Kang Changwoo, Kim Dong Hoon, Kim Seong Chun, Lee Soo Hoon, Jeong Jin Hee, Kang Tae-Sin, Shin Il-Woo, Kim Rock Bum, Lee Dong Hoon
Department of Emergency Medicine, Gyeongsang National University School of Medicine , Jinju , Korea.
Clin Toxicol (Phila). 2015 Jul;53(6):540-4. doi: 10.3109/15563650.2015.1045979. Epub 2015 May 18.
Intravenous lipid emulsion (ILE) has been shown to ameliorate the toxicity of lipid-soluble agents in animal studies and clinical cases.
To investigate the therapeutic effects of ILE in a rat model of toxicity from calcium channel blockers (CCBs), including diltiazem and nicardipine.
Two sets of experiments of CCB poisoning were conducted. In the first set, 14 male Sprague-Dawley rats were sedated and treated with ILE or normal saline (NS), followed by continuous intravenous infusion of diltiazem (20 mg/kg/h). In the second experiment, the study protocol was the same except the infusion of nicardipine (20 mg/kg/h). The total dose of infused drug and the duration of survival were measured. In addition, mean arterial pressure and heart rate were monitored.
Survival was prolonged in the ILE group (48.4 ± 11.3 vs. 25.0 ± 3.7 min; p = 0.002). Furthermore, the cumulative mean lethal dose of diltiazem was higher in the ILE group (16.1 ± 3.8 mg/kg) than in the NS group (8.3 ± 1.1 mg/kg) (p = 0.002). With nicardipine poisoning, survival was also prolonged in the ILE group (71.0 ± 8.3 min vs. 30.6 ± 6.1 min; p = 0.002). The cumulative mean lethal dose was higher in the ILE group than in the NS group (23.7 ± 2.8 mg/kg vs. 10.2 ± 2.0 mg/kg; p = 0.002).
ILE pretreatment prolonged survival and increased the lethal dose in a rat model of CCB poisoning using diltiazem and nicardipine.
在动物研究和临床病例中,静脉注射脂质乳剂(ILE)已被证明可改善脂溶性药物的毒性。
研究ILE对钙通道阻滞剂(CCB)(包括地尔硫䓬和尼卡地平)中毒大鼠模型的治疗效果。
进行了两组CCB中毒实验。在第一组实验中,14只雄性Sprague-Dawley大鼠被麻醉并接受ILE或生理盐水(NS)治疗,随后持续静脉输注地尔硫䓬(20mg/kg/h)。在第二个实验中,研究方案相同,只是输注尼卡地平(20mg/kg/h)。测量输注药物的总剂量和存活时间。此外,监测平均动脉压和心率。
ILE组的存活时间延长(48.4±11.3分钟对25.0±3.7分钟;p=0.002)。此外,ILE组地尔硫䓬的累积平均致死剂量高于NS组(16.1±3.8mg/kg对8.3±1.1mg/kg)(p=0.002)。在尼卡地平中毒时,ILE组的存活时间也延长(71.0±8.3分钟对30.6±6.1分钟;p=0.002)。ILE组的累积平均致死剂量高于NS组(23.7±2.8mg/kg对10.2±2.0mg/kg;p=0.002)。
在使用地尔硫䓬和尼卡地平的CCB中毒大鼠模型中,ILE预处理可延长存活时间并增加致死剂量。