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首页> 外文期刊>Advances in Experimental Medicine and Biology >Evaluation of Anti-Epileptic Effect of New Indole Derivatives by Estimation of Biogenic Amines Concentrations in Rat Brain
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Evaluation of Anti-Epileptic Effect of New Indole Derivatives by Estimation of Biogenic Amines Concentrations in Rat Brain

机译:新吲哚衍生物通过估计大鼠脑血液胺浓度的抗癫痫作用

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Abstract The new heterocyclic compounds are used to treat epilepsy. In the present work new indole derivatives i.e. 5-[2(3)-di alkyl amino alkoxy] Indole 2,3-di-one derivatives are synthesized and characterized and these compounds was subjected to acute toxicity and then screened for antiepileptic activity on Maximal Electroshock (MES) seizures model in albino wistar rats. In that study 5-[2-dimethyl amino ethoxy] Indole 2,3 dione and 5-[2-dimethyl amino ethoxy] Indole 2-one,3-semicarbazone(IVa) showed good antiepileptic activity and less neurotoxicity compared to phenytoin. The purpose of the present study is to investigate the effect of 5-[2-dimethyl amino ethoxy] Indole 2,3-di one and 5-[2-dimethyl amino ethoxy] Indole 2-one,3-semicarbazone(IVa) derivatives on biogenic amines concentrations in rat brain after induction of seizures by Maximal Electro Shock(MES) method. Our aim of study was relationship between seizure activities and altered the monoamines such as noradrenaline (NA), dopamine (DA), serotonin (5-HT) in forebrain of rats in MES seizure models. In MES model, study of 5-[2-dimethyl amino ethoxy] Indole 2,3 dione(IIIa) and 5-[2-dimethyl amino ethoxy] Indole 2-one,3-semicarbazone(IVa) (100 mg/kg) showed significantly restored the decreased levels of brain monoamines such as Noradrenaline, Dopamine & 5-Hydroxy Triptamine. Thus, this study suggests that study of 5-[2-Dimethyl amino ethoxy] Indole 2,3-dione(HIa) and 5-[2-dimethyl amino ethoxy] Indole 2-one,3-semicarbazone(IVa) increased the monoamines on rat brain, which may be decreased the susceptibility to MES induced seizure in rats.
机译:摘要新的杂环化合物用于治疗癫痫。在本工作中,新的吲哚衍生物IE 5- [2(3)-DI烷基氨基烷氧基]吲哚2,3-二 - 一种衍生物被合成并表征,并对这些化合物进行急性毒性,然后对最大的抗癫痫活性进行筛选Albino Wistar大鼠中的闪管(MES)癫痫发作模型。在该研究中,5- [2-二甲基氨基乙氧基]吲哚2,3迪酮和5- [2-二甲基氨基乙氧基]吲哚2-1,与苯妥英相比显示出良好的抗癫痫活性和较少的神经毒性。本研究的目的是研究5- [2-二甲基氨基乙氧基]吲哚2,3-DI一个和5- [2-二甲基氨基乙氧基]吲哚2-on,3-胚肼(IVA)衍生物的作用基于最大电击(MES)法诱导癫痫发作后大鼠脑浓度的生物胺浓度。我们的研究目的是癫痫发作活动之间的关系,并改变了MES癫痫发作模型中大鼠的大鼠前脑中的甘露那氨基(DA),多巴胺(DA),血清酮(5-HT)的单胺。在MES模型中,研究5- [2-二甲基氨基乙氧基]吲哚2,3迪酮(IIIa)和5- [2-二甲基氨基乙氧基]吲哚2-on,3-缩氨基脲(IVA)(100mg / kg)表现明显恢复了脑单胺等下降水平,例如去甲肾上腺素,多巴胺和5-羟基胎胺。因此,该研究表明,研究5- [2-二甲基氨基乙氧基]吲哚2,3-二酮(Hia)和5- [2-二甲基氨基乙氧基]吲哚2-on,3-胚肼(IVA)增加单胺在大鼠大脑上,这可能会降低对大鼠诱导的MES诱导的敏感性。

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