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Vol. 301, Issue 1, 152-159, April 2002
Department of Pharmacology and Experimental Therapeutics (K.J.V.,
B.A.O.), Department of Cell Biology and Anatomy (J.D.), Louisiana State
University Health Sciences Center, New Orleans, Louisiana; and
Department of Pathology (S.M.-S.), Tulane School of Medicine, New
Orleans, Louisiana
Methamphetamine (METH) abuse is often characterized by a repeated
pattern of frequent drug administrations (binge) followed by a period
of abstinence. The effect of this pattern of METH use on cardiovascular
function has not been characterized. Radiotelemetry was used to record
the cardiovascular responses elicited during three successive METH
binges (3 mg/kg, b.i.d. for 4 days) in conscious rats. Each binge was
followed by a 10-day METH-free period. The effects of METH
administration on vascular reactivity, Bezold-Jarisch reflex function,
and cardiac morphology were also evaluated. The pressor responses
elicited by the first three doses of METH in the second and third
binges were significantly larger than those elicited by the
corresponding doses in the first binge. The heart rate (HR) responses
elicited by METH were similar within and among the three binges. Ten
days after the last binge, the depressor responses elicited by the i.v.
injection of sodium nitroprusside, isoproterenol, and acetylcholine
were significantly smaller than those elicited before each binge. The
arterial pressure and HR responses elicited by phenylephrine
were unchanged. Bezold-Jarisch reflex function evoked by i.v. serotonin
(10 µg/kg) was significantly altered. The hearts from treated rats
showed focal inflammatory infiltrates with abundant monocytes and
occasional necrotic foci. These results indicate that this binge
pattern of METH administration can significantly alter cardiovascular
function and cardiovascular reflex function and produce serious cardiac pathology.
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