Mamelak M, Scharf M B, Woods M
Sleep. 1986;9(1 Pt 2):285-9. doi: 10.1093/sleep/9.1.285.
Previous studies on the effects of gamma-hydroxybutyrate (GHB) on the sleep and clinical response of patients with narcolepsy are reviewed. New information on 48 patients treated with GHB for as long as 9 years is presented. These studies indicate that 2.25 to 3.00 g of GHB, taken in conjunction with a low dose of a stimulant during the day, rapidly alleviate the symptoms of narcolepsy in most patients. Tolerance does not develop to this treatment regimen; neither have any patients discontinued the treatment because of side effects. In poor responders, daytime drowsiness and not cataplexy has been the most common residual symptom. Sleep studies reveal that GHB induces REM followed by slow wave sleep. Although total sleep time at night may be unchanged, sleep is less fragmented. GHB appears to be effective because it can induce the symptoms of narcolepsy and contain them at night. It is noteworthy, therefore, that the central biochemical changes induced by GHB also appear comparable to those found naturally in narcolepsy.
本文回顾了以往关于γ-羟基丁酸(GHB)对发作性睡病患者睡眠及临床反应影响的研究。文中呈现了48例接受GHB治疗长达9年的患者的新信息。这些研究表明,在白天服用2.25至3.00克GHB并结合低剂量兴奋剂,能迅速缓解大多数发作性睡病患者的症状。对这种治疗方案不会产生耐受性;也没有患者因副作用而停止治疗。在反应不佳的患者中,白天嗜睡而非猝倒是最常见的残留症状。睡眠研究显示,GHB可诱导快速眼动睡眠,随后是慢波睡眠。虽然夜间总睡眠时间可能不变,但睡眠碎片化程度降低。GHB似乎有效,因为它能诱发发作性睡病症状并在夜间抑制这些症状。因此,值得注意的是,GHB诱导的中枢生化变化似乎也与发作性睡病患者自然出现的变化相当。