Biaglow J E, Greenstock C L, Durand R E
Br J Cancer Suppl. 1978 Jun;3:145-9.
We have investigated the effects of 24 nitrocompounds, differing in their half-reduction potential, on the respiration in vitro of Ehrlich ascites tumour cells and cultured V79 lung cells. Many drugs with redox potentials more positive than--0.35 stimulated oxygen utilization in the presence of glucose. Glucose had little effect on the inhibition of respiration by drugs with oxidation-reduction potentials more negative than--0.38. Nitrocompounds that inhibited Ehrilch cell respiration in the presence of glucose, also inhibited intracellular reduction of ferricytochrome (c+c1). Drugs that stimulated oxygen utilization also stimuated intracellular (c " c1). Drugs that stimulated oxygen utilization also stimulated intracellular reduction of ferricytochrome (c + c1). A correlation between drug oxidation-reduction potential and stimulation of oxygen utilization in KCN-inhibited cells was found.
我们研究了24种半还原电位不同的硝基化合物对艾氏腹水瘤细胞和培养的V79肺细胞体外呼吸的影响。许多氧化还原电位比-0.35更正的药物在有葡萄糖存在的情况下会刺激氧气的利用。葡萄糖对氧化还原电位比-0.38更负的药物对呼吸的抑制作用影响很小。在有葡萄糖存在的情况下抑制艾氏细胞呼吸的硝基化合物,也会抑制细胞内铁细胞色素(c+c1)的还原。刺激氧气利用的药物也会刺激细胞内(c“c1)。发现药物氧化还原电位与KCN抑制细胞中氧气利用的刺激之间存在相关性。