Yokoyama H, Iinuma K
Department of Pediatrics, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-77, Japan.
CNS Drugs. 1996 May;5(5):321-30. doi: 10.2165/00023210-199605050-00002.
Experimental studies have indicated that the central histaminergic neuron system plays an important role in the inhibition of seizures through stimulation of histamine H1 receptors, especially in the developmental period. This has therapeutic implications for currently available drugs that act at histamine receptors. H1 receptor antagonists, including classical antihistamines and anti-allergy drugs, occasionally induce convulsions in healthy children and patients with epilepsy. In particular, promethazine, carbinoxamine, mepyramine (pyrilamine) and ketotifen should be used with caution in these patients. These drugs are widely used as components of over-the-counter medications. The use of the d-chlorphenamine (d-chlorpheniramine) activation study with EEG monitoring is useful for assessing the seizure susceptibility of patients who have had convulsions secondary to administration of H1 receptor antagonists.H2 receptor antagonists have also occasionally been reported to induce convulsions in critically ill and polymedicated patients, and patients with chronic renal or hepatic failure. However, experimental findings have not been consistent with these clinical reports, such that the role of these receptors and their ligands in inducing seizures cannot be confirmed.Recently, H3 receptor antagonists, which enhance endogenous histamine release in the brain, have been demonstrated to have a potent anticonvulsant action. Therefore, these compounds may represent a new avenue for the development of antiepileptic drugs. Considering that H3 receptor antagonists also induce arousal patterns on the EEG, it is possible that they will not be associated with the sedative effects of many conventional antiepileptic drugs.
实验研究表明,中枢组胺能神经元系统在通过刺激组胺H1受体抑制癫痫发作中起重要作用,尤其是在发育阶段。这对于目前作用于组胺受体的药物具有治疗意义。H1受体拮抗剂,包括经典抗组胺药和抗过敏药,偶尔会在健康儿童和癫痫患者中诱发惊厥。特别是,在这些患者中应谨慎使用异丙嗪、卡比沙明、美吡拉敏(吡拉明)和酮替芬。这些药物作为非处方药的成分被广泛使用。使用右旋氯苯那敏(右氯苯那敏)激活研究并进行脑电图监测,有助于评估因服用H1受体拮抗剂继发惊厥的患者的癫痫易感性。H2受体拮抗剂也偶尔被报道在重症和多药治疗的患者以及慢性肾或肝功能衰竭患者中诱发惊厥。然而,实验结果与这些临床报告并不一致,因此这些受体及其配体在诱发癫痫发作中的作用无法得到证实。最近,已证明可增强脑内内源性组胺释放的H3受体拮抗剂具有强大的抗惊厥作用。因此,这些化合物可能代表了抗癫痫药物开发的新途径。考虑到H3受体拮抗剂也会在脑电图上诱发觉醒模式,它们可能不会产生许多传统抗癫痫药物的镇静作用。