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抗癫痫药物左乙拉西坦对培养的皮质神经元中AMPA受体的调节作用。

Modulation of AMPA receptors in cultured cortical neurons induced by the antiepileptic drug levetiracetam.

作者信息

Carunchio Irene, Pieri Massimo, Ciotti Maria Teresa, Albo Federica, Zona Cristina

机构信息

Department of Neuroscience, University of Rome Tor Vergata, Rome, Italy.

出版信息

Epilepsia. 2007 Apr;48(4):654-62. doi: 10.1111/j.1528-1167.2006.00973.x. Epub 2007 Feb 5.

Abstract

PURPOSE

The present study explores the hypothesis that the antiepileptic mechanism of action of levetiracetam (LEV) is related to effects on alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor channels in mouse cortical neurons in culture.

METHODS

The neurons were subjected to the whole-cell configuration of the patch-clamp recording technique and were 8-12 days old in culture.

RESULTS

Kainate elicited concentration-dependent (EC(50)= 80 microM) inward currents in all the patched cells. LEV (5-200 microM) itself did not induce inward or outward currents on all patched neurons, whereas it was effective on the kainate- and AMPA-induced current because it significantly decreased the amplitude of these currents. LEV was also able to significantly decrease the total membrane conductance during kainate perfusion, indicating that its effect was not dependent on the cellular voltage membrane potential. Further evidence that LEV modulated the ionotropic non-NMDA receptors came from the analysis of miniature excitatory postsynaptic currents (mEPSCs). In fact, LEV significantly decreased both the amplitude and the frequency of mEPSCs, as shown by the relative cumulative distributions.

CONCLUSIONS

These results reveal that AMPA receptors are modulated by LEV because a significant decrease in the kainate- and AMPA-induced currents and a decrease in amplitude and in frequency of mEPSCs have been observed in cortical neurons in culture. The described effect of LEV on AMPA receptors in cortical neurons is probably due to the etheromeric composition of the receptors and may be considered as a possible new antiepileptic mechanism of action.

摘要

目的

本研究探讨左乙拉西坦(LEV)的抗癫痫作用机制是否与对培养的小鼠皮质神经元中α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体通道的影响有关。

方法

采用膜片钳记录技术的全细胞模式对培养8至12天的神经元进行研究。

结果

在所有膜片钳记录的细胞中,海人酸可引起浓度依赖性(EC50 = 80微摩尔)内向电流。LEV(5至200微摩尔)本身在所有膜片钳记录的神经元上均未诱导内向或外向电流,然而它对海人酸和AMPA诱导的电流有效,因为它显著降低了这些电流的幅度。在海人酸灌注期间,LEV还能够显著降低总膜电导,表明其作用不依赖于细胞的电压膜电位。对微小兴奋性突触后电流(mEPSCs)的分析进一步证明LEV调节了离子型非NMDA受体。事实上,如相对累积分布所示,LEV显著降低了mEPSCs的幅度和频率。

结论

这些结果表明,在培养的皮质神经元中,由于观察到海人酸和AMPA诱导的电流显著降低以及mEPSCs的幅度和频率降低,AMPA受体受到LEV的调节。LEV对皮质神经元中AMPA受体的上述作用可能归因于受体的异构体组成,并可被视为一种可能的新的抗癫痫作用机制。

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