Alteration by phenobarbital and 3-methyl-cholanthrene of functional and structural changes in rat liver due to carbon tetrachloride inhalation
- PMID: 1133769
Alteration by phenobarbital and 3-methyl-cholanthrene of functional and structural changes in rat liver due to carbon tetrachloride inhalation
Abstract
The effect of carbon tetracholoride (CCl4) inhalation (1100 ppm, 30 minutes) on rat hepatic polyribosomal profile, amino acid incorporation and endoplasmic reticulum were studied in phenobarbital or 3-methylcholanthrene (3-MC) pretreated rats. The inhalation of CCl4 alone caused a partial disruption of the hepatic polyribosomal profile. Rats pretreated with phenobarbital or 3-MC showed complete disruption of the hepatic polyribosomal profile. The hepatic polyribosomal profile returned to normal within 24 hours after exposure to CCl4 in saline and 3-MC-pretreated rats as compared to 48 hours in phenobarbital-pretreated rats. The incorporation of 14-C(U)-L-leucine into 9000 x g liver supernatant fraction protein was decreased in phenobarbital-pretreated rats when measured immediately following or 24 hours after inhalation of CCl4. The incorporation was also decreased in 3-MC-pretreated rats when measured immediately after exposure but not at 6 or 24 hours. The centrolobular hepatocytes of phenobarbital-pretreated rats exposed to CCl4 showed dilation and vesiculation of cisternae of the rough endoplasmic reticulum and striking changes in the nuclear double membrane. Partial recovery occurred within 24 hours and complete recovery within 48 hours after exposure. There were no observable changes in these parameters 0, 6, or 24 hours after exposure to CCl4 in 3-MC-pretreated rats. A new hypothesis is put forward which states that the activation of CCl4 to trichloromethyl free radicals takes place at two sites on the reduced nicotinamide adenine dinucleotide phosphate-cytochrome P-450 electron-transport chain of liver microsomes.
Similar articles
-
Further studies on the mechanism of the carbon tetrachloride induced polysome breakdown.Res Commun Chem Pathol Pharmacol. 1976 Apr;13(4):731-41. Res Commun Chem Pathol Pharmacol. 1976. PMID: 131362
-
[A selective decrease in cytochrome P450 in the liver microsomes of male rats following phenobarbital and 3-methylcholanthrene induction and acute tetrachloromethane poisoning].Eksp Med Morfol. 1993;31(3-4):1-15. Eksp Med Morfol. 1993. PMID: 7805614 Bulgarian.
-
Differential inhibitory effects of carbon tetrachloride on the hepatic plasma membrane, mitochondrial and endoplasmic reticular calcium transport systems: implications to hepatotoxicity.Cell Biochem Funct. 2002 Mar;20(1):47-59. doi: 10.1002/cbf.934. Cell Biochem Funct. 2002. PMID: 11835270
-
Hyperbaric oxygen treatment for carbon tetrachloride poisoning.Drug Saf. 1991 Sep-Oct;6(5):332-8. doi: 10.2165/00002018-199106050-00003. Drug Saf. 1991. PMID: 1930739 Review.
-
Autoprotection: stimulated tissue repair permits recovery from injury.J Biochem Toxicol. 1994 Jun;9(3):131-9. doi: 10.1002/jbt.2570090304. J Biochem Toxicol. 1994. PMID: 7983678 Review.
Cited by
-
Characterization of the glucose-induced inactivation of maltose permease in Saccharomyces cerevisiae.J Bacteriol. 1996 Apr;178(8):2245-54. doi: 10.1128/jb.178.8.2245-2254.1996. J Bacteriol. 1996. PMID: 8636025 Free PMC article.
-
Functional domains of Pho81p, an inhibitor of Pho85p protein kinase, in the transduction pathway of Pi signals in Saccharomyces cerevisiae.Mol Cell Biol. 1995 Feb;15(2):997-1004. doi: 10.1128/MCB.15.2.997. Mol Cell Biol. 1995. PMID: 7823964 Free PMC article.
-
Multiple mechanisms provide rapid and stringent glucose repression of GAL gene expression in Saccharomyces cerevisiae.Mol Cell Biol. 1994 Jun;14(6):3834-41. doi: 10.1128/mcb.14.6.3834-3841.1994. Mol Cell Biol. 1994. PMID: 8196626 Free PMC article.
-
Two different repressors collaborate to restrict expression of the yeast glucose transporter genes HXT2 and HXT4 to low levels of glucose.Mol Cell Biol. 1996 Oct;16(10):5536-45. doi: 10.1128/MCB.16.10.5536. Mol Cell Biol. 1996. PMID: 8816466 Free PMC article.
-
Heat shock transcription factor activates yeast metallothionein gene expression in response to heat and glucose starvation via distinct signalling pathways.Mol Cell Biol. 1994 Dec;14(12):8155-65. doi: 10.1128/mcb.14.12.8155-8165.1994. Mol Cell Biol. 1994. PMID: 7969152 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources