Journal of Pharmacy and Pharmacology · 1985 · 22 citations · 17 references
MedicinePharmacologyToxicologyBiochemical PharmacologyExperimental PharmacologyHepatotoxicologyChemical-induced HepatotoxicityCytochrome P450 EnzymesCytochrome P450-mediated MetabolismEnzyme InductionHepatotoxicity MechanismsOxidative Stress In HepatotoxicityCytochrome P450 Enzyme ActivityCytochrome P450 Enzyme InhibitionCytochrome P450 OxidationEnzymesHepatotoxic Plant CompoundsLipid Peroxidation In HepatotoxicityLiver Microsomal MetabolismNadph Oxidase Activity
The effects of saikosaponin-d extracted from the roots of Buplerum falcatum L. on increased toxicity of CCl4 and increased activities of microsomal enzymes induced by phenobarbitone have been examined. Saikosaponin-d showed protection against the CCl4-hepatotoxicity enhanced by phenobarbitone. It also inhibited increases in the content of cytochrome P450 and NADPH-cytochrome c reductase activity, which are induced by the phenobarbitone treatment, but the spectral characteristics of P450 were not altered. The rate of microsomal lipid peroxidation by NADPH and CCl4 was significantly lowered in-vitro in rats pretreated with phenobarbitone and saikosaponin-d compared with those pretreated with phenobarbitone alone.
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The Carbon Monoxide-binding Pigment of Liver Microsomes
Tsuneo Omura, Ryo Sato · Journal of Biological Chemistry · 1964 · 3.5K citations · Full text
Sten Orrenius, Jan L. E. Ericsson, Lars Ernster · The Journal of Cell Biology · 1965 · 533 citations · Full text
Medicine, Biochemistry, Pharmacology +17