dc.contributor.author | Bozkurt, M.F. | |
dc.contributor.author | Bhaya, M.N. | |
dc.contributor.author | Dibekoğlu, C. | |
dc.contributor.author | Akat, A. | |
dc.contributor.author | Ateş, U. | |
dc.contributor.author | Erbaş, O. | |
dc.date.accessioned | 2022-11-04T19:55:47Z | |
dc.date.available | 2022-11-04T19:55:47Z | |
dc.date.issued | 2022 | |
dc.identifier.issn | 0102-8650 | |
dc.identifier.uri | https://doi.org/10.1590/acb370704 | |
dc.identifier.uri | http://hdl.handle.net/11446/4626 | |
dc.description.abstract | Purpose: To evaluate the ameliorative effect of mesenchymal stem cells (MSCs) on acetic acid colitis model via Nrf2/HO-1 pathway in rats. Methods: In this study, 30 rats were divided into three groups. Acute colitis was induced by rectal administration of 4% solution of acetic acid. MSCs were injected intraperitoneally in the treatment group. Results: Increased levels of tumor necrosis factor-α (TNF-α), pentraxin-3, and malondialdehyde (MDA) in colitis group were revealed biochemically. Increased level of TNF-α and decreased levels of Nrf2 and interleukin-10 (IL-10) were observed in rectum tissues. Increased fibrous tissue proliferation, vascularization and inflammatory cell infiltration were described in the colitis group. Significant improvement was observed in MSCs treated group histopathologically. Increased immunopositivity of TNF-α, vascular endothelial growth factor (VEGF) and CD68 markers was observed in the colitis group cells, and decreased level of this positivity was observed in MSCs treated group. Conclusion: Biochemical, histopathological and immunohistochemical results strongly support the ameliorative effect of MSCs against acetic induced colitis model via Nrf2/HO-1 pathway in rats. © 2022, Sociedade Brasileira para o Desenvolvimento de Pesquisa em Cirurgia. All rights reserved. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Sociedade Brasileira para o Desenvolvimento de Pesquisa em Cirurgia | en_US |
dc.relation.ispartof | Acta Cirurgica Brasileira | en_US |
dc.identifier.doi | 10.1590/acb370704 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Acetic Acid | en_US |
dc.subject | Inflammation | en_US |
dc.subject | Mesenchymal Stem Cells | en_US |
dc.subject | NF-E2-Related Factor 2 | en_US |
dc.subject | Vascular Endothelial Growth Factor A | en_US |
dc.subject | acetic acid | en_US |
dc.subject | beta1 integrin | en_US |
dc.subject | CD68 antigen | en_US |
dc.subject | endoglin | en_US |
dc.subject | interleukin 10 | en_US |
dc.subject | ketasol | en_US |
dc.subject | malonaldehyde | en_US |
dc.subject | microsomal aminopeptidase | en_US |
dc.subject | penicillin derivative | en_US |
dc.subject | pentraxin 3 | en_US |
dc.subject | streptomycin | en_US |
dc.subject | transcription factor Nrf2 | en_US |
dc.subject | tumor necrosis factor | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | vasculotropin | en_US |
dc.subject | xylazine | en_US |
dc.subject | interleukin 10 | en_US |
dc.subject | malonaldehyde | en_US |
dc.subject | transcription factor Nrf2 | en_US |
dc.subject | tumor necrosis factor | en_US |
dc.subject | vasculotropin A | en_US |
dc.subject | adipose tissue | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | animal tissue | en_US |
dc.subject | Article | en_US |
dc.subject | cell growth | en_US |
dc.subject | cell infiltration | en_US |
dc.subject | cell isolation | en_US |
dc.subject | cell proliferation | en_US |
dc.subject | colitis | en_US |
dc.subject | controlled study | en_US |
dc.subject | cryopreservation | en_US |
dc.subject | disease severity | en_US |
dc.subject | enzyme linked immunosorbent assay | en_US |
dc.subject | histopathology | en_US |
dc.subject | immunofluorescence assay | en_US |
dc.subject | immunohistochemistry | en_US |
dc.subject | inflammation | en_US |
dc.subject | lipid peroxidation | en_US |
dc.subject | macrophage | en_US |
dc.subject | male | en_US |
dc.subject | mesenchymal stem cell | en_US |
dc.subject | morphology | en_US |
dc.subject | nonhuman | en_US |
dc.subject | Nrf2 signaling | en_US |
dc.subject | photography | en_US |
dc.subject | protein expression | en_US |
dc.subject | rat | en_US |
dc.subject | rectal tissue | en_US |
dc.subject | vascularization | en_US |
dc.subject | animal | en_US |
dc.subject | colitis | en_US |
dc.subject | metabolism | en_US |
dc.subject | Animals | en_US |
dc.subject | Colitis | en_US |
dc.subject | Interleukin-10 | en_US |
dc.subject | Malondialdehyde | en_US |
dc.subject | Mesenchymal Stem Cells | en_US |
dc.subject | NF-E2-Related Factor 2 | en_US |
dc.subject | Rats | en_US |
dc.subject | Tumor Necrosis Factor-alpha | en_US |
dc.subject | Vascular Endothelial Growth Factor A | en_US |
dc.title | Mesenchymal stem cells have ameliorative effect on the colitis model via Nrf2/HO-1 pathway | en_US |
dc.type | article | en_US |
dc.identifier.issue | 7 | en_US |
dc.identifier.volume | 37 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.department-temp | Bozkurt, M.F., Afyon Kocatepe University, Department of Pathology, Faculty of Veterinary Medicine, Afyonkarahisar, Turkey; Bhaya, M.N., Afyon Kocatepe University, Department of Pathology, Faculty of Veterinary Medicine, Afyonkarahisar, Turkey; Dibekoğlu, C., Istanbul Florence Nightingale Hospital, Department of General Surgery, Istanbul, Turkey; Akat, A., Stembio Cell and Tissue Technologies Inc, Istanbul, Turkey; Ateş, U., Stembio Cell and Tissue Technologies Inc, Istanbul, Turkey; Erbaş, O., Demiroğlu Bilim University, Department of Physiology, Cephalink Institute, Gebze, Turkey | en_US |
dc.identifier.pmid | 36228298 | en_US |
dc.identifier.scopus | 2-s2.0-85139470289 | en_US |
dc.authorscopusid | 56511367200 | |
dc.authorscopusid | 57225073351 | |
dc.authorscopusid | 6505797608 | |
dc.authorscopusid | 55986085900 | |
dc.authorscopusid | 6506910118 | |
dc.authorscopusid | 55469991100 | |