Related Experiment Video
Updated: Aug 19, 2026

Single Cell Measurement of Dopamine Release with Simultaneous Voltage-clamp and Amperometry
Published on: November 21, 2012
Release of met-enkephalin from rat striatal slices: effect of amphetamine and fipexide
Abstract:
The release of Met-enkephalin immunoreactive material (ME-IR) from rat striatal slices is affected by exposure to amphetamine and fipexide (chloro-4-phenoxy)-2-acetyl-1-(methylene-dioxy 3, 4-benzyl-4-piperazine) a psychostimulant drug with mild dopaminomimetic activity. Both amphetamine and fipexide inhibited in vitro the release of ME-IR. The same effect was observed after in vivo acute administration and is also maintained after chronic treatment. The action of fipexide and amphetamine is still present after reserpine pretreatment. The results indicate that fipexide may facilitate dopamine neurotransmission by inhibition of an enkephalinergic inhibitory feed-back circuit.
Insights
Psychostimulants amphetamine and fipexide reduce Met-enkephalin release in rats. This effect, observed both in vitro and in vivo, suggests fipexide may enhance dopamine neurotransmission by inhibiting enkephalinergic feedback.
Area of Science:
- Neuroscience
- Pharmacology
- Neurochemistry
Background:
- Met-enkephalin immunoreactive material (ME-IR) plays a role in regulating neurotransmission.
- Psychostimulants like amphetamine are known to affect dopamine pathways.
- Fipexide is a psychostimulant with mild dopaminomimetic activity.
Purpose of the Study:
- To investigate the effect of amphetamine and fipexide on ME-IR release from rat striatal slices.
- To determine if these effects differ between in vitro and in vivo administration.
- To explore the mechanism underlying fipexide's action on dopamine neurotransmission.
Main Methods:
- In vitro studies using rat striatal slices to measure ME-IR release.
- In vivo acute and chronic administration of amphetamine and fipexide.
- Reserpine pretreatment to assess the role of catecholamines.
Main Results:
- Both amphetamine and fipexide significantly inhibited ME-IR release in vitro.
- This inhibitory effect was consistent with both acute and chronic in vivo administration.
- The action of both drugs persisted after reserpine pretreatment, indicating a non-catecholaminergic mechanism.
Conclusions:
- Fipexide, similar to amphetamine, inhibits ME-IR release.
- This inhibition suggests that fipexide may facilitate dopamine neurotransmission.
- The mechanism likely involves the disinhibition of an enkephalinergic inhibitory feedback circuit.
More Related Videos
06:40Combined Infusion and Stimulation with Fast-Scan Cyclic Voltammetry (CIS-FSCV) to Assess Ventral Tegmental Area Receptor Regulation of Phasic Dopamine
Published on: April 23, 2020
07:56A Plate-Based Assay for the Measurement of Endogenous Monoamine Release in Acute Brain Slices
Published on: August 11, 2021