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Mitochondria-targeted antioxidant mitoquinone attenuates liver inflammation and fibrosis in cirrhotic rats
- Publication Year :
- 2020
- Publisher :
- American Physiological Society, 2020.
-
Abstract
- In liver cirrhosis, oxidative stress plays a major role in promoting liver inflammation and fibrosis. Mitochondria dysregulation is responsible for excessive reactive oxygen species production. Therefore, in an experimental model of cirrhosis, we investigated the effect of mitochondria-targeted antioxidant mitoquinone. Liver cirrhosis was induced in Spraque-Dawley rats by common bile duct ligation (CBDL). Mitoquinone (10 mg·kg−1·day−1, oral gavage) or vehicle was administered from 3rd to 28th day after CBDL, when animals were euthanized; liver oxidative stress, inflammation, fibrosis, mitophagy were evaluated; and in vivo and ex vivo hemodynamic studies were performed. In cirrhotic rats, mitoquinone prevented liver inflammation, hepatocyte necrosis, and fibrosis at histological examination; decreased circulating TNF-α, gene expression of transforming growth factor-β1, collagen type 1a1, TNF-α, IL-6, IL-1β, tissue inhibitor of metalloproteinase-1, matrix metalloproteinase (MMP)-2, and MMP-13; and reduced hepatic oxidative stress, as shown by reduced oxidative carbonylation of the proteins, by modulating antioxidants catalase, Mn superoxide dismutase, and Cu/Zn superoxide dismutase. Furthermore, mitoquinone attenuated apoptosis by reducing hepatic protein expression of cleaved caspase-3. A selective removal of dysfunctional mitochondria was improved by mitoquinone, as shown by the increase in Parkin translocation to mitochondria. Treatment with mitoquinone normalized the weight of the spleen; however, it increased portal blood flow and reduced splenic artery intrahepatic resistance, suggesting an effect on resistance index. Mitochondria-targeted antioxidant mitoquinone improves liver inflammation and fibrosis in cirrhotic rats by reducing hepatic oxidative stress, preventing apoptosis, and promoting removal of dysfunctional mitochondria. Therefore, it may represent a promising strategy for the prevention and treatment of liver cirrhosis.
- Subjects :
- collagen
Liver Cirrhosis
Male
Cirrhosis
antioxidant
interleukin 1beta
Physiology
collagenase 3
Ubiquinone
ex vivo study
Mitochondria dysfunction
antioxidant activity
transforming growth factor beta1
Apoptosis
Mitochondria, Liver
Pharmacology
Mitochondrion
reactive oxygen metabolite
medicine.disease_cause
hemodynamics
manganese superoxide dismutase
Antioxidants
Hepatitis
Rats, Sprague-Dawley
spleen artery
liver mitochondrion
biochemical analysis
Fibrosis
cytokine
tissue inhibitor of metalloproteinase 1
mitochondrion
oxidative stress
rat
animal
parkin
liver fibrosis
chemistry.chemical_classification
Sprague Dawley rat
catalase
drug effect
Gastroenterology
liver cell
liver cirrhosis
mitochondria dysfunction
mitoquinone
organophosphorus compound
unclassified drug
cell death
priority journal
Liver
histopathology
Cytokines
liver protein
medicine.symptom
tumor necrosis factor
animal experiment
portal vein blood flow
interleukin 6
Inflammation
Article
animal tissue
histology
in vivo study
protein carbonylation
copper zinc superoxide dismutase
disorders of mitochondrial functions
liver weight
Organophosphorus Compounds
blood
Physiology (medical)
medicine
Animals
collagen type 1a1
Mitoquinone
protein expression
gelatinase A
Reactive oxygen species
nonhuman
Hepatology
animal model
fibrosis
medicine.disease
Rats
spleen weight
mitophagy
chemistry
gene expression
pathology
spleen
Mitochondria targeted antioxidant
Oxidative stress
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....7efe7ce0a737d7c12088845e11cf647c