[琥珀酸乙酯对地塞米松给药过程中老龄大鼠脑部慢性神经炎症参数和塑性过程的影响]。

Q3 Medicine
O L Terekhina, Yu I Kirova
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引用次数: 0

摘要

研究目的研究旨在评估琥珀酸/SUCNR1信号传导对老龄大鼠大脑皮层(CC)糖皮质激素受体(GR)激活的非基因组免疫抑制和基因介导的炎症-退行性作用的潜在调节作用:通过Western印迹分析,我们评估了促炎细胞因子(TNF-α、IL-1β)、抗炎细胞因子(IL-10、TGF-β1)、线粒体生成标志物(PGC-1α、NDUFV2、SDHA、cyt c1、在 18 个月大鼠的 CC 中,分离给予高度特异性 GR 配体地塞米松(1 mg/kg,i.p.,结果表明:地塞米松会导致大鼠CC中琥珀酸拮抗剂的浓度升高,而琥珀酸拮抗剂的浓度升高会导致大鼠CC中琥珀酸拮抗剂的浓度降低:结果:地塞米松导致 18 月龄大鼠 CC 中所有可检测到的参数含量下降,包括抗炎 IL-10、TGF-β1、PGC-1α、VEGF、BDNF、这与有关 GR 转抑关键促炎因子(NFkB、AP1、STAT1)、抗炎因子(PPARγ、ERRα)、促合成代谢转录因子(雌激素、雄激素受体)的文献数据一致。每天在注射地塞米松一小时后服用美西多不会影响地塞米松对促炎细胞因子的抑制作用,但会增加抗炎细胞因子、线粒体、血管和突触生成蛋白标志物的表达水平:该研究首次证明了在衰老机体中联合使用地塞米松和美西多的前景和病理基础,其目的是最大限度地减少旨在抑制促合成代谢程序和炎症消解机制的 GC 活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The effect of ethylmethylhydroxypyridine succinate on the parameters of chronic neuroinflammation and plastic processes in the brain of old rats during course of dexamethasone administration].

Objective: To study was to evaluate the potential modulatory impact of succinate/SUCNR1 signaling on the non-genomic immunosuppressive and gene-mediated inflammatory-degenerative effects of glucocorticoid receptor (GR) activation in the cerebral cortex (CC) of aging rats.

Material and methods: Using Western blot analysis, we assessed the expression level of pro-inflammatory (TNF-α, IL-1β), anti-inflammatory cytokines (IL-10, TGF-β1), mitochondriogenesis markers (PGC-1α, NDUFV2, SDHA, cyt c1, COX2, ATP5A), angiogenesis marker VEGF, neurotrophin BDNF, GR, succinate receptor SUCNR1 in the CC of 18-month-old rats with isolated administration of the highly specific GR ligand dexamethasone (1 mg/kg, i.p., daily, 10 days) and its combined administration with the succinate-containing drug Mexidol (100 mg/kg, i.p., daily, 10 days).

Results: Dexamethasone caused a decrease in the content of all detectable parameters in the CC of 18-month-old rats, including anti-inflammatory IL-10, TGF-β1, PGC-1α, VEGF, BDNF, which progressed by 10 days, amounting to 40-60%, which is consistent with the literature data on transrepression by GR of key pro-inflammatory (NFkB, AP1, STAT1), anti-inflammatory (PPARγ, ERRα), pro-anabolic transcription factors (estrogen, androgen receptors). The administration of Mexidol daily an hour after the injection of dexamethasone did not affect the dexamethasone-induced suppression of pro-inflammatory cytokines, but increased the expression levels of anti-inflammatory cytokines, protein markers of mitochondrio-, angio- and synaptogenesis.

Conclusion: The study demonstrates for the first time the prospect and pathogenetic foundation of the combined use of dexamethasone and Mexidol in an aging body in order to minimize the activity of GC aimed at suppressing pro-anabolic programs and mechanisms for resolving inflammation.

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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
287
审稿时长
3-6 weeks
期刊介绍: Одно из старейших медицинских изданий России, основанное в 1901 году. Создание журнала связано с именами выдающихся деятелей отечественной медицины, вошедших в историю мировой психиатрии и неврологии, – С.С. Корсакова и А.Я. Кожевникова. Широкий диапазон предлагаемых журналом материалов и разнообразие форм их представления привлекают внимание научных работников и врачей, опытных и начинающих медиков, причем не только неврологов и психиатров, но и специалистов смежных областей медицины.
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