Title : Pivotal role of hepatocellular regeneration in the ultimate hepatotoxicity of CCl4 in chlordecone-, mirex-, or phenobarbital-pretreated rats.

Pub. Date : 1992

PMID : 1284994






6 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Pivotal role of hepatocellular regeneration in the ultimate hepatotoxicity of CCl4 in chlordecone-, mirex-, or phenobarbital-pretreated rats. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
2 Our earlier histomorphometric and biochemical studies suggested that the progressive phase of the interactive toxicity of chlordecone (CD) + CCl4 involves suppression of hepatocellular regeneration. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
3 Dietary 10 ppm CD potentiated the hepatotoxicity of CCl4 to a greater extent than PB or M, as evidenced by elevations in plasma enzymes. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
4 Actual liver injury by CCl4 was greater in PB- than in CD-pretreated rats, as evidenced by histopathological observations. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
5 A 100% mortality occurred in CD-pretreated rats at 60 hr after CCl4 administration, whereas no mortality occurred in either N-, M-, or PB-pretreated rats, indicating recovery from liver injury. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
6 Hepatocellular nuclear DNA levels were significantly decreased starting at 6 hr after CCl4 administration to CD-pretreated rats, but not in M- or PB-pretreated rats. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus