Cardiac effects of MDMA on the metabolic profile determined with 1H‐magnetic resonance spectroscopy in the rat

MDMA (ecstasy) dose-dependently increased body temperature and decreased serotonin levels in heart tissue of rats. The drug altered cardiac metabolites, increasing carnitine while decreasing choline, with no change in other energy-related compounds. These effects suggest MDMA disrupts energy regulation in heart tissue, potentially shifting metabolism toward fatty acid use, and affects cardiovascular serotonergic signaling.

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Abstract

Abstract Despite the potential for deleterious (even fatal) effects on cardiac physiology, 3,4‐methylenedioxymethamphetamine (MDMA; ecstasy) abuse abounds driven mainly by its euphoric effects. Acute exposure to MDMA has profound cardiovascular effects on blood pressure and heart rate in humans and animals. To determine the effects of MDMA on cardiac metabolites in rats, MDMA (0, 5, or 10 mg/kg) was injected every 2 h for a total of four injections; animals were sacrificed 2 h after the last injection (8 h drug exposure), and their hearts removed and tissue samples from left ventricular wall dissected. High resolution magic angle spinning proton magnetic resonance spectroscopy ( 1 H‐MRS) at 11.7 T, a specialized version of MRS aptly suited for analysis of semi‐solid materials such as intact tissue samples, was used to measure the cardiac metabolomic profile, including alanine, lactate, succinate, creatine, and carnitine, in heart tissue from rats treated with MDMA. MDMA effects on MR‐visible choline, glutamate, glutamine, and taurine were also determined. Body temperature was measured following each MDMA administration and serotonin and norepinephrine (NE) levels were measured by high pressure liquid chromatography (HPLC) in heart tissue from treated animals. MDMA significantly and dose‐dependently increased body temperature, a hallmark of amphetamines. Serotonin, but not NE, levels were significantly and dose‐dependently decreased by MDMA in the heart wall. MDMA significantly altered the MR‐visible profile with an increase in carnitine and no change in other key compounds involved in cardiomyocyte energy metabolomics. Finally, choline levels were significantly decreased by MDMA in heart. The results are consistent with the notion that MDMA has significant effects on cardiovascular serotonergic tone and disrupts the metabolic homeostasis of energy regulation in cardiac tissue, potentially increasing utilization of fatty acid metabolism. The contributions of serotonergic signaling on MDMA‐induced changes in cardiac metabolism remain to be determined. Copyright © 2008 John Wiley & Sons, Ltd.