Adrenal GRK2 lowering is an underlying mechanism for the beneficial sympathetic effects of exercise training in heart failure

Giuseppe Rengo, Dario Leosco, Carmela Zincarelli, Massimo Marchese, Graziamaria Corbi, Daniela Liccardo, Amelia Filippelli, Nicola Ferrara, Michael P. Lisanti, Walter J. Koch, Anastasios Lymperopoulos

    Research output: Contribution to journalArticlepeer-review


    Exercise training has been reported to exert beneficial effects on cardiac function and to reduce morbidity and mortality of chronic heart failure (HF). Augmented sympathetic nervous system (SNS) activity, leading to elevated circulating catecholamine (CA) levels, is a hallmark of chronic HF that significantly aggravates this disease. Exercise training has been shown to also reduce SNS overactivity in HF, but the underlying molecular mechanism(s) remain unidentified. We recently reported that adrenal G protein-coupled receptor kinase-2 (GRK2), an enzyme that regulates the sympathoinhibitory α2-adrenoceptors (α2-ARs) present in the CA-producing adrenal medulla, is upregulated in HF, contributing to the chronically elevated CA levels and SNS activity of the disease. In the present study, we tested whether exercise training can affect the adrenal GRK2-α2-AR-CA production system in the context of HF. For this purpose, a 10-wk-long exercise training regimen of adult male Sprague-Dawley rats starting at 4 wk postmyocardial infarction (post-MI) was employed, and examination at the end of this treatment period revealed significant amelioration of β-AR-stimulated contractility in response to exercise training, accompanied by cardiac GRK2 reduction and restoration of circulating plasma CA levels. Importantly, adrenal GRK2 expression (72 ± 5% reduction vs. post-MI untrained) and α2-AR number were also restored after exercise training in post-MI animals. These results suggest that exercise training restores the adrenal GRK2-α2-AR-CA production axis, and this might be part of the mechanism whereby this therapeutic modality normalizes sympathetic overdrive and impedes worsening of the failing heart. Copyright © 2010 the American Physiological Society.
    Original languageEnglish
    Pages (from-to)H2032-H2038
    JournalAmerican Journal of Physiology: Heart and Circulatory Physiology
    Issue number6
    Publication statusPublished - Jun 2010


    • Adrenal G protein-coupled receptor kinase-2
    • Catecholamines
    • Sympathetic overactivity


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