TBARS公司
CYP2E1
对乙酰氨基酚
肝损伤
药理学
脂质过氧化
CYP1A2
医学
HMOX1型
化学
细胞色素P450
氧化应激
内科学
生物化学
酶
新陈代谢
血红素
血红素加氧酶
作者
Aline Meireles Coelho,Isabela Ferreira Queiroz,Wanderson Geraldo de Lima,André Talvani,Luíza Oliveira Perucci,Melina Oliveira de Souza,Daniela Caldeira Costa
标识
DOI:10.1080/01480545.2022.2052891
摘要
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.
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