Title : Altered hepatic energy status in chlordecone (Kepone)-potentiated CCl4 hepatotoxicity.

Pub. Date : 1990 Aug 15

PMID : 1696822






7 Functional Relationships(s)
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Protein Name
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1 Altered hepatic energy status in chlordecone (Kepone)-potentiated CCl4 hepatotoxicity. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
2 Altered hepatic energy status in chlordecone (Kepone)-potentiated CCl4 hepatotoxicity. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
3 Previous studies have demonstrated that increased intracellular calcium, depletion of glycogen, and suppressed hepatocellular division resulting in progression of hepatic lesion without recovery are associated with chlordecone (CD)-potentiated CCl4 hepatotoxicity. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
4 Previous studies have demonstrated that increased intracellular calcium, depletion of glycogen, and suppressed hepatocellular division resulting in progression of hepatic lesion without recovery are associated with chlordecone (CD)-potentiated CCl4 hepatotoxicity. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
5 However, CCl4 administration to CD pretreated rats resulted in significantly decreased hepatic ATP content as early as 1 hr (36%), and this decrease was irreversibly progressive with time (81% at 6 hr). Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
6 These findings indicate that CCl4 administration to CD but not to PB or mirex pretreated rats results in a severely compromised energy status of the liver. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus
7 The progressive and early depletion of liver ATP and the inhibition of Mg2(+)-ATPase in CD + CCl4 treated rats indicate the association of compromised energy status with altered Ca2+ homeostasis, depletion of glycogen, and suppressed cell division in CD-potentiated CCl4 toxicity. Chlordecone C-C motif chemokine ligand 4 Rattus norvegicus