Atkinson R L, Suratt P M, Wilhoit S C, Recant L
Int J Obes. 1985;9(4):233-9.
To test the hypothesis that endogenous opiates play a role in the etiology of the sleep apnea syndrome, we administered naloxone, an opiate antagonist, to ten obese humans with sleep apnea. On two separate nights we measured the frequency and severity of sleep apnea during naloxone infusion vs saline control infusion. The number of oxyhemoglobin desaturation episodes was not significantly lowered but the average maximal oxyhemoglobin desaturation fell significantly (P less than 0.01) with naloxone. The desaturation index (average maximal oxyhemoglobin desaturation times desaturations per hour) fell by 21 percent (P less than 0.05) on the night of naloxone infusion. Nine of the ten patients had a lower desaturation index with naloxone. REM sleep decreased by 80 percent (P less than 0.05) in the subjects in whom it was measured. We conclude that opiate antagonists hold promise in the treatment of sleep apnea and that the endogenous opiate system may be involved in the production of sleep apnea.
为了验证内源性阿片类物质在睡眠呼吸暂停综合征病因学中起作用这一假说,我们对10名患有睡眠呼吸暂停的肥胖者给予了阿片类拮抗剂纳洛酮。在两个不同的夜晚,我们测量了输注纳洛酮与输注生理盐水对照期间睡眠呼吸暂停的频率和严重程度。氧合血红蛋白去饱和事件的数量没有显著降低,但使用纳洛酮时平均最大氧合血红蛋白去饱和度显著下降(P小于0.01)。在输注纳洛酮的当晚,去饱和指数(平均最大氧合血红蛋白去饱和度乘以每小时去饱和度次数)下降了21%(P小于0.05)。10名患者中有9名使用纳洛酮时去饱和指数较低。在进行测量的受试者中,快速眼动睡眠减少了80%(P小于0.05)。我们得出结论,阿片类拮抗剂在睡眠呼吸暂停的治疗中具有前景,并且内源性阿片系统可能参与了睡眠呼吸暂停的产生。