositol on Neuroinflammatory Responses in Primary Neuronal Cultures.

Douglas E Brenneman, Dean Petkanas, Michael Ippolito, Sara Jane Ward

Abstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Douglas E BrennemanPennsylvania Biotechnology Center, Kannalife Sciences, Inc, 3805 Old Easton Road, Doylestown, PA, 18902, USA. doug@kannalife.com.
Dean PetkanasPennsylvania Biotechnology Center, Kannalife Sciences, Inc, 3805 Old Easton Road, Doylestown, PA, 18902, USA.
Michael IppolitoCenter for Substance Abuse Research, Department of Neural Science, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, 19140, USA.
Sara Jane WardCenter for Substance Abuse Research, Department of Neural Science, Lewis Katz School of Medicine, Temple University, Philadelphia, PA, 19140, USA.

Funding

Development of KLS-13019 for Neuropathic PainR42NS120548 · NINDS · KANNALIFE SCIENCES, INC. · PI BRENNEMAN, DOUGLAS ERIC, WARD, SARA J · 2021 to 2023
$3.0M
NINDS NIH HHS R42 NS120548NINDS NIH HHS R42NS120548
6 · The paper itself

Abstract

Lysophosphatidylinositol (LPI) is an endogenous signaling molecule for the GPR55 receptor. Previous studies have shown that arachidonoyl-lysophosphatidylinositol (LPI-20:4) produced an increase in the inflammatory mediators NLPR3 (inflammasome-3 marker) and IL-1b in neurons from both rat dorsal root ganglion (DRG) and hippocampal cultures. Because LPI is comprised of a family of lipid structures that vary in fatty acyl composition, the current work examined neuroinflammatory responses to various LPI structures in DRG and hippocampal cultures as assessed by high-content fluorescent imaging. Major endogenous LPI fatty acyl structures consisting of 16:0, 18:0, 18:1, or 20:4 were compared for their effects on IL-1b, NLRP3, and GPR55 immunoreactive areas of neurites and cell bodies after a 6-h treatment. Among these four LPI structures, only LPI-20:4 treatment produced increases in immunoreactive areas for GPR55, NLRP3, and IL-1b in DRG and hippocampal neurites. In contrast, all other LPI structures tested produced a decrease in all of these inflammatory immunoreactive areas in both neurites and cell bodies. Additional studies with LPI-20:4 treatment indicated that IL-6, IL-18, and TNF-α were significantly increased in neurites of DRG and hippocampal cultures. However, oleoyl-lysophosphatidylinositol (LPI-18:1) treatment produced decreases in these three cytokines. Using the viability dye Alamar blue, LPI-20:4 was shown to produce concentration-dependent decreases, whereas all other endogenous LPI structures produced increases with this assay. These studies indicate that fatty acyl structure is the major determinant of LPI for neuroinflammatory responses in DRG and hippocampal cultures, with LPI-20:4 showing pro-inflammatory effects and all other endogenous LPIs tested exhibiting anti-inflammatory responses.

Indexed as

LysophospholipidsNeuronsAnimalsCells, CulturedGanglia, SpinalHippocampusInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinRatsRats, Sprague-DawleyReceptors, CannabinoidReceptors, G-Protein-CoupledGPR55 protein, ratInterleukin-1betalysophosphatidylinositolLysophospholipidsNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratReceptors, CannabinoidReceptors, G-Protein-CoupledCytokinesDorsal root ganglionGPR55HippocampusLysophosphatidylinositolNeuroinflammation

Identifiers

PMID40085305
PMCPMC13147479

What Socratic holds

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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 Socratic graph.