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[髓过氧化物酶作为心肌氧化损伤的一个因素:二氢硫辛酰胺脱氢酶的失活]

[Myeloperoxidase as a factor of oxidative damage of the myocardium: inactivation of dihydrolipoamide dehydrogenase].

作者信息

Gutiérrez Correa J, Stoppani A O

机构信息

Centro de Investigaciones Bioenergéticas, Facultad de Medicina (UBA-CONICET), Universidad de Buenos Aires, Argentina.

出版信息

Medicina (B Aires). 1998;58(2):171-8.

PMID:9706251
Abstract

Myocardial dihydrolipoamide dehydrogenase (LADH) is inactivated after incubation at 30 degree C, with myeloperoxidase (MPO)-dependent systems. The enzyme inactivation was a function of the pro-oxidant system composition and the time of incubation. The standard inactivating system contained 50 mM KH2PO4-K2HPO44, pH 7.4, 0.5-1.0 muM LADH, and pro-oxidant system. After 30 or 60 min of incubation with the MPO/H2O2/NaCl system, LADH inactivation was 64 and 87%, respectively (Figure 1). In the absence of NaCl, inactivation values were 9 and 27%, respectively, whereas in the absence of MPO the inactivation values were 4.0 and 11%, respectively (Figure 1). Under similar experimental conditions, sodium hypochlorite significantly inactivated LADH, thus supporting the role of hipochlorous acid as agent of the MPO/H2O2/CINa system. With the MPO/H2O2/Kl, MPO/H2O2/SCN or the MPO/H2O2/NaNO2 systems LADH inactivation depended on the anion nature, 1-being the most effective (Figure 2). NaNo2 effectively replaced halides as pro-oxidant (Figure 3). The MPO/NADH/halide systems, where NADH replaced H2O2, also inactivated LADH. Native (not denatured) catalase completely prevented the MPO/NADH/Kl system effect (Table 1), in close agreement with H2O2 production by the LADH-catalysed NADH oxidation and the role of H2O2 in LADH inactivation. LADH was also inactivated after incubation with MPO-generated free radicals such as the Chloropromazine and Paracetamol radicals (Table 2). Thiol compounds (Captopril, penicillamine, cysteine, N-acetylcysteine and mercaptopropionylglycine) (Table 3 and Figure 4), as well as taurine, ascorbate (Table 4), GSSG and trypanothione (Figure 5), protected LADH against the MPO-dependent oxidizing systems, and also against NaCIO (Table 4). The summarized observations are discussed in relation to MPO function in free radical production and pathologies such as ischemia-reperfusion injury and inflammation.

摘要

心肌二氢硫辛酰胺脱氢酶(LADH)在30℃下与髓过氧化物酶(MPO)依赖性系统孵育后会失活。酶失活是促氧化系统组成和孵育时间的函数。标准失活系统包含50 mM KH2PO4-K2HPO44,pH 7.4,0.5-1.0 μM LADH和促氧化系统。与MPO/H2O2/NaCl系统孵育30或60分钟后,LADH失活率分别为64%和87%(图1)。在没有NaCl的情况下,失活值分别为9%和27%,而在没有MPO的情况下,失活值分别为4.0%和11%(图1)。在类似的实验条件下,次氯酸钠显著使LADH失活,从而支持次氯酸作为MPO/H2O2/NaCl系统的作用因子。对于MPO/H2O2/KI、MPO/H2O2/SCN或MPO/H2O2/NaNO2系统,LADH失活取决于阴离子的性质,I-是最有效的(图2)。NaNO2有效地替代卤化物作为促氧化剂(图3)。MPO/NADH/卤化物系统中,NADH替代了H2O2,也使LADH失活。天然(未变性)过氧化氢酶完全阻止了MPO/NADH/KI系统的作用(表1),这与LADH催化的NADH氧化产生H2O2以及H2O2在LADH失活中的作用密切相关。LADH与MPO产生的自由基如氯丙嗪和对乙酰氨基酚自由基孵育后也会失活(表2)。硫醇化合物(卡托普利、青霉胺、半胱氨酸、N-乙酰半胱氨酸和巯基丙酰甘氨酸)(表3和图4)以及牛磺酸、抗坏血酸(表4)、谷胱甘肽二硫化物和锥虫硫醇(图5)可保护LADH免受MPO依赖性氧化系统以及NaClO的影响(表4)。结合MPO在自由基产生以及诸如缺血再灌注损伤和炎症等病理过程中的作用,对总结的观察结果进行了讨论。

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