Wong Benjamin, Perkins Michael W, Tressler Justin, Rodriguez Ashley, Devorak Jennifer, Sciuto Alfred M
a Biochemistry and Toxicology Branch , US Army Medical Research Institute of Chemical Defense , Aberdeen Proving Ground , MD , USA.
Inhal Toxicol. 2017 Feb;29(2):65-74. doi: 10.1080/08958378.2017.1282065. Epub 2017 Mar 3.
This study examined the real-time exposure-response effects of aerosolized carfentanil (CRF) on opioid-induced toxicity, respiratory dynamics and cardiac function in mice. Unrestrained, conscious male CD-1 mice (25-30 g) were exposed to 0.4 or 4.0 mg/m of aerosolized CRF for 15 min (Ct = 6 or 60 mg min/m) in a whole-body plethysmograph chamber. Minute volume (MV), core body temperature (T), mean arterial blood pressure (MAP) and heart rate (HR) were evaluated in animals exposed to CRF or sterile HO. Loss of consciousness and Straub tail were observed in before 1 min following initiation of exposure to 6 or 60 mg min/m of CRF. Clinical signs of opioid-induced toxicity were observed in a dose-dependent manner. Exposure to 6 or 60 mg min/m of CRF resulted in significant decrease in MV as compared to the controls. MAP, HR and T decreased 24 h in animals exposed to either 6 or 60 mg min/m of CRF as compared to the controls. Post-exposure administration of naloxone (NX, 0.05 mg/kg, i.m.) did not increase the MV of animals exposed to CRF to control levels within 24 h, but decreased clinical signs of opioid-induced toxicity and the duration of respiratory depression. This is the first study to evaluate real-time respiratory dynamics and cardiac function during exposure and up to 24 h post-exposure to CRF. The evaluation of toxicological signs and respiratory dynamics following exposure to CRF will be useful in the development of therapeutic strategies to counteract the ongoing threat of abuse and overuse of opioids and their synthetic variants.
本研究考察了雾化卡芬太尼(CRF)对小鼠阿片类药物所致毒性、呼吸动力学和心脏功能的实时暴露-反应效应。将未束缚的清醒雄性CD-1小鼠(25-30克)置于全身体积描记箱中,暴露于0.4或4.0毫克/立方米的雾化CRF中15分钟(Ct = 6或60毫克·分钟/立方米)。对暴露于CRF或无菌水的动物评估每分通气量(MV)、核心体温(T)、平均动脉血压(MAP)和心率(HR)。在暴露于6或60毫克·分钟/立方米的CRF开始后1分钟内观察到意识丧失和 Straub 尾。观察到阿片类药物所致毒性的临床体征呈剂量依赖性。与对照组相比,暴露于6或60毫克·分钟/立方米的CRF导致MV显著降低。与对照组相比,暴露于6或60毫克·分钟/立方米的CRF的动物在24小时内MAP、HR和T均降低。暴露后给予纳洛酮(NX,0.05毫克/千克,肌肉注射)在24小时内未将暴露于CRF的动物的MV提高到对照水平,但降低了阿片类药物所致毒性的临床体征和呼吸抑制的持续时间。这是第一项评估暴露于CRF期间及暴露后长达24小时的实时呼吸动力学和心脏功能的研究。评估暴露于CRF后的毒理学体征和呼吸动力学将有助于制定治疗策略,以应对阿片类药物及其合成变体滥用和过度使用带来的持续威胁。