TY - JOUR
T1 - Contribution of high-mobility group box-1 to the development of ventilator-induced lung injury
AU - Ogawa, Eileen N.
AU - Ishizaka, Akitoshi
AU - Tasaka, Sadatomo
AU - Koh, Hidefumi
AU - Ueno, Hiroshi
AU - Amaya, Fumimasa
AU - Ebina, Masahito
AU - Yamada, Shingo
AU - Funakoshi, Yosuke
AU - Soejima, Junko
AU - Moriyama, Kiyoshi
AU - Kotani, Toru
AU - Hashimoto, Satoru
AU - Morisaki, Hiroshi
AU - Abraham, Edward
AU - Takeda, Junzo
PY - 2006/8/15
Y1 - 2006/8/15
N2 - Rationale: Proinflammatory cytokines play an important role in ventilator-induced lung injury (VILI). High-mobility group box-1 (HMGB1) is a macrophage-derived proinflammatory cytokine that can cause lung injury. Objectives: This study tested the hypothesis that HMGB1 is released in intact lungs ventilated with large VT. A second objective was to identify the source of HMGB1. A third objective was to examine the effects of blocking HMGB1 on the subsequent development of VILI. Methods: Bronchoalveolar lavage fluid (BALF) and lung tissues were obtained from rabbits mechanically ventilated for 4 h with a small (8 ml/kg) versus a large (30 ml/kg) VT. BALF was also obtained from rabbits with intratracheal instillation of anti-HMGB1 antibody before the initiation of large VT ventilation. Measurements and Main Results: The concentrations of HMGB1 in BALF were fivefold higher in the large than in the small VT group. Immunohistochemistry and immunofluorescence studies revealed expression of HMGB1 in the cytoplasm of macrophages and neutrophils in lungs ventilated with large VT. Blocking HMGB1 improved oxygenation, limited microvascular permeability and neutrophil influx into the alveolar lumen, and decreased concentrations of tumor necrosis factor-α in BALF. Conclusions: These observations suggest that HMGB1 could be one of the deteriorating factors in the development of VILI.
AB - Rationale: Proinflammatory cytokines play an important role in ventilator-induced lung injury (VILI). High-mobility group box-1 (HMGB1) is a macrophage-derived proinflammatory cytokine that can cause lung injury. Objectives: This study tested the hypothesis that HMGB1 is released in intact lungs ventilated with large VT. A second objective was to identify the source of HMGB1. A third objective was to examine the effects of blocking HMGB1 on the subsequent development of VILI. Methods: Bronchoalveolar lavage fluid (BALF) and lung tissues were obtained from rabbits mechanically ventilated for 4 h with a small (8 ml/kg) versus a large (30 ml/kg) VT. BALF was also obtained from rabbits with intratracheal instillation of anti-HMGB1 antibody before the initiation of large VT ventilation. Measurements and Main Results: The concentrations of HMGB1 in BALF were fivefold higher in the large than in the small VT group. Immunohistochemistry and immunofluorescence studies revealed expression of HMGB1 in the cytoplasm of macrophages and neutrophils in lungs ventilated with large VT. Blocking HMGB1 improved oxygenation, limited microvascular permeability and neutrophil influx into the alveolar lumen, and decreased concentrations of tumor necrosis factor-α in BALF. Conclusions: These observations suggest that HMGB1 could be one of the deteriorating factors in the development of VILI.
KW - High-mobility group box-1
KW - Macrophage, rabbit model
KW - Ventilator-induced lung injury
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U2 - 10.1164/rccm.200605-699OC
DO - 10.1164/rccm.200605-699OC
M3 - Article
C2 - 16728713
AN - SCOPUS:33747112388
SN - 1073-449X
VL - 174
SP - 400
EP - 407
JO - American journal of respiratory and critical care medicine
JF - American journal of respiratory and critical care medicine
IS - 4
ER -