Related Experiment Videos
Ventral tegmental self-stimulation selectively induces opioid peptide release in rat CNS
1Department of Psychiatry, Medical College of Wisconