Departments of Pharmacology (L.R.G., D.R.M., J.H.W., C.P.F.) and Psychiatry (C.P.F.) and Addiction Research, Treatment & Training Center of Excellence (L.R.G., D.R.M., J.H.W., C.P.F.), University of Texas Health Science Center at San Antonio, San Antonio, Texas; and Department of Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom (S.M.H., A.D.).
Departments of Pharmacology (L.R.G., D.R.M., J.H.W., C.P.F.) and Psychiatry (C.P.F.) and Addiction Research, Treatment & Training Center of Excellence (L.R.G., D.R.M., J.H.W., C.P.F.), University of Texas Health Science Center at San Antonio, San Antonio, Texas; and Department of Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom (S.M.H., A.D.)
J Pharmacol Exp Ther. 2019 Feb;368(2):229-236. doi: 10.1124/jpet.118.253286. Epub 2018 Nov 21.
One consequence of the ongoing opioid epidemic is a large number of overdose deaths. Naloxone reverses opioid-induced respiratory depression; however, its short duration of action limits the protection it can provide. Methocinnamox (MCAM) is a novel opioid receptor antagonist with a long duration of action. This study examined the ability of MCAM to prevent and reverse the respiratory-depressant effects (minute volume [V]) of heroin in five monkeys. MCAM (0.32 mg/kg) was given before heroin to determine whether it prevents respiratory depression; heroin dose-effect curves were generated 1, 2, 4, and 8 days later, and these effects were compared with those of naltrexone (0.032 mg/kg). Heroin dose dependently decreased V MCAM and naltrexone prevented respiratory depression, shifting the heroin dose-effect curve rightward at least 10-fold. MCAM, but not naltrexone, attenuated these effects of heroin for 4 days. MCAM (0.1-0.32 mg/kg) was given 30 minutes after heroin to determine whether it reverses respiratory depression; heroin dose-effect curves were generated 1, 2, 4, 8, and 16 days later, and these effects were compared with those of naloxone (0.0032-0.1 mg/kg). MCAM and naloxone reversed respiratory depression within 30 minutes, although only MCAM antagonized heroin on subsequent days. Thus, MCAM prevents and reverses respiratory depression, the potentially lethal effect of heroin, longer than opioid receptor antagonists currently in use. Because of its sustained effects, MCAM might provide more effective rescue from and protection against the fatal respiratory-depressant effects of opioids, thereby improving treatment of opioid overdose.
阿片类药物流行的一个后果是大量过量死亡。纳洛酮逆转阿片类药物引起的呼吸抑制;然而,其作用持续时间短限制了它所能提供的保护。美沙酮(MCAM)是一种新型的阿片受体拮抗剂,作用持续时间长。本研究考察了 MCAM 预防和逆转 5 只猴子海洛因呼吸抑制作用(分钟通气量[V])的能力。在给予海洛因之前给予 MCAM,以确定它是否预防呼吸抑制;1、2、4 和 8 天后生成海洛因剂量-效应曲线,并将这些效应与纳曲酮(0.032mg/kg)进行比较。海洛因剂量依赖性地降低 V MCAM 和纳曲酮预防呼吸抑制,至少将海洛因剂量-效应曲线向右移动 10 倍。MCAM 但不是纳曲酮,减弱了这些海洛因的作用,持续 4 天。30 分钟后给予 MCAM(0.1-0.32mg/kg),以确定它是否逆转呼吸抑制;1、2、4、8 和 16 天后生成海洛因剂量-效应曲线,并将这些效应与纳洛酮(0.0032-0.1mg/kg)进行比较。MCAM 和纳洛酮在 30 分钟内逆转呼吸抑制,尽管只有 MCAM 在随后的日子里拮抗海洛因。因此,MCAM 预防和逆转呼吸抑制,海洛因的潜在致命作用,比目前使用的阿片受体拮抗剂更长。由于其持续的效果,MCAM 可能提供更有效的救援和保护免受致命的呼吸抑制作用的阿片类药物,从而改善治疗阿片类药物过量。