Boison Detlev
R.S. Dow Neurobiology Laboratories, Legacy Research, Portland, OR 97232, USA.
Handb Exp Pharmacol. 2011(200):251-66. doi: 10.1007/978-3-642-13443-2_9.
Clinical evidence, in particular the wide use of theophylline as a bronchodilator, suggests that methylxanthines can cause seizures in patients without known underlying epilepsy. Theophylline is also known to be an added risk factor for seizure exacerbation in patients with epilepsy. The proconvulsant activity of methylxanthines can best be explained by their antagonizing the brain's own anticonvulsant adenosine. Recent evidence suggests that adenosine dysfunction is a pathological hallmark of epilepsy contributing to seizure generation and seizure spread. Conversely, adenosine augmentation therapies are effective in seizure suppression and prevention, whereas adenosine receptor antagonists such as methylxanthines generally exacerbate seizures. The impact of the methylxanthines caffeine and theophylline on seizures and excitotoxicity depends on timing, dose, and acute versus chronic use. New findings suggest a role of free radicals in theophylline-induced seizures, and adenosine-independent mechanisms for seizure generation have been proposed.
临床证据,尤其是氨茶碱作为支气管扩张剂的广泛使用,表明甲基黄嘌呤可在无已知潜在癫痫的患者中引发癫痫发作。氨茶碱也是癫痫患者癫痫发作加剧的一个额外风险因素。甲基黄嘌呤的促惊厥活性最好用其拮抗大脑自身的抗惊厥腺苷来解释。最近的证据表明,腺苷功能障碍是癫痫的一个病理标志,有助于癫痫发作的产生和传播。相反,腺苷增强疗法在癫痫抑制和预防方面是有效的,而腺苷受体拮抗剂如甲基黄嘌呤通常会加剧癫痫发作。甲基黄嘌呤咖啡因和氨茶碱对癫痫发作和兴奋性毒性的影响取决于时间、剂量以及急性与慢性使用情况。新的研究结果表明自由基在氨茶碱诱导的癫痫发作中起作用,并且已经提出了与腺苷无关的癫痫发作产生机制。