Factors of inflammatory, adhesiveness and thrombosis in acute lower limb ischemia and dexamethasone therapy

I. D. Magamedov, L. Pivovarova, S. P. Nokhrin, V. Soroka, O. Ariskina, I. V. Osipova, I. M. Radjabov, K. Fomin, S. L. Potskhor-ogly, L. V. Kolichenko, E. Markelova, O. Goncharova
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引用次数: 0

Abstract

Lymphocyte-to-platelet adhesion during hypoxia, tissue damage, activation of inflammation and coagulation is associated with expression of ICAM-1 membrane molecules by blood and tissue cells. At the same time, the platelet adhesion receptors determine their adherence to endothelium and recruited lymphocytes. Moreover, the role of platelets in pathogenesis of ischemic cardiovascular diseases comprises their ability to modulate both hemostasis and inflammatory reactions, which are accompanied by secretion of inflammatory mediators and some factors that promote recruitment of leukocytes to tissue damage sites. Creatine kinase activity is a sensitive marker of tissue damage and tissue ischemia. The purpose of the present study was to assess the effect of anti-inflammatory therapy with dexamethasone upon the intensity of inflammation and adhesive properties of lymphocytes, number of platelets in peripheral blood of the patients with acute lower limb ischemia (ALLI), as well as to evaluate the effectiveness of treatment. To study the effect of anti-inflammatory therapy, a group of 32 patients treated with dexamethasone was selected; the control group was represented by 71 patients with basic therapy, the comparison group consisted of 15 volunteers. After revascularization, all patients received antiplatelet and anticoagulant therapy. Dexamethasone infusions were carried out as a course of 4 to 6 days after reconstructive surgery. In all patients, the content of C-reactive protein in blood, the activity of creatine kinase, the content of platelets and, especially, of enlarged platelets were determined. The numbers of lymphocytes expressing ICAM-1 (CD54+) adhesion molecules were counted using immunocytochemical technique. The studies were performed before surgery and 1, 3, 5, 7, 10 days after surgery. During exacerbation of the limb ischemia and damage to endothelium, the accumulation of cytolysis products was noted. Expression of adhesion molecules was increased both on endotheliocytes and on inflammation effector cells, i.e., leukocytes and platelets. The adhesion molecules transmit the activating signal inside the cell, thus promoting adhesion of leukocytes and platelets to endothelium, lymphocytic-platelet adhesion, formation of parietal thrombi, and possible occlusion of damaged vessels. Increased expression of adhesion molecules is associated with activation of metabolism, inflammation, coagulation and oxidative stress. It may stimulate all hematopoietic lineages, including platelets. The involvement level of cellular reactions in pathogenesis of the disease affects effectiveness and duration of treatment, risk of recurrent thrombosis and lethal outcome. Anti-inflammatory therapy with dexamethasone contributed to earlier remission, it was associated with lower frequency of infectious and thrombotic complications, decreased mortality, and reduced duration of treatment. Inflammation, adhesiveness of effector cells and thrombosis are important factors in pathogenesis of acute lower limb ischemia. Additional anti-inflammatory therapy with dexamethasone contributes to earlier remission, decreased proportion of infectious and thrombotic complications, lower frequency of deaths, and reduced duration of treatment.
急性下肢缺血与地塞米松治疗的炎症、粘连和血栓形成因素
在缺氧、组织损伤、炎症激活和凝血过程中,淋巴细胞与血小板的粘附与血液和组织细胞表达ICAM-1膜分子有关。同时,血小板粘附受体决定其对内皮和募集淋巴细胞的粘附。此外,血小板在缺血性心血管疾病发病机制中的作用包括其调节止血和炎症反应的能力,这些反应伴随着炎症介质的分泌和一些促进白细胞向组织损伤部位募集的因子。肌酸激酶活性是组织损伤和组织缺血的敏感标志。本研究旨在评价地塞米松抗炎治疗对急性下肢缺血(ALLI)患者外周血淋巴细胞的炎症强度、黏附特性、血小板数量的影响,并评价其治疗效果。为了研究抗炎治疗的效果,选择32例接受地塞米松治疗的患者;对照组71例患者接受基础治疗,对照组15例患者接受基础治疗。血运重建术后,所有患者均接受抗血小板和抗凝治疗。重建术后4 ~ 6天进行地塞米松输注。在所有患者中,测定血液中c反应蛋白的含量、肌酸激酶的活性、血小板的含量,特别是扩大的血小板的含量。采用免疫细胞化学技术计数表达ICAM-1 (CD54+)粘附分子的淋巴细胞数量。研究分别于术前、术后1、3、5、7、10天进行。在肢体缺血加剧和内皮损伤期间,细胞溶解产物的积累被注意到。粘附分子在内皮细胞和炎症效应细胞(即白细胞和血小板)上的表达均增加。粘附分子在细胞内传递激活信号,从而促进白细胞和血小板粘附内皮,淋巴细胞-血小板粘附,形成壁血栓,并可能阻塞受损血管。黏附分子表达的增加与代谢、炎症、凝血和氧化应激的激活有关。它可以刺激所有的造血系统,包括血小板。细胞反应在疾病发病机制中的参与程度影响治疗的有效性和持续时间、血栓复发的风险和致死结果。地塞米松抗炎治疗有助于早期缓解,感染和血栓并发症的发生率较低,死亡率降低,治疗时间缩短。炎症反应、效应细胞粘附和血栓形成是急性下肢缺血发病的重要因素。额外的地塞米松抗炎治疗有助于早期缓解,减少感染和血栓并发症的比例,降低死亡频率,缩短治疗时间。
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