Left ventricular dysfunction and associated cellular injury in rats exposed to chronic intermittent hypoxia

Ling Chen, Jin Zhang, Tracey X. Gan, Ye Chen-Izu, Jeffrey D. Hasday, Morris Karmazyn, C. William Balke, Steven M. Scharf

Research output: Contribution to journalArticle

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Abstract

Obstructive sleep apnea (OSA) increases cardiovascular morbidity and mortality. We have reported that chronic intermittent hypoxia (CIH), a direct consequence during OSA, leads to left ventricular (LV) remodeling and dysfunction in rats. The present study is to determine LV myocardial cellular injury that is possibly associated with LV global dysfunction. Fifty-six rats were exposed either to CIH (nadir O2 4-5%) or sham (handled normoxic controls, HC), 8 h/day for 6 wk. At the end of the exposure, we studied LV global function by cardiac catheterization, and LV myocardial cellular injury by in vitro analyses. Compared with HC, CIH animals demonstrated elevations in mean arterial pressure and LV end-diastolic pressure, but reductions in cardiac output (CIH 141.3 ± 33.1 vs. HC 184.4 ± 21.2 ml·min -1·kg-1, P < 0.01), maximal rate of LV pressure rise in systole (+dP/dt), and maximal rate of LV pressure fall in diastole (-dP/dt). CIH led to significant cell injury in the left myocardium, including elevated LV myocyte size, measured by cell surface area (CIH 3,564 ± 354 vs. HC 2,628 ± 242 μm2, P < 0.05) and cell length (CIH 148 ± 23 vs. HC 115 ± 16 μm, P < 0.05), elevated terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL)-stained positive cell number (CIH 98 ± 45 vs. HC 15 ± 13, P < 0.01), elevated caspase-3 activity (906 ± 249 vs. 2,275 ± 1,169 pmol·min-1·mg-1, P < 0.05), and elevated expression of several remodeling gene markers, including c-fos, atrial natriuretic peptide, β-myosin heavy chain, and myosin light chain-2. However, there was no difference between groups in sarcomere contractility of isolated LV myocytes, or in LV collagen deposition on trichrome-stained slices. In conclusion, CIH-mediated LV global dysfunction is associated with myocyte hypertrophy and apoptosis at the cellular level.

Original languageEnglish (US)
Pages (from-to)218-223
Number of pages6
JournalJournal of Applied Physiology
Volume104
Issue number1
DOIs
StatePublished - Jan 2008
Externally publishedYes

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Left Ventricular Dysfunction
Wounds and Injuries
Muscle Cells
Obstructive Sleep Apnea
Ventricular Pressure
Hypoxia
Sarcomeres
Ventricular Remodeling
Diastole
DNA Nucleotidylexotransferase
Myosin Heavy Chains
Systole
Atrial Natriuretic Factor
Cardiac Catheterization
Cell Size
Left Ventricular Function
Caspase 3
Cardiac Output
Hypertrophy
Myocardium

Keywords

  • Apoptosis
  • Cardiac hypertrophy
  • Obstructive sleep apnea

ASJC Scopus subject areas

  • Physiology
  • Endocrinology
  • Orthopedics and Sports Medicine
  • Physical Therapy, Sports Therapy and Rehabilitation

Cite this

Left ventricular dysfunction and associated cellular injury in rats exposed to chronic intermittent hypoxia. / Chen, Ling; Zhang, Jin; Gan, Tracey X.; Chen-Izu, Ye; Hasday, Jeffrey D.; Karmazyn, Morris; Balke, C. William; Scharf, Steven M.

In: Journal of Applied Physiology, Vol. 104, No. 1, 01.2008, p. 218-223.

Research output: Contribution to journalArticle

Chen, Ling ; Zhang, Jin ; Gan, Tracey X. ; Chen-Izu, Ye ; Hasday, Jeffrey D. ; Karmazyn, Morris ; Balke, C. William ; Scharf, Steven M. / Left ventricular dysfunction and associated cellular injury in rats exposed to chronic intermittent hypoxia. In: Journal of Applied Physiology. 2008 ; Vol. 104, No. 1. pp. 218-223.
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