Correction of neurodegenerative retinal damage with dimethylaminoethanol derivatives

A. Pobeda
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Abstract

Glaucoma occupies a leading place among the pathologies of the eye, leading to irreversible consequences. Many researchers assign glutamate excitotoxicity a key role in retinal neurodegeneration. This allows us to consider the model of NMDA-induced retinal degeneration as one of the main ones in experimental studies aimed at studying the neuroprotective properties of compounds. We have studied the pharmacological activity of dimethylaminoethanol derivatives in the model of NMDA-induced retinal excitotoxicity. 7 days after the modeling of the pathology, ophthalmoscopic changes in the fundus and the level of microcirculation were assessed. According to the results of the study, it was found that the compound under the laboratory code DMAE 10-19 had the highest activity. The introduction of the compound provided an improvement in the picture of the fundus by 24.4 %, relative to the group with a pathology model, which is a significant difference (p < 0.05). And also there was an increase in the level of microcirculation in the retina, up to 625.4 p.u., which is 37.6 % higher than in the group with the pathology model (p < 0.05). Thus, it was found that the compound under the laboratory code DMAE 10-19 has the highest pharmacological activity, which is characterized by an improvement in the fundus picture and an increase in the level of microcirculation in the retina. Keywords: dimethylaminoethanol derivatives, NMDA, excitotoxicity, retina, rats, the level of microcirculation, ophthalmoscopy
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二甲氨基乙醇衍生物矫正视网膜神经退行性损伤
青光眼在眼部疾病中占主导地位,导致不可逆转的后果。许多研究者认为谷氨酸兴奋性毒性在视网膜神经变性中起关键作用。这使得我们可以考虑将nmda诱导的视网膜变性模型作为研究化合物神经保护特性的实验研究的主要模型之一。我们研究了二甲氨基乙醇衍生物在nmda诱导视网膜兴奋性毒性模型中的药理活性。病理造模7 d后,观察眼底变化及微循环水平。根据研究结果,发现实验室代码为DMAE 10-19的化合物具有最高的活性。与病理模型组相比,该化合物的引入使眼底图像改善24.4%,差异有统计学意义(p < 0.05)。视网膜微循环水平升高,达625.4 p.u,比病理模型组高37.6% (p < 0.05)。因此,我们发现实验室代码为DMAE 10-19的化合物具有最高的药理活性,其特征是改善眼底图像和增加视网膜微循环水平。关键词:二甲氨基乙醇衍生物,NMDA,兴奋毒性,视网膜,大鼠,微循环水平,检眼镜
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