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Investigation of Compositional, Structural, and Dynamical Changes of Pentylenetetrazol-Induced Seizures on a Rat Brain by FT-IR Spectroscopy

机译:FT-IR光谱研究P四唑诱发的大鼠癫痫发作的成分,结构和动态变化

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To accomplish the appropriate treatment strategies of epilepsy action mechanisms underlying epileptic seizures should be lightened. The identification of epileptic seizure-induced alterations on the brain related to their pathologies may provide information for its action mechanism. Therefore, the current study determined molecular consequences of seizures induced by pentylenetetrazol (PTZ), which is a widely used convulsant agent, on rat brain. The rats were administered subconvulsant (25 mg/kg) and convulsant (60 mg/kg) doses of PTZ during a week, and brain tissues were studied by Fourier transform infrared (FT-IR) spectroscopy. Results revealed a decrease in lipid fluidity and lipid and protein content and also the differences in membrane packing by changing the nature of hydrogen bonding as indicated by the C=O, the PO_2~- symmetric, and asymmetric bands. Monitoring of the olefinic band elicited seizure-induced lipid peroxidation further confirmed by the thiobarbituric acid (TBAR) assay. Additionally, PTZ-induced convulsions led to alterations in protein structures obtained by neural network (NN) predictions like an increase in random coils. On the basis of the spectral changes, treated samples could be successfully differentiated from the controls by cluster analysis. Consequently, the convulsive dose of PTZ caused more significant molecular variations compared to the subconvulsive one. All findings might have an important role in understanding the molecular mechanisms underlying epileptic activities.
机译:为了完成适当的治疗策略,应减轻癫痫发作的潜在癫痫作用机制。癫痫性癫痫发作诱发的大脑病变与其病理相关的鉴定可能为其作用机制提供信息。因此,当前的研究确定了由戊四氮(PTZ)引起的癫痫发作的分子后果,这是一种广泛使用的惊厥剂,对大鼠大脑有影响。在一周内给大鼠施用亚惊厥药(25 mg / kg)和惊厥药(60 mg / kg)剂量的PTZ,并通过傅里叶变换红外(FT-IR)光谱学研究脑组织。结果表明,通过改变氢键的性质,脂质流动性和脂质和蛋白质含量降低,并且膜堆积的差异也发生了改变,如C = O,PO_2〜-对称和不对称带所示。通过硫代巴比妥酸(TBAR)测定进一步证实了对烯烃带的监测引起癫痫发作诱导的脂质过氧化。此外,PTZ诱发的惊厥导致通过神经网络(NN)预测获得的蛋白质结构发生变化,例如随机线圈数增加。根据光谱变化,可以通过聚类分析成功地将处理后的样品与对照区分开。因此,与亚惊厥药相比,PTZ惊厥药引起更大的分子变异。所有发现都可能在理解癫痫活动的分子机制中起重要作用。

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