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α1-Adrenergic Receptors Contribute to the Acute Effects of 3,4-Methylenedioxymethamphetamine in Humans

Cédric M. Hysek, Anja E. Fink, Linda D. Simmler, Massimiliano Donzelli, Eric Grouzmann, Matthias E. Liechti

Journal of Clinical Psychopharmacology July 13, 2013 DOI: 10.1097/jcp.0b013e3182979d32 via OpenAlex

Summary

Blocking α₁-noradrenergic receptors with the drug doxazosin reduces MDMA-induced increases in blood pressure and body temperature, and moderately lessens positive mood, but enhances rapid heart rate. In a randomized, double-blind, placebo-controlled crossover study with 16 healthy participants, doxazosin (8 mg daily for 3 days before MDMA 125 mg) altered several acute effects of MDMA. The findings suggest that α₁-adrenergic receptors play a role in the cardiovascular stimulant effects of MDMA and, to a minor extent, its thermogenic and euphoric effects in humans.

Study at a glance

Characteristics Randomized, double-blind, placebo-controlled, 4-session crossover study Peer reviewed
Sample size 16
Population Healthy subjects
Interventions Doxazosin MDMA Placebo
Dose 8 mg/d doxazosin, 125 mg MDMA
Duration 3 days of doxazosin or placebo before each MDMA or placebo session
Topics MDMA
Keywords Doxazosin Placebo Pharmacology
Citations 57
Key finding Doxazosin reduced MDMA-induced elevations in blood pressure and body temperature and moderately attenuated positive mood but enhanced tachycardia.

Abstract

Preclinical studies implicate a role for α₁-noradrenergic receptors in the effects of psychostimulants, including 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy"). The present study evaluated the effects of the α₁-noradrenergic receptor antagonist doxazosin on the acute pharmacodynamic and pharmacokinetic response to MDMA in 16 healthy subjects. Doxazosin (8 mg/d) or placebo was administered for 3 days before MDMA (125 mg) or placebo using a randomized, double-blind, placebo-controlled, 4-session, crossover design. Doxazosin reduced MDMA-induced elevations in blood pressure, body temperature, and moderately attenuated positive mood but enhanced tachycardia associated with MDMA. The results indicate that α₁-adrenergic receptors contribute to the acute cardiostimulant and to a minor extent possibly also to the thermogenic and euphoric effects of MDMA in humans.

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