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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Glutamate transport in rat cerebellar granule cells is impaired by inorganic epileptogenic agents.
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Glutamate transport in rat cerebellar granule cells is impaired by inorganic epileptogenic agents.

机译:无机致癫痫剂会损害大鼠小脑颗粒细胞中的谷氨酸转运。

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摘要

There is evidence that extracellular glutamate levels are elevated in certain brain regions immediately prior to and during induction and propagation of seizures. There appears to be a correlation between the capacity of removing released glutamate and the genesis of epileptiform activity. Some models make use of metals, such as Co(2+) and Ni(2+), to induce epilepsy. We used patch-clamp recordings to measure the electrogenic glutamate transport in neuronal cells. The present results indicate that Co(2+) (1 mM) and Ni(2+) (5 mM) blocked glutamate transport by 17.6+/-3.9% (n=5, P<0.05) and by 31.8+/-6.2% (n=7, P<0.05), respectively. Ni(2+) inhibited glutamate uptake in a dose-dependent manner. The IC(50) value obtained was 66.6 microM and the maximum inhibition was 40%. We conclude that one mechanism that may explain the seizures induced by exposure to those divalent cations is inhibition of the glutamate transporter.
机译:有证据表明,在癫痫发作和传播之前和之中,某些大脑区域的细胞外谷氨酸水平升高。去除释放的谷氨酸的能力与癫痫样活性的发生之间似乎存在相关性。一些模型利用金属,例如Co(2+)和Ni(2+)诱发癫痫。我们使用膜片钳记录来测量神经元细胞中的谷氨酸转运。目前的结果表明Co(2+)(1 mM)和Ni(2+)(5 mM)阻止谷氨酸转运17.6 +/- 3.9%(n = 5,P <0.05)和31.8 +/- 6.2 %(n = 7,P <0.05)。 Ni(2+)以剂量依赖的方式抑制谷氨酸的摄取。获得的IC(50)值为66.6 microM,最大抑制率为40%。我们得出结论,可以解释暴露于那些二价阳离子引起的癫痫发作的一种机制是谷氨酸转运蛋白的抑制。

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