Toxic Alkaloids and their Interaction with Microsomal Cytochrome P-450 in vitro

被引:21
作者
Peeples, A. [1 ]
Dalvi, R. R. [1 ]
机构
[1] Tuskegee Inst, Sch Vet Med, Dept Physiol & Pharmacol, Tuskegee, AL 36088 USA
基金
美国国家科学基金会;
关键词
alkaloids; rat liver microsomes; cytochrome P-450; binding spectra; drug metabolism;
D O I
10.1002/jat.2550020607
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Studies on the binding spectra of certain alkaloids with rat liver microsomes revealed that brucine, scopolamine and strychnine are type I compounds, whereas boldine, emetine, nicotine, reserpine and sanguinarine show type I1 binding. In contrast, colchicine and solanine failed to produce any measurable binding spectra. In vitro incubation of colchicine, nicotine or scopolamine with microsomal suspensions and NADPH resulted in demethylation of these alkaloids, while the incubation of boldine, brucine, emetine, reserpine, sanguinarine or solanine showed little or no dealkylation reaction. Furthermore, the effect of these alkaloids on the in vitro microsomal metabolism of a drug, benzphetamine, has also been studied.
引用
收藏
页码:300 / 302
页数:3
相关论文
共 18 条