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褪黑素在实验性癫痫发作和癫痫中的作用。

Melatonin in experimental seizures and epilepsy.

机构信息

Experimental Neuropathophysiology Unit, Department of Pathophysiology, Medical University, PL 20-090 Lublin, Jaczewskiego 8, Poland.

出版信息

Pharmacol Rep. 2011;63(1):1-11. doi: 10.1016/s1734-1140(11)70393-0.

Abstract

Although melatonin is approved only for the treatment of jet-lag syndrome and some types of insomnia, clinical data suggest that it is effective in the adjunctive therapy of osteoporosis, cataract, sepsis, neurodegenerative diseases, hypertension, and even cancer. Melatonin also modulates the electrical activity of neurons by reducing glutamatergic and enhancing GABA-ergic neurotransmission. The indoleamine may also be metabolized to kynurenic acid, an endogenous anticonvulsant. Finally, the hormone and its metabolites act as free radical scavengers and antioxidants. The vast majority of experimental data indicates anticonvulsant properties of the hormone. Melatonin inhibited audiogenic and electrical seizures, as well as reduced convulsions induced by pentetrazole, pilocarpine, L-cysteine and kainate. Only a few studies have shown direct or indirect proconvulsant effects of melatonin. For instance, melatonin enhanced low Mg2+-induced epileptiform activity in the hippocampus, whereas melatonin antagonists delayed the onset of pilocarpine-induced seizures. However, the relatively high doses of melatonin required to inhibit experimental seizures can induce some undesired effects (e.g., cognitive and motor impairment and decreased body temperature). In humans, melatonin may attenuate seizures, and it is most effective in the treatment of juvenile intractable epilepsy. Its additional benefits include improved physical, emotional, cognitive, and social functions. On the other hand, melatonin has been shown to induce electroencephalographic abnormalities in patients with temporal lobe epilepsy and increase seizure activity in neurologically disabled children. The hormone showed very low toxicity in clinical practice. The reported adverse effects (nightmares, hypotension, and sleep disorders) were rare and mild. However, more placebo-controlled, double-blind randomized clinical trials are needed to establish the usefulness of melatonin in the adjunctive treatment of epilepsy.

摘要

尽管褪黑素仅被批准用于治疗时差综合征和某些类型的失眠症,但临床数据表明,它在骨质疏松症、白内障、脓毒症、神经退行性疾病、高血压甚至癌症的辅助治疗中也具有疗效。褪黑素通过减少谷氨酸能和增强 GABA 能神经传递来调节神经元的电活动。这种吲哚胺也可能代谢为犬尿氨酸,一种内源性抗惊厥药。最后,该激素及其代谢物充当自由基清除剂和抗氧化剂。绝大多数实验数据表明该激素具有抗惊厥特性。褪黑素抑制听觉性和电发性癫痫发作,并减少戊四唑、毛果芸香碱、L-半胱氨酸和海人酸诱导的癫痫发作。只有少数研究表明褪黑素具有直接或间接的致惊厥作用。例如,褪黑素增强了低镁诱导的海马癫痫样活动,而褪黑素拮抗剂则延迟了毛果芸香碱诱导的癫痫发作的发作。然而,抑制实验性癫痫发作所需的褪黑素相对较高剂量可能会引起一些不良影响(例如认知和运动障碍以及体温下降)。在人类中,褪黑素可能会减轻癫痫发作,在治疗青少年难治性癫痫方面最为有效。它的额外益处包括改善身体、情绪、认知和社会功能。另一方面,褪黑素已被证明会引起颞叶癫痫患者的脑电图异常,并增加神经发育障碍儿童的癫痫发作活动。该激素在临床实践中显示出非常低的毒性。报告的不良反应(噩梦、低血压和睡眠障碍)很少且轻微。然而,需要更多的安慰剂对照、双盲随机临床试验来确定褪黑素在癫痫辅助治疗中的有效性。

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