Evidence map›Paper›PMID 39408803›Full record

ArticleInternational journal of molecular sciences2024

Hyperbaric Treatment Stimulates Chaperone-Mediated Macroautophagy and Autophagy in the Liver Cells of Healthy Female Rats.

Agnieszka Pedrycz, Mariusz Kozakiewicz, Mansur Rahnama, Marek Kos, Ewelina Grywalska, Marietta Bracha, Anna Grzywacz, Iwona Bojar

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

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

8 authors.

Agnieszka PedryczFaculty of Medicine and Health Sciences, University of Applied Sciences in Tarnow, Mickiewicza 8, 33-100 Tarnów, Poland.
Mariusz KozakiewiczLudwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Jagiellońska 13/15, 85-067 Bydgoszcz, Poland.ORCID 0000-0002-6988-3038
Mansur RahnamaDepartament of Dental Surgery, Medical University of Lublin, Chodźki 6, 20-093 Lublin, Poland.ORCID 0000-0002-5622-7330
Marek KosDepartment of Public Health, Medical University of Lublin, Chodźki 1, 20-093 Lublin, Poland.
Ewelina GrywalskaDepartment of Experimental Immunology, Medical University of Lublin, Chodźki 4a, 20-093 Lublin, Poland.ORCID 0000-0002-0451-4741
Marietta BrachaDepartment of Geriatrics, Faculty of Health Sciences, Nicolaus Copernicus University in Toruń, Jagiellońska 15, 85-067 Bydgoszcz, Poland.
Anna GrzywaczIndependent Laboratory of Behaviour Genetics and Epigenetics, Pomeranian Medical University in Szczecin, Rybacka 1, 70-204 Szczecin, Poland.
Iwona BojarDepartment of Women's Health, Institute of Rural Health, 20-093 Lublin, Poland.ORCID 0000-0002-3171-225X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of autophagy goes far beyond the elimination of damaged cellular components and the quality control of proteins. It also cleanses cells from inclusions, including pathogenic viruses, and provides energy-forming components. The liver, which is an organ with increased metabolism, is made up of cells that are particularly vulnerable to damage. Therefore, detoxification of liver cells in the process of autophagy has become a very important issue clinically. The aim of this study was an immunohistochemical evaluation of proteins activated in rat liver cells at different stages of hyperbaric autophagy. The rats used for the study were randomly divided into six equivalent groups-three control groups and three experimental groups. Animals from the experimental groups were subjected to hyperbaric treatment in a hyperbaric chamber, with a pressure of 1.6 ATA for 120 min. They breathed atmospheric air. Rats were decapitated within 5 or 10 days after removal from the chamber. Immunohistochemical reactions with beclin 1, LC3B, RAB7, and HSC73 proteins were carried out on preparations made from liver slices. A three-step labeled streptavidin-biotin detection method of paraffin blocks (LSAB three-step) was used for immunohistochemical research. The results were evaluated using computer programs for morphometric analysis of microscopic images by calculating the mean surface areas occupied by a positive immunohistochemical reaction in individual groups for all antibodies tested. Increased closure of substrates in the autophagosome (beclin 1) induced late endosome transport and accelerated autophagosome maturation process (RAB7). Furthermore, a larger number of autophagosomes (LC3B) was observed in liver cells immediately after the cessation of hyperbaric activity; however, this decreased after 5 days. During this time, chaperone-mediated autophagy (HSC73) was observed on a larger scale. This means that increased macroautophagy induced by hyperbaric treatment weakens with time that has elapsed since the cessation of high pressure, whereas similarly induced chaperone-mediated autophagy intensifies over time.

Indexed as

AutophagyLiverAnimalsAutophagosomesBeclin-1Chaperone-Mediated AutophagyFemaleHepatocytesHyperbaric OxygenationMacroautophagyMicrotubule-Associated ProteinsRatsBeclin-1Microtubule-Associated Proteinsautophagychaperones (HSC73)hyperbaric treatmentliverviruses

Identifiers

PMID39408803
PMCPMC11476916

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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.