Diacerein protects rats with liver ischemia/reperfusion damage: Down-regulation of TLR4/ NFκ-B signaling pathway.
Alanine Transaminase
/ metabolism
Animals
Anthraquinones
/ pharmacology
Anti-Inflammatory Agents
/ pharmacology
Antioxidants
/ pharmacology
Down-Regulation
Fatty Acid-Binding Proteins
/ metabolism
Liver
/ drug effects
Liver Diseases
/ drug therapy
Male
NF-kappa B
/ metabolism
Oxidative Stress
/ drug effects
Protective Agents
/ pharmacology
Rats
Reperfusion Injury
/ drug therapy
Signal Transduction
/ drug effects
Toll-Like Receptor 4
/ metabolism
Tumor Necrosis Factor-alpha
/ metabolism
Vascular Cell Adhesion Molecule-1
/ metabolism
Diacerein
Inflammatory pathway
L-FABP
Liver ischemia-reperfusion
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
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
111063Informations de copyright
Published by Elsevier Masson SAS.