Chinese Journal of Tissue Engineering Research ›› 2015, Vol. 19 ›› Issue (43): 6913-6917.doi: 10.3969/j.issn.2095-4344.2015.43.005

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Chitosan nanoparticles enfolding antisense endothelin converting enzyme RNA expression plasmid and airway hyperresponsiveness in asthmatic mouse models

Liu Jia   

  1. Department of Respiratory Medicine, General Hospital of Shenyang Military Region, Shenyang 110016, Liaoning Province, China
  • Received:2015-09-10 Online:2015-10-15 Published:2015-10-15
  • About author:Liu Jia, Master, Physician, Department of Respiratory Medicine, General Hospital of Shenyang Military Region, Shenyang 110016, Liaoning Province, China

Abstract:

BACKGROUND: Studies have reported that under in vitro experimental environment, antisense endothelin nucleic acid nanometer carrier can express target nucleic acid and produce RNA interference effect after enfolding by 12-alkylated chitosan nanoparticles, which can effectively inhibit the excessive generation of endothelin from inflammatory cytokines induced by allergen.

OBJECTIVE: To investigate the effect of 12-alkylated chitosan nanoparticles enfolding antisense endothelin converting enzyme RNA expression plasmid on airway hyperresponsiveness in asthmatic mouse models.
METHODS: Forty Balb/c mice were randomly divided into four groups: control, chitosan nanoparticles, normal saline and plasmid groups. Mice in the chitosan nanoparticles, normal saline and plasmid groups were subjected to sensitization by an intraperitoneal injection with ovalbumin (0, 14 days) and motivation by aerosol inhalation of ovalbumin (24, 25, 26 days) to induce asthma models. Mice in the control group were subjected to sensitization and motivation by the perfusion of normal saline. At 24hours before the first excitation, mice in the control, chitosan nanoparticles, normal saline and plasmid groups were perfused with normal saline via airway, 12-alkylated chitosan nanoparticles, normal saline and antisense endothelin converting enzyme RNA. At 48 hours after the last excitation, the airway reactivity of mice was detected. After 28 days, bronchoalveolar lavage  fluid cytology, lung histopathology, cytokines in spleen cell culture supernatant were detected.
RESULTS AND CONCLUSION: Compared with the control group, the total number of plasmid cells, the percentage of eosinophils, eosinophil absolute counts, interleukin-4 levels, endothelin levels and airway hyperresponsiveness of mice in chitosan nanoparticles, normal saline and plasmid groups were increased (P < 0.05), and the lung inflammation was more severe. These indicators in the chitosan nanoparticles group were all lower than those in the normal saline and plasmid groups (P < 0.05) and the degree of inflammation was lighter than that in the saline and plasmid groups. These results demonstrate that 12-alkylated chitosan nanoparticles enfolding antisense endothelin converting enzyme RNA expression plasmid can reduce the synthetic amount of asthma endothelin and inhibit airway responsiveness.
 

Key words: Chitosan, Nanoparticles, Asthma, Tissue Engineering