Evidence map›Paper›PMID 38203447›Full record

ArticleInternational journal of molecular sciences2023

Prednisolone Targets Claudins in Mouse Brain Blood Vessels.

Alexander G Markov, Anastasia E Bikmurzina, Arina A Fedorova, Ekaterina P Vinogradova, Natalia M Kruglova, Igor I Krivoi, Salah Amasheh

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 76% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 2 countries.

Alexander G MarkovDepartment of General Physiology, St. Petersburg State University, 199034 St. Petersburg, Russia.
Anastasia E BikmurzinaDepartment of General Physiology, St. Petersburg State University, 199034 St. Petersburg, Russia.
Arina A FedorovaDepartment of General Physiology, St. Petersburg State University, 199034 St. Petersburg, Russia.ORCID 0000-0001-8080-7426
Ekaterina P VinogradovaDepartment of Higher Nervous Activity and Psychophysiology, St. Petersburg State University, 199034 St. Petersburg, Russia.
Natalia M KruglovaDepartment of General Physiology, St. Petersburg State University, 199034 St. Petersburg, Russia.
Igor I KrivoiDepartment of General Physiology, St. Petersburg State University, 199034 St. Petersburg, Russia.ORCID 0000-0002-2690-9226
Salah AmashehInstitute of Veterinary Physiology, Freie Universität Berlin, 14163 Berlin, Germany.ORCID 0000-0002-6365-1949
St Petersburg University · RUFreie Universität Berlin · DE

Funding

Freie Universität Berlin Open access funds
6 · The paper itself

Abstract

Endothelial cells in brain capillaries are crucial for the function of the blood-brain barrier (BBB), and members of the tight junction protein family of claudins are regarded to be primarily responsible for barrier properties. Thus, the analysis of bioactive substances that can affect the BBB's permeability is of great importance and may be useful for the development of new therapeutic strategies for brain pathologies. In our study, we tested the hypothesis that the application of the glucocorticoid prednisolone affects the murine blood-brain barrier in vivo. Isolated brain tissue of control and prednisolone-injected mice was examined by employing immunoblotting and confocal laser scanning immunofluorescence microscopy, and the physiological and behavioral effects were analyzed. The control tissue samples revealed the expression of barrier-forming tight junction proteins claudin-1, -3, and -5 and of the paracellular cation and water-channel-forming protein claudin-2. Prednisolone administration for 7 days at doses of 70 mg/kg caused physiological and behavioral effects and downregulated claudin-1 and -3 and the channel-forming claudin-2 without altering their localization in cerebral blood vessels. Changes in the expression of these claudins might have effects on the ionic and acid-base balance in brain tissue, suggesting the relevance of our findings for therapeutic options in disorders such as cerebral edema and psychiatric failure.

Indexed as

ClaudinsPrednisoloneAnimalsBrainClaudin-1Claudin-2Endothelial CellsMiceClaudin-1Claudin-2ClaudinsPrednisolonebehaviorblood–brain barrierclaudinsprednisolonetight junctions

Identifiers

PMID38203447
PMCPMC10779016
OpenAlexW4390176362

What OpenQuestion holds

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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.