Diacerein protects rats with liver ischemia/reperfusion damage: Down-regulation of TLR4/ NFκ-B signaling pathway.


Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 09 09 2020
revised: 17 11 2020
accepted: 20 11 2020
pubmed: 22 12 2020
medline: 2 7 2021
entrez: 21 12 2020
Statut: ppublish

Résumé

Liver ischemia-reperfusion (I/R) injury is an inescapable problem. Diacerein, a chondro-protective drug, has antioxidant and anti-inflammatory effects. Its effect on liver I/R injury has not yet been fully clarified. Therefore, the current study aimed to detect its hepatic protective effect with the explanation of possible underlying mechanisms. Adult male albino rats were assigned to 4 groups: sham group, diacerein pretreated sham group, I/R non-treated group, and I/R diacerein pretreated group. Serum liver enzymes, hepatic tissue oxidative stress parameters, inflammatory biomarkers mainly Toll-like receptors-4 (TLR4), and liver fatty acid binding protein (L-FABP) levels were determined. Histopathological examination of liver tissues and immunohistochemical studies of heat shock protein 70, nuclear factor-kappa B, and Cluster of Differentiation 68 were also done. Diacerein pretreatment has the ability to restore the hepatic I/R damaging effect, proved by the reduction of serum liver enzymes, the decrease of the oxidative stress and hepatic inflammation via down-regulation of TLR4/ NFκ-B signaling pathway together with the restoration of L-FABP level and improvement of the histopathological and immunohistochemical study findings in the hepatic tissue. These results suggested the hepatoprotective effect of diacerein relies on its antioxidant and anti-inflammatory effects reducing TLR4/ NFκ-B signaling pathway.

Identifiants

pubmed: 33348310
pii: S0753-3322(20)31255-5
doi: 10.1016/j.biopha.2020.111063
pii:
doi:

Substances chimiques

Anthraquinones 0
Anti-Inflammatory Agents 0
Antioxidants 0
Fatty Acid-Binding Proteins 0
NF-kappa B 0
Protective Agents 0
Tlr4 protein, rat 0
Toll-Like Receptor 4 0
Tumor Necrosis Factor-alpha 0
Vascular Cell Adhesion Molecule-1 0
diacerein 4HU6J11EL5
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111063

Informations de copyright

Published by Elsevier Masson SAS.

Auteurs

Mohamed Abdellah Ibrahim (MA)

Department of Pharmacology, Faculty of Medicine, Minia University, Minia, Egypt. Electronic address: maim69@yahoo.com.

Walaa Yehia Abdelzaher (WY)

Department of Pharmacology, Faculty of Medicine, Minia University, Minia, Egypt. Electronic address: walaayehia22@yahoo.com.

Yasmine F Ibrahim (YF)

Department of Pharmacology, Faculty of Medicine, Minia University, Minia, Egypt. Electronic address: jasy3000@yahoo.com.

Amira F Ahmed (AF)

Department of Histology and Cell Biology, Faculty of Medicine, Minia University, Minia, Egypt; Department of Histology and Cell Biology, Misr University for Science and Technology, Egypt. Electronic address: amirabehery@gmail.com.

Nermeen N Welson (NN)

Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Beni-Suef University, Beni-Suef, 62511, Egypt. Electronic address: nermeennerm@yahoo.com.

Sarah Al-Rashed (S)

Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, 11451, Saudi Arabia. Electronic address: salrashed@ksu.edu.sa.

Gaber El-Saber Batiha (GE)

Department of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour 22511, AlBeheira, Egypt. Electronic address: gaberbatiha@gmail.com.

Asmaa Mohamed Abdel-Aziz (AM)

Department of Pharmacology, Faculty of Medicine, Minia University, Minia, Egypt. Electronic address: asmaaabdelaziz303@yahoo.com.

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Classifications MeSH