{"title":"Influence of ketanserin on the effects of methylenedioxymethamphetamine on body temperature in the mouse","authors":"J. R. Docherty, S. Bexis","doi":"10.1111/aap.12009","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>\n \n </p><ol>\n \n \n <li>We have investigated the ability of the 5HT<sub>2</sub>-receptor antagonist ketanserin to affect the hyperthermia produced by methylenedioxymethamphetamine (MDMA) in conscious mice and examined whether α<sub>1</sub>-adrenoceptor antagonist actions are involved.</li>\n \n \n <li>Mice were implanted with intra-abdominal temperature probes under anaesthesia and allowed 2 weeks recovery. MDMA (20 mg kg<sup>−1</sup>) was administered subcutaneously 30 min after vehicle or test antagonist and effects on body temperature monitored by telemetry.</li>\n \n \n <li>Following vehicle, MDMA produced a slowly developing hyperthermia, reaching a maximum increase of 1.24 °C at 150 min postinjection. Ketanserin (0.5 mg kg<sup>−1</sup>) revealed a significant and marked early hypothermia to MDMA, an effect that is mimicked by the α<sub>1</sub>-adrenoceptor antagonist prazosin (0.1 mg kg<sup>−1</sup>).</li>\n \n \n <li>Functional studies revealed antagonist actions of ketanserin at α<sub>1</sub>-adrenoceptors in rat aorta and rat vas deferens <i>in vitro</i> indicative of α<sub>1</sub>-adrenoceptor antagonist actions at the concentration used <i>in vivo</i>.</li>\n \n \n <li>In conclusion, ketanserin (0.5 mg kg<sup>−1</sup>) modulates the hyperthermic actions of MDMA in mice. Although we cannot rule out additional actions at 5HT<sub>2</sub>-receptors, the actions of ketanserin are consistent with α<sub>1</sub>-adrenoceptor antagonism. There is no clear evidence from this study that 5HT<sub>2</sub>-receptors mediate the hyperthermic response to MDMA.</li>\n </ol>\n \n </div>","PeriodicalId":100151,"journal":{"name":"Autonomic and Autacoid Pharmacology","volume":"33 3-4","pages":"35-41"},"PeriodicalIF":0.0000,"publicationDate":"2013-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/aap.12009","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Autonomic and Autacoid Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/aap.12009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9
Abstract
We have investigated the ability of the 5HT2-receptor antagonist ketanserin to affect the hyperthermia produced by methylenedioxymethamphetamine (MDMA) in conscious mice and examined whether α1-adrenoceptor antagonist actions are involved.
Mice were implanted with intra-abdominal temperature probes under anaesthesia and allowed 2 weeks recovery. MDMA (20 mg kg−1) was administered subcutaneously 30 min after vehicle or test antagonist and effects on body temperature monitored by telemetry.
Following vehicle, MDMA produced a slowly developing hyperthermia, reaching a maximum increase of 1.24 °C at 150 min postinjection. Ketanserin (0.5 mg kg−1) revealed a significant and marked early hypothermia to MDMA, an effect that is mimicked by the α1-adrenoceptor antagonist prazosin (0.1 mg kg−1).
Functional studies revealed antagonist actions of ketanserin at α1-adrenoceptors in rat aorta and rat vas deferens in vitro indicative of α1-adrenoceptor antagonist actions at the concentration used in vivo.
In conclusion, ketanserin (0.5 mg kg−1) modulates the hyperthermic actions of MDMA in mice. Although we cannot rule out additional actions at 5HT2-receptors, the actions of ketanserin are consistent with α1-adrenoceptor antagonism. There is no clear evidence from this study that 5HT2-receptors mediate the hyperthermic response to MDMA.