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Overview
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Background
Carmustine is a nitrogen mustard β-chloro-nitrosourea compound that is used as an antitumor chemotherapeutic agent[1].
In rat glial tumor cytosol and intact cells, carmustine (8, 80, and 800 µM) reduces N-acetyltransferase activities for 2-aminofluorene and p-aminobenzoic acid. In rat glioma cells, carmustine reduces the formation of DNA-AF adducts[1].
Intraperitoneal administration of carmustine 25 mg/kg in rat, which increases liver-to-weight ratio, significantly reduces bile flow, and decreases GSSG and GSH/GSSG values, and mild fibrous edema and monocyte infiltration in the liver of rats[2].[1].Hung C F. Effects of carmustine and lomustine on arylamine N-acetyltransferase activity and 2-aminofluorene-DNA adducts in rat glial tumor cells. Neurochem Res, 2000, 25(6): 845-51.
[2].Demir A, et al. The effect of trimetazidine on intrahepatic cholestasis caused by carmustine in rats. Hepatol Res, 2001, 20(1): 133-143.
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Overview