Diaphragm unloading via controlled mechanical ventilation alters the gene expression profile

Am J Respir Crit Care Med. 2005 Nov 15;172(10):1267-75. doi: 10.1164/rccm.200503-403OC. Epub 2005 Aug 26.

Abstract

Rationale: Prolonged controlled mechanical ventilation results in diaphragmatic inactivity and promotes oxidative injury, atrophy, and contractile dysfunction in this important inspiratory muscle. However, the impact of controlled mechanical ventilation on global mRNA alterations in the diaphragm remains unknown.

Objectives: In these experiments, we used an Affymetrix oligonucleotide array to identify the temporal changes in diaphragmatic gene expression during controlled mechanical ventilation in the rat.

Methods: Adult Sprague-Dawley rats were assigned to either control or mechanical ventilation groups (n = 5/group). Mechanically ventilated animals were anesthetized, tracheostomized, and ventilated with room air for 6 or 18 h. Animals in the control group were acutely anesthetized but not exposed to mechanical ventilation.

Measurements and main results: Compared with control diaphragms, microarray analysis identified 354 differentially expressed, unique gene products after 6 and 18 h of mechanical ventilation. In general, genes in the cell growth/cell maintenance, stress response, and nucleic acid metabolism categories showed predominant upregulation, whereas genes in the structural protein and energy metabolism categories were predominantly downregulated.

Conclusions: We conclude that mechanical ventilation results in rapid changes in diaphragmatic gene expression, and subsequently, many of these changes may contribute to atrophy and muscle fiber remodeling associated with unloading this primary inspiratory muscle. Importantly, this study also provides new insights into why the diaphragm, after the onset of contractile inactivity, atrophies more rapidly than locomotor skeletal muscles and also highlights unique differences that exist between these muscles in the mRNA response to inactivity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Diaphragm / metabolism
  • Diaphragm / pathology
  • Diaphragm / physiology*
  • Energy Metabolism / physiology
  • Female
  • Gene Expression Profiling
  • Gene Expression*
  • Muscle Contraction / physiology
  • Muscle, Skeletal / physiology
  • Oxidative Stress / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Respiration, Artificial
  • Transcription, Genetic

Substances

  • Calcium