Holst Sebastian C, Werth Esther, Landolt Hans-Peter
1 Copenhagen University Hospital, Rigshospitalet, Department of Neurology and Neurobiology Research Unit, Kopenhagen, Dänemark.
2 Sleep and Health Zürich (SHZ), Universität Zürich.
Praxis (Bern 1994). 2019 Jan;108(2):131-138. doi: 10.1024/1661-8157/a003189.
Pharmacotherapy of Sleep-Wake Disorders Abstract. Sleep is a complex behavior, coordinated by many different brain regions and neurotransmitters. These neurochemical systems can be pharmacologically influenced to modulate wakefulness and sleep. Excessive daytime sleepiness (EDS) is often treated with dopaminergic drugs, which in mild cases range from caffeine via (ar)modafinil to amphetamine derivatives. Tricyclic antidepressants and melatonin-based drugs are also used to promote alertness, but to a lesser extent. The drugs used to promote sleep include GABA-ergic drugs such as benzodiazepines and Z-hypnotics as well as histamine H1 receptor antagonists. Exogenous melatonin or a pharmacological combination of melatonin receptor agonists and 5-HT2C receptor antagonists are also used in mild cases. Selective and dual orexin (hypocretin) receptor antagonists (DORA) as well as drugs binding to specific 5-HT receptors are currently being investigated as future sleep-promoting drugs. However, pharmacological treatment is not always the primary treatment option, insomnia is treated first-line with cognitive behavioral therapy, and continuous positive airway pressure is used to treat sleep apnea.
睡眠-觉醒障碍的药物治疗 摘要。睡眠是一种复杂的行为,由许多不同的脑区和神经递质协调。这些神经化学系统可通过药理学手段加以影响,以调节觉醒和睡眠。白天过度嗜睡(EDS)通常用多巴胺能药物治疗,在轻度病例中,药物范围从咖啡因到(阿)莫达非尼再到苯丙胺衍生物。三环类抗抑郁药和褪黑素类药物也用于提高警觉性,但程度较轻。用于促进睡眠的药物包括GABA能药物,如苯二氮䓬类和Z类催眠药以及组胺H1受体拮抗剂。轻度病例也使用外源性褪黑素或褪黑素受体激动剂与5-HT2C受体拮抗剂的药理学组合。选择性和双重食欲素(下丘脑分泌素)受体拮抗剂(DORA)以及与特定5-HT受体结合的药物目前正作为未来的促眠药物进行研究。然而,药物治疗并非总是主要的治疗选择,失眠的一线治疗是认知行为疗法,持续气道正压通气用于治疗睡眠呼吸暂停。