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Studies on the effect of MDMA (‘ecstasy’) on the body temperature of rats housed at different ambient room temperatures
Author(s) -
Green A Richard,
O'Shea Esther,
Saadat Kathryn S,
Elliott J Martin,
Colado M Isabel
Publication year - 2005
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0706318
Subject(s) - mdma , hypothermia , chemistry , hyperthermia , antagonist , endocrinology , ecstasy , dopamine , medicine , thermoregulation , amphetamine , pharmacology , receptor , psychiatry
3,4‐Methylenedioxymethamphetamine (MDMA, ‘ecstasy’) administration to rats produces hyperthermia if they are housed in normal or warm ambient room temperature ( T a ) conditions (20°C), but hypothermia when in cool conditions ( T a 17°C). We have now investigated some of the mechanisms involved. MDMA (5 mg kg −1 i.p.) produced a rapid decrease in rectal temperature in rats at T a 15°C. This response was blocked by pretreatment with the dopamine D 2 receptor antagonist remoxipride (10 mg kg −1 i.p.), but unaltered by pretreatment with the D 1 antagonist SCH23390 (1.1 mg kg −1 i.p.). MDMA (5 mg kg −1 ) did not alter the tail temperature of rats at T a 15°C, but decreased the tail temperature of rats at T a 30°C. A neurotoxic dose of MDMA (three doses of 5 mg kg −1 given 3 h apart) decreased cortical and hippocampal 5‐HT content by approximately 30% 7 days later. This lesion did not influence the rise in tail temperature when rats were moved from T a 20°C to 30°C compared to nonlesioned controls, but did result in a lower tail temperature than that of controls when they were returned to T a 24°C. Acute administration of MDMA (5 mg kg −1 ) to MDMA‐lesioned rats produced a sustained decrease in tail temperature in rats housed at T a 30°C compared to nonlesioned controls. These data suggest that the thermoregulatory problems previously observed in MDMA‐lesioned rats housed at T a 30°C result, partially, from their inability to lose heat by vasodilation of the tail, a major heat‐loss organ in this species.British Journal of Pharmacology (2005) 146 , 306–312. doi: 10.1038/sj.bjp.0706318

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