Anesthesia may alter mRNA expression of certain wound healing-associated genes in dermal wound environment of the rats.


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 07 12 2018
accepted: 27 02 2019
pubmed: 7 3 2019
medline: 18 12 2019
entrez: 7 3 2019
Statut: ppublish

Résumé

Some anesthetics including ketamine/xylazine and thiopental have been shown to alter the expression of genes related with inflammatory cytokines and chemokines in previous studies unassociated with wound healing, arising the question of whether commonly used anesthetics in wound healing models could interfere with the transcriptional responses of the genes associated with skin wound healing. The gene expression profile in wound biopsies of rats who received widely used anesthetics doses of intraperitoneal ketamine/xylazine (50 mg/kg and 10 mg/kg) or thiopental (50 mg/kg) in comparison with control rats was analyzed by monitoring the expression of genes effective on various phases of wound healing. The expression levels of 84 genes were determined on 3rd, 7th and 14th days of post-wounding using a qPCR array system. Of the genes either up or downregulated fivefolds or more, three (Egf, Col5a1 and Cxcl3) and two (Tgfa and Il2) genes were found to be the most responsive ones to ketamine/xylazine or thiopental anesthesia respectively in a period of 14 days after correction for multiple testing. However, up to 22 and 24 genes for ketamine/xylazine and thiopental were found to be differentially expressed in the same period without correction for multiple-comparisons testing (p < 0.05). In conclusion, our data suggest that ketamine/xylazine and thiopental may alter the transcriptional responses of some genes associated with wound healing in rats. We strongly suggest to consider the possible alteration effect of these anesthetics on gene expression in animal models of dermal wound healing.

Identifiants

pubmed: 30838502
doi: 10.1007/s11033-019-04728-4
pii: 10.1007/s11033-019-04728-4
doi:

Substances chimiques

RNA, Messenger 0
Xylazine 2KFG9TP5V8
Ketamine 690G0D6V8H
Thiopental JI8Z5M7NA3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2819-2827

Subventions

Organisme : Istanbul Üniversitesi
ID : 156.2015-YL-35/2709

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Auteurs

Muhammed Akif Altun (MA)

Department of Medical Biology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Fatih, Istanbul, Turkey.

Ahmet Ozaydin (A)

Department of Medical Biology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Fatih, Istanbul, Turkey. aozaydin@istanbul.edu.tr.

Hülya Arkan (H)

Department of Medical Biology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Fatih, Istanbul, Turkey.

Suleyman Demiryas (S)

Department of General Surgery, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Fahri Akbas (F)

Department of Medical Biology, Faculty of Medicine, Bezmialem Vakif University, Istanbul, Turkey.

Nurten Bahtiyar (N)

Department of Biophysics, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Ilhan Onaran (I)

Department of Medical Biology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Fatih, Istanbul, Turkey.

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Classifications MeSH