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免疫吸附特异性清除循环肿瘤坏死因子—α对内毒素休克时一氧化氮?…
引用本文:Long H,Zhang X,Hou F. 免疫吸附特异性清除循环肿瘤坏死因子—α对内毒素休克时一氧化氮?…[J]. 中华医学杂志, 1998, 78(1): 23-26
作者姓名:Long H  Zhang X  Hou F
摘    要:目的 观察免疫吸附特异性清除循环肿瘤坏死因子α(TNF-α)对内毒素休克时一氧化氮(NO)的生成及其作用的影响。方法 利用新西兰白兔内毒素休克模型,观察经抗TNFα-单克隆抗体亲和免疫吸附血液灌注重对血压、血浆NTF-α活性、NO2含量、脏器NO合酶(NOS)活性及肝、肾功能等的影响,结果 免疫吸附治疗后,血浆TNF-α水平迅速下降,2小时即为44±10U/ml,低血压状态明显改善,NO的生成与释

关 键 词:休克 脓毒性休克 TNF-2 一氧化氮 免疫吸附

Effects of specific removal of circulating tumor necrosis factor-alpha by immunoadsorption on nitric oxide in endotoxin shock
Long H,Zhang X,Hou F. Effects of specific removal of circulating tumor necrosis factor-alpha by immunoadsorption on nitric oxide in endotoxin shock[J]. Zhonghua yi xue za zhi, 1998, 78(1): 23-26
Authors:Long H  Zhang X  Hou F
Affiliation:Department of Nephrology, Nanfang Hospital, First Military Medical College, Guangzhou.
Abstract:OBJECTIVES: To evaluate the effects of specific removal of circulating TNF-alpha by immunoadsorption on nitric oxide (NO) in endotoxin shock. METHODS: Immunoadsorbent against TNF-alpha was produced by the attachment of anti-TNF-alpha monoclonal antibody (McAb) to agarose beads. Blank columns were made of agarose beads without the attachment of anti-TNF-alpha McAb. New Zealand white rabbits were injected intravenously with Lipopolysaccharide (LPS, Escherichia coli O111: B4, 8.0 x 10(9) cfu/kg. B.W), and then were randomly divided into three groups: (1) control group(n = 25); without other treatment. (2) pseudoperfusion group(n = 25): rabbits underwent hemoperfusion through the blank columns. (3) perfusion group (n = 15): rabbits underwent hemoperfusion through the immunoadsorbent columns. Hemoperfusion was started at 1 h after the injection of LPS, and was sustained for two hours with blood flow rate of 5 ml/min. RESULTS: Mean arterial pressure in the perfusion group was significantly increased at 30 min after hemoperfusion (P < 0.05). It maintained a level higher than that before hemoperfusion (P < 0.05), and was higher (P < 0.05) than that in the control and pseudoperfusion groups at 3 h (end of the monitoring period). The plasma TNF-alpha level in the perfusion group was significantly lower than that in the other two groups at 2, 3 and 6 hour after LPS injection (P < 0.05). Although the concentration of plasma nitrite (NO2-, one of the stable end products of NO) in the perfusion group was significantly lower (P < 0.05) than that in the other two groups from 3 h after LPS infusion, it was significantly higher (P < 0.05) than the baseline value from 30 min to 12 h. The activities of NO synthase (NOS) in the heart and lung were significantly lower (P < 0.05) in the perfusion group than in the other two groups at 24 h. The serum levels of alanine transaminase, aspartate transaminase, urea nitrogen, creatinine, lactate dehydrogenase, alpha-hydrobulyric dehydrogenase and alkaline phosphatase in the perfusion group were significantly lower (P < 0.05) than those in the other two groups at 24 h. Moreover, the survival rate of rabbits in the perfusion group was higher (P < 0.05) than that of the other two groups at 24 h. CONCLUSION: Specific removal of circulating TNF-alpha by immunoadsorption actually acts as the selective inhibition of the inducible NOS(iNOS) and may be a new and effective therapy for endotoxin shock.
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