From the Heart, Trauma and Sepsis Research Laboratory, Australian Institute of Tropical Health and Medicine, College of Medicine, James Cook University, Townsville, Queensland, Australia.
J Trauma Acute Care Surg. 2014 Sep;77(3):471-8. doi: 10.1097/TA.0000000000000361.
No drug therapy has demonstrated improved clinical outcomes in the treatment of sepsis. A bolus of adenosine, lidocaine, and magnesium (ALM) has been shown to be cardioprotective and restore coagulopathy in different trauma states. We hypothesized that ALM therapy may improve hemodynamics, protect the lung, and prevent coagulopathy in the rat sepsis model.
Nonheparinized, anesthetized Sprague-Dawley rats (350-450 g, n = 32) were randomly assigned to (1) shams (without sepsis), (2) saline controls, and (3) ALM treatment. Sepsis was induced by cecal ligation and puncture. A 0.3-mL bolus was administered intravenously, followed by a 4-hour intravenous infusion (1 mL/kg/h), and hemodynamics (mean arterial pressure [MAP], systolic arterial pressure, diastolic arterial pressure, and heart rate [HR]) and body temperature (BT) were monitored. Coagulation was assessed using prothrombin time and activated partial thromboplastin time (aPTT).
Shams displayed progressive falls in MAP, HR, and BT as well as a prolonged aPTT, which were related to surgery, not infection. At 4 hours, controls showed more pronounced falls in MAP (33%), HR (17%), and BT (3.3°C), and MAP continued to fall after the infusion was stopped. In contrast, ALM treatment resulted in a rapid fall in MAP from 111 mm Hg to 73 mm Hg at 30 minutes (p < 0.05 all groups) and was 59 mm Hg at 240 minutes (p < 0.05 shams), which immediately corrected after 4 hours (p < 0.05 controls). HR paralleled MAP changes in ALM rats, and BT was significantly higher than that of the controls but not that of shams. ALM rats had no arrhythmias compared with the controls or shams and had significantly lower lung wet-dry ratios. Prothrombin time in saline controls at 1 hour and 5 hours was prolonged but not in the shams or ALM rats. aPTT at 1 hour in the sham, control, and ALM groups was 158 ± 41 seconds, 161 ± 41 seconds, and 54 ± 23 seconds and at 5 hours was 104 ± 43 seconds, 205 ± 40 seconds, and 33 ± 3 seconds (p < 0.05), respectively.
An ALM bolus/infusion induces a stable, hypotensive hemodynamic state with no arrhythmias, significantly less pulmonary edema, and a higher BT and prevents coagulopathy compared with the controls.
目前尚无药物疗法能够改善脓毒症的临床预后。腺苷、利多卡因和镁(ALM)推注已被证明在不同的创伤状态下具有心脏保护作用并能恢复凝血功能障碍。我们假设 ALM 治疗可能改善血流动力学、保护肺部并预防脓毒症大鼠模型中的凝血功能障碍。
非肝素化麻醉的 Sprague-Dawley 大鼠(350-450g,n=32)随机分为(1)假手术(无脓毒症)、(2)生理盐水对照和(3)ALM 治疗。通过结扎和穿刺盲肠来诱导脓毒症。静脉内给予 0.3mL 推注,随后静脉内输注 4 小时(1mL/kg/h),监测血流动力学(平均动脉压[MAP]、收缩压、舒张压和心率[HR])和体温(BT)。使用凝血酶原时间和激活部分凝血活酶时间(aPTT)评估凝血。
假手术组 MAP、HR 和 BT 逐渐下降,aPTT 延长,这与手术有关,而与感染无关。4 小时时,对照组 MAP(下降 33%)、HR(下降 17%)和 BT(下降 3.3°C)下降更明显,且输注停止后 MAP 继续下降。相比之下,ALM 治疗在 30 分钟时使 MAP 从 111mmHg 迅速下降至 73mmHg(所有组均 p<0.05),在 240 分钟时下降至 59mmHg(shams 组 p<0.05),4 小时后立即得到纠正(对照组 p<0.05)。HR 与 ALM 大鼠的 MAP 变化平行,BT 明显高于对照组但低于 sham 组。与对照组或 sham 组相比,ALM 大鼠无心律失常,肺湿干重比明显降低。生理盐水对照组在 1 小时和 5 小时时的凝血酶原时间延长,但 sham 组和 ALM 组无此变化。sham、control 和 ALM 组在 1 小时的 aPTT 分别为 158±41 秒、161±41 秒和 54±23 秒,在 5 小时的 aPTT 分别为 104±43 秒、205±40 秒和 33±3 秒(p<0.05)。
与对照组相比,ALM 推注/输注诱导出稳定的、低血压性血流动力学状态,无心律失常,肺水肿明显减少,BT 较高,且可预防凝血功能障碍。