Published ahead of print on September 16, 2004, doi:10.1164/rccm.200407-939OC
American Journal of Respiratory and Critical Care Medicine Vol 170. pp. 1179-1184, (2004)
© 2004 American Thoracic Society
doi: 10.1164/rccm.200407-939OC
Trolox Attenuates Mechanical Ventilationinduced Diaphragmatic Dysfunction and Proteolysis
Jenna L. Betters,
David S. Criswell,
R. Andrew Shanely,
Darin Van Gammeren,
Darin Falk,
Keith C. DeRuisseau,
Melissa Deering,
Tossaporn Yimlamai and
Scott K. Powers
Department of Applied Physiology and Kinesiology and Department of Physiology, Center for Exercise Science, University of Florida, Gainesville, Florida
Correspondence and requests for reprints should be addressed to Correspondence and requests for reprints should be addressed to David S. Criswell, Ph.D., P.O. Box 118206, Center for Exercise Science, University of Florida, Gainesville, FL 32611. E-mail: dcriswell{at}hhp.ufl.edu
Prolonged mechanical ventilation results in diaphragmatic oxidative injury, elevated proteolysis, fiber atrophy, and reduced force-generating capacity. We tested the hypothesis that antioxidant infusion during mechanical ventilation would function as an antioxidant to maintain redox balance within diaphragm muscle fibers and therefore prevent oxidative stress and subsequent proteolysis and contractile dysfunction. Sprague-Dawley rats were anesthetized, tracheostomized, and mechanically ventilated with 21% O2 for 12 hours. The antioxidant Trolox was intravenously infused in a subset of ventilated animals. Compared with acutely anesthetized, nonventilated control animals, mechanical ventilation resulted in a significant reduction (17%) in diaphragmatic maximal tetanic force. Importantly, Trolox completely attenuated this mechanical ventilation-induced diaphragmatic contractile deficit. Total diaphragmatic proteolysis was increased 105% in mechanical ventilation animals compared with controls. In contrast, diaphragmatic proteolysis did not differ between controls and mechanical ventilationTrolox animals. Moreover, 20S proteasome activity in the diaphragm was elevated in the mechanical ventilation animals (+76%); Trolox treatment attenuated this mechanical ventilation-induced rise in protease activity. These results are consistent with the hypothesis that mechanical ventilation-induced oxidative stress is an important factor regulating mechanical ventilation-induced diaphragmatic proteolysis and contractile dysfunction. Our findings suggest that antioxidant therapy could be beneficial during prolonged mechanical ventilation.
Key Words: antioxidant protein degradation rat weaning
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Copyright © 2004 American Thoracic Society
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