Regional expression of endothelin-1, ANP, IGF-1, and LV wall stress in the infarcted rat heart

JP Loennechen, A Støylen, V Beisvag… - American Journal …, 2001 - journals.physiology.org
JP Loennechen, A Støylen, V Beisvag, U Wisløff, Ø Ellingsen
American Journal of Physiology-Heart and Circulatory Physiology, 2001journals.physiology.org
We hypothesized that myocardial infarction induces regional and temporal differences in
endothelin-1 (ET-1), atrial natriuretic peptide (ANP), and insulin-like growth factor-1 (IGF-1)
gene expression that correlate with left ventricular (LV) wall stress. Echocardiography and
LV pressure measurements were performed in coronary artery-ligated or sham-operated
rats. Gene expression was measured by competitive RT-PCR in the infarct, border zone, and
remote area and in regionally isolated cardiomyocytes. ET-1 and IGF-1 expression was …
We hypothesized that myocardial infarction induces regional and temporal differences in endothelin-1 (ET-1), atrial natriuretic peptide (ANP), and insulin-like growth factor-1 (IGF-1) gene expression that correlate with left ventricular (LV) wall stress. Echocardiography and LV pressure measurements were performed in coronary artery-ligated or sham-operated rats. Gene expression was measured by competitive RT-PCR in the infarct, border zone, and remote area and in regionally isolated cardiomyocytes. ET-1 and IGF-1 expression was highest in the infarcted myocardium, whereas ANP expression was highest in noninfarcted myocardium. For all genes, remote area expression was highest after 7 days. At 42 days, ANP maintained maximum expression, ET-1 decreased to 50% of peak levels, and IGF-1 was normalized. Cardiomyocyte expression followed the same pattern as in the myocardium except for a markedly lower IGF-1 expression. Diastolic wall stress was the best hemodynamic variable to predict ET-1 and ANP expression in the remote area. We conclude that ET-1, ANP, and IGF-1 are expressed in different patterns in the infarcted heart in relation to time, functional regions, cellular distribution, and mechanical load.
American Physiological Society