Evidence map›Paper›PMID 39690422›Full record

ArticleFluids and barriers of the CNS2024

Brain endothelial permeability, transport, and flow assessed over 10 orders of magnitude using the in situ brain perfusion technique.

Quentin R Smith, Haritha Mandula, Jagan Mohan R Parepally, Jun Oki, Fancy Thomas, Helen R Thorsheim, Abraham J Al-Ahmad, Thomas J Abbruscato, Per Ask, David S Hage and 1 more

Abstract read
In one paragraph

Article in Fluids and barriers of the CNS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Quentin R SmithDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA. quentin.smith@ttuhsc.edu.
Haritha MandulaDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Jagan Mohan R ParepallyDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Jun OkiDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Fancy ThomasDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Helen R ThorsheimDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Abraham J Al-AhmadDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Thomas J AbbruscatoDepartment of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.
Per AskDepartment of Biomedical Engineering, Linköping University, Linköping, Sweden.
David S HageDepartment of Chemistry, University of Nebraska-Lincoln, Lincoln, NE, USA.
Peter J RobinsonNational Institute on Aging, National Institutes of Health, Bethesda, MD, USA.

Funding

Role of plasma protein binding in brain drug deliveryR01NS052484 · NINDS · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI SMITH, QUENTIN R. · 2006 to 2009
$1.4M
NIH HHS 5RO1 NS052484
6 · The paper itself

Abstract

backgroundCerebral blood flow normally places a limit on the magnitude of brain vascular permeability (P) that can be measured in vivo. At normal cerebral blood flow, this limit falls at the lower end of lipophilicity for most FDA-approved CNS drugs. In this study, we report on two methods that can be used to overcome this limitation and measure brain vascular permeability values that are up to ~1000 times higher using the in situ brain perfusion technique.

methodsRat brain was perfused with physiological saline at increased flow rate and in the presence of various concentrations of plasma protein, serum albumin or alpha-acid glycoprotein. Plasma protein was added to the saline perfusion fluid to lower extraction into the measurable range using the Crone Renkin "diffusion-flow" equation to calculate brain P

resultsCerebrovascular P

conclusionsThe results show that brain vascular permeability can be measured directly in vivo for highly lipophilic solutes and the PS values obtained match reasonably with that predicted by the Crone-Renkin flow diffusion equation with care taken to validate the accuracy for the component measurements and with no need to invoke "enhanced" or "induced" dissociation.

Indexed as

Blood-Brain BarrierBrainCapillary PermeabilityCerebrovascular CirculationPerfusionAnimalsMaleRatsRats, Sprague-DawleyAlbuminAlpha-1 acid glycoproteinBlood brain barrierDiazepamEnhanced dissociationNeurovascular unitPharmaceutical screening

Identifiers

PMID39690422
PMCPMC11650849

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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.