抗癫痫药物的生物分子机制

M. Husna, S. Kurniawan
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引用次数: 1

摘要

癫痫治疗几乎总是慢性的,并且经常使用一种以上的药物。目前,抗癫痫药物仍是治疗癫痫的主要药物。了解这些药物的药效学和药代动力学将有助于选择正确的药物,并开展进一步确定药物机制的研究。抗癫痫药的作用机制可分为四大类:(1)调节钠、钙、钾等电压门控离子通道;(2)通过GABA- a受体、GABA转运体GAT-1或GABA转氨酶的作用,GABA抑制增加;(3)直接调节SV2A和α2δ的突触释放;(4)通过包括AMPA受体在内的谷氨酸离子受体抑制兴奋性突触。AED的工作是平衡大脑中的抑制和兴奋过程,因此它既可以用于癫痫,也可以用于与癫痫病理生理相似的其他疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BIOMOLECULAR MECHANISM OF ANTI EPILEPTIC DRUGS
Epilepsy therapy is almost always chronic and often used more than one drug. Currently, antiepileptic drugs are still the mainstay of therapy for epilepsy. An understanding of the pharmacodynamics and pharmacokinetics of these drugs would be very helpful in choosing the right medication and develop a study to determine the drug's mechanism further. Mechanism of action of AED (anti epileptic drug) can be categorized into four main groups: (1) modulation of voltage-gated ion channels, including sodium, calcium, and potassium; (2) increase in GABA inhibition through an effect on GABA-A receptors, the GAT-1 GABA transporter, or GABA transaminase; (3) direct modulation of the synaptic release of such SV2A and α2δ; and (4) inhibition of excitatory synapses through ionotropik glutamate receptors including AMPA receptors. AED work to balance the process of inhibition and excitation in the brain, so it can be used both for epilepsy and other diseases with similarities with the pathophysiology of epilepsy.
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