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微粒体中脂质过氧化物的形成。一般考虑因素。

Lipid peroxide formation in microsomes. General considerations.

作者信息

Wills E D

出版信息

Biochem J. 1969 Jun;113(2):315-24. doi: 10.1042/bj1130315.

Abstract
  1. Liver microsomes form lipid peroxide when incubated with ascorbate or NADPH, but not with NADH. Increasing the concentration of ascorbate beyond the optimum (0.5mm) decreases the rate of lipid peroxide formation, but this effect does not occur with NADPH. Other reducing agents such as p-phenylenediamine or ferricyanide were not able to replace ascorbate and induce lipid peroxide formation. 2. The rate of ascorbate-induced peroxidation is optimum at pH6.0 whereas the rate of the NADPH system is optimum at pH7.0. Both systems require phosphate for maximum activity. 3. Lipid peroxide formation occurs at the maximum specific rate in very dilute microsome suspensions (0.15mg. of protein/ml.). 4. Treatment of microsomes with deoxycholate and other detergents causes membrane disintegration and inhibits lipid peroxide formation. 5. Lipid peroxide formation is accompanied by a rapid uptake of oxygen and there is a large excess of oxygen utilized for each molecule of malonaldehyde measured in the peroxide method. 6. Boiled microsomes form lipid peroxide in the presence of ascorbate, but not if NADPH is added. 7. Lipid peroxide formation induced by NADPH is strongly inhibited by p-chloromercuribenzoate, weakly inhibited by N-ethylmaleimide and unaffected by iodoacetamide. Ascorbate-induced peroxidation in untreated microsomes is unaffected by p-chloromercuribenzoate, but inhibited if boiled microsomes are used. These experiments may be interpreted on the basis that a ferredoxin-type protein forms part of the system in which NADPH induces lipid peroxide formation. 8. Most heavy-metal ions, with the exception of inorganic iron (Fe(2+) or Fe(3+)), which activates, inhibit both ascorbate-induced and NADPH-induced peroxidation. Mg(2+) increases the rate of peroxidation whereas Ca(2+) inhibits it. 9. Lipid peroxide formation is inhibited strongly by GSH and weakly by cysteine. Ascorbate-induced peroxidation is much more sensitive than NADPH-induced peroxidation. 10. Peroxidation is strongly inhibited by addition of low concentrations (0.01-0.1mm) of cytochrome c or of haemoglobin. 11. It is considered that lipid peroxide formation occurs as a result of the operation of the microsomal electron-transport chain switching from hydroxylation to oxidize unsaturated lipids of the endoplasmic reticulum.
摘要
  1. 肝微粒体与抗坏血酸或NADPH一起温育时会形成脂质过氧化物,但与NADH一起温育时则不会。将抗坏血酸浓度提高到超过最佳浓度(0.5mM)会降低脂质过氧化物的形成速率,但NADPH不存在这种效应。其他还原剂如对苯二胺或铁氰化物不能替代抗坏血酸并诱导脂质过氧化物的形成。2. 抗坏血酸诱导的过氧化速率在pH6.0时最佳,而NADPH系统的速率在pH7.0时最佳。两个系统都需要磷酸盐以达到最大活性。3. 在非常稀的微粒体悬浮液(0.15mg蛋白质/ml)中,脂质过氧化物以最大比速率形成。4. 用脱氧胆酸盐和其他去污剂处理微粒体会导致膜崩解并抑制脂质过氧化物的形成。5. 脂质过氧化物的形成伴随着氧气的快速摄取,并且在过氧化物法中每测量一分子丙二醛就有大量过量的氧气被利用。6. 煮沸的微粒体在有抗坏血酸存在时会形成脂质过氧化物,但添加NADPH时则不会。7. NADPH诱导的脂质过氧化物形成受到对氯汞苯甲酸的强烈抑制,受到N - 乙基马来酰亚胺的弱抑制,而不受碘乙酰胺的影响。未处理的微粒体中抗坏血酸诱导的过氧化不受对氯汞苯甲酸的影响,但使用煮沸的微粒体时会受到抑制。这些实验可以基于铁氧还蛋白型蛋白质是NADPH诱导脂质过氧化物形成系统的一部分这一观点来解释。8. 除了能激活的无机铁(Fe(2+)或Fe(3+))外,大多数重金属离子都会抑制抗坏血酸诱导的和NADPH诱导的过氧化。Mg(2+)会增加过氧化速率,而Ca(2+)会抑制它。9. 脂质过氧化物的形成受到谷胱甘肽的强烈抑制和半胱氨酸的弱抑制。抗坏血酸诱导的过氧化比NADPH诱导的过氧化更敏感。10. 添加低浓度(0.01 - 0.1mM)的细胞色素c或血红蛋白会强烈抑制过氧化。11. 据认为,脂质过氧化物的形成是微粒体电子传递链从羟基化转变为氧化内质网不饱和脂质的结果。

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