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Metformin treatment reverses high fat diet- induced non-alcoholic fatty liver diseases and dyslipidemia by stimulating multiple antioxidant and anti-inflammatory pathways
- Source :
- Biochemistry and Biophysics Reports, Vol 28, Iss, Pp 101168-(2021), Biochemistry and Biophysics Reports
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- Purpose This current study investigated the effect of metformin treatment on hepatic oxidative stress and inflammation associated with nonalcoholic fatty liver disease (NADLD) in high fat diet (HFD) fed rats. Method Wistar rats were fed with a HFD or laboratory chow diet for 8 weeks. Metformin was administered orally at a dose of 200 mg/kg. Body weight, food and water intake were recorded on daily basis. Oral glucose tolerance test (OGTT), biochemical analysis and histological examinations were conducted on plasma and tissue samples. Antioxidant and anti-inflammatory mRNA expression was analyzed using reverse transcription polymeric chain reaction (RT-PCR). Results Metformin treatment for 8 weeks prevented HFD-induced weight gain and decreased fat deposition in HFD fed rats. Biochemical analysis revealed that metformin treatment significantly attenuated nitro-oxidative stress markers malondialdehyde (MDA), advanced protein oxidation product (APOP), and excessive nitric oxide (NO) levels in the liver of HFD fed rats. Gene expression analysis demonestrated that metformin treatment was associated with an enhanced expression of antioxidant genes such as Nrf-2, HO-1, SOD and catalase in liver of HFD fed rats. Metformin treatment also found to modulate the expression of fat metabolizing and anti-inflammatory genes including PPAR--γ, C/EBP-α, SREBP1c, FAS, AMPK and GLUT-4. Consistent with the biochemical and gene expression data, the histopathological examination unveiled that metformin treatment attenuated inflammatory cells infiltration, steatosis, hepatocyte necrosis, collagen deposition, and fibrosis in the liver of HFD fed rats. Conclusion In conclusion, this study suggests that metformin might be effective in the prevention and treatment of HFD-induced steatosis by reducing hepatic oxidative stress and inflammation in the liver.<br />Highlights • High fat diet in rats developed glucose intolerance and oxidative stress in liver. • Metformin restored antioxidant genes expression in liver of HFD fed rats. • Metformin also inhibited the inflammatory genes expression and fibrosis in liver. • Moreover, metformin treatment may ameliorate fatty liver in HFD fed rats.
- Subjects :
- AST, aspartate aminotransferase
Protein oxidation
medicine.disease_cause
Biochemistry
LDL, low density lipoprotein
SOD, Superoxide dismutase
Lipid peroxidation
AUC, area under the curve
chemistry.chemical_compound
TBARS, Thiobarbituric acid reactive substances
Nonalcoholic fatty liver disease
OGTT, Oral glucose tolerance test
Biology (General)
IL-6, interleukin-6
digestive, oral, and skin physiology
Fatty liver
PBS, Phosphate buffer saline
SREBP1c, sterol regulatory element-binding protein 1c
Malondialdehyde
Metformin
PGC-1α, peroxisome proliferator-activated receptor γ coactivator 1
ATP, Adinosine triphosphate
Research Article
medicine.drug
medicine.medical_specialty
QH301-705.5
HSCs, Hepatic stellate cells
MPO, Myeloperoxidase
Biophysics
QD415-436
IACUC, Institutional Animal Care and Use Committee
ROS, reactive oxygen species
ALT, alanine aminotransferase
Internal medicine
medicine
FAS, Fatty acid synthase
Obesity
MDA, Malondialdehyde
PPAR-γ, peroxisome proliferator-activated receptor γ
Inflammation
APOP, advanced protein oxidation product
NO, nitric oxide
ALP, alkaline phosphatase
business.industry
TBA, Thiobarbituric acid
nutritional and metabolic diseases
medicine.disease
HDL, high density lipoprotein
Met, Metformin
AMPK, AMP-activated protein kinase
Endocrinology
chemistry
HF, High fat
NAFLD, nonalcoholic fatty liver disease
CAT, catalase
Steatosis
business
Oxidative stress
Non-alcoholic fatty liver disease
Subjects
Details
- ISSN :
- 24055808
- Volume :
- 28
- Database :
- OpenAIRE
- Journal :
- Biochemistry and Biophysics Reports
- Accession number :
- edsair.doi.dedup.....71282b5e76c3ceeef714c367923f6132
- Full Text :
- https://doi.org/10.1016/j.bbrep.2021.101168