University of Texas Medical Branch, Galveston, TX, USA.
Shock. 2010 Sep;34(3):261-8. doi: 10.1097/shk.0b013e3181d8e2a6.
Anesthetics used in burn and trauma animal models may be influencing results by modulating inflammatory and acute-phase responses. Accordingly, we determined the effects of various anesthetics, analgesia, and euthanasia techniques in a rodent burn model. Isoflurane (ISO), ketamine-xylazine (KX), or pentobarbital (PEN) with or without buprenorphine were administered before scald-burn in 72 rats that were euthanized without anesthesia by decapitation after 24 h and compared with unburned shams. In a second experiment, 120 rats underwent the same scald-burn injury using KX, and 24 h later were euthanized under anesthesia or carbon dioxide (CO2). In addition, we compared euthanasia by exsanguination with that of decapitation. Serum cytokine levels were determined by an enzyme-linked immunosorbent assay. In the first experiment, ISO was associated with elevation of cytokine-induced neutrophil chemoattractant 2 (CINC-2) and monocyte chemotactic protein 1 (MCP-1), and KX and PEN was associated with elevation of CINC-1,CINC-2, IL-6, and MCP-1. Pentobarbital also decreased IL-1". IL-6 increased significantly when ISO or PEN were combined with buprenorphine. In the second experiment, euthanasia performed by exsanguination under ISO was associated with reduced levels of IL-1", CINC-1, CINC-2, and MCP-1, whereas KX reduced CINC-2 and increased IL-6 levels. Meanwhile, PEN reduced levels of IL-1" and MCP-1, and CO2 reduced CINC-2 and MCP-1. In addition,decapitation after KX, PEN, or CO2 decreased IL-1" and MCP-1, although we found no significant difference between ISO and controls. Euthanasia by exsanguination compared with decapitation using the same agent also led to modulation of several cytokines. Differential expression of inflammatory markers with the use of anesthetics and analgesics should be considered when designing animal studies and interpreting results because these seem to have a significant modulating impact. Our findings indicate that brief anesthesia with ISO immediately before euthanasia by decapitation exerted the least dampening effect on the cytokines measured. Conversely, KX with buprenorphine may offer a better balance during longer procedures to avoid significant modulation. Standardization across all experiments that are compared and awareness of these findings are essential for those investigating the pathophysiology of inflammation in animal models.
用于烧伤和创伤动物模型的麻醉剂可能通过调节炎症和急性期反应来影响结果。因此,我们在啮齿动物烧伤模型中确定了各种麻醉剂、镇痛剂和安乐死技术的影响。在对 72 只大鼠进行烫伤烧伤之前,用异氟烷(ISO)、氯胺酮-二甲苯胺(KX)或戊巴比妥(PEN)联合或不联合丁丙诺啡进行处理,24 小时后未经麻醉断头安乐死,并与未烧伤的假手术组进行比较。在第二个实验中,120 只大鼠使用 KX 进行相同的烫伤烧伤,24 小时后在麻醉或二氧化碳(CO2)下安乐死。此外,我们还比较了放血安乐死和断头安乐死。通过酶联免疫吸附试验测定血清细胞因子水平。在第一个实验中,ISO 与细胞因子诱导的中性粒细胞趋化因子 2(CINC-2)和单核细胞趋化蛋白 1(MCP-1)的升高有关,而 KX 和 PEN 与 CINC-1、CINC-2、IL-6 和 MCP-1 的升高有关。戊巴比妥还降低了 IL-1。当 ISO 或 PEN 与丁丙诺啡联合使用时,IL-6 显著增加。在第二个实验中,在 ISO 下进行的放血安乐死与 IL-1、CINC-1、CINC-2 和 MCP-1 水平降低有关,而 KX 降低了 CINC-2 并增加了 IL-6 水平。同时,PEN 降低了 IL-1 和 MCP-1 的水平,CO2 降低了 CINC-2 和 MCP-1 的水平。此外,与使用相同药物进行断头安乐死相比,KX、PEN 或 CO2 后,IL-1 和 MCP-1 降低,但与 ISO 和对照组相比,我们未发现差异有统计学意义。
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