Temporal analysis of paracetamol-induced hepatotoxicity.
Aline Meireles CoelhoIsabela Ferreira QueirozWanderson Geraldo de LimaAndré TalvaniLuiza Oliveira PerucciMelina Oliveira de SouzaDaniela Caldeira CostaPublished in: Drug and chemical toxicology (2022)
Paracetamol-induced hepatotoxicity (APAP) causes severe damage that may be irreversible. Understanding the evolution of liver injury caused by overdose of the drug is important to assist in the treatment. In the present study, we evaluated the acute intoxication by APAP (500 mg/kg) in periods of 3 and 12 hours in C57BL/6 mice through biochemical, histological, inflammatory parameters, and the redox status. The results showed that in the 3-hour period there was an increase in creatinine dosage and lipid peroxidation (TBARS) compared to the control group. In the period of 12 hours after APAP intoxication all parameters evaluated were altered; there was an increase of ALT, AST, and necrosis, besides the increase of redox status biomarkers as carbonylated protein, TBARS, and MMP-9. We also observed activation of the inflammasome pathway as well as a reduction in the regenerative capacity of hepatocytes with a decrease in binucleated liver cells. In cytochrome gene expression, the mRNA level increased in CYP2E1 isoenzyme and reduced CYP1A2 expression. This study indicated that early treatment is necessary to mitigate APAP-induced acute liver injury, and alternative therapies capable of controlling the progression of intoxication in the liver are needed.
Keyphrases
- drug induced
- liver injury
- gene expression
- adverse drug
- stem cells
- oxidative stress
- poor prognosis
- binding protein
- induced apoptosis
- dna methylation
- emergency department
- blood pressure
- liver failure
- type diabetes
- uric acid
- long non coding rna
- metabolic syndrome
- hepatitis b virus
- signaling pathway
- combination therapy
- small molecule
- electronic health record
- replacement therapy