Respirology · 2010 · 33 citations · 31 references
PharmacyImmunologyPharmacologyApoptosisInflammationPulmonary Drug DeliveryAcute Lung InjuryInhalation Drug DeliveryInhalation InjuryPulmonary ToxicityPulmonary ToxicologyRespiratory ToxicologyAcute Lung Injury PathophysiologyEpithelial ApoptosisHyaluronan BiologyInflammatory Lung InjuryInhalational Lung InjuryNeutrophil-mediated Lung InjuryNeutrophilic Lung InflammationPulmonary Epithelial Injury
BACKGROUND AND OBJECTIVE: High MW hyaluronan (HMW HA) as opposed to low MW hyaluronan (LMW HA) has been shown to have anti-inflammatory and anti-apoptotic effects. We hypothesized that treatment with HMW HA would block smoke inhalation lung injury by inhibiting smoke-induced lung inflammation and airway epithelial cell apoptosis. METHODS: Anesthetized, intubated male rats were randomly allocated to either control or smoke inhalation injury groups. Rats were treated with 3-mL subcutaneous normal saline solution (sham) or LMW HA (35 kDa) or HMW HA (1600 kDa) 18 h before exposure to 15 min of cotton smoke (n = 5 each). Rats were also treated post smoke inhalation with 1600 kDa HA by intra-peritoneal injection (3 mL) or intra-tracheal nebulization (200 µL). Lung neutrophil infiltration, airway apoptosis, airway mucous plugging and lung injury were assessed 4 h after smoke inhalation injury. RESULTS: Rats pretreated with 1600 kDa HA had significantly less smoke-induced neutrophil infiltration, lung oedema, airway apoptosis and mucous plugging. Pretreatment with 35 kDa HA, in contrast, increased smoke-induced neutrophil infiltration and lung injury score. Intra-tracheal administration of a single dose 1600 kDa HA, but not intra-peritoneal injection, significantly improved survival post smoke inhalation. CONCLUSIONS: High MW hyaluronan (1600 kDa) may prove to be a beneficial therapy for smoke inhalation through inhibition of smoke-induced inflammation, lung oedema, airway epithelial cell apoptosis and airway mucous plugging.
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Regulation of lung injury and repair by Toll-like receptors and hyaluronan
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Hyaluronan Fragments Act as an Endogenous Danger Signal by Engaging TLR2
Kara Scheibner, Michael A. Lutz, Sada Boodoo et al. · The Journal of Immunology · 2006 · 698 citations · Full text