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叔丁基对羟基茴香醚作为肿瘤细胞呼吸抑制剂

t-butyl-4-hydroxyanisole as an inhibitor of tumor cell respiration.

作者信息

Fones E, Amigo H, Gallegos K, Guerrero A, Ferreira J

机构信息

Department of Experimental Medicine, Faculty of Medicine, Universidad de Chile, Santiago.

出版信息

Biochem Pharmacol. 1989 Oct 15;38(20):3443-51. doi: 10.1016/0006-2952(89)90113-5.

Abstract

The effect of t-butyl-4-hydroxyanisole (BHA), a widely used food antioxidant additive, on the culture growth, oxygen consumption, and redox state of some electron carriers of intact TA3 and 786A ascites tumor cells has been studied. BHA inhibited culture growth and respiration of these two tumor cell lines, by inhibiting the electron flow through the respiratory chain. Experiments to determine its site of action showed that BHA did not inhibit noticeably the electron flow through cytochrome oxidase, due to the ability of N,N,N',N'-tetramethyl-p-phenylenediamine to bypass the BHA inhibition of the respiration. Electron flow through the ubiquinone-cytochrome b-c1 complex also was unaffected by BHA; in fact, BHA failed to inhibit the oxidation of duroquinol. Spectrophotometric experiments are in accordance with studies carried out using synthetic electron donors. The redox state of NAD(P)+, determined in steady-state conditions, changed to a more reduced level, and the redox states of ubiquinone, cytochrome b, cytochromes c + c1 and cytochromes a + a3 changed to a more oxidized level. These observations suggest that the electron transport in the tumor mitochondria was inhibited by BHA at the NADH-dehydrogenase-ubiquinone level (energy-conserving site 1). These findings could explain, in part, the cytotoxic effect of BHA.

摘要

已研究了广泛使用的食品抗氧化剂添加剂叔丁基对羟基茴香醚(BHA)对完整的TA3和786A腹水肿瘤细胞的培养生长、氧气消耗以及某些电子载体氧化还原状态的影响。BHA通过抑制电子通过呼吸链的流动,抑制了这两种肿瘤细胞系的培养生长和呼吸作用。确定其作用位点的实验表明,由于N,N,N',N'-四甲基对苯二胺能够绕过BHA对呼吸作用的抑制,BHA并未显著抑制电子通过细胞色素氧化酶的流动。电子通过泛醌-细胞色素b-c1复合体的流动也不受BHA的影响;事实上,BHA未能抑制硬脂醌醇的氧化。分光光度实验与使用合成电子供体进行的研究一致。在稳态条件下测定的NAD(P)+的氧化还原状态变为更还原的水平,而泛醌、细胞色素b、细胞色素c + c1和细胞色素a + a3的氧化还原状态变为更氧化的水平。这些观察结果表明,肿瘤线粒体中的电子传递在NADH-脱氢酶-泛醌水平(能量保存位点1)受到BHA的抑制。这些发现可以部分解释BHA的细胞毒性作用。

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