TY - JOUR
T1 - Exacerbation of Bleomycin-Induced Injury and Fibrosis by Pneumonectomy in the Residual Lung of Mice
AU - Kakizaki, Toru
AU - Kono, Mitsutomo
AU - Watanabe, Masazumi
AU - Tajima, Atsushi
AU - Izumi, Yotaro
AU - Miyasho, Taku
AU - Tasaka, Sadatomo
AU - Fukunaga, Koichi
AU - Maruyama, Ikuro
AU - Ishizaka, Akitoshi
AU - Kobayashi, Koichi
N1 - Funding Information:
This study was supported in part by a Grant-in-Aid for Scientific Research (no. 18120101, 2006, for I. Maruyama and K. Kobayashi) from the Ministry of Education, Science, Sports and Culture.
PY - 2009/6/15
Y1 - 2009/6/15
N2 - Background: Lung resection after induction chemotherapy and/or radiotherapy for down-staging of locally advanced lung cancer can be complicated with lethal interstitial pneumonia. We studied the effects of pneumonectomy on bleomycin-induced lung injury and fibrosis in mice. Methods: The mice underwent left pneumonectomy or a sham thoracotomy after intratracheal administration of saline or bleomycin. Lung permeability index, wet-to-dry weight ratio, histological changes, collagen contents, and concentrations of inflammatory mediators and cell counts in broncho-alveolar lavage (BAL) fluid were assessed in the residual right lung 7 d after surgery. Results: The index of capillary permeability, lung water content, and inflammatory cell counts in BAL fluid were significantly increased by pneumonectomy. These measurements were highest in the mice with both pneumonectomy and intratracheal administration of bleomycin. Similarly, fibrotic change in lung pathology, as well as an increase in lung collagen content, was most prominent in the mice exposed to both interventions. The BAL fluid concentrations of interleukin-1β, interleukin-6, RANTES, and high mobility group box 1 were significantly increased by pneumonectomy and enhanced by the additional administration of bleomycin. Conclusions: The results of this study indicate that pneumonectomy alone causes noncritical lung injury, which amplifies the inflammatory response to bleomycin and promotes lung fibrosis. Several inflammatory mediators appear to be involved in the exacerbation of bleomycin-induced lung injury and fibrosis.
AB - Background: Lung resection after induction chemotherapy and/or radiotherapy for down-staging of locally advanced lung cancer can be complicated with lethal interstitial pneumonia. We studied the effects of pneumonectomy on bleomycin-induced lung injury and fibrosis in mice. Methods: The mice underwent left pneumonectomy or a sham thoracotomy after intratracheal administration of saline or bleomycin. Lung permeability index, wet-to-dry weight ratio, histological changes, collagen contents, and concentrations of inflammatory mediators and cell counts in broncho-alveolar lavage (BAL) fluid were assessed in the residual right lung 7 d after surgery. Results: The index of capillary permeability, lung water content, and inflammatory cell counts in BAL fluid were significantly increased by pneumonectomy. These measurements were highest in the mice with both pneumonectomy and intratracheal administration of bleomycin. Similarly, fibrotic change in lung pathology, as well as an increase in lung collagen content, was most prominent in the mice exposed to both interventions. The BAL fluid concentrations of interleukin-1β, interleukin-6, RANTES, and high mobility group box 1 were significantly increased by pneumonectomy and enhanced by the additional administration of bleomycin. Conclusions: The results of this study indicate that pneumonectomy alone causes noncritical lung injury, which amplifies the inflammatory response to bleomycin and promotes lung fibrosis. Several inflammatory mediators appear to be involved in the exacerbation of bleomycin-induced lung injury and fibrosis.
KW - acute lung injury/acute respiratory distress syndrome (ALI/ARDS)
KW - bleomycin
KW - high mobility group box 1
KW - induction therapy
KW - lung cancer
KW - lung resection
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U2 - 10.1016/j.jss.2008.06.021
DO - 10.1016/j.jss.2008.06.021
M3 - Article
C2 - 19118846
AN - SCOPUS:67349207414
SN - 0022-4804
VL - 154
SP - 336
EP - 344
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 2
ER -