A(1) adenosine receptor upregulation accompanies decreasing myocardial adenosine levels in mice with left ventricular dysfunction

Article

关键词: CARDIAC-SPECIFIC OVEREXPRESSION;    NITRIC-OXIDE SYNTHASE;    DILATED CARDIOMYOPATHY;    ENDOGENOUS ADENOSINE;    TRANSGENIC MICE;    HEART-FAILURE;    RAT-HEART;    REPERFUSION;    DESENSITIZATION;    EXPRESSION;   

DOI  :  10.1161/CIRCULATIONAHA.107.694596

来源: SCIE

【 摘 要 】

Background - It is well known that adenosine levels are increased during ischemia and protect the heart during ischemia/reperfusion. However, less is known about the role of adenosine - adenosine receptor (AR) pathways in hearts with left ventricular dilation and dysfunction. Therefore, we assessed adenosine levels and selective AR expression in transgenic mice with left ventricular systolic dysfunction secondary to overexpression of tumor necrosis factor-alpha (TNF 1.6). Methods and Results - Cardiac adenosine levels were reduced by 70% at 3 and 6 weeks of age in TNF 1.6 mice. This change was accompanied by a 4-fold increase in the levels of A(1)-AR and a 50% reduction in the levels of A(2A)-AR. That the increase in A1-AR density was of physiological significance was shown by the fact that chronotropic responsiveness to the A(1)-AR selective agonist 2-chloro-N-6-cyclopentanyladenosine was enhanced in the TNF 1.6 mice. Similar changes in adenosine levels were found in 2 other models of heart failure, mice overexpressing calsequestrin and mice after chronic pressure overload, suggesting that the changes in adenosine-AR signaling were secondary to myocardial dysfunction rather than to TNF overexpression. Conclusions - Cardiac dysfunction secondary to the overexpression of TNF is associated with marked alterations in myocardial levels of adenosine and ARs. Modulation of the myocardial adenosine system and its signaling pathways may be a novel therapeutic target in patients with heart failure.

【 授权许可】

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