Unraveling Hepatic Metabolomic Profiles and Morphological Outcomes in a Hybrid Model of NASH in Different Mouse Strains.
Gabriel Bacil PrataGuilherme Ribeiro RomualdoPriscila M F D PiaggeDaniel Rodrigues CardosoMathieu VinkenBruno CogliatiLuis Fernando BarbisanPublished in: Antioxidants (Basel, Switzerland) (2023)
Nonalcoholic fatty liver disease (NAFLD) encompasses nonalcoholic steatohepatitis (NASH) and affects 25% of the global population. Although a plethora of experimental models for studying NASH have been proposed, still scarce findings regarding the hepatic metabolomic/molecular profile. In the present study, we sought to unravel the hepatic metabolomic profile of mice subjected to a hybrid model of NASH, by combining a Western diet and carbon tetrachloride administration, for 8 weeks, in male C57BL/6J and BALB/c mice. In both mouse strains, the main traits of NASH-metabolic (glucose intolerance profile), morphologic (extensive microvesicular steatosis and fibrosis, lobular inflammation, and adipose tissue-related inflammation/hypertrophy), and molecular (impaired Nrf2/NF-κB pathway dynamics and altered metabolomic profile)-were observed. The hepatic metabolomic profile revealed that the hybrid protocol impaired, in both strains, the abundance of branched chain-aromatic amino acids, carboxylic acids, and glycosyl compounds, that might be linked to the Nrf2 pathway activation. Moreover, we observed a strain-dependent hepatic metabolomic signature, in which the tricarboxylic acid metabolites and pyruvate metabolism were dissimilarly modulated in C57BL/6J and BALB/c mice. Thus, we provide evidence that the strain-dependent hepatic metabolomic profile might be linked to the distinct underlying mechanisms of NASH, also prospecting potential mechanistic insights into the corresponding disease.
Keyphrases
- oxidative stress
- adipose tissue
- escherichia coli
- high fat diet induced
- amino acid
- insulin resistance
- randomized controlled trial
- type diabetes
- high fat diet
- signaling pathway
- dna methylation
- genome wide
- metabolic syndrome
- cell proliferation
- immune response
- physical activity
- inflammatory response
- single molecule
- blood glucose
- toll like receptor
- preterm birth
- gestational age