Moss I R, Scott S C, Inman J D
Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas 75235.
Am J Physiol. 1993 Apr;264(4 Pt 2):R754-60. doi: 10.1152/ajpregu.1993.264.4.R754.
The role of mu- vs. delta-opioid receptors in modulating cardiorespiratory and sleep/wake behavior was studied in sixteen 4- to 11-, and 26- to 33-day-old chronically instrumented piglets. Each underwent 1.5-h recordings of sleep/wake state, diaphragmatic and posterior cricoarytenoid electromyogram (EMGdi, EMGpca), heart rate, and arterial pressure, pH, and gas tensions, before and after either naltrexone (2 mg/kg i.v.), a predominantly mu antagonist, or naltrindole (4 mg/kg i.v.), a specific delta antagonist. In younger piglets, 1) naltrindole, but not naltrexone, decreased percent of time spent in active and quite sleep and increased that in wakefulness, and 2) naltrexone, but not naltrindole, increased respiratory frequency, decreased the duration of EMGdi and EMGpca activity, and increased initial summed EMGdi activity, all independently of state. Older piglets exhibited 1) increased arousal with both drugs and 2) weaker stimulation of respiratory timing and no stimulation of EMGdi or EMGpca with naltrexone and enhanced EMGpca activity with naltrindole during transitional sleep only. Thus, in early neonatal life, delta-opioid systems modulate sleep/wake behavior, whereas mu systems modulate respiration. With age, these influences change and become less specific.
在16只4至11日龄以及26至33日龄长期植入仪器的仔猪中,研究了μ型与δ型阿片受体在调节心肺功能及睡眠/觉醒行为方面的作用。每只仔猪在静脉注射纳曲酮(2毫克/千克)(一种主要的μ型拮抗剂)或纳曲吲哚(4毫克/千克)(一种特异性δ型拮抗剂)前后,均进行了1.5小时的睡眠/觉醒状态、膈肌和环杓后肌肌电图(EMGdi、EMGpca)、心率、动脉压、pH值以及气体张力的记录。在幼龄仔猪中,1)纳曲吲哚而非纳曲酮可减少活跃睡眠和安静睡眠的时间百分比,并增加觉醒时间百分比;2)纳曲酮而非纳曲吲哚可增加呼吸频率,缩短EMGdi和EMGpca活动的持续时间,并增加初始EMGdi活动总和,且这些均与状态无关。老龄仔猪表现为:1)两种药物均可增加觉醒;2)纳曲酮对呼吸节律的刺激较弱,对EMGdi或EMGpca无刺激作用,而纳曲吲哚仅在过渡睡眠期间增强EMGpca活动。因此,在新生儿早期,δ型阿片系统调节睡眠/觉醒行为,而μ型系统调节呼吸。随着年龄增长,这些影响发生变化且特异性降低。