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丙泊酚对烧冲复合伤犬外周血单个核细胞及细胞间黏附分子的影响 被引量:5

Effects of continuous sedation with propofol on peripheral blood mononuclear cell and intercellular adhesion molecule in beagles with combined burn-blast injuries
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摘要 目的 观察丙泊酚对烧冲复合伤犬外周血单个核细胞(PBMC)及细胞间黏附分子(ICAM-1)的影响.方法 将32只雄性比格犬按随机数字表法分为:正常对照组、复合伤对照组、丙泊酚1组、丙泊酚2组各8只,除正常对照组外其余3组均致重度烧冲复合伤,4组犬均按Parkland公式补充乳酸钠林格注射液,丙泊酚1组、丙泊酚2组在补液同时分别连续输注2、5 mg·kg^-1·h^-1丙泊酚注射液,持续72 h.4组犬在伤前及伤后6、24、48、72 h分别采取外周静脉血,酶联免疫吸附(ELISA)法检测各组ICAM-1和淋巴细胞功能相关抗原1(LFA-1)水平;流式细胞仪检测各组CD14^+单核细胞犬主要组织相容性复合体(MHC)抗原表达率;CD4^+/CD8^+T淋巴细胞比值和PBMC凋亡率.结果 复合伤对照组伤后24、48、72 h的ICAM-1水平分别为(10.5±1.1)、(10.8±1.3)、(12.3±1.4) ng/ml,均显著高于正常对照组的(7.4±1.4)、(7.4±1.1)、(7.4±1.6)ng/ml(均P<0.05);丙泊酚1组、丙泊酚2组伤后72 h的ICAM-1水平分别为(10.7±1.3)、(8.8±1.4) ng/ml,均显著低于复合伤对照组(均P<0.05),且丙泊酚2组显著低于与丙泊酚1组(P<0.05).复合伤对照组伤后24、48、72 h的LFA-1水平分别为(7.3±1.3)、(8.4±1.3)、(9.6±1.7) ng/ml,均显著高于正常对照组的(5.1±1.2)、(5.4±1.3)、(5.8±1.2) ng/ml(均P<0.05).丙泊酚2组伤后72 h的MHC表达率均显著高于复合伤对照组和丙泊酚1组[(46±13)%比(26±15)%和(32±12)%](均P<0.05).丙泊酚1组和丙泊酚2组伤后48、72 h的CD4 +/CD8^+T淋巴细胞比值分别为(1.71±0.26)、(1.82±0.31)和(1.81±0.24)、(1.96±0.24),均显著高于复合伤对照组的(1.41±0.34)、(1.34±0.26) (P <0.05).伤后72 h复合伤对照组、丙泊酚1组凋亡率分别为(2.57±0.21)%、(1.64±0.10)%,均显著高于正常对照组的(0.81±0.11)%(均P<0.01);丙泊酚2组的凋亡率(1.09±0.15)%显著低于复合伤对照组和丙泊酚1组(均P<0.01).结论 丙泊酚可能通过剂量依赖性的方式抑制ICAM-1过度释放和PBMC凋亡,从而改善烧冲复合伤后免疫功能. Objective To observe the effects of continuous sedation with propofol on peripheral blood mononuclear cell (PBMC) and intercellular adhesion molecule 1 (ICAM-1) in beagles with combined bum-blast injuries.Methods A total of 32 male beagles were randomly divided into 4 groups of normal control (NC),combined injury control (CC),propofol 1 (P1) and propofol 2 (P2) (n =8 each).Except for NC group,the other 3 groups were subject to severe combined bum-blast injury.And sodium lactate Ringer's solution was infused after trauma according to the Parkland formula,including NC group.At the same time,P1 and P2 groups received continuous intravenous infusions of 2 mg · kg^-1 · h^-1,5 mg · kg^-1 · h^-1doses of propofol respectively for 72 hours.The serum concentrations of ICAM-1 and lymphocyte function associated antigen-1 (LFA-1) were measured by enzyme-linked immunosorbent assay (ELISA) at 6,24,48,72 h post-injury.Flow cytometry was used to detect the major histocompatibility complex (MHC) antigen expression on CD14^+ monocytes,CD4^+/CD8^+ T lymphocyte rate and PBMC apoptosis rate.Results The level of ICAM-1 in CC group ((10.5 ± 1.1),(10.8 ± 1.3),(12.3 ± 1.4) ng/ml) was significantly higher than that in NC group ((7.4±1.4),(7.4±1.1),(7.4±1.6) ng/ml) at 12,24,48 h postinjury (all P 〈 0.05).The level of ICAM-1 in P1 group was significantly lower than that in CC group ((10.7 ± 1.3) vs (12.3 ± 1.4) ng/ml) while the level of ICAM-1 in P2 group was significantly lower than that in P1 group at 72 h post-injury ((8.8 ± 1.4) vs (10.7 ± 1.3) ng/ml) (both P 〈0.05).The level of LFA-1 in CC group ((7.3 ± 1.3),(8.4 ± 1.3),(9.6 ± 1.7) ng/ml) was significantly higher than that in NC group ((5.1 ± 1.2),(5.4 ± 1.3),(5.8 ± 1.2) ng/ml) at 24,48,72 h post-injury (all P 〈 0.05).MHC antigen expression on the CD14^+ monocytes of P2 group was obviously higher than that of CC and P1 groups ((46 ± 13) % vs (26 ± 15) % and (32 ± 12) %,both P 〈 0.05).The CD4/CD8 rate in P1 and P2 was significantly higher than that in CC group (1.71 ±0.26,1.82 ±0.31 and 1.81 ±0.24,1.96 ±0.24 vs 1.41 ±0.34,1.34 ±0.26) at 48,72 h post-injury (all P 〈0.05).At 72 h post injury,the PBMC apoptosis rate in CC and P1 group was obviously higher than that of the NC group ((2.57 ± 0.21) % and (1.64 ± 0.10)% vs (0.81 ± 0.11)%) (both P 〈 0.01) ; the apoptosis rate in P2 group was significantly lower thanthat in P1 group ((1.09±0.15)% vs (1.64±0.10)%) (P〈0.01).Conclusion Propofol may improve the immune function after combined burn-blast injuries through suppressing an excessive release of ICAM-1 and PBMC apoptosis in a concentration-dependent manner.
出处 《中华医学杂志》 CAS CSCD 北大核心 2014年第20期1573-1576,共4页 National Medical Journal of China
基金 首都医学发展科研基金(2009-2040)
关键词 创伤和损伤 二异泊酚 烧冲复合伤 细胞黏附分子 淋巴细胞功能相关抗原1 Wound and injuries Propofol Burn-blast combined injuries Cell adhesion molecules Lymphocyte function-associated antigen-1
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