ENDOTHELIAL DYSFUNCTION UNDER EXPERIMENTAL SUBARACHNOID HEMORRHAGE. POSSIBLE WAYS OF PHARMACOCORRECTION

O. Polkovnikov, S. Pavlov, I. Belenichev, N. Matolinets
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Motor and exploratory activity determination was carried out following SAH with the “Open Field” technique. Determination of biochemical markers of endothelial dysfunction was performed in a rat brain homogenate. Results and discussion. It was found that modeling of subarachnoid hemorrhage (SAH) led to the oxidative stress development development and the product of oxidative modification of proteins (nitrotyrosine (Ntz) on the 4th and especially on the 7th day of the experiment) increase in the brain tissues. Starting from the 4th day, we registered a compensatory increase in the activity of NO-synthase (NOS) - by 56%, followed by a decrease in its activity on the 7th day, by more than 33% against the intact group of animals. It was registered a compensatory increase in VEGF-A in rats with SAH modeling on the 4th day of the experiment and its further decrease on the 7th day. The established pathobiochemical changes in the brain tissue were accompanied by the cognitive deficit development in experimental animals, especially on the 7th day of the SAH. SAH led to a significant decrease in the total activity of animals by 2.63 times, a decrease in the distance traveled by animals by 1.89 times, the number of freezes increased by 1.86 times and the immobility of animals increased when moving from the periphery to the center and immobility in the center of the arena (anxiety, fear, disorientation), as well as a decrease in the distance traveled and the speed of movement in illuminated center of the arena 2 and 2.6 times, respectively. Experimental therapy with acelysine 15 mg/kg led to the normalization of biochemical indicators of endothelial dysfunction: concentration of nitrotyrosine, starting from the 4th day of the experiment, increased eNOS activity and VEGF-A concentration (by 75% and 64% on 7th day). The administration of namidopine led to less pronounced effects, statistically significant changes occurred only in relation to the VEGF-A concentration. Administration of namidopine resulted in only a slight increase in VEGF-A concentration. Acelysine and nimotope significantly increased the total activity of rats on the 7th day after SAH by 76.3% and 48.8%, respectively. In animals treated with acelysine, anxiety and fear decreased. The animals were less aggressive and more empathic - long-term grooming increased 3 times. The administration of nimotop in rats survived SAH had a less pronounced positive effect on behavior. Nimotop did not effect on indicators of general activity and did not increase the total distance traveled. Animals received nimtop were inactive by the 7th day of treatment. Conclusions: Experimental therapy with acelysine led to the normalization of biochemical parameters of endothelial dysfunction, namely nitrotyrosine concentration, starting from the 4th day of the experiment and increased eNOS activity and VEGF-A concentration. It should be noted that, in contrast to the rats of the control group, under prescription of acelysine, there was an increase in the concentration of eNOS and VEGF-A both on the 4th and 7th days of the experiment. The administration of namidopine led to less pronounced effects, statistically significant changes occurred only in relation to the VEGF-A concentration. The administration of acelysin to animals after SAH had a beneficial effect on the emotional status and behavior of animals, and also led to the normalization of their general activity and orientation-exploratory activity. The mechanism of edotheliotropic effect of acelysine, in our opinion, is associated with its antioxidant effects, modulating impact on endothelial NOS, as well as its property, indirectly, to influence on increase VEGF content. Nimotope therapy had no effect on the emotional status and behavior of the animals. The use of calcium channel blockers revealed such side effects as depression, drowsiness, diplopia, and disorientation","PeriodicalId":140699,"journal":{"name":"Proceedings of the Shevchenko Scientific Society. Medical Sciences","volume":"42 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Shevchenko Scientific Society. 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引用次数: 1

