Department of Anesthesiology, Leiden University Medical Center, Leiden, Netherlands.
Centre for Human Drug Research, Leiden, Netherlands.
JCI Insight. 2022 May 9;7(9):e156973. doi: 10.1172/jci.insight.156973.
BACKGROUNDPotent synthetic opioids, such as fentanyl, are increasingly abused, resulting in unprecedented numbers of fatalities from respiratory depression. Treatment with the high-affinity mu-opioid receptor partial agonist buprenorphine may prevent fatalities by reducing binding of potent opioids to the opioid receptor, limiting respiratory depression.METHODSTo characterize buprenorphine-fentanyl interaction at the level of the mu-opioid receptor in 2 populations (opioid-naive individuals and individuals who chronically use high-dose opioids), the effects of escalating i.v. fentanyl doses with range 0.075-0.35 mg/70 kg (opioid naive) and 0.25-0.70 mg/70 kg (chronic opioid use) on iso-hypercapnic ventilation at 2-3 background doses of buprenorphine (target plasma concentrations range: 0.2-5 ng/mL) were quantified using receptor association/dissociation models combined with biophase distribution models.RESULTSBuprenorphine produced mild respiratory depression, while high doses of fentanyl caused pronounced respiratory depression and apnea in both populations. When combined with fentanyl, buprenorphine produced a receptor binding-dependent reduction of fentanyl-induced respiratory depression in both populations. In individuals with chronic opioid use, at buprenorphine plasma concentrations of 2 ng/mL or higher, a protective effect against high-dose fentanyl was observed.CONCLUSIONOverall, the results indicate that when buprenorphine mu-opioid receptor occupancy is sufficiently high, fentanyl is unable to activate the mu-opioid receptor and consequently will not cause further respiratory depression in addition to the mild respiratory effects of buprenorphine.TRIAL REGISTRATIONTrialregister.nl, no. NL7028 (https://www.trialregister.nl/trial/7028)FUNDINGIndivior Inc., North Chesterfield, Virginia, USA.
芬太尼等强效合成阿片类药物的滥用情况日益严重,导致因呼吸抑制而死亡的人数前所未有。高亲和力μ-阿片受体部分激动剂丁丙诺啡的治疗可能通过减少强效阿片类药物与阿片受体的结合,从而预防死亡,限制呼吸抑制。
为了在 2 个人群(阿片类药物未使用者和长期使用高剂量阿片类药物的人群)中描述丁丙诺啡-芬太尼相互作用在μ-阿片受体水平上的作用,使用受体结合/解离模型结合生物相分布模型,量化了递增静脉内芬太尼剂量(范围为 0.075-0.35 mg/70 kg(阿片类药物未使用者)和 0.25-0.70 mg/70 kg(慢性阿片类药物使用者))对丁丙诺啡(目标血浆浓度范围:0.2-5 ng/mL)2-3 个背景剂量下等碳酸血症通气的影响。
丁丙诺啡产生轻度呼吸抑制,而高剂量芬太尼在这两个人群中均引起明显的呼吸抑制和呼吸暂停。当与芬太尼联合使用时,丁丙诺啡在这两个人群中产生了一种受体结合依赖性的芬太尼引起的呼吸抑制减少。在慢性阿片类药物使用者中,当丁丙诺啡的血浆浓度达到 2 ng/mL 或更高时,观察到对高剂量芬太尼的保护作用。
总体而言,结果表明,当丁丙诺啡μ-阿片受体占有率足够高时,芬太尼无法激活μ-阿片受体,因此除了丁丙诺啡的轻度呼吸作用外,不会导致进一步的呼吸抑制。
Trialregister.nl,编号 NL7028(https://www.trialregister.nl/trial/7028)
美国弗吉尼亚州北切斯特菲尔德的 Indivior Inc.