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Article Open Access

Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model

  • Authors:
    • Li-Yan Jin
    • Cong-Feng Li
    • Guang-Fa Zhu
    • Chun-Ting Wu
    • Jun Wang
    • Shu-Feng Yan
  • View Affiliations / Copyright

    Affiliations: Department of Infectious Disease, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing 100029, P.R. China, Department of Respiratory and Critical Care Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing 100029, P.R. China
    Copyright: © Jin et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY_NC 3.0].
  • Pages: 631-637
    |
    Published online on: June 5, 2014
       https://doi.org/10.3892/mmr.2014.2299
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Abstract

The aim of the present study was to explore the protective effect of small interfering RNA (siRNA) against nuclear factor κB (NF-κB) p65 on sepsis-induced acute lung injury (ALI) in mice. In total, 70 male Kunming mice were randomly divided into a healthy control group, a sepsis group, a specific interfering group and a scrambled control group (Sc), and the latter three groups were divided into post-operational 6 and 12 h subgroups, each of which consisted of 10 mice. The mice were administered with NF-κB siRNA, scrambled siRNA and normal saline via tail vein injection. Following 1 h, a mouse model of septic ALI was produced by cecal ligation and puncture (CLP) in the two siRNA groups and the sepsis control group. At 6 and 12 h post‑operation, the experimental mice were sacrificed and the lung tissue samples were collected. Histopathological changes, wet/dry ratio of lung weight, NF-κB protein and NF-κB p65 mRNA levels, matrix metalloproteinase-9 (MMP-9) mRNA and protein activity were detected. Compared with the sepsis group and the Sc at the corresponding time, the expression levels of NF-κB p65 mRNA, the lung injury of experimental mice, the wet/dry ratio and the levels of MMP-9 mRNA and protein activity decreased, and significant differences were observed at 6 h post-operation (P<0.05). RNA interference against NF-κB p65 was able to decrease the expression of NF-κB and further inhibit the early phasic excessive inflammatory reaction in sepsis, which may alleviate ALI.
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Copy and paste a formatted citation
Spandidos Publications style
Jin L, Li C, Zhu G, Wu C, Wang J and Yan S: Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model. Mol Med Rep 10: 631-637, 2014.
APA
Jin, L., Li, C., Zhu, G., Wu, C., Wang, J., & Yan, S. (2014). Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model. Molecular Medicine Reports, 10, 631-637. https://doi.org/10.3892/mmr.2014.2299
MLA
Jin, L., Li, C., Zhu, G., Wu, C., Wang, J., Yan, S."Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model". Molecular Medicine Reports 10.2 (2014): 631-637.
Chicago
Jin, L., Li, C., Zhu, G., Wu, C., Wang, J., Yan, S."Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model". Molecular Medicine Reports 10, no. 2 (2014): 631-637. https://doi.org/10.3892/mmr.2014.2299
Copy and paste a formatted citation
x
Spandidos Publications style
Jin L, Li C, Zhu G, Wu C, Wang J and Yan S: Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model. Mol Med Rep 10: 631-637, 2014.
APA
Jin, L., Li, C., Zhu, G., Wu, C., Wang, J., & Yan, S. (2014). Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model. Molecular Medicine Reports, 10, 631-637. https://doi.org/10.3892/mmr.2014.2299
MLA
Jin, L., Li, C., Zhu, G., Wu, C., Wang, J., Yan, S."Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model". Molecular Medicine Reports 10.2 (2014): 631-637.
Chicago
Jin, L., Li, C., Zhu, G., Wu, C., Wang, J., Yan, S."Effect of siRNA against NF-κB on sepsis‑induced acute lung injury in a mouse model". Molecular Medicine Reports 10, no. 2 (2014): 631-637. https://doi.org/10.3892/mmr.2014.2299
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