Circulation, Vol 87, 1687-1697, Copyright © 1993 by American Heart Association
BS Stambler, K Komamura, T Ihara and RP Shannon
BACKGROUND. Prior studies in experimental canine models have demonstrated
that intravenous cocaine administration causes myocardial depression. The
purpose of the present study was to establish the mechanisms of cocaine's
actions on myocardial and left ventricular performance after single
intravenous bolus doses in conscious, chronically instrumented dogs, in
which the full autonomic influences of cocaine would be manifest. METHODS
AND RESULTS. In the intact state, cocaine (1 mg/kg) caused a transient
decrease in left ventricular dP/dt (baseline; 3,086 +/- 107 mm Hg/sec; 2.5
minutes, 2,649 +/- 114 mm Hg; p < 0.05) followed by a 25 +/- 4% increase
in left ventricular dP/dt that peaked at 15 minutes (left ventricular
dP/dt, 3,751 +/- 127 mm Hg/sec, p < 0.01) and remained elevated during
the 30-minute period of observation. Both the initial depression and the
sustained increase in left ventricular contractile response were dose
related. The increase in left ventricular dP/dt persisted under
circumstances in which the responses were normalized for changes in heart
rate and preload that accompanied cocaine administration. The positive
inotropic effects were abolished by full autonomic or selective
beta-adrenergic blockades. Finally, both cardiac output (baseline, 2,461
+/- 142 min/mL; peak [5 minutes], 3,434 +/- 218 mL/min; p < 0.05) and
left ventricular stroke work (baseline, 39 +/- 5 g.m; peak, 49 +/- 6 g.m; p
< 0.05) were increased at all times after cocaine administration,
suggesting that pump performance was enhanced, despite early reductions in
myocardial contractility. Similarly, indexes of early diastolic filling
were enhanced despite transient early prolongation in isovolumic
relaxation. CONCLUSIONS. Acute intravenous cocaine administration (0.1-2
mg/kg) has a biphasic effect on myocardial and left ventricular function
with a transient depression followed by significant sustained increases in
left ventricular contractility. The results are in keeping with an early
local effect followed by significant adrenergic stimulation, which may be
obscured by anesthesia or masked by changes in loading conditions.
ARTICLES
Acute intravenous cocaine causes transient depression followed by enhanced left ventricular function in conscious dogs
Department of Medicine, Harvard Medical School, Beth Israel Hospital, Boston, Mass.
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