Abstract

Purpose of the article: to study the effect of acelysine and nimodipine on certain endothelial dysfunction indicators and to evaluate their therapeutic efficacy after subarachnoid hemorrhage in rats. Materials and Methods: an experimental study was carried out using 50 Wistar rats of both sexes. Spontaneous subarachnoid hemorrhage was modeled in animals. Three groups of animals were identified: a control group, a group of animals received a standard therapeutic dose of acelysine, and a group received a standard therapeutic dose of nimotop. Each group included 15 animals. There were also 5 intact animals. The animals were withdrawn from the experiment on days 4 and 7 after the motor and exploratory activity determination. Motor and exploratory activity determination was carried out following SAH with the “Open Field” technique. Determination of biochemical markers of endothelial dysfunction was performed in a rat brain homogenate. Results and discussion. It was found that modeling of subarachnoid hemorrhage (SAH) led to the oxidative stress development development and the product of oxidative modification of proteins (nitrotyrosine (Ntz) on the 4th and especially on the 7th day of the experiment) increase in the brain tissues. Starting from the 4th day, we registered a compensatory increase in the activity of NO-synthase (NOS) - by 56%, followed by a decrease in its activity on the 7th day, by more than 33% against the intact group of animals. It was registered a compensatory increase in VEGF-A in rats with SAH modeling on the 4th day of the experiment and its further decrease on the 7th day. The established pathobiochemical changes in the brain tissue were accompanied by the cognitive deficit development in experimental animals, especially on the 7th day of the SAH. SAH led to a significant decrease in the total activity of animals by 2.63 times, a decrease in the distance traveled by animals by 1.89 times, the number of freezes increased by 1.86 times and the immobility of animals increased when moving from the periphery to the center and immobility in the center of the arena (anxiety, fear, disorientation), as well as a decrease in the distance traveled and the speed of movement in illuminated center of the arena 2 and 2.6 times, respectively. Experimental therapy with acelysine 15 mg/kg led to the normalization of biochemical indicators of endothelial dysfunction: concentration of nitrotyrosine, starting from the 4th day of the experiment, increased eNOS activity and VEGF-A concentration (by 75% and 64% on 7th day). The administration of namidopine led to less pronounced effects, statistically significant changes occurred only in relation to the VEGF-A concentration. Administration of namidopine resulted in only a slight increase in VEGF-A concentration. Acelysine and nimotope significantly increased the total activity of rats on the 7th day after SAH by 76.3% and 48.8%, respectively. In animals treated with acelysine, anxiety and fear decreased. The animals were less aggressive and more empathic - long-term grooming increased 3 times. The administration of nimotop in rats survived SAH had a less pronounced positive effect on behavior. Nimotop did not effect on indicators of general activity and did not increase the total distance traveled. Animals received nimtop were inactive by the 7th day of treatment. Conclusions: Experimental therapy with acelysine led to the normalization of biochemical parameters of endothelial dysfunction, namely nitrotyrosine concentration, starting from the 4th day of the experiment and increased eNOS activity and VEGF-A concentration. It should be noted that, in contrast to the rats of the control group, under prescription of acelysine, there was an increase in the concentration of eNOS and VEGF-A both on the 4th and 7th days of the experiment. The administration of namidopine led to less pronounced effects, statistically significant changes occurred only in relation to the VEGF-A concentration. The administration of acelysin to animals after SAH had a beneficial effect on the emotional status and behavior of animals, and also led to the normalization of their general activity and orientation-exploratory activity. The mechanism of edotheliotropic effect of acelysine, in our opinion, is associated with its antioxidant effects, modulating impact on endothelial NOS, as well as its property, indirectly, to influence on increase VEGF content. Nimotope therapy had no effect on the emotional status and behavior of the animals. The use of calcium channel blockers revealed such side effects as depression, drowsiness, diplopia, and disorientation
实验性蛛网膜下腔出血后内皮功能障碍。可能的药物校正方法
本文目的:研究乙酰赖氨酸和尼莫地平对大鼠蛛网膜下腔出血后内皮功能障碍某些指标的影响,评价其治疗效果。材料与方法:采用Wistar大鼠50只,雌雄不限。建立动物自发性蛛网膜下腔出血模型。实验确定了三组动物:对照组,一组接受标准治疗剂量的乙酰赖氨酸,一组接受标准治疗剂量的尼莫托。每组15只。还有5只完整的动物。在进行运动和探索性活动测定后,于第4天和第7天退出实验。在SAH后用“Open Field”技术进行运动和探索性活动测定。在大鼠脑匀浆中测定内皮功能障碍的生化标志物。结果和讨论。结果发现,蛛网膜下腔出血(SAH)模型导致大鼠脑组织氧化应激发展和氧化修饰蛋白产物(硝基酪氨酸(Ntz))在实验第4天,特别是在第7天增加。从第4天开始,我们发现NO-synthase (NOS)的活性代偿性增加了56%,随后在第7天,NO-synthase (NOS)的活性下降了33%以上。SAH模型大鼠VEGF-A在实验第4天代偿性升高,第7天进一步降低。在实验动物中,脑组织病理生化变化伴随着认知缺陷的发展,尤其是在SAH的第7天。SAH导致的总活性明显降低动物的2.63倍,减少动物的距离的1.89倍,冻结的数量增长了1.86倍和静止的动物增加当从边缘到中心和静止中心的舞台(焦虑、恐惧、定向障碍),以及减少照明的距离和速度运动的中心舞台2和2.6倍,分别。以乙酰赖氨酸15 mg/kg作为实验治疗,内皮功能障碍的生化指标恢复正常:硝基酪氨酸浓度从实验第4天开始,eNOS活性和VEGF-A浓度升高(第7天分别增加75%和64%)。服用奈米多平导致的影响不太明显,统计学上显著的变化仅与VEGF-A浓度有关。服用奈米多平只导致VEGF-A浓度轻微升高。乙酰赖氨酸和烟碱能显著提高SAH后第7天大鼠的总活性,分别提高76.3%和48.8%。在用乙酰赖氨酸治疗的动物中,焦虑和恐惧减少了。这些动物的攻击性更低,移情能力更强——长期梳理毛发的次数增加了3倍。在SAH存活的大鼠中给予nimotop对行为的积极影响不太明显。Nimotop对一般活动指标没有影响,也没有增加总行驶距离。给药第7天,nimtop组动物无活动。结论:乙酰赖氨酸实验治疗导致内皮功能障碍生化参数硝基酪氨酸浓度从实验第4天开始正常化,eNOS活性和VEGF-A浓度升高。值得注意的是,与对照组大鼠相比,在乙酰赖氨酸的处方下,在实验第4天和第7天,eNOS和VEGF-A的浓度都有所增加。服用奈米多平导致的影响不太明显,统计学上显著的变化仅与VEGF-A浓度有关。在SAH后给动物注射茜素对动物的情绪状态和行为有有益的影响,也导致动物的一般活动和定向探索活动的正常化。我们认为,乙酰赖氨酸的增脂作用机制与其抗氧化作用、对内皮细胞NOS的调节作用以及间接影响VEGF含量的增加有关。Nimotope治疗对动物的情绪状态和行为没有影响。钙通道阻滞剂的使用显示出诸如抑郁、嗜睡、复视和定向障碍等副作用
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