Behavioral Neuroscience Branch, National Institute on Drug Abuse - Intramural Research Program, National Institutes of Health, DHHS, Baltimore, MD, 21224, USA.
Behavioral Neuroscience Branch, National Institute on Drug Abuse - Intramural Research Program, National Institutes of Health, DHHS, Baltimore, MD, 21224, USA.
Neuropharmacology. 2023 Jun 15;231:109507. doi: 10.1016/j.neuropharm.2023.109507. Epub 2023 Mar 20.
Opioids induce respiratory depression resulting in coma or even death during overdose. Naloxone, an opioid antagonist, is the gold standard reversal agent for opioid intoxication, but this treatment is often less successful for fentanyl. While low dosing is thought to be a factor limiting naloxone's efficacy, the timing between fentanyl exposure and initiation of naloxone treatment may be another important factor. Here, we used oxygen sensors coupled with amperometry to examine the pattern of oxygen responses in the brain and periphery induced by intravenous fentanyl in freely moving rats. At both doses (20 and 60 μg/kg), fentanyl induced a biphasic brain oxygen response-a rapid, strong, and relatively transient decrease (8-12 min) followed by a weaker and prolonged increase. In contrast, fentanyl induced stronger and more prolonged monophasic oxygen decreases in the periphery. When administered before fentanyl, intravenous naloxone (0.2 mg/kg) fully blocked the hypoxic effects of moderate-dose fentanyl in both the brain and periphery. However, when injected 10 min after fentanyl, when most of hypoxia had already ceased, naloxone had minimal effect on central and peripheral oxygen levels, but at a higher dose, it strongly attenuated hypoxic effects in the periphery with only a transient brain oxygen increase associated with behavioral awakening. Therefore, due to the rapid, strong but transient nature of fentanyl-induced brain hypoxia, the time window when naloxone can attenuate this effect is relatively short. This timing limitation is critical, making naloxone most effective when used quickly and less effective when used during the post-hypoxic comatose state after brain hypoxia has already ceased and harm for neural cells already done.
阿片类药物会导致呼吸抑制,在过量使用时会导致昏迷甚至死亡。纳洛酮是阿片类药物中毒的金标准解毒剂,但这种治疗方法在芬太尼中毒时往往效果较差。虽然低剂量被认为是限制纳洛酮疗效的一个因素,但芬太尼暴露与纳洛酮治疗开始之间的时间可能是另一个重要因素。在这里,我们使用氧传感器结合安培法来检查静脉注射芬太尼在自由活动的大鼠中引起的大脑和外周氧反应模式。在两个剂量(20 和 60μg/kg)下,芬太尼诱导双相脑氧反应-快速、强烈且相对短暂的降低(8-12 分钟),随后是较弱且延长的增加。相比之下,芬太尼在外周引起更强且更持久的单相氧降低。当在芬太尼之前给予时,静脉内纳洛酮(0.2mg/kg)完全阻断了中等剂量芬太尼在大脑和外周的缺氧作用。然而,当在芬太尼注射 10 分钟后给予时,当大部分缺氧已经停止时,纳洛酮对中枢和外周氧水平几乎没有影响,但在更高剂量下,它强烈减弱了外周的缺氧作用,仅短暂地增加了与行为觉醒相关的脑氧。因此,由于芬太尼诱导的脑缺氧具有快速、强烈但短暂的性质,纳洛酮可以减轻这种作用的时间窗口相对较短。这种时间限制至关重要,使得纳洛酮在快速使用时最有效,在脑缺氧已经停止并且已经对神经细胞造成损害的缺氧后昏迷状态下使用时效果较差。