稳定铯对哺乳动物横纹肌组织(心肌和骨骼肌)影响的生态学和毒理学特征

IF 0.5 Q4 BIOLOGY
O. Yermishev
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引用次数: 0

摘要

最近,辐射危险大大增加。这与对乌克兰发动全面战争以及拥有世界第二大核武库的俄罗斯联邦夺取扎波罗热核电站有关。大多数关于放射性辐射对人体和动物影响的研究绝对没有考虑到载体和化学元素的生态毒性效应。同时,人体并不区分化学元素的放射性同位素和非放射性同位素,并在交换过程中与它们相互作用。这项工作的目的是研究稳定铯对横纹肌组织(包括骨骼肌和心肌)微观结构的影响。我们的研究结果表明,在所有受检器官和组织中,铯都会在 24 天内大量蓄积。事实上,最密集的蓄积过程出现在心脏中,与完整大鼠相比,分别增加了 214.9 倍和 695.3 倍,骨骼肌中的钾含量也同时分别减少了 19.2% 和 29.1%。铯对包括横纹肌在内的组织有两种作用机制:铯是钾的拮抗剂,与钾的运输系统有关;铯是一种有毒元素,会引发过氧化过程,进而改变膜及其钾通道。在横纹肌细胞内铯增加的情况下,可兴奋组织的钾通道在复极化阶段的功能会发生紊乱。这些紊乱可根据获得性 "钾 "通道病的类型进行,在心肌中可表现为心律紊乱、QT 延长综合征等。这将导致受检组织的组织学结构出现严重破坏。铯对骨骼肌和心肌横纹肌组织都有明显的破坏作用,骨骼肌和心肌横纹肌组织的形态变化基本相似。心肌细胞和横纹肌细胞核和细胞质的萎缩性变化、微循环通道中血液循环受损的迹象,以及血管壁水肿的形成、内皮细胞的破坏、各种类型的出血和纤维基质的淋巴组织细胞浸润,这些都是铯对组织产生毒性作用的后果。因此,我们获得的氯化铯作用下横纹肌组织学结构变化的结果表明,稳定铯具有相当高的杀细胞活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ecological and toxicological features of the effect of stable cesium on striated muscle tissue (myocardium and skeletal muscles) of mammals
Recently, the risks of radiation danger have significantly increased. This is connected with the start of a full-scale war against Ukraine and the seizure of the Zaporizhzhya NPP by the Russian Federation, which has the second most powerful arsenal of nuclear weapons in the world. The majority of studies devoted to the effect of radioactive radiation on the human body and animals absolutely do not take into account the ecotoxic effect of the carrier and a chemical element. At the same time, the body does not distinguish between radioactive and non-radioactive isotopes of chemical elements and interacts with them during exchange processes. The aim of the work was to study the influence of stable cesium on the microscopic structure of striated muscle tissue, both skeletal and cardiac ones. The results of our research revealed that intensive accumulation of cesium for 24 days occurred in all the examined organs and tissues. In fact, the most intensive accumulative process appeared to be in the heart by 214.9 times and by 695.3 times with skeletal muscles, with a simultaneous decrease in potassium content by 19.2% and 29.1%, respectively, compared to intact rats. We can talk about the presence of two mechanisms of action of cesium on tissues, including striated muscles: as an antagonist of potassium, which concerns the transport system of the latter and as a toxic element that initiates peroxide processes with subsequent modification of membranes and their potassium channels. Functional disturbances in the work of potassium channels of excitable tissues in the repolarization phase occur in the conditions of an increase in intracellular cesium in striated muscles. These disorders can proceed according to the type of acquired "potassium" channelopathies, which in the myocardium can manifest in the form of rhythm disorders, prolonged QT syndrome, etc. This leads to the appearance of significant violations of the histological structure of the examined tissues. Cesium has pronounced damaging effects on both skeletal and cardiac striated muscle tissue, with morphological changes in skeletal and cardiac striated muscle tissue being generally similar. Dystrophic changes in the nuclei and cytoplasm of cardiomyocytes and striated muscles, signs of impaired blood circulation in the microcirculatory channel with the formation of vascular wall edema, destruction of endothelial cells, various types of hemorrhages and lymphohistiocytic infiltration of the stroma of fibers are the consequences of the toxic effect of cesium on tissues. Thus, the results of changes in the histological structure of striated muscles under the action of cesium chloride obtained by us indicate a fairly high cytocidal activity of stable cesium.
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CiteScore
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