Faingold C L, Browning R A
Eur J Pediatr. 1987 Jan;146(1):8-14. doi: 10.1007/BF00647274.
The usefulness of the anticonvulsant drugs is determined by the mechanisms by which the agent acts and its pharmacokinetics. The general mechanisms of action of these agents include (1) effects on neurotransmitter action, (2) effects on repetitive neuronal firing mechanisms, (3) effects on neuronal networks, and (4) effects on neuronal ionic transport. Ethosuximide, valproic acid and clonazepam are used primarily in absence epilepsy. Valproic acid is also effective against generalized tonic-clonic epilepsy. Diazepam is used primarily in status epilepticus. Valproic acid enhances gamma aminobutyric acid (GABA)-mediated inhibition, reduces repetitive firing, and reduces both inhibition and excitation in neuronal networks. Clonazepam and diazepam enhance the inhibitory action of GABA, decrease inhibition in neuronal networks and affect calcium ion transport with lesser effects on repetitive firing. Ethosuximide reduces inhibition in neuronal networks, may interact with dopamine, and possibly affects sodium and potassium ion transport. Further work is needed to assess the degree of involvement of these effects in the anticonvulsant action versus the adverse effects of these agents.
抗惊厥药物的效用取决于其作用机制和药代动力学。这些药物的一般作用机制包括:(1)对神经递质作用的影响;(2)对神经元重复放电机制的影响;(3)对神经元网络的影响;(4)对神经元离子转运的影响。乙琥胺、丙戊酸和氯硝西泮主要用于失神性癫痫。丙戊酸对全身性强直阵挛性癫痫也有效。地西泮主要用于癫痫持续状态。丙戊酸增强γ-氨基丁酸(GABA)介导的抑制作用,减少重复放电,并减少神经元网络中的抑制和兴奋。氯硝西泮和地西泮增强GABA的抑制作用,减少神经元网络中的抑制,并影响钙离子转运,对重复放电的影响较小。乙琥胺减少神经元网络中的抑制,可能与多巴胺相互作用,并可能影响钠和钾离子转运。需要进一步开展工作,以评估这些作用在抗惊厥作用与这些药物不良反应中所涉及的程度。