Aerosolized bovine lactoferrin reduces lung injury and fibrosis in mice exposed to hyperoxia

Biometals. 2014 Oct;27(5):1057-68. doi: 10.1007/s10534-014-9750-7. Epub 2014 May 20.

Abstract

This study investigated the ability of aerosolized bovine lactoferrin (bLF) to protect the lungs from injury induced by chronic hyperoxia. Female CD-1 mice were exposed to hyperoxia (FiO2 = 80 %) for 7 days to induce lung injury and fibrosis. The therapeutic effects of bLF, administered via an aerosol delivery system, on the chronic lung injury induced by this period of hyperoxia were measured by bronchoalveolar lavage, lung histology, cell apoptosis, and inflammatory cytokines in the lung tissues. After exposure to hyperoxia for 7 days, the survival of the mice was significantly decreased to 20 %. The protective effects of bLF against hyperoxia were further confirmed by significant reductions in lung edema, total cell numbers in bronchoalveolar lavage fluid, inflammatory cytokines (IL-1β and IL-6), pulmonary fibrosis, and apoptotic DNA fragmentation. The aerosolized bLF protected the mice from oxygen toxicity and increased the survival fraction to 66.7 % in the hyperoxic model. The results support the use of an aerosol therapy with bLF in intensive care units to reduce oxidative injury in patients with severe hypoxemic respiratory failure or chronic obstructive pulmonary disease.

MeSH terms

  • Administration, Inhalation
  • Animals
  • Apoptosis / drug effects
  • Cattle
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Disease Models, Animal
  • Drug Delivery Systems
  • Female
  • Humans
  • Hyperoxia / complications
  • Hyperoxia / drug therapy*
  • Hyperoxia / pathology
  • Immunologic Factors / administration & dosage
  • Inflammation / pathology
  • Inflammation / prevention & control
  • Lactoferrin / administration & dosage*
  • Lung Injury / etiology
  • Lung Injury / pathology
  • Lung Injury / prevention & control*
  • Mice
  • Mice, Inbred ICR
  • Pulmonary Fibrosis / etiology
  • Pulmonary Fibrosis / pathology
  • Pulmonary Fibrosis / prevention & control

Substances

  • Cytokines
  • Immunologic Factors
  • Lactoferrin