Miko M, Drobnica L, Jindra A, Semonský M
Neoplasma. 1979;26(4):449-60.
The effect of nine chloro- and bromoderivatives of isocrotonic acid on some bioenergetic processes in both Ehrlich ascites cells and isolated rat liver mitochondria has been investigated. Substances studied in the concentration range 25--200 microM significantly inhibited incorporation of both 14C-adenine and 14C-valine into acid-insoluble material of Ehrlich ascites cells. The rate of 14C-precursors incorporation being directly related to the concentration of the inhibitor. Gamma,gamma-bis-4-ethylphenyl-alpha,beta-dichloroisocrotonic acid fully inhibits both aerobic glucose utilization and lactic acid formation at 200 microM concentration. At lower concentrations, however, glycolysis is stimulated. Maximal stimulation of rat liver mitochondrial respiration in state 4 with succinate as substrate was reached at concentrations as low as 10 microM. On the other hand, these substances were able to release by the oligomycin inhibited respiration of rat liver mitochondria. Our data suggest that cytotoxic and cancerostatic action of isocrotonic acid derivatives lies primarily in the exclusion of key processes in the energy metabolism of Ehrlich ascites cells and isolated mitochondria.
研究了异巴豆酸的九种氯代和溴代衍生物对艾氏腹水癌细胞和离体大鼠肝线粒体中某些生物能过程的影响。在所研究的25 - 200微摩尔浓度范围内的物质显著抑制了14C - 腺嘌呤和14C - 缬氨酸掺入艾氏腹水癌细胞的酸不溶性物质中。14C - 前体掺入率与抑制剂浓度直接相关。γ,γ - 双 - 4 - 乙基苯基 - α,β - 二氯异巴豆酸在200微摩尔浓度时完全抑制有氧葡萄糖利用和乳酸形成。然而,在较低浓度时,糖酵解受到刺激。以琥珀酸为底物时,在低至10微摩尔的浓度下达到了对大鼠肝线粒体状态4呼吸的最大刺激。另一方面,这些物质能够使大鼠肝线粒体被寡霉素抑制的呼吸恢复。我们的数据表明,异巴豆酸衍生物的细胞毒性和抗癌作用主要在于排除艾氏腹水癌细胞和离体线粒体能量代谢中的关键过程。