Jönsson A, Brofeldt B T, Nellgård P, Tarnow P, Cassuto J
Department of Physiology, Göteborg University, Sweden.
J Burn Care Rehabil. 1998 Jan-Feb;19(1 Pt 1):50-6. doi: 10.1097/00004630-199801000-00011.
Deep partial-thickness burn injury was induced in the abdominal skin of anesthetized rats. Dermal perfusion was assessed by laser Doppler flowmetry. In the first set of experiments, one group of rats (n = 15) was topically treated with a lidocaine-prilocaine cream 5% (25 mg of each in 1 g) for 6 hours, starting 5 minutes after inducing the burn injury. In one control group (n = 14), the thermal injury was treated with placebo cream. Results showed a markedly reduced perfusion in the skin of the control animals within the first hour after burn injury, with further decrease during the following 5 hours of observation. In animals treated with the lidocaine-prilocaine cream, skin perfusion in the burned area was significantly increased during the first 30 minutes after the burn injury compared to before the burn (p < 0.01), followed by a decrease to a level below the preburn stage but significantly higher than that of control animals during the first hour after burn injury (p < 0.05). As opposed to burned control animals, skin perfusion gradually recovered toward preburn levels at the end of the experiment in local anesthetic-treated animals. In the second experimental set, four groups of animals were burned and subsequently treated with a bolus dose of lidocaine intravenously (2 mg/kg), followed by continuous intravenous lidocaine infusions at a rate of 50 (n = 10), 100 (n = 11), or 150 (n = 10) micrograms.kg-1.min-1. The infusions were started 5 minutes after the burn injury and lasted for 6 hours. Corresponding volumes of saline solution were given to burned control animals (n = 10). Results showed a significantly improved skin perfusion in the lidocaine-treated group in a dose-response fashion as compared to control animals. A maximum improvement of dermal perfusion in the burned area was induced by intravenous lidocaine at an infusion rate of 150 micrograms.kg-1.min-1 as compared to burned controls treated with isotonic saline solution infusions (p < 0.01). Results showed that topical or systemic administration of local anesthetics can prevent progressive dermal ischemia after thermal injury.
在麻醉大鼠的腹部皮肤造成深度部分厚度烧伤。通过激光多普勒血流仪评估皮肤灌注。在第一组实验中,一组大鼠(n = 15)在烧伤损伤后5分钟开始,用5%利多卡因-丙胺卡因乳膏(每1克含各25毫克)局部治疗6小时。在一个对照组(n = 14)中,热损伤用安慰剂乳膏治疗。结果显示,对照动物皮肤在烧伤损伤后的第一小时内灌注明显降低,在随后5小时的观察期间进一步下降。在用利多卡因-丙胺卡因乳膏治疗的动物中,烧伤区域的皮肤灌注在烧伤损伤后的前30分钟内与烧伤前相比显著增加(p < 0.01),随后下降至低于烧伤前阶段的水平,但在烧伤损伤后的第一小时内显著高于对照动物(p < 0.05)。与烧伤对照动物相反,在实验结束时,局部麻醉治疗的动物皮肤灌注逐渐恢复到烧伤前水平。在第二组实验中,四组动物烧伤后静脉注射一剂利多卡因(2毫克/千克),随后以50(n = 10)、100(n = 11)或150(n = 10)微克·千克⁻¹·分钟⁻¹的速率持续静脉输注利多卡因。输注在烧伤损伤后5分钟开始,持续6小时。给烧伤对照动物(n = 10)输注相应体积的生理盐水。结果显示,与对照动物相比,利多卡因治疗组的皮肤灌注以剂量反应方式显著改善。与用等渗盐水输注治疗的烧伤对照相比,静脉输注利多卡因以150微克·千克⁻¹·分钟⁻¹的速率可使烧伤区域的皮肤灌注得到最大改善(p < 0.01)。结果表明,局部麻醉药的局部或全身给药可预防热损伤后进行性皮肤缺血。