新型gaba和谷氨酸衍生物对慢性酒精中毒大鼠心肌形态的影响

A. Nesterova, I. I. Prokofiev, V. Perfilova, O. Y. Evsyukov, M. V. Kustova, I. Tyurenkov
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摘要

的目标。目的研究新型谷氨酸衍生物glufimet (compound RSPU-238)和新型γ -氨基丁酸(GABA)衍生物(compound RSPU-260)对慢性酒精中毒(CAI)大鼠心肌的病理组织学改变。材料和方法。实验以10月龄雌性Wistar大鼠为实验对象。将大鼠分为以下组:1组为完整雌性;第2组为对照组,采用10%乙醇溶液代替饮用水进行CAI模拟,持续24周;第3组和第4组为实验组,雌性小鼠在停止饮用酒精溶液后,每天1次腹腔注射剂量为28.7 mg / kg的格菲美特和剂量为25 mg / kg的RSPU260,持续14天;第5组:一组动物按照与所研究化合物类似的治疗方案,以50mg / kg的剂量服用参考药物米屈酸钠。光镜下观察左心室心肌显微结构和形态学参数的变化。心肌细胞体积分数降低,而间质和血管体积分数升高。心肌细胞变性,如波状变形、横纹丧失、质溶解灶和肌纤维断裂。大鼠经格菲美特治疗后,心肌细胞的结构变化很小。观察到下肢血管过多;血管呈单一瘀血、淤血特征。心肌细胞体积分数比对照组大9.7%,而间质和血管体积分数分别比对照组小66.0和70.0%。用RSPU-260化合物处理的动物心肌细胞和小血管没有明显的退行性变化,类似于注射了glufimet的实验动物。米屈酸钠的心脏保护作用不那么明显。与对照组大鼠相比,给予模拟慢性酒精中毒动物新的GABA和谷氨酸衍生物可改善心肌细胞的微结构。这表明所研究的神经活性氨基酸衍生物具有明显的心脏保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Morphological changes in the myocardium of rats with chronic alcohol intoxication after treatment with new GABAand glutamic acid derivatives
Aim. To study pathohistological changes in the myocardium of rats with chronic alcohol intoxication (CAI) after treatment with a new glutamic acid derivative glufimet (compound RSPU-238) and a new gamma-aminobutyric acid (GABA) derivative (compound RSPU-260).Materials and methods. Experiments were performed on female Wistar rats aged 10 months. The rats were divided into the following groups: group 1 – intact females; group 2 – a control group which included animals after CAI simulated by replacing drinking water with 10% ethanol solution for 24 weeks; groups 3 and 4 – experimental groups, in which females were intraperitoneally administered with glufimet at a dose of 28.7 mg / kg and RSPU260 at a dose of 25 mg / kg once a day for 14 days after cessation of alcohol solution consumption; group 5 – a group of animals receiving a reference listed drug mildronate at a dose of 50 mg / kg according to a regimen similar to that of the studied compounds. Changes in microstructural and morphometric parameters of the left ventricular myocardium were assessed using light microscopy.Results. In animals after CAI, the cardiomyocyte volume fraction decreased, while the interstitial and vascular volume fractions increased. Degeneration of cardiomyocytes, such as their wave-like deformation, loss of transverse striation, foci of plasmolysis, and fragmentation of muscle fibers were revealed. In rats treated with glufimet, the structural changes in cardiomyocytes were minimal. Lower vascular plethora was observed; blood vessels were characterized by single stasis and sludge. The cardiomyocyte volume fraction was 9.7% greater than in control animals, while the interstitial and vascular volume fractions were 66.0 and 70.0% smaller, respectively. The animals treated with the RSPU-260 compound had no significant degenerative changes in cardiomyocytes and small vessels similar to the experimental animals injected with glufimet. Mildronate had a less pronounced cardioprotective effect.Conclusion. Administration of new GABA and glutamic acid derivatives to animals with simulated chronic alcohol intoxication leads to improvement of the microstructure in cardiomyocytes compared with control rats. This indicates pronounced cardioprotective effects of the studied neuroactive amino acid derivatives.
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