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前列腺素生物合成中过氧化物引发的自由基机制的证据。

Evidence for a peroxide-initiated free radical mechanism of prostaglandin biosynthesis.

作者信息

Hemler M E, Lands W E

出版信息

J Biol Chem. 1980 Jul 10;255(13):6253-61.

PMID:6771268
Abstract

High levels of NaCN (20 to 250 mM) were required to inhibit cyclooxygenase catalysis and cause extended lag periods (up to 1.6 min), whereas CO failed to inhibit catalysis. This NaCN inhibition was easily overcome by endogenous or exogenous hydroperoxides. Added hydroperoxides acted to eliminate lag periods without undergoing net conversion to other chemical species. In addition, experiments with glutathione peroxidase inhibition showed that hydroperoxides were essential not only in the early phases, but throughout catalysis. In spectrophotometric experiments, NaCN formed a complex with ferriheme cyclooxygenase (Kd = 1.3 mM) and inhibited hydroperoxide interaction with this form of the enzyme. Phenolic antioxidants, only slightly extended lag periods while inhibiting oxygenation rates more than 50%. Low levels of phenol (which is normally stimulatory) or alpha-naphthol when combined with NaCN or glutathione peroxidase (agents which interfere with peroxide activation) resulted in potent synergistic inhibition with long lag times. A mechanism consistent with all of the above properties of cyclooxygenase has been elucidated, Further mechanistic explanation was sought for reaction-catalyzed self-inactivation of cyclooxygenase. This phenomenon could not be explained simply by heme lability, or cyclooxygenase sensitivity to destruction by ambient hydroperoxides, Rather, it appears to involve a destructive reaction intermediate intrinsic to involve a destructive reaction intermediate intrinsic to the cyclooxygenase mechanism.

摘要

需要高浓度的氰化钠(20至250 mM)来抑制环氧化酶催化并导致延长的延迟期(长达1.6分钟),而一氧化碳未能抑制催化作用。这种氰化钠抑制作用很容易被内源性或外源性氢过氧化物克服。添加的氢过氧化物可消除延迟期,而不会净转化为其他化学物质。此外,谷胱甘肽过氧化物酶抑制实验表明,氢过氧化物不仅在早期阶段,而且在整个催化过程中都是必不可少的。在分光光度实验中,氰化钠与高铁血红素环氧化酶形成复合物(解离常数Kd = 1.3 mM),并抑制氢过氧化物与这种形式的酶相互作用。酚类抗氧化剂仅略微延长延迟期,同时抑制氧化速率超过50%。低水平的苯酚(通常具有刺激作用)或α-萘酚与氰化钠或谷胱甘肽过氧化物酶(干扰过氧化物活化的试剂)结合时,会导致具有长延迟时间的强效协同抑制作用。已经阐明了一种与环氧化酶上述所有特性一致的机制,进一步寻求对环氧化酶反应催化的自我失活的机制解释。这种现象不能简单地用血红素不稳定性或环氧化酶对环境氢过氧化物破坏的敏感性来解释,相反,它似乎涉及环氧化酶机制固有的一种破坏性反应中间体。

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