Dynamics of pathomorphological changes of ultrastructural organization of intervertebral disc at different terms of experimental opioid influence and with its cancellation

M. Pankiv, Z. Z. Masna, I. Chelpanova, O. Dudok, M. Kovalska
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Abstract

Background. Patients with degenerative diseases of the spine - "difficult patients". Often, exhausted by long-term pain, they have a dependence, and sometimes tolerance to various analgesics, which greatly reduces the effectiveness of routinely used in the hospital anesthesia. Objective. The aim of our work was to study the features of pathomorphological manifestations of the structural components of the intervertebral disc at different terms of opioid influence and at the difference at the ultrastructural level in the experiment. Methods. The material of the study were sexually mature, white, nonlinear rats - males in the amount of 90 hundred animals, weighing 92 - 103 g, aged 4.5 months. Animals were injected with Nalbuphine at home, once daily for one day (10-11 am) for 42 days. The initial dose of Nalbuphine was 8 mg / kg during the first week, 15 mg / kg during the second week; 20 mg / kg during the third week; 25 mg / kg during the fourth week; 30 mg / kg during the fifth week and 35 mg / kg during the sixth week of the experimental opioid effect. Thus created the conditions for chronic opioid exposure. Intervertebral discs of rats were used as material for ultrastructural study. Results and conclusion. As a result of our study, we found that at the end of 21 days we found the progression of alternative changes in the cellular elements of the gelatinous nucleus, characterized by the development of necrotic changes in notochondral cells, as well as chondroptosis of chondrocytes. Preserved notochondral cells were rarely visualized. In some places, there were notochondral cells in which the nucleus disintegrated into separate fragments filled with heterochromatin, and the remains of organelle membranes were localized in the enlightened cytoplasm. Pronounced destructive changes were found in chondrocytes. After 28 days, the changes progressed, this was manifested by the fact that in the pulpal nucleus there were extensive cell-free zones filled with a significant amount of granular intensely osmophilic mass. Notochondral cells and most chondrocytes underwent necrotic changes. After 35 days at the ultrastructural level revealed pronounced changes in the structural elements of the gelatinous nucleus and fibrous ring. Extensive cell-free zones were localized in the gelatinous nucleus, with a somewhat compacted matrix in which an intensely osmophilic fine-grained deep mass accumulated. With the abolition of opioid exposure at the end of 56 days, we found pronounced changes in notochondral cells and in the vast majority of chondrocytes. The matrix of the gelatinous nucleus was compacted, it showed thickened collagen fibrils. Most of the cellular elements of the gelatinous nucleus were at different stages of necrosis, and some chondrocytes - chondroptosis. Vacuoles filled with enlightened contents also appeared in the cytoplasm. The nucleus was compacted, condensation of chromatin was observed. In such areas, the fibrils of collagen fibers were loose, stratified, disintegrated and lysed.
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实验性阿片类药物影响及其消除不同时期椎间盘超微结构组织病理形态学变化的动态
背景。脊柱退行性疾病患者——“难治患者”。通常,由于长期疼痛的疲惫,他们对各种镇痛药产生依赖,有时甚至耐受,这大大降低了医院常规使用麻醉的有效性。目标。我们的工作目的是在实验中研究阿片类药物影响不同条件下椎间盘结构成分的病理形态学表现特征和超微结构水平的差异。方法。该研究的材料是性成熟的白色非线性大鼠——雄性动物数量为9000只,体重为92 - 103克,年龄为4.5个月。动物在家注射纳布芬,每天1次,连续1天(上午10-11点),共42天。第一周纳布啡初始剂量为8mg / kg,第二周为15mg / kg;第三周20 mg / kg;第四周25 mg / kg;在实验阿片类药物效应的第5周和第6周分别为30 mg / kg和35 mg / kg。从而创造了慢性阿片类药物暴露的条件。以大鼠椎间盘为材料进行超微结构研究。结果与结论。在我们的研究中,我们发现在21天结束时,我们发现凝胶核的细胞成分发生了变化,其特征是无软骨细胞的坏死变化,以及软骨细胞的软骨病。保存完好的软骨细胞很少可见。在某些地方,有非软骨细胞,其中细胞核分裂成充满异染色质的碎片,细胞器膜的残留物定位在启蒙的细胞质中。软骨细胞有明显的破坏性改变。28天后,这种变化进一步发展,表现为髓核内有广泛的无细胞区,充满大量的颗粒状强渗透性团块。软骨细胞和大部分软骨细胞发生坏死改变。35天后,超微结构水平显示凝胶核和纤维环的结构成分发生了明显变化。广泛的无细胞区位于胶状细胞核内,基质有点压实,其中积聚了强烈的亲渗透细粒深团块。在56天结束时停止阿片类药物暴露,我们发现notochondral细胞和绝大多数软骨细胞发生了明显变化。胶质核基质致密,胶原原纤维增厚。胶质核的大部分细胞成分处于不同阶段的坏死,部分软骨细胞-软骨萎缩。细胞质中还可见充满启迪内容物的空泡。细胞核被压缩,染色质被凝结。在这些区域,胶原纤维的原纤维松散,分层,解体和裂解。
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