Protein Information

ID 132
Name CYP2E1
Synonyms CPE 1; Flavoprotein linked monooxygenase; Xenobiotic monooxygenase; Microsomal monooxygenase; CPE1; CYP2E; CYP2E1; CYP2E1 protein…

Compound Information

ID 1392
Name carbon tetrachloride
CAS tetrachloromethane

Reference

PubMed Abstract RScore(About this table)
17084009 Avasarala S, Yang L, Sun Y, Leung AW, Chan WY, Cheung WT, Lee SS: A temporal study on the histopathological, biochemical and molecular responses of CCl (4)-induced hepatotoxicity in Cyp2e1-null mice. Toxicology. 2006 Dec 7;228(2-3):310-22. Epub 2006 Oct 6.
Previous study using Cyp2e1-null mice showed that Cyp2e1 is required in CCl (4)-induced liver injury at 24h, what remains unclear are the temporal changes in liver damage and the spectrum of genes involved in this process. We investigated the time-dependent liver changes that occurred at morphological, histopathological, biochemical and molecular levels in both Cyp2e1 (+/+) and Cyp2e1 (-/-) mice after treating with either corn oil or CCl (4) (1 ml/kg) for 2, 6, 12, 24 and 48 h. A pale orange colored liver, indicative of fatty infiltration, was observed in Cyp2e1 (+/+) mice treated with CCl (4) for 24 and 48 h, while the Cyp2e1 (+/+) mice treated with corn oil and Cyp2e1 (-/-) mice treated with either corn oil or CCl (4) showed normal reddish brown colored liver. Ballooned hepatocytes with multiple vacuoles in their cytoplasm were observed in the livers of Cyp2e1 (+/+) mice 24 and 48 h after treating with CCl (4). The levels of serum alanine aminotransferase and aspartate aminotransferase, markers for liver injury, were significantly higher at 12h, peaked at 24h and gradually decreased at 48 h after CCl (4) intoxication. In contrast, this kind of damage was not apparent in the Cyp2e1 (-/-) mice treated with CCl (4). Altered expressions of genes related to liver cirrhosis, apoptosis, oxidative stress, xenobiotic detoxification, lipid metabolism, chemsensory signaling or tumorigenesis, structural organization, regeneration and inflammatory response were identified, and the time-dependent changes in expression of these genes were varied. Overall, the present study provides insights into the mechanism of CCl (4)-induced hepatotoxicity in animal models.
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