(Circulation. 2000;102:2396.)
© 2000 American Heart Association, Inc.
Basic Science Reports |
From San Diego VA Healthcare System (D.M.R., B.P.H., J.Z., C.K., H.K.H.); the Departments of Medicine (N.D., H.K.H.) and Anesthesia (D.M.R.), University of California at San Diego; the Department of Cardiovascular Medicine, Hokkaido University School of Medicine, Sapporo, Japan (K.U.); and Collateral Therapeutics, Inc, San Diego, Calif (N.C.L., M.H.G., S.F., M.D.M., D.A.R.).
Correspondence to H. Kirk Hammond, MD, VAMC-San Diego (111-A), 3350 La Jolla Village Drive, San Diego, CA 92161. E-mail khammond{at}ucsd.edu
BackgroundWe tested the hypothesis that intracoronary injection of a recombinant adenovirus encoding adenylyl cyclase type VI (ACVI) would increase cardiac function in pigs.
Methods and ResultsLeft ventricular (LV) dP/dt and cardiac output in response to isoproterenol and NKH477 stimulation were assessed in normal pigs before and 12 days after intracoronary delivery of histamine followed by intracoronary delivery of an adenovirus encoding lacZ (control) or ACVI (1.4x1012 vp). Animals that had received ACVI gene transfer showed increases in peak LV dP/dt (average increase of 1267±807 mm Hg/s; P=0.0002) and cardiac output (average increase of 39±20 mL · kg-1 · min-1; P<0.0001); control animals showed no changes. Increased LV dP/dt was evident 6 days after gene transfer and persisted for at least 57 days. Basal heart rate, blood pressure, and LV dP/dt were unchanged, despite changes in cardiac responsiveness to catecholamine stimulation. Twenty-three hour ECG recordings showed no change in mean heart rate or ectopic beats and no arrhythmias. LV homogenates from animals receiving ACVI gene transfer showed increased ACVI protein content (P=0.0007) and stimulated cAMP production (P=0.0006), confirming transgene expression and function; basal LV AC activity was unchanged. Increased cAMP-generating capacity persisted for at least 18 weeks (P<0.0002).
ConclusionsIntracoronary injection of a recombinant adenovirus encoding AC provides enduring increases in cardiac function.
Key Words: receptors, adrenergic, beta gene transfer heart failure histamine myocardial contraction
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