Good find on dangers o XTC
JNM - The Journal of Nuclear Medicine
Clinical Investigations
Long-Term Effects of "Ecstasy" Use on Serotonin Transporters of the Brain Investigated by PET
Ralph Buchert, PhD1, Rainer Thomasius, MD2, Bruno Nebeling, PhD1, Kay Petersen, PhD2, Jost Obrocki, MD2, Lars Jenicke, MD1, Florian Wilke1, Lutz Wartberg2, Pavlina Zapletalova, MS2 and Malte Clausen, MD1
1 Department of Nuclear Medicine, University Hospital Hamburg-Eppendorf, Hamburg, Germany
2 Department of Psychiatry and Psychotherapy, University Hospital Hamburg-Eppendorf, Hamburg, Germany
Alterations of the serotonergic system due to ecstasy consumption have been extensively documented in recent literature. However, reversibility of these neurotoxic effects still remains unclear. To address this question, PET was performed using the serotonin transporter (SERT) ligand 11C-(+)-McN5652 in a total of 117 subjects subdivided into 4 groups: actual ecstasy users (n = 30), former ecstasy users (n = 29), drug-naive control subjects (n = 29), and subjects with abuse of psychoactive agents other than ecstasy (n = 29). Methods: About 500 MBq 11C-(+)-McN5652 were injected intravenously. Thirty-five scans were acquired according to a dynamic scan protocol of 90 min using a full-ring whole-body PET system. Transaxial slices were reconstructed using an iterative method. Individual brains were transformed to a template defined earlier. Distribution volume ratios (DVRs) were derived by application of a reference tissue approach for reversible binding. Gray matter of the cerebellum served as reference. SERT-rich brain regions—mesencephalon, putamen, caudate, and thalamus—were selected for the evaluation of SERT availability using volumes of interest predefined in the template. Results: Compared with drug-naive control subjects, the DVR in actual ecstasy users was significantly reduced in the mesencephalon (P = 0.004) and the thalamus (P = 0.044). The DVR in former ecstasy users was very close to the DVR in drug-naive control subjects in all brain regions. The DVR in polydrug users was slightly higher than that in the drug-naive control subjects in all SERT-rich regions (not statistically significant). Conclusion: Our findings further support the hypothesis of ecstasy-induced protracted alterations of the SERT. In addition, they might indicate reversibility of the availability of SERT as measured by PET. However, this does not imply full reversibility of the neurotoxic effects.
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In other words. Seritonin levels in the group of current ecstacy users was unnaturally low. But, it shows that the former ecstacy users, after abstaining from the drug for about 3 monthes, seritonin function was somewhat lessened, but very minutely. maybe 4-5% below natural production.
In other words. The long-term effects of ecstacy are not what the us. gov't says. they base their findings on a very bad study by Dr. George A. Ricaurte of Johns Hopkins University. http://www.mdma.net/toxicity/research.html He is also the basis of the govt's campaign to persuade people that ecstacy is an extremely dangerous drug. Saying, one recreational use can cause parkinson's disease, "holes in the brain". they base these claims on the studies by Dr. Ricaurte.
The truth is, if u stop taking ecstacy for a relatively short time, your seritonin levels come back to practically normal levels. with my a 4-5% difference from before. ecstacy does not put holes in your brain, make u paranoid, give u parkinsons' disease or very rarely kills u.
The danger comes from dehydration, and overheating. not the drug itself. There was another study that out of 19,000 deaths in new york city in one year. 22 were related to ectasy. 19 had ectasy in their systems, and 3 died as a result of the MDMA itself. 3, out of the hundreds of thousands of pills taken every year in new york city.
another danger is of course the purity. some try to make an easy buck, and make fake pills. some are laced with far more dangerous drugs like coke and herione or lsd.
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