Related Experiment Video
Updated: Aug 11, 2026

Investigating Long-term Synaptic Plasticity in Interlamellar Hippocampus CA1 by Electrophysiological Field Recording
Published on: August 11, 2019
[Long-term neurotoxic effects of MDMA result in cortical and hippocampal structural changes]
Abstract:
3,4-Methylenedioxymethamphetamine (MDMA) is a substituted amphetamine with stimulating and hallucinogenic properties. Since MDMA induces "ecstasy" it is extensively used as a "recreational" drug. It has been well established that MDMA is neurotoxic and can result in long-term degeneration of cerebral 5-hydroxytryptamine (5-HT) nerve terminals in many species. The present study was undertaken to investigate the long-term neurotoxic effects of MDMA on cortical and hippocampal structures, by repeatedly administering MDMA in short time. Male Wistar rats were randomly assigned to control group and MDMA-treated group. MDMA (10 mg/kg) was administered to rats of MDMA-treated group, once per hour, total 40 mg/kg; rats of control group were treated with the same volume of saline. Thirty-two weeks after administering MDMA, the expression of serotonin transporter (SERT) mRNA and diazepam binding inhibitor (DBI) mRNA was detected by in situ hybridization. The expression of glial fibrillary acidic protein (GFAP) was detected by immunohistochemistry, and the degeneration of nerve terminals was demonstrated by Bielschowsky and Glee Marsland silver staining. The results showed that the expression of SERT mRNA in hippocampus decreased by 31.96%, while expression of DBI mRNA in neocortex increased by 40.51%, compared with the control group (P<0.05). The expression of GFAP in the brain tissue increased (P<0.05), while significant reduction of the nerve terminals in neocortex was demonstrated by silver staining, compared with the control group. These results suggest that the neurotoxicity of MDMA results in sustained cortical and hippocampal structural changes, which in turn result in disorder of the brain functions.
Insights
Repeated exposure to 3,4-Methylenedioxymethamphetamine (MDMA) causes long-term neurotoxic effects on rat brains, including decreased serotonin transporter mRNA and nerve terminal degeneration in the cortex and hippocampus.
Area of Science:
- Neuroscience
- Pharmacology
- Toxicology
Context:
- 3,4-Methylenedioxymethamphetamine (MDMA), known as "ecstasy," is a recreational drug with known neurotoxic properties.
- Previous research indicates MDMA can cause long-term degeneration of serotonin nerve terminals.
Purpose:
- To investigate the sustained neurotoxic effects of repeated MDMA administration on cortical and hippocampal structures in a rat model.
- To assess changes in serotonin transporter (SERT) mRNA, diazepam binding inhibitor (DBI) mRNA, glial fibrillary acidic protein (GFAP), and nerve terminal integrity.
Summary:
- Rats treated repeatedly with MDMA showed a significant decrease in SERT mRNA expression in the hippocampus (31.96%) and an increase in DBI mRNA in the neocortex (40.51%).
- Increased GFAP expression indicated neuroinflammation, and silver staining revealed significant nerve terminal degeneration in the neocortex compared to controls.
- These structural changes persisted 32 weeks after MDMA administration.
Impact:
- The study demonstrates that MDMA-induced neurotoxicity leads to lasting structural alterations in the cortex and hippocampus.
- These persistent changes suggest a mechanism for long-term disruption of brain functions following MDMA use.
Related Concept Videos
Long-term Depression
Calcium Ion Concentration Mechanism
If over time, all...
Long-term Depression
Alzheimer Disease ll: Pathophysiology
Long-term Potentiation
Long-term Potentiation
Hebbian LTP
LTP can occur when presynaptic neurons...
Role of Hippocampus in Memory

