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  1. Article: Methylenedioxymethamphetamine (MDMA, 'Ecstasy'): a stressor on the immune system.

    Connor, Thomas J

    Immunology

    2004  Volume 111, Issue 4, Page(s) 357–367

    Abstract: ... as a 'chemical stressor' on the immune system. Finally, the potential of MDMA-induced immunosuppression ... derivative, methylenedioxymethamphetamine (MDMA; 'Ecstasy') on immunity. Research conducted over the last 5 ... years, in both laboratory animals and humans, has demonstrated that MDMA has immunosuppressive actions ...

    Abstract Drug abuse is a global problem of considerable concern to health. One such health concern stems from the fact that many drugs of abuse have immunosuppressive actions and consequently have the potential to increase susceptibility to infectious disease. This article is focused on the impact of the amphetamine derivative, methylenedioxymethamphetamine (MDMA; 'Ecstasy') on immunity. Research conducted over the last 5 years, in both laboratory animals and humans, has demonstrated that MDMA has immunosuppressive actions. Specifically, MDMA suppresses neutrophil phagocytosis, suppresses production of the pro-inflammatory cytokines tumour necrosis factor-alpha (TNF-alpha) and interleukin (IL)-1beta, and increases production of the endogenous immunosuppressive cytokine (IL-10), thereby promoting an immunosuppressive cytokine phenotype. MDMA also suppresses circulating lymphocyte numbers, with CD4+ T cells being particularly affected, and alters T-cell function as indicated by reduced mitogen-stimulated T-cell proliferation, and a skewing of T-cell cytokine production in a T helper 2 (Th2) direction. For the most part, the aforementioned effects of MDMA are not the result of a direct action of the drug on immune cells, but rather caused by the release of endogenous immunomodulatory substances. Consequently, the physiological mechanisms that are thought to underlie the immunosuppressive effects of MDMA will be discussed. As many of the physiological changes elicited by MDMA closely resemble those induced by acute stress, it is suggested that exposure to MDMA could be regarded as a 'chemical stressor' on the immune system. Finally, the potential of MDMA-induced immunosuppression to translate into significant health risks for abusers of the drug will be discussed.
    MeSH term(s) Animals ; Disease Models, Animal ; Hallucinogens/toxicity ; Humans ; Immune System/drug effects ; Immune Tolerance/drug effects ; N-Methyl-3,4-methylenedioxyamphetamine/toxicity ; Substance-Related Disorders/immunology
    Chemical Substances Hallucinogens ; N-Methyl-3,4-methylenedioxyamphetamine (KE1SEN21RM)
    Language English
    Publishing date 2004-04
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 80124-0
    ISSN 1365-2567 ; 0019-2805 ; 0953-4954
    ISSN (online) 1365-2567
    ISSN 0019-2805 ; 0953-4954
    DOI 10.1111/j.0019-2805.2004.01847.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Acute 3,4-methylenedioxymethamphetamine(MDMA) administration produces a rapid and sustained suppression of immune function in the rat.

    Connor, T J / McNamara, M G / Finn, D / Currid, A / O'Malley, M / Redmond, A M / Kelly, J P / Leonard, B E

    Immunopharmacology

    1998  Volume 38, Issue 3, Page(s) 253–260

    Abstract: 3,4-Methylenedioxymethamphetamine (MDMA;'Ecstasy') is a ring substituted phenylisopropylamine ... established toxic effects of MDMA on the central serotonergic system, a single administration of this widely ... function. However, to date the effects of MDMA on immune function have been restricted to in vitro ...

    Abstract (+)-3,4-Methylenedioxymethamphetamine (MDMA;'Ecstasy') is a ring substituted phenylisopropylamine that is structurally related to both amphetamines and hallucinogens. The unique behavioural activating properties of MDMA have led to its widespread abuse. MDMA induces many neurochemical, behavioural and endocrine alterations which closely resemble those elicited by exposure to acute stress, suggesting that MDMA could be regarded as a 'chemical stressor'. In addition to the neurochemical, behavioural and endocrine effects of stressor exposure, it has been reported that stress produces alterations in immune function. However, to date the effects of MDMA on immune function have been restricted to in vitro investigations. In this study we report, for the first time, that acute in vivo administration of MDMA (20 mg/kg, i.p.) produced a rapid (within 30 min) suppression of Con A-induced lymphocyte proliferation and a profound reduction in the total leucocyte count in rats that persisted for at least 6 h following injection. These alterations in immune function were accompanied by a significant increase in plasma corticosterone concentrations 30 min post MDMA administration which had returned to baseline values within 6 h of drug administration. In addition, there was a significant depletion in cortical 5-HT concentrations both 30 min and 6 h after MDMA administration. The results of this study provide evidence that in addition to the well established toxic effects of MDMA on the central serotonergic system, a single administration of this widely abused drug induces a rapid and sustained suppression of immune function.
    MeSH term(s) Animals ; Cerebral Cortex/drug effects ; Cerebral Cortex/metabolism ; Concanavalin A ; Corticosterone/blood ; Female ; Hallucinogens/administration & dosage ; Hallucinogens/toxicity ; Hydroxyindoleacetic Acid/analysis ; Hydroxyindoleacetic Acid/metabolism ; Immunity, Cellular/drug effects ; Leukocyte Count/drug effects ; Lymphocyte Activation/drug effects ; N-Methyl-3,4-methylenedioxyamphetamine/administration & dosage ; N-Methyl-3,4-methylenedioxyamphetamine/toxicity ; Rats ; Rats, Sprague-Dawley ; Serotonin/analysis ; Serotonin/metabolism ; Serotonin Agents/administration & dosage ; Serotonin Agents/toxicity ; T-Lymphocytes/drug effects ; T-Lymphocytes/immunology ; Time Factors
    Chemical Substances Hallucinogens ; Serotonin Agents ; Concanavalin A (11028-71-0) ; Serotonin (333DO1RDJY) ; Hydroxyindoleacetic Acid (54-16-0) ; N-Methyl-3,4-methylenedioxyamphetamine (KE1SEN21RM) ; Corticosterone (W980KJ009P)
    Language English
    Publishing date 1998-01
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 424423-0
    ISSN 1879-047X ; 0162-3109
    ISSN (online) 1879-047X
    ISSN 0162-3109
    DOI 10.1016/s0162-3109(97)00084-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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