作者: Damiano Cottalasso , Cinzia Domenicotti , Nicola Traverso , Maria Adelaide Pronzato , Giorgio Nanni
DOI: 10.1016/S0300-483X(02)00235-4
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摘要: Abstract Our previous investigations demonstrated that 1,2-dichloroethane (DCE) and chronic ethanol treatment separately are able to impair glycoprotein metabolism secretion, reduce dolichol concentration in liver membranes. The purpose of this study was investigate whether consumption can induce potentiation rat damage due DCE haloalkane used several chemical processes agriculture. Rats were given 36% their total energy as the Lieber–DeCarli liquid diet for 8 weeks (CH group). pair-fed control group received an isocaloric amount dextrine-maltose (PF ‘In vitro’ experiments: (6.5 mM) isolated hepatocytes from CH rats enhanced retention further reduced secretion 14 C-glucosamine incorporation compared or PF treated rats. vivo’ a marked decrease microsomes (in which dolichyl phosphate is rate-limiting initial glycosylation protein) Golgi membranes very important membrane permeability, fluidity vesicle fusion) observed acutely with 628 mg/kg bw (CH+DCE) PF+DCE These data suggest increases toxicity by affecting protein impairing glycolipoprotein concomitant at level apparatus.