Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption.
Ecstasy is a drug that is usually consumed by young people at the weekends and frequently, in combination with cannabis. In the present study we have investigated the long-term effects of administering increasing doses of delta-9-tetrahydrocannabinol [THC; 2.5, 5, 10 mg/kg; i.p.] from postnatal day...
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oai:doaj.org-article:e71ae0e04d994ad0aac180a8587aaff32021-11-18T08:48:33ZSex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption.1932-620310.1371/journal.pone.0078386https://doaj.org/article/e71ae0e04d994ad0aac180a8587aaff32013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24223797/?tool=EBIhttps://doaj.org/toc/1932-6203Ecstasy is a drug that is usually consumed by young people at the weekends and frequently, in combination with cannabis. In the present study we have investigated the long-term effects of administering increasing doses of delta-9-tetrahydrocannabinol [THC; 2.5, 5, 10 mg/kg; i.p.] from postnatal day (pnd) 28 to 45, alone and/or in conjunction with 3,4-methylenedioxymethamphetamine [MDMA; two daily doses of 10 mg/kg every 5 days; s.c.] from pnd 30 to 45, in both male and female Wistar rats. When tested one day after the end of the pharmacological treatment (pnd 46), MDMA administration induced a reduction in directed exploration in the holeboard test and an increase in open-arm exploration in an elevated plus maze. In the long-term, cognitive functions in the novel object test were seen to be disrupted by THC administration to female but not male rats. In the prepulse inhibition test, MDMA-treated animals showed a decrease in prepulse inhibition at the most intense prepulse studied (80 dB), whereas in combination with THC it induced a similar decrease at 75 dB. THC decreased hippocampal Arc expression in both sexes, while in the frontal cortex this reduction was only evident in females. MDMA induced a reduction in ERK1/2 immunoreactivity in the frontal cortex of male but not female animals, and THC decreased prepro-orexin mRNA levels in the hypothalamus of males, although this effect was prevented when the animals also received MDMA. The results presented indicate that adolescent exposure to THC and/or MDMA induces long-term, sex-dependent psychophysiological alterations and they reveal functional interactions between the two drugs.Alvaro Llorente-BerzalEmma PuighermanalAurelijus BurokasAndrés OzaitaRafael MaldonadoEva M MarcoMaria-Paz ViverosPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 11, p e78386 (2013) |
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Medicine R Science Q Alvaro Llorente-Berzal Emma Puighermanal Aurelijus Burokas Andrés Ozaita Rafael Maldonado Eva M Marco Maria-Paz Viveros Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption. |
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Ecstasy is a drug that is usually consumed by young people at the weekends and frequently, in combination with cannabis. In the present study we have investigated the long-term effects of administering increasing doses of delta-9-tetrahydrocannabinol [THC; 2.5, 5, 10 mg/kg; i.p.] from postnatal day (pnd) 28 to 45, alone and/or in conjunction with 3,4-methylenedioxymethamphetamine [MDMA; two daily doses of 10 mg/kg every 5 days; s.c.] from pnd 30 to 45, in both male and female Wistar rats. When tested one day after the end of the pharmacological treatment (pnd 46), MDMA administration induced a reduction in directed exploration in the holeboard test and an increase in open-arm exploration in an elevated plus maze. In the long-term, cognitive functions in the novel object test were seen to be disrupted by THC administration to female but not male rats. In the prepulse inhibition test, MDMA-treated animals showed a decrease in prepulse inhibition at the most intense prepulse studied (80 dB), whereas in combination with THC it induced a similar decrease at 75 dB. THC decreased hippocampal Arc expression in both sexes, while in the frontal cortex this reduction was only evident in females. MDMA induced a reduction in ERK1/2 immunoreactivity in the frontal cortex of male but not female animals, and THC decreased prepro-orexin mRNA levels in the hypothalamus of males, although this effect was prevented when the animals also received MDMA. The results presented indicate that adolescent exposure to THC and/or MDMA induces long-term, sex-dependent psychophysiological alterations and they reveal functional interactions between the two drugs. |
format |
article |
author |
Alvaro Llorente-Berzal Emma Puighermanal Aurelijus Burokas Andrés Ozaita Rafael Maldonado Eva M Marco Maria-Paz Viveros |
author_facet |
Alvaro Llorente-Berzal Emma Puighermanal Aurelijus Burokas Andrés Ozaita Rafael Maldonado Eva M Marco Maria-Paz Viveros |
author_sort |
Alvaro Llorente-Berzal |
title |
Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption. |
title_short |
Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption. |
title_full |
Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption. |
title_fullStr |
Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption. |
title_full_unstemmed |
Sex-dependent psychoneuroendocrine effects of THC and MDMA in an animal model of adolescent drug consumption. |
title_sort |
sex-dependent psychoneuroendocrine effects of thc and mdma in an animal model of adolescent drug consumption. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2013 |
url |
https://doaj.org/article/e71ae0e04d994ad0aac180a8587aaff3 |
work_keys_str_mv |
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