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[依莫昔平、雷美替胺和美西多宁在实验性糖尿病中的抗焦虑和抗抑郁作用]

[Anxiolytic and antidepressant effects of emoxipine, reamberin and mexidol in experimental diabetes mellitus].

作者信息

Volchegorskii I A, Miroshnichenko I Yu, Rassokhina L M, Faizullin R M, Pryakhina K E

机构信息

South Ural State Medical University, Pharmacology Department, Chelyabinsk, Russia.

出版信息

Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(5):52-57. doi: 10.17116/jnevro20171175152-57.

Abstract

AIM

To perform a comparative study of anxiolytic and antidepressant effects of derivatives of 3-oxypyridine and succinic acid (emoxipine, reamberin and mexidol) in experimental diabetes mellitus.

MATERIAL AND METHODS

An effect of emoxipine, reamberin and mexidol on manifestations of anxiety in 'elevated plus maze' (EPM) and duration of 'desperate behavior' (DB) in Porsolt test in rats with alloxan diabetes during medication course was studied. Alpha-lipoic (thioctic) acid (α-LA) was used as a reference drug. In additional experimental series, an effect of emoxipine, reamberin, mexidol and α-LA on the intensity of hyperglycemia in experimental DM was investigated.

RESULTS AND CONCLUSION

All studied medications used in doses equivalent to therapeutic range in humans and administered for 14 days significantly reduced manifestations of anxiety and depression in rats with alloxan diabetes. The most pronounced anxiolytic potential was demonstrated for emoxipine that emerged as the only medication in the study that reduced manifestations of anxiety not only in comparison with 'alloxan diabetes-control' groups but also in comparison to 'intact control'. The intensity of tranquilizing activity of derivatives of 3-oxypyridine and succinic acid was similar to that of α-LA while the thymoanaleptic activity, when the drugs were administered in maximal doses to rats with experimental DM, was higher. Both emoxipine and mexidol as well as α-LA in all studied doses significantly decreased hyperglycemia in alloxan diabetes. Reamberin demonstrated only insignificant tendencies of the same trend.

摘要

目的

对3-氧代吡啶和琥珀酸衍生物(依莫昔平、瑞香巴林和美西多宁)在实验性糖尿病中的抗焦虑和抗抑郁作用进行比较研究。

材料与方法

研究了依莫昔平、瑞香巴林和美西多宁在用药过程中对四氧嘧啶糖尿病大鼠“高架十字迷宫”(EPM)中焦虑表现和Porsolt试验中“绝望行为”(DB)持续时间的影响。α-硫辛酸(α-LA)用作对照药物。在额外的实验系列中,研究了依莫昔平、瑞香巴林、美西多宁和α-LA对实验性糖尿病中高血糖强度的影响。

结果与结论

所有研究药物以相当于人类治疗范围的剂量给药14天,均显著降低了四氧嘧啶糖尿病大鼠的焦虑和抑郁表现。依莫昔平表现出最显著的抗焦虑潜力,它是该研究中唯一一种不仅与“四氧嘧啶糖尿病-对照”组相比,而且与“正常对照”相比都能降低焦虑表现的药物。3-氧代吡啶和琥珀酸衍生物的镇静活性强度与α-LA相似,而当以最大剂量给实验性糖尿病大鼠给药时,其兴奋精神活性更高。依莫昔平和美西多宁以及所有研究剂量的α-LA均显著降低了四氧嘧啶糖尿病中的高血糖。瑞香巴林仅表现出相同趋势的不显著倾向。

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