Endotoxin-induced lung injury in mice: structural, functional, and biochemical responses

Division of Pulmonary, Allergy and Critical Care, Center for Translational Research of the Lung, McKelvey Center for Lung Transplantation, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia Submitted 7 September 2004 ; accepted in final form 5 October 2004 Acute lung injury is usually a complication of sepsis, and endotoxin treatment of mice is a frequently used experimental model. To define this model and to clarify pathogenesis of the lung injury, we injected with 1 mg/kg endotoxin ip and measured pulmonary function, pulmonary edema, serum concentrations of cytokines and growth factors, and lung histology over 48 h. During the first 6 h, tidal volume and minute volume increased and respiratory frequency decreased. Serum concentrations of cytokines showed three patterns: 10 cytokines peaked at 2 h and declined rapidly, two peaked at 6 h and declined, and two had biphasic peaks at 2 and 24 h. Growth factors increased later and remained elevated longer. Both collagen and fibronectin were deposited in the lungs beginning within hours of endotoxin and resolving over 48 h. Histologically, lungs showed increased cellularity at 6 h with minimal persistent inflammation at 48 h. Lung water peaked at 6 h and gradually decreased over 48 h. We conclude that intraperitoneal administration of endotoxin to mice causes a transient systemic inflammatory response and transient lung injury and dysfunction. The response is characterized by successive waves of cytokine release into the circulation, early evidence of lung fibrogenesis, and prolonged increases in growth factors that may participate in lung repair. acute lung injury; acute respiratory distress syndrome; cytokines; growth factors; lipopolysaccharide; animal model Address for reprint requests and other correspondence: M. Rojas, Div. of Pulmonary, Allergy and Critical Care, Center for Translational Research of the Lung, Emory Univ. School of Medicine, Atlanta, GA 30322 (E-mail: mrojas{at}emory.edu )