Adenosine, a purine nucleoside and a "retaliatory metabolite" in ischemia, is ubiquitous in the body and increases 100-fold during ischemia. Its biological actions are mediated by four adenosine receptors (ARs): A(1), A(2A), A(2B) and A(3). The aim of this study was to determine possible myocardial alterations in AR expression in an experimental animal model of myocardial infarction (MI) with a preserved left ventricular (LV) ejection fraction. LV tissue was collected from sexually mature male farm pigs with MI (n = 6) induced by permanent surgical ligation of the left anterior descending coronary artery and from five healthy pigs (C). mRNA expression of A(1)R, A(2A)R, A(2B)R, A(3)R and TNF-alpha was determined by real-time PCR in tissue collected from border (BZ) and remote zones (RZ) of the infarcted area and from LV of C. BZ, RZ and samples of C were stained immunohistochemically to investigate A(3)R immunoreaction. After 4 weeks a different regulation of ARs was observed. A(1)R mRNA expression was significantly lower in the infarct regions than in controls (C = 0.75 +/- A 0.2, BZ = 0.05 +/- A 0.2, RZ = 0.07 +/- A 0.02 p = 0.0025, p = 0.0016, C vs. BZ and RZ, respectively). Conversely A(3)R was higher in infarct areas (C = 0.94 +/- A 0.2, BZ = 2.85 +/- A 0.5, RZ = 3.48 +/- A 1.0, p = 0.048 C vs. RZ). No significant differences were observed for A(2A)R (C = 1.58 +/- A 0.6, BZ = 0.42 +/- A 0.1, RZ = 1.37 +/- A 0.6) and A(2B)R (C = 1.66 +/- A 0.2, BZ = 1.54 +/- A 0.5, RZ = 1.25 +/- A 0.4). A(3)R expression was confirmed by immunohistochemical analysis and was principally localized in cardiomyocytes. TNF-alpha mRNA results were: C 0.41 +/- A 0.25; BZ 1.60 +/- A 0.19; RZ 0.17 +/- A 0.04. The balance between A(1)R and A(3)R as well as between A(2A)R and A(2B)R was consistent with adaptative retaliatory anti-ischemic adenosinergic changes in the infarcted heart with preserved LV function.
Adenosine receptor expression in an experimental animal model of myocardial infarction with preserved left ventricular ejection fraction
Cabiati Manuela;Caselli Chiara;Prescimone Tommaso;Del Ry Silvia
2013
Abstract
Adenosine, a purine nucleoside and a "retaliatory metabolite" in ischemia, is ubiquitous in the body and increases 100-fold during ischemia. Its biological actions are mediated by four adenosine receptors (ARs): A(1), A(2A), A(2B) and A(3). The aim of this study was to determine possible myocardial alterations in AR expression in an experimental animal model of myocardial infarction (MI) with a preserved left ventricular (LV) ejection fraction. LV tissue was collected from sexually mature male farm pigs with MI (n = 6) induced by permanent surgical ligation of the left anterior descending coronary artery and from five healthy pigs (C). mRNA expression of A(1)R, A(2A)R, A(2B)R, A(3)R and TNF-alpha was determined by real-time PCR in tissue collected from border (BZ) and remote zones (RZ) of the infarcted area and from LV of C. BZ, RZ and samples of C were stained immunohistochemically to investigate A(3)R immunoreaction. After 4 weeks a different regulation of ARs was observed. A(1)R mRNA expression was significantly lower in the infarct regions than in controls (C = 0.75 +/- A 0.2, BZ = 0.05 +/- A 0.2, RZ = 0.07 +/- A 0.02 p = 0.0025, p = 0.0016, C vs. BZ and RZ, respectively). Conversely A(3)R was higher in infarct areas (C = 0.94 +/- A 0.2, BZ = 2.85 +/- A 0.5, RZ = 3.48 +/- A 1.0, p = 0.048 C vs. RZ). No significant differences were observed for A(2A)R (C = 1.58 +/- A 0.6, BZ = 0.42 +/- A 0.1, RZ = 1.37 +/- A 0.6) and A(2B)R (C = 1.66 +/- A 0.2, BZ = 1.54 +/- A 0.5, RZ = 1.25 +/- A 0.4). A(3)R expression was confirmed by immunohistochemical analysis and was principally localized in cardiomyocytes. TNF-alpha mRNA results were: C 0.41 +/- A 0.25; BZ 1.60 +/- A 0.19; RZ 0.17 +/- A 0.04. The balance between A(1)R and A(3)R as well as between A(2A)R and A(2B)R was consistent with adaptative retaliatory anti-ischemic adenosinergic changes in the infarcted heart with preserved LV function.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.