Researchers
have demonstrated that binge use of MDMA (ecstasy) can significantly
alter cardiovascular function, including inducing cardiac arrhythmia
and myocarditis, inflammation of the heart wall.
In rats injected
with MDMA, the risk of cardiac arrhythmia increased and the pattern
of mean arterial pressure (MAP) and fluctuations in heart rate changed
after repeated MDMA binges. This finding indicates that MDMA has the
potential to significantly alter cardiovascular function and to produce
potentially serious cardiovascular toxicity.
Scientists
employed radiotelemetry to chart the changes in the rats’ arterial blood
pressure and heart rate during three MDMA binges. Each binge was separated
by a 10-day period of abstinence and consisted of administering 3 or
9 mg/kg of MDMA twice daily for four days. Researchers say that the
3-mg/kg dose of MDMA used in the study is within the range of human
recreational doses. The pattern of drug bingeing followed by a period
of abstinence also is characteristic of the drug’s use by humans.
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No
significant differences were seen in the resting levels of MAP or heart
rate before each of the three MDMA binges or 10 days after the third
binge. In the first binge, the intravenous administration of 3 or 9
mg/kg of MDMA increased MAP and produced an episode of slowed heart
rate (bradycardia) followed by rapid heart rate (tachycardia). After
repeated dosing, the pattern of MAP and heart rate responses elicited
by MDMA changed from that typically induced by a stimulant to one resembling
the vasovagal reflex—a decrease in heartbeat and in MAP.
What it means: This is the first study to examine the cardiovascular
responses elicited by the binge pattern of chronic MDMA use and the
first report showing that the binge administration of MDMA can produce
toxic inflammation in the ventricles of the heart. The study’s findings
indicate that MDMA users may be risking damage to their cardiovascular
systems. The study was reported in the September 2002 issue of The
Journal of Pharmacology and Experimental Therapeutics by a research
team headed by Kurt J. Varner of the Louisiana State University Health
Sciences Center.
NIDA NewsScan,
March 5, 2002 |