Department of Psychiatry and Human Behavior, Center for Innovation and Discovery in Addictions, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Department of Psychiatry and Human Behavior, Center for Innovation and Discovery in Addictions, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Drug Alcohol Depend. 2024 Nov 1;264:112434. doi: 10.1016/j.drugalcdep.2024.112434. Epub 2024 Sep 6.
Recent studies have proposed the use of dual orexin receptor antagonists, such as suvorexant, for the treatment of opioid use disorder (OUD) and opioid-related sleep disturbances because of orexin's role in sleep-wake regulation and addiction. Accumulating evidence suggests that orexin is also an important modulator of respiratory function, raising the possibility of adverse respiratory events when combining orexin antagonists and opioids. The aim of the present study was to investigate the effects of suvorexant, alone or in combination with the opioid oxycodone, on pulmonary ventilation in male rats.
Adult, male Sprague Dawley rats received treatments with vehicle, oxycodone (3 and 10mg/kg, i.p.) or suvorexant (10 and 18mg/kg, i.p.), and respiratory measures were obtained using whole-body plethysmography. We then tested the effects of a combination of suvorexant (10 and 18mg/kg, i.p.) and the highest dose of oxycodone that did not suppress respiration alone (3mg/kg, i.p).
Oxycodone induced respiratory depression at 10mg/kg, but not 3.0mg/kg; as evident by significant decreases in minute volume (mls/min) and tidal volume (mls). Suvorexant alone did not alter any respiratory measures at the doses tested. When combined, 18mg/kg (but not 10mg/kg) suvorexant plus an ineffective dose of oxycodone significantly decreased minute and tidal volume compared with vehicle and either drug alone, whereas respiratory frequency was significantly decreased compared with vehicle.
Our findings show that suvorexant, at a dose associated with sleep promotion and blockade of oxycodone self-administration, robustly enhanced oxycodone-induced respiratory depression in male rats.
最近的研究提出使用双重食欲素受体拮抗剂,如苏沃雷生,治疗阿片类药物使用障碍(OUD)和与阿片类药物相关的睡眠障碍,因为食欲素在睡眠-觉醒调节和成瘾中起作用。越来越多的证据表明,食欲素也是呼吸功能的重要调节剂,当食欲素拮抗剂和阿片类药物结合使用时,可能会引起呼吸不良事件。本研究旨在探讨苏沃雷生(单独或与阿片类药物羟考酮合用)对雄性大鼠肺通气的影响。
成年雄性 Sprague Dawley 大鼠接受 vehicle、羟考酮(3 和 10mg/kg,ip)或苏沃雷生(10 和 18mg/kg,ip)治疗,并使用全身 plethysmography 获得呼吸测量值。然后,我们测试了苏沃雷生(10 和 18mg/kg,ip)与单独使用不抑制呼吸的最高剂量羟考酮(3mg/kg,ip)的组合的效果。
羟考酮在 10mg/kg 时引起呼吸抑制,但在 3.0mg/kg 时没有;这表现为分钟通气量(mls/min)和潮气量(mls)显著下降。单独使用苏沃雷生在测试剂量下不会改变任何呼吸测量值。当联合使用时,18mg/kg(但不是 10mg/kg)苏沃雷生加无效剂量的羟考酮与 vehicle 和单独使用任何一种药物相比,显著降低了分钟通气量和潮气量,而呼吸频率与 vehicle 相比显著降低。
我们的研究结果表明,苏沃雷生在与促进睡眠和阻断羟考酮自我给药相关的剂量下,可显著增强雄性大鼠羟考酮引起的呼吸抑制。