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Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats

The present study aimed to identify the possible protective effect of diacerein (DIA) on gentamicin (GNT)‐induced parotid toxicity in rats. DIA was administered in the presence and absence of GNT. Thirty‐two Wistar adult male rats were randomly arranged into four groups: control, DIA (50 mg/kg/day),...

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Autores principales: Ali, Dalia Mohamed, Mahmoud, Mohamed H., Rifaai, Rehab Ahmed, Fawzy, Michael Atef, Atta, Medhat, Welson, Nermeen N., Batiha, Gaber El‐Saber, Alexiou, Athanasios, Papadakis, Marios, Abdelzaher, Walaa Yehia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273056/
https://www.ncbi.nlm.nih.gov/pubmed/37257043
http://dx.doi.org/10.1111/jcmm.17791
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author Ali, Dalia Mohamed
Mahmoud, Mohamed H.
Rifaai, Rehab Ahmed
Fawzy, Michael Atef
Atta, Medhat
Welson, Nermeen N.
Batiha, Gaber El‐Saber
Alexiou, Athanasios
Papadakis, Marios
Abdelzaher, Walaa Yehia
author_facet Ali, Dalia Mohamed
Mahmoud, Mohamed H.
Rifaai, Rehab Ahmed
Fawzy, Michael Atef
Atta, Medhat
Welson, Nermeen N.
Batiha, Gaber El‐Saber
Alexiou, Athanasios
Papadakis, Marios
Abdelzaher, Walaa Yehia
author_sort Ali, Dalia Mohamed
collection PubMed
description The present study aimed to identify the possible protective effect of diacerein (DIA) on gentamicin (GNT)‐induced parotid toxicity in rats. DIA was administered in the presence and absence of GNT. Thirty‐two Wistar adult male rats were randomly arranged into four groups: control, DIA (50 mg/kg/day), GNT (100 mg/kg) and GNT+DIA groups for 8 days. Parotid oxidative stress parameters, besides inflammatory and apoptotic biomarkers, were evaluated. Salivary flow rate, transient receptor potential canonical 1 (TRCP1), and C/EBP homologous protein (CHOP) in parotid tissue were measured. A parotid histopathological examination and an interleukin‐1 beta (IL‐1β) immunohistochemical study were also performed. GNT significantly increased parotid oxidative stress, inflammatory, apoptotic and CHOP biomarkers with decreased salivary flow rate and TRCP1 level. A histopathological picture of parotid damage and high IL‐1β immunoexpression were detected. DIA significantly normalized the distributed oxidative, inflammatory and apoptotic indicators, CHOP and TRCP1, with a prompt improvement in the histopathological picture and a decrease in IL‐1β immunoexpression. These results reported that DIA protects against GNT‐induced parotid toxicity via modulation of TLR4/NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways.
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spelling pubmed-102730562023-06-17 Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats Ali, Dalia Mohamed Mahmoud, Mohamed H. Rifaai, Rehab Ahmed Fawzy, Michael Atef Atta, Medhat Welson, Nermeen N. Batiha, Gaber El‐Saber Alexiou, Athanasios Papadakis, Marios Abdelzaher, Walaa Yehia J Cell Mol Med Original Articles The present study aimed to identify the possible protective effect of diacerein (DIA) on gentamicin (GNT)‐induced parotid toxicity in rats. DIA was administered in the presence and absence of GNT. Thirty‐two Wistar adult male rats were randomly arranged into four groups: control, DIA (50 mg/kg/day), GNT (100 mg/kg) and GNT+DIA groups for 8 days. Parotid oxidative stress parameters, besides inflammatory and apoptotic biomarkers, were evaluated. Salivary flow rate, transient receptor potential canonical 1 (TRCP1), and C/EBP homologous protein (CHOP) in parotid tissue were measured. A parotid histopathological examination and an interleukin‐1 beta (IL‐1β) immunohistochemical study were also performed. GNT significantly increased parotid oxidative stress, inflammatory, apoptotic and CHOP biomarkers with decreased salivary flow rate and TRCP1 level. A histopathological picture of parotid damage and high IL‐1β immunoexpression were detected. DIA significantly normalized the distributed oxidative, inflammatory and apoptotic indicators, CHOP and TRCP1, with a prompt improvement in the histopathological picture and a decrease in IL‐1β immunoexpression. These results reported that DIA protects against GNT‐induced parotid toxicity via modulation of TLR4/NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways. John Wiley and Sons Inc. 2023-05-31 /pmc/articles/PMC10273056/ /pubmed/37257043 http://dx.doi.org/10.1111/jcmm.17791 Text en © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ali, Dalia Mohamed
Mahmoud, Mohamed H.
Rifaai, Rehab Ahmed
Fawzy, Michael Atef
Atta, Medhat
Welson, Nermeen N.
Batiha, Gaber El‐Saber
Alexiou, Athanasios
Papadakis, Marios
Abdelzaher, Walaa Yehia
Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats
title Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats
title_full Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats
title_fullStr Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats
title_full_unstemmed Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats
title_short Diacerein modulates TLR4/ NF‐κB/IL‐1β and TRPC1/CHOP signalling pathways in gentamicin‐induced parotid toxicity in rats
title_sort diacerein modulates tlr4/ nf‐κb/il‐1β and trpc1/chop signalling pathways in gentamicin‐induced parotid toxicity in rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273056/
https://www.ncbi.nlm.nih.gov/pubmed/37257043
http://dx.doi.org/10.1111/jcmm.17791
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