Oxidative stress in the molecular mechanism of pathogenesis at different diseased states of organism in clinics and experiment.

Konstantin G Karageuzyan
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Data of publications represented testify exceptional efficiency of sodium thiosulfate (STS) as a powerful synergist for endogenous factors of antioxidant effect, particularly alpha-tocopherol (alpha-T), which is the main component for the system of cell antiradical defence. Detoxicating effect of STS can be demonstrated indeed on the example of zearalenon intoxication during the first two hours with the reduction of metabolism disturbances of PL and products of its peroxidation. Comparative evaluation of molecular mechanisms of STS normalizing effect as a supplier for hydrogen and sulphur ions, as well as an effective synergist for alpha-T on the level of various formations of the live cell in compare with the effects of alpha-T and ubiquinone, allowed to make a special accent on the role of STS in interaction with energy-dependent enzymatic systems of cell antiradical defence, as well as accumulation and transformation of energy on the level of mitochondrial membranes. 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引用次数: 35

Abstract

According to modern images and results of our observations the oxidative stress (OS) is a non-specific though certain component of pathogenesis at numerous diseased states of organism having in the basis the thoroughness of pathogenic disturbances of phospholipids (PL) metabolism and processes of their free radical oxidation (FRO), which takes place in the membrane formations of as the whole cell, as well as the mitochondrial and microsomal fractions (MCF and MSF) of the white rat brain, liver mitochondria, lung shadows, at the same time erythrocyte and lymphocyte shadows at brain acute edema, ischemia, reperfusion and desympathization, infarction of myocardium, tuberculosis of lungs, diabetes, Familial Mediterranean Fever (FMF), intoxications under halothane anaesthesia (HA) and with micotoxin zearalenon. The regularities observed promote to understand from the point of view of modern approaches the molecular mechanisms of initiation, development and generalization of factors for OS formation under pathologic conditions. It is more obvious at zearalenon intoxication with intensification of lipids FRO processes and failures in PL-PL ratio phenomena. The lymphocytes membranes of the white rats spleen subjected OS induced by zearalenon intoxication permit us conclude that the general immune status of the organism decreases. It is generally peculiar to the states under conditions of generalized intoxication. The observed increase of phospholipase A(2) activity induces the release of high concentrations of lysophosphatidylcholines (LPC) and non-etherified fatty acids (NEFA) of polyenic range with prevail of arachidonic acid as a pathogenic factor, namely, at modelling brain acute edema by tetraethylolovo to white rats. Formation of the above mentioned disturbances to some extent depends on hydrophobic properties of toxins, particularly, zearalenon. The latter gives certain tropism to dopamine-beta-monooxygenase (DBM), and ability to stimulate functional activity of the enzyme. Striking haemolytic properties of phospholipase A(2) induced by existence of LPC and NEFA high concentrations, and products of their peroxidation, promote elimination of separate protein fractions of erythrocyte membranes (EM) responsible for OS formation and decrease of erythrocytes resistance to peroxide hemolysis. Increase of DBM activity under the effect of relatively moderate doses of zearalenon (1-15 microg/ml) is accompanied with extra intensification of catecholamine synthesizing function of the organism with lethal result. Data of publications represented testify exceptional efficiency of sodium thiosulfate (STS) as a powerful synergist for endogenous factors of antioxidant effect, particularly alpha-tocopherol (alpha-T), which is the main component for the system of cell antiradical defence. Detoxicating effect of STS can be demonstrated indeed on the example of zearalenon intoxication during the first two hours with the reduction of metabolism disturbances of PL and products of its peroxidation. Comparative evaluation of molecular mechanisms of STS normalizing effect as a supplier for hydrogen and sulphur ions, as well as an effective synergist for alpha-T on the level of various formations of the live cell in compare with the effects of alpha-T and ubiquinone, allowed to make a special accent on the role of STS in interaction with energy-dependent enzymatic systems of cell antiradical defence, as well as accumulation and transformation of energy on the level of mitochondrial membranes. The results obtained by us confirm a number of clinical experimental observations, which demonstrate treatment and prophylactic role of STS at different pathologic states of the organism. STS protectory role at toxic injuries of the organism is higher at its preliminary introduction to the organism before modelling of the studied diseased states, especially at zearalenon and halothane (H) intoxication (in the last case before HA). These data serve a sound affirmation for protectory function of STS, detailed revelation of molecular properties of pathogenesis of the studied intoxication to which a part of our clinical and experimental studies at present is devoted.

氧化应激在机体不同病变状态下的分子发病机制的临床及实验研究。
根据现代图像和我们的观察结果,氧化应激(OS)是一种非特异性的,但在许多生物体患病状态下的发病机制的某些组成部分,基于对磷脂(PL)代谢及其自由基氧化(FRO)过程的致病性干扰的彻彻性,这发生在整个细胞的膜形成中,以及线粒体和微粒体部分(MCF和MSF)。肝线粒体、肺影,同时在脑急性水肿、缺血、再灌注和去交感、心肌梗死、肺结核、糖尿病、家族性地中海热(FMF)、氟烷麻醉(HA)中毒和微毒素赤霉烯酸中毒时出现红细胞和淋巴细胞影。观察到的规律有助于从现代方法的角度理解病理条件下OS形成因素的发生、发展和推广的分子机制。在玉米霉烯酸中毒时,随着脂质FRO过程的加剧和PL-PL比现象的失效,这种现象更为明显。玉米赤霉烯酸中毒引起的大鼠脾脏淋巴细胞膜使我们得出结论,机体的总体免疫状态下降。它通常是在全身性中毒的情况下所特有的。所观察到的磷脂酶A(2)活性的增加诱导高浓度溶血磷脂酰胆碱(LPC)和非醚化脂肪酸(NEFA)的释放,以花生四烯酸为致病因子,即四乙基olovo模拟大鼠脑急性水肿。上述干扰的形成在一定程度上取决于毒素的疏水性,特别是赤霉烯酸。后者使多巴胺- β -单加氧酶(DBM)具有一定的趋向性,并能刺激该酶的功能活性。高浓度LPC和NEFA及其过氧化产物诱导的磷脂酶A(2)具有显著的溶血特性,促进了红细胞膜(EM)中负责OS形成的分离蛋白组分的消除,并降低了红细胞对过氧化溶血的抵抗力。相对中等剂量(1 ~ 15 μ g/ml)的玉米赤霉烯酸作用下,DBM活性增加,机体儿茶酚胺合成功能额外增强,具有致死作用。发表的数据表明,硫代硫酸钠(STS)作为内源性抗氧化因子的强大增效剂,特别是α -生育酚(α -t),它是细胞抗自由基防御系统的主要成分,具有卓越的效率。STS的解毒作用确实可以通过前两个小时的赤霉烯酸中毒的例子来证明,因为它减少了PL及其过氧化产物的代谢紊乱。与α - t和泛素的作用相比,STS作为氢和硫离子的供应商,以及在活细胞的各种形态水平上作为α - t的有效增效剂的分子机制的比较评估,允许特别强调STS在与细胞抗自由基防御的能量依赖性酶系统相互作用中的作用。以及线粒体膜水平上能量的积累和转化。我们得到的结果证实了一些临床实验观察,证明了STS在生物体不同病理状态下的治疗和预防作用。在对所研究的病变状态进行建模之前,STS对生物体毒性损伤的保护作用更高,特别是在过氧化氢和氟化烷(H)中毒(在HA之前的最后一个病例中)。这些数据充分肯定了STS的保护作用,详细揭示了我们目前部分临床和实验研究所研究的中毒发病机制的分子特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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