Literature DB >> 17289273

High ambient temperature increases 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy")-induced Fos expression in a region-specific manner.

G A Hargreaves1, G E Hunt, J L Cornish, I S McGregor.   

Abstract

3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy") is a popular drug that is often taken under hot conditions at dance clubs. High ambient temperature increases MDMA-induced hyperthermia and recent studies suggest that high temperatures may also enhance the rewarding and prosocial effects of MDMA in rats. The present study investigated whether ambient temperature influences MDMA-induced expression of Fos, a marker of neural activation. Male Wistar rats received either MDMA (10 mg/kg i.p.) or saline, and were placed in test chambers for 2 h at either 19 or 30 degrees C. MDMA caused significant hyperthermia at 30 degrees C and a modest hypothermia at 19 degrees C. The 30 degrees C ambient temperature had little effect on Fos expression in vehicle-treated rats. However MDMA-induced Fos expression was augmented in 15 of 30 brain regions at the high temperature. These regions included (1) sites associated with thermoregulation such as the median preoptic nucleus, dorsomedial hypothalamus and raphe pallidus, (2) the supraoptic nucleus, a region important for osmoregulation and a key mediator of oxytocin and vasopressin release, (3) the medial and central nuclei of the amygdala, important in the regulation of social and emotional behaviors, and (4) the shell of the nucleus accumbens and (anterior) ventral tegmental area, regions associated with the reinforcing effects of MDMA. MDMA-induced Fos expression was unaffected by ambient temperature at many other sites, and was diminished at high temperature at one site (the islands of Calleja), suggesting that the effect of temperature on MDMA-induced Fos expression was not a general pharmacokinetic effect. Overall, these results indicate that high temperatures accentuate key neural effects of MDMA and this may help explain the widespread use of the drug under hot conditions at dance parties as well as the more hazardous nature of MDMA taken under such conditions.

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Year:  2007        PMID: 17289273     DOI: 10.1016/j.neuroscience.2006.12.023

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  14 in total

Review 1.  The prosocial effects of 3,4-methylenedioxymethamphetamine (MDMA): Controlled studies in humans and laboratory animals.

Authors:  Philip Kamilar-Britt; Gillinder Bedi
Journal:  Neurosci Biobehav Rev       Date:  2015-09-25       Impact factor: 8.989

Review 2.  The preclinical pharmacology of mephedrone; not just MDMA by another name.

Authors:  A R Green; M V King; S E Shortall; K C F Fone
Journal:  Br J Pharmacol       Date:  2014-05       Impact factor: 8.739

3.  Aversive effects of ethanol in adolescent versus adult rats: potential causes and implication for future drinking.

Authors:  Nicole L Schramm-Sapyta; Alexandra G DiFeliceantonio; Ethan Foscue; Susan Glowacz; Naadeyah Haseeb; Nancy Wang; Cathy Zhou; Cynthia M Kuhn
Journal:  Alcohol Clin Exp Res       Date:  2010-09-22       Impact factor: 3.455

4.  Heat increases MDMA-enhanced NAcc 5-HT and body temperature, but not MDMA self-administration.

Authors:  Allison A Feduccia; Nundhun Kongovi; Christine L Duvauchelle
Journal:  Eur Neuropsychopharmacol       Date:  2010-12       Impact factor: 4.600

Review 5.  Evaluation of reward from pain relief.

Authors:  Edita Navratilova; Jennifer Yanhua Xie; Tamara King; Frank Porreca
Journal:  Ann N Y Acad Sci       Date:  2013-03-15       Impact factor: 5.691

6.  Synthetic studies and pharmacological evaluations on the MDMA ('Ecstasy') antagonist nantenine.

Authors:  Onica Legendre; Stevan Pecic; Sandeep Chaudhary; Sarah M Zimmerman; William E Fantegrossi; Wayne W Harding
Journal:  Bioorg Med Chem Lett       Date:  2009-11-20       Impact factor: 2.823

Review 7.  From ultrasocial to antisocial: a role for oxytocin in the acute reinforcing effects and long-term adverse consequences of drug use?

Authors:  I S McGregor; P D Callaghan; G E Hunt
Journal:  Br J Pharmacol       Date:  2008-05       Impact factor: 8.739

Review 8.  Cortisol and 3,4-methylenedioxymethamphetamine: neurohormonal aspects of bioenergetic stress in ecstasy users.

Authors:  A C Parrott
Journal:  Neuropsychobiology       Date:  2009-11-05       Impact factor: 2.328

9.  Independent of 5-HT1A receptors, neurons in the paraventricular hypothalamus mediate ACTH responses from MDMA.

Authors:  Dmitry V Zaretsky; Maria V Zaretskaia; Joseph A Dimicco; Pamela J Durant; Christian T Ross; Daniel E Rusyniak
Journal:  Neurosci Lett       Date:  2013-08-08       Impact factor: 3.046

10.  Pain relief produces negative reinforcement through activation of mesolimbic reward-valuation circuitry.

Authors:  Edita Navratilova; Jennifer Y Xie; Alec Okun; Chaoling Qu; Nathan Eyde; Shuang Ci; Michael H Ossipov; Tamara King; Howard L Fields; Frank Porreca
Journal:  Proc Natl Acad Sci U S A       Date:  2012-11-26       Impact factor: 11.205

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