文章摘要
右美托咪定经门静脉预处理对肝部分切除术患者术中炎症反应和氧化应激的影响
Effects of dexmedetomidine via portal vein preconditioning on inflammatory response and oxidative stress in hepatic ischemia-reperfusion injury
  
DOI:10.12089/jca.2020.04.001
中文关键词: 右美托咪定  门静脉  肝脏缺血-再灌注损伤  氧化应激  炎症反应
英文关键词: Dexmedetomidine  Portal vein  Hepatic ischemia-reperfusion injury  Oxidative stress  Inflammatory response
基金项目:
作者单位E-mail
邢现良 330006,南昌大学第二附属医院麻醉科  
朱妍梦 南昌大学玛丽女王学院  
汤斌铨 330006,南昌大学第二附属医院麻醉科  
邓欢玲 330006,南昌大学第二附属医院麻醉科  
邓福谋 330006,南昌大学第二附属医院麻醉科  
胡衍辉 330006,南昌大学第二附属医院麻醉科 1282254282@qq.com 
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中文摘要:
      
目的 探讨右美托咪定经门静脉预处理对肝部分切除术患者术中肝脏缺血-再灌注损伤中炎症反应和氧化应激的影响。
方法 拟在全麻下行肝部分切除术患者60例,男34例,女26例,年龄25~64岁,体重55~70 kg,ASAⅡ级,肝功能Child-Pugh A级。采用随机数字表法将患者分为三组,每组20例。DP组在游离出门静脉后经门静脉输注右美托咪定1.0 μg/kg,DJ组在游离出门静脉后经颈内静脉输注右美托咪定1.0 μg/kg,C组给予等容量生理盐水。分别于肝门阻断前10 min、肝门开放后1、6、12、24 h经颈内静脉采血检测血清ALT、AST、TNF-α、IL-33、高迁移率族蛋白1(HMGB1)、血红素氧合酶-1(HO-1)浓度和超氧化物歧化酶(SOD)活性。
结果 与肝门阻断前10 min比较,肝门开放后1、6、12、24 h三组血清ALT、AST、TNF-α、IL-33、HMGB1和HO-1浓度明显升高,SOD活性明显降低(P<0.05)。与C组比较,肝门开放后1、6、12、24 h DP组和DJ组血清ALT、AST、TNF-α、IL-33、HMGB1浓度明显降低,HO-1浓度和SOD活性明显升高(P<0.05)。与DJ组比较,肝门开放后1、6、12、24 h DP组血清ALT、AST、TNF-α、IL-33、HMGB1浓度明显降低,HO-1浓度和SOD活性明显升高(P<0.05)。
结论 经门静脉输注右美托咪定能更有效抑制炎症反应和氧化应激,增强机体抗炎抗氧化能力,减轻肝部分切除术患者肝缺血-再灌注损伤。
英文摘要:
      
Objective To investigate the effects of dexmedetomidine via portal vein preconditioning on inflammatory response and oxidative stress in hepatic ischemia-reperfusion injury.
Methods Sixty patients with partial hepatectomy under general anesthesia, 34 males and 26 females, aged 25-64 years, weighing 55-70 kg, ASA physical status Ⅱ, and liver function Child-Pugh grade A, were divided into three groups (n = 20 ecah) by using a random number table method: dexmedetomidine via the portal vein infusion group (group DP), dexmedetomidine via the internal infusion group (group DJ) and control group (group C). In group DP, dexmedetomidine 1.0 μg/kg was infused via the portal vein after the portal vein was released. In group DJ, dexmedetomidine was 1.0 μg/kg via the internal jugular vein after the portal vein was released. Group C was given an equal volume of normal saline. Serum ALT, AST, TNF-α, IL-33, high mobility group protein 1 (HMGB1), heme oxygenase-1 (HO-1) and superoxide dismutase (SOD) activity were detected at internal jugular vein 10 min before hepatic portal occlusion and 1, 6, 12 and 24 hours after hepatic portal opening.
Results Compared with 10 min before hepatic portal occlusion, the serum concentrations of ALT, AST, TNF-α, IL-33, HMGB1 and HO-1 were significantly increased and the activity of SOD was significantly decreased in the three groups at 1, 6, 12 and 24 hours after hepatic portal occlusion (P < 0.05). Compared with group C, the serum concentrations of ALT, AST, TNF-α, IL-33 and HMGB1 were decreased significantly, while HO-1 concentration and SOD activity were increased significantly in group DP and group DJ at 1, 6, 12 and 24 hours after porta hepatis opening (P < 0.05). Compared with group DJ, the concentration of ALT, AST, TNF-α, IL-33 and HMGB1 were decreased significantly, while the concentration of HO-1 and the activity of SOD were increased significantly in group DP at 1, 6, 12 and 24 hours after porta hepatis opening (P < 0.05).
Conclusion Portal intravenous infusion of dexmetomidine can more effectively inhibit inflammatory reaction and oxidative stress, enhance the ability of anti-inflammation and antioxidation, and reduce hepatic ischemia-reperfusion injury in patients with partial hepatectomy.
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