Inhibition of mouse liver respiration by Chelidonium majus isoquinoline alkaloids

被引:52
作者
Barreto, MC
Pinto, RE
Arrabaça, JD
Pavao, ML
机构
[1] Univ Acores, Dept Ciencias Tecnol & Desenvolvimento, Ctr Invest Recursos Nat, P-9502 Ponta Delgada, Portugal
[2] Inst Bento Rocha Cabral, Grp Bioquim & Biol Teor, P-1250047 Lisbon, Portugal
[3] Univ Lisbon, Fac Ciencias, Dept Quim & Bioquim, Ctr Estudos Bioquim & Fisiol, P-1749016 Lisbon, Portugal
[4] Univ Lisbon, Fac Ciencias, Dept Biol Vegetal, Ctr Engn Biol, P-1749016 Lisbon, Portugal
关键词
protoberberine alkaloids; benzophenanthridine alkaloids; structure-activity relationship; mitochondrial respiration; NADH dehydrogenase; succinate dehydrogenase;
D O I
10.1016/j.toxlet.2003.09.007
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The alkaloids from Chelidonium majus L. which had a significant inhibitory effect in mitochondrial respiration were those which contain a positive charge due to a quaternary nitrogen atom, i.e., chelerythrine, sanguinarine, berberine and coptisine, both with malate + glutamate or with succinate as substrates. When malate + glutamate was used as substrate, chelerythrine and berberine, which contain methoxy groups, were particularly more active, since they had a strong effect even at low concentrations. In submitochondrial particles, berberine and coptisine had a marked inhibitory effect on NADH dehydrogenase activity but practically no effect on succinate dehydrogenase activity, whereas chelerythrine and sanguinarine inhibited more strongly succinate dehydrogenase than NADH dehydrogenase, which is in agreement with the results found for mitochondrial respiration. Protopine and allocryptopine, which did not inhibit mitochondrial respiration, strongly inhibited NADH dehydrogenase in submitochondrial particles, but had no effect on succinate dehydrogenase activity. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:37 / 47
页数:11
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