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Natural surfactant and hyperoxic lung injury in primates. I. Physiology and biochemistry.

Publication ,  Journal Article
Huang, YC; Caminiti, SP; Fawcett, TA; Moon, RE; Fracica, PJ; Miller, FJ; Young, SL; Piantadosi, CA
Published in: J Appl Physiol (1985)
March 1994

Surfactant dysfunction contributes to the pathophysiology of adult respiratory distress syndrome (ARDS), and we hypothesized that surfactant treatment would improve experimental ARDS produced by continuous exposure to hyperoxia. Twelve healthy male baboons (10-15 kg) were anesthetized, paralyzed, and mechanically ventilated with 2.5 cmH2O positive end-expiratory pressure (PEEP) for 96 h. Baboons were divided into three groups: 1) the O2 group (n = 5) received 100% O2, 2) the surfactant group (n = 5) received 100% O2 and aerosolized porcine surfactant, and 3) a control group (n = 2) was ventilated at fractional concentration of inspired O2 of 0.21 for 96 h to control for effects of anesthesia and mechanical ventilation. Hemodynamic parameters were obtained every 12 h, and ventilation-perfusion (VA/Q) distribution was measured daily by multiple inert gas elimination technique. PEEP was increased once or twice daily to 10 cmH2O for 30 min to study its effects on measurements of VA/Q. At the end of experiments, lungs were obtained for biochemical analysis. Prolonged hyperoxia resulted in progressive worsening in VA/Q, hemodynamic deterioration, severe lung edema, and altered surfactant metabolism. Surfactant administration increased disaturated phosphatidylcholine in lavage fluid but did not improve lung edema or gas exchange. In the surfactant group, however, the addition of 10 cmH2O PEEP resulted in a greater degree of shunt reduction than did 2.5 cmH2O PEEP (47 vs. 31% in the O2 group, P < 0.05). We conclude that aerosolized porcine surfactant did not prevent pulmonary O2 injury in baboons, but it potentiated the shunt-reducing effect of PEEP.

Duke Scholars

Published In

J Appl Physiol (1985)

DOI

ISSN

8750-7587

Publication Date

March 1994

Volume

76

Issue

3

Start / End Page

991 / 1001

Location

United States

Related Subject Headings

  • Ventilation-Perfusion Ratio
  • Swine
  • Respiratory Function Tests
  • Respiratory Distress Syndrome
  • RNA, Messenger
  • Pulmonary Surfactants
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Edema
  • Pulmonary Circulation
  • Proteolipids
 

Citation

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MLA
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Huang, Y. C., Caminiti, S. P., Fawcett, T. A., Moon, R. E., Fracica, P. J., Miller, F. J., … Piantadosi, C. A. (1994). Natural surfactant and hyperoxic lung injury in primates. I. Physiology and biochemistry. J Appl Physiol (1985), 76(3), 991–1001. https://doi.org/10.1152/jappl.1994.76.3.991
Huang, Y. C., S. P. Caminiti, T. A. Fawcett, R. E. Moon, P. J. Fracica, F. J. Miller, S. L. Young, and C. A. Piantadosi. “Natural surfactant and hyperoxic lung injury in primates. I. Physiology and biochemistry.J Appl Physiol (1985) 76, no. 3 (March 1994): 991–1001. https://doi.org/10.1152/jappl.1994.76.3.991.
Huang YC, Caminiti SP, Fawcett TA, Moon RE, Fracica PJ, Miller FJ, et al. Natural surfactant and hyperoxic lung injury in primates. I. Physiology and biochemistry. J Appl Physiol (1985). 1994 Mar;76(3):991–1001.
Huang, Y. C., et al. “Natural surfactant and hyperoxic lung injury in primates. I. Physiology and biochemistry.J Appl Physiol (1985), vol. 76, no. 3, Mar. 1994, pp. 991–1001. Pubmed, doi:10.1152/jappl.1994.76.3.991.
Huang YC, Caminiti SP, Fawcett TA, Moon RE, Fracica PJ, Miller FJ, Young SL, Piantadosi CA. Natural surfactant and hyperoxic lung injury in primates. I. Physiology and biochemistry. J Appl Physiol (1985). 1994 Mar;76(3):991–1001.

Published In

J Appl Physiol (1985)

DOI

ISSN

8750-7587

Publication Date

March 1994

Volume

76

Issue

3

Start / End Page

991 / 1001

Location

United States

Related Subject Headings

  • Ventilation-Perfusion Ratio
  • Swine
  • Respiratory Function Tests
  • Respiratory Distress Syndrome
  • RNA, Messenger
  • Pulmonary Surfactants
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Edema
  • Pulmonary Circulation
  • Proteolipids