Sex-Dependent Psychoneuroendocrine Effects of THC and MDMA in an Animal Model of Adolescent Drug Consumption
Alvaro Llorente‐berzal, Emma Puighermanal, Aurelijus Burokas, Andrés Ozaita, Rafaël Maldonado, Eva M. Marco, María‐paz Viveros
PLoS One November 4, 2013 DOI: 10.1371/journal.pone.0078386 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Animal experiment Peer reviewed |
|---|---|
| Population | Male and female Wistar rats |
| Interventions | THC MDMA |
| Dose | THC: 2.5, 5, 10 mg/kg i.p.; MDMA: 10 mg/kg s.c. twice daily every 5 days |
| Duration | From postnatal day 28 to 45 (THC) and from postnatal day 30 to 45 (MDMA); tested on postnatal day 46 and later |
| Measures | holeboard test, elevated plus maze, novel object test, prepulse inhibition |
| Topics | Cannabis MDMA |
| Keywords | Prepulse inhibition Hallucinogen Endocrinology Hippocampal formation Pharmacology Delta-9-tetrahydrocannabinol |
| Citations | 43 |
| Key findings | Adolescent exposure to THC and/or MDMA induces long-term, sex-dependent psychophysiological alterations and reveals functional interactions between the two drugs. |
Abstract
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.