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Neuroadaptive Changes in 5-HT1A Autoreceptor Sensitivity Following High-Dose MDMA Treatment

Simon David Fisher

2011 DOI: 10.26686/wgtn.16985362.v1 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study
Population Rats
Interventions MDMA 8-OH-DPAT
Dose MDMA: 4x 10 mg/kg i.p. at 2-hour intervals; 8-OH-DPAT: 0, 0.025, 0.05, 0.1 mg/kg s.c. (Experiment 2) and 0.0125 and 0.00625 mg/kg s.c. (Experiment 2b)
Duration Two weeks between MDMA pretreatment and testing
Measures 5-HTP accumulation, body temperature
Topics MDMA Serotonin
Key findings No significant changes in 5-HTP accumulation or hypothermic response to 8-OH-DPAT were found between MDMA-pretreated rats and controls, and no substantial serotonin deficits were observed. The authors conclude that the results do not indicate increased 5-HT1A autoreceptor sensitivity, but methodological issues prevent a firm conclusion.

Abstract

Rationale: There is evidence that the serotonin (5-HT) deficits and related cognitive and mood impairments caused by +/-3,4- methylenedioxymethamphetamine (MDMA) may be mediated by neuroadaptations of the 5-HT1A autoreceptor.

Objectives: The increase in sensitivity of the 5-HT1A autoreceptor caused by highdose, repeated MDMA treatment was assessed neurochemically, by measuring 5- HTP accumulation, and physiologically, via changes in body temperature.

Methods: Experiment 1 confirmed the effects of 8-hydroxy-2-(di-npropylamino) tetralin (8-OH-DPAT) (0, 0.025, 0.05, 0.1 mg/kg s.c.) on 5- hydroxytryptophan (5-HTP) accumulation following 3-hydroxybenzylhydrazine dihydrochloride (NSD-1015) administration as a valid measure of 5-HT synthesis and hence 5-HT1A autoreceptor sensitivity in rats. Experiment 2 performed these procedures in additional animals, with half receiving MDMA (4x 10 mg/kg i.p. at 2 hour intervals) two weeks before testing. Body temperature changes due to the 8-OH-DPAT hypothermic response were tested using a rectal probe. Experiment 2b repeated the procedures in additional groups with lower doses of 8-OH-DPAT (0.0125 and 0.00625 mg/kg s.c.).

Results: No significant changes in 5-HTP accumulation levels or changes in the hypothermic response to 8-OH-DPAT were found between MDMA pretreated rats and controls in Experiments 2 and 2b. Moreover, there was no substantial evidence of expected 5-HT deficits due to high-dose MDMA treatment.

Conclusion: The results do not indicate an increase in sensitivity of the 5-HT1A autoreceptor, and hence the original hypothesis is not supported. However, there were a number of methodological issues, as indicated by the lack of MDMAinduced 5-HT deficits, which prevent a firm conclusion from being drawn. Future research is outlined to overcome these issues.

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