Journal of Capital Medical University ›› 2006, Vol. 27 ›› Issue (1): 9-13.

• 专题报道 • Previous Articles     Next Articles

Tumor Necrosis Factor-α Expression and Nuclear Factor- kappa B Activation in Ventilator-Induced Lung Injury in Rabbits

Zhang Jun, Wang Chen, Pang Baosen, Qin Zhiqiang, Niu Shujie, Ma Li, Mao Yanling   

  1. Beijing Chaoyang Hospital, Beijing Institute of Respiratory Medicine, Capital University of Medical Sciences
  • Received:2005-12-16 Revised:1900-01-01 Online:2006-02-24 Published:2006-02-24

Abstract: Objective The expression of tumor necrosis factor-α(TNF-α) and the activation of nuclear factor-kappa B(NF-κB) were examined in order to investigate the molecular mechanism of ventilator-induced lung injury(VILI).Methods The VILI model was established by mechanical ventilation with a VT of 40 mL/kg. Forty healthy male New Zealand rabbits were randomly divided into control group,conventional ventilation group and VILI group.The concentrations of TNF-α in lung homogenate were measured by enzyme-linked immunosorbent assay(ELISA).The TNF-α mRNA was measured by semi-quantitative transcription-polymerase chain reaction(RT-PCR).The DNA-binding activity of NF-κB was detected by electrophoretic mobility shift assay(EMSA).The partial arterial blood pressure of oxygen(PaO2),wet lung weight to dry lung weight ratio(W/D) and histological changes of lung tissue were also investigated. Results 1) After 4 h of injurious ventilation,PaO2 was significantly reduced compared with conventional ventilation group(P<0.05).In contrast,the W/D was significantly increased compared with control group(P<0.01) and conventional ventilation group(P<0.01).2) The concentrations of TNF-α proteins in lung homogenates were significantly increased by the injurious ventilation for 2 h or 4 h,compare to control group and conventional ventilation group (all P<0.01).The TNF-α mRNA levels in all injurious ventilation groups were significantly higher than control group(all P<0.01) and conventional ventilation group((P<)(0.01)).The TNF-α mRNA levels induced by injurious ventilation for 4 h were significantly higher than that induced by injurious ventilation for 1 h(P<0.01) and 2 h(P<0.05).3) The DNA-binding activity of oxymatrine was significantly increased in all injurious ventilation groups compared with that of control and conventional ventilation group(P<0.01).The DNA-binding activity of NF-κB reached to maximal level at 2 h and remained until 4 h.Conclusion The mRNA and protein level of TNF-α and DNA binding activity of NFκB were up-regulated by VILI.Increased NF-κB activity in the lung may be involved in the transcriptional up-regulation of TNF-α.

Key words: ventilator-induced lung injury, nuclear factor-kappa B, tumor necrosis factor-α

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