Evidence map›Paper›PMID 39827410›Full record

ArticleThe Journal of physiology2025

Inhibition of diacylglycerol lipase α induced blood-brain barrier breach in female Sprague-Dawley rats.

Erika Liktor-Busa, Aidan A Levine, Sally J Young, Colin Bader, Seph M Palomino, Felipe D Polk, Sarah A Couture, Paulo W Pires, Trent Anderson, Tally M Largent-Milnes

Abstract read
In one paragraph

Article in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Erika Liktor-BusaCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Aidan A LevineCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Sally J YoungCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Colin BaderCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Seph M PalominoCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Felipe D PolkCollege of Medicine, Department of Physiology, University of Arizona, Tucson, AZ, USA.
Sarah A CoutureCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Paulo W PiresCollege of Medicine, Department of Physiology, University of Arizona, Tucson, AZ, USA.
Trent AndersonCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.
Tally M Largent-MilnesCollege of Medicine, Department of Pharmacology, University of Arizona, Tucson, AZ, USA.

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Jennifer Wright Bea · 1985 to 2026
$110.2M
The Center of Excellence in Addiction Studies (CEAS)P30DA051355 · NIDA · UNIVERSITY OF ARIZONA · PI PORRECA, FRANK, VANDERAH, TODD W · 2021 to 2025
$6.7M
Role of Endothelial K+ Channels in Age-Related DementiaR01AG073230 · NIA · LOMA LINDA UNIVERSITY · PI Erik J. Behringer, Paulo W Pires · 2022 to 2026
$3.3M
Targeting the Endocannabinoid System for Headache InterventionR01NS126752 · NINDS · UNIVERSITY OF ARIZONA · PI Tally Marie Milnes · 2023 to 2026
$2.4M
Blood Brain Barrier and Migraine: Effect on Therapy (Diversity Supplement)R01NS099292 · NINDS · UNIVERSITY OF ARIZONA · PI MILNES, TALLY MARIE · 2017 to 2021
$1.7M
Primary Afferent Transmission in the Trigeminal Dorsal HornF32DE022499 · NIDCR · OREGON HEALTH & SCIENCE UNIVERSITY · PI MILNES, TALLY MARIE · 2011 to 2014
$127k
NCI NIH HHS P30 CA023074NIA NIH HHS R01 AG073230NIDA NIH HHS P30 DA051355NIDCR NIH HHS F32 DE022499NINDS NIH HHS R01 NS099292NINDS NIH HHS R01 NS126752
6 · The paper itself

Abstract

The endocannabinoid system's significance in maintaining blood-brain barrier (BBB) integrity under physiological and pathological conditions is suggested by several reports, but the underlying molecular mechanisms are not well understood. In this paper, we investigated the effects of depletion of 2-arachidonoylglycerol (2-AG), one of the main endocannabinoids in the central nervous system, on BBB integrity using pharmacological tools. Female Sprague-Dawley rats were injected with the diacylglycerol lipase α (DAGLα) inhibitor LEI-106 (40 mg/kg, i.p.), followed by assessment of BBB integrity via in situ brain perfusion. Liquid chromatography-mass spectrometry, western immunoblotting, light transmittance experiments and pressure myography were also used to further examine the results of DAGLα blockade on the BBB and vascular reactivity. We found that DAGLα inhibition caused BBB opening in cortical brain areas, manifesting as increased sucrose transport measured by in situ brain perfusion. This was accompanied by reduced levels of 2-AG and decreased detection of the tight junction protein zonula occludens-1 (ZO-1). The protein level in cortical areas of neuronal PAS domain protein 4 (NPAS4), encoded by an activity-dependent immediate early gene, was increased without the presence of cortical spreading depression after LEI-106 administration. We also observed a significant increase in pressure-induced constriction within the parenchymal microcirculation after inhibition of DAGLα, possibly altering shear stress in the microcirculation. These results support the role of endogenous 2-AG in maintaining normal tight junction function. This improved understanding of the molecular mechanisms of endocannabinoid system function at the neurovascular unit can help to unlock the therapeutic potentials of cannabinoids in central nervous system disorders associated with BBB dysfunction. KEY POINTS: The administration of the diacylglycerol lipase α (DAGLα) inhibitor LEI-106 (40 mg/kg, i.p.) induced blood-brain barrier (BBB) opening of cortical brain areas in female Sprague-Dawley rats. This BBB disruption was accompanied by reduced levels of 2-arachidonoylglycerol (2-AG) and decreased detection of the tight junction protein zonula occludens-1 (ZO-1). The protein level in cortical areas of neuronal PAS domain protein 4 (NPAS4), encoded by an activity-dependent immediate early gene, was increased without the presence of cortical spreading depression after LEI-106 administration. A significant increase in pressure-induced constriction within the parenchymal microcirculation was also observed after inhibition of DAGLα, possibly altering shear stress. These results support the role of endogenous 2-AG in maintaining normal tight junction function.

Indexed as

Blood-Brain BarrierLipoprotein LipaseAnimalsArachidonic AcidsEndocannabinoidsEnzyme InhibitorsFemaleGlyceridesRatsRats, Sprague-DawleyZonula Occludens-1 ProteinArachidonic AcidsEndocannabinoidsEnzyme InhibitorsGlyceridesglyceryl 2-arachidonateLipoprotein LipaseZonula Occludens-1 Protein2‐AGblood–brain barrierDAGLαendocannabinoid systemZO‐1

Identifiers

PMID39827410
PMCPMC11826068

What OpenQuestion 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 OpenQuestion graph.