振动影响下心肌结构重塑的机制

O. Levchenkova, V. V. Vorobieva
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引用次数: 0

摘要

本综述介绍了专门研究振动病患者心脏结构变化的文献数据分析,通过超声心动图方法确定了左心室腔同心重塑和舒张功能紊乱的形式,与健康人相比,心脏结构工作强度降低了1.2倍(P0.05)。在各种实验振动模式(频率为 8 赫兹的 7 次和 56 次)背景下,心肌细胞形态计量和生物能参数的变化证实,心腔的空间结构、收缩能力和能量供应潜力之间的理想关系受到了破坏。心肌纤维的损失象征着心肌肥大向失代偿阶段的转化和退化(萎缩)迹象的增加,特别是心肌细胞肌节的损失。在振动介导的血流动力学因素和缺血因素影响下,要实现组织的病理结构(形态)和能量重组过程,就必须让众多调节新陈代谢、增殖、生长和存活的介质参与其中,如细胞、细胞核和细胞膜、如 STIM(基质相互作用分子)、SERCA(肌浆网内的钙 ATP 酶)、IP3R(肌醇-1,4,5-三磷酸受体)、Orai(形成 CRAC 通道的蛋白质)、TRPC(瞬时受体电位)等。心脏结构重塑的最重要环节之一是细胞外基质降解系统,包括基质金属蛋白酶(MMPs)及其组织抑制剂(TIMPs),它们通过与控制心脏营养和可塑性的特定 DNA 区域结合,调节 DNA 基质上 mRNA 的合成速度。通过分析大量事实,可以解释振动病患者心脏重塑的一些发展模式,并确定基于病因的治疗方法的方向,不仅要考虑到药物的振动保护作用,还要考虑到药物抑制和缓解心肌重塑的能力。
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MECHANISMS OF STRUCTURAL MYOCARDIAL REMODELING UNDER THE INFLUENCE OF VIBRATION
The review presents literature data analysis devoted to the study of structural changes in the heart in patients with vibration disease, identified by echocardiographic methods in the form of concentric remodeling of the left ventricle chambers and disturbance of its diastolic function, a decrease in the intensity of the heart structure work compared to healthy ones in 1.2 times (p0.05). The changes in morphometric and bioenergetic parameters of cardiomyocytes against the background of various experimental vibration modes (7 and 56 sessions with a frequency of 8 Hz) confirms the violation of the ideal relationship between the spatial configuration of the heart cavities, the ability to contract and the energy supply potential. The loss of cardiac myofibrils symbolizes the convertion of myocardial hypertrophy to the decompensation stage and the increase in degenerative (dystrophic) signs, in particular the loss of sarcomeres of cardiomyocytes. To realize the processes of pathological structural (morphological) and energy restructuring of tissue under the influence of vibration-mediated hemodynamic and ischemic factors, it is necessary to involve in the process numerous mediators that regulate metabolism, proliferation, growth and survival of cells, such as STIM (stromal interaction molecule), SERCA (calcium ATPase of the endo(sarco)plasmic reticulum), IP3R (inositol-1,4,5-triphosphate receptor), Orai (protein that forms CRAC channels), TRPC (transient receptor potential canonical), etc. As one of the most important link of structural cardiac remodeling is performed by the degradation system of the extracellular matrix, including matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs), which regulate the rate of mRNA synthesis on the DNA matrix by binding to specific DNA regions that control cardiac nutrition and plasticity. A lot of analyzed facts make it possible to explain some patterns of the development of cardiac remodeling in patients with vibration disease and to determine the direction of pathogenetically based approaches to therapy, taking into account not only the vibration-protective effect of drugs, but also their ability to inhibit and regress myocardial remodeling.
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