实用医学杂志
實用醫學雜誌
실용의학잡지
The Journal of Practical Medicine
2015年
19期
3166-3168
,共3页
应激障碍, 创伤后%细胞因子%环氧化酶-2%氧化应激
應激障礙, 創傷後%細胞因子%環氧化酶-2%氧化應激
응격장애, 창상후%세포인자%배양화매-2%양화응격
Stress disorders,post-traumatic%Cytokine%Cyclooxygenase-2%Oxidativestress
目的:初步探讨创伤后应激障碍(PTSD)患者血清中白细胞介素(IL)-1、IL-6、肿瘤坏死因子-α(TNF-α)与环氧化酶-2(COX-2)的表达变化及意义。方法:收集32例PTSD患者(PTSD组)与26例健康体检者(对照组),采用酶联免疫吸附法(ELISA)与Western blot法对PTSD组血清中IL-1、IL-6、TNF-α及COX-2进行检测,并与对照组进行比较。结果:PTSD 组血清 IL-1、IL-6及 TNF-α水平明显高于对照组(P <0.01);COX-2含量水平也明显高于对照组(P <0.01)。结论:PTSD患者存在显著的免疫功能紊乱,IL-1、IL-6、TNF-α及COX-2可能在PTSD的发病机制中起着重要作用。
目的:初步探討創傷後應激障礙(PTSD)患者血清中白細胞介素(IL)-1、IL-6、腫瘤壞死因子-α(TNF-α)與環氧化酶-2(COX-2)的錶達變化及意義。方法:收集32例PTSD患者(PTSD組)與26例健康體檢者(對照組),採用酶聯免疫吸附法(ELISA)與Western blot法對PTSD組血清中IL-1、IL-6、TNF-α及COX-2進行檢測,併與對照組進行比較。結果:PTSD 組血清 IL-1、IL-6及 TNF-α水平明顯高于對照組(P <0.01);COX-2含量水平也明顯高于對照組(P <0.01)。結論:PTSD患者存在顯著的免疫功能紊亂,IL-1、IL-6、TNF-α及COX-2可能在PTSD的髮病機製中起著重要作用。
목적:초보탐토창상후응격장애(PTSD)환자혈청중백세포개소(IL)-1、IL-6、종류배사인자-α(TNF-α)여배양화매-2(COX-2)적표체변화급의의。방법:수집32례PTSD환자(PTSD조)여26례건강체검자(대조조),채용매련면역흡부법(ELISA)여Western blot법대PTSD조혈청중IL-1、IL-6、TNF-α급COX-2진행검측,병여대조조진행비교。결과:PTSD 조혈청 IL-1、IL-6급 TNF-α수평명현고우대조조(P <0.01);COX-2함량수평야명현고우대조조(P <0.01)。결론:PTSD환자존재현저적면역공능문란,IL-1、IL-6、TNF-α급COX-2가능재PTSD적발병궤제중기착중요작용。
Objective To investigate the significance of variation of concentrations of serum IL-1,IL-6, TNF-α and cyclooxygenase-2 in patients with post-traumatic stress disorder (PTSD). Methods Thirty-two PTSD patients were chosen as the observation group and another 26 normal patients were taken as the control group. The concentrations of serum IL-1,IL-6,TNF-α and COX-2 in patients of both groups were detected by Enzyme-linked immunosorbent assay (ELISA) and Western blot and were compared in these 2 groups. Results The concentrations of serum IL-1 , IL-6 and TNF-α were significantly higher in the observation group than those in the control group (P < 0.01);and the level of COX-2 in the observation group was significantly higher than that of the control group(P < 0.01). Conclusions Abnormal immune states are awared in PTSD patients and the IL-1,IL-6,TNF-α and COX-2 might play an important role in the pathogenesis of PTSD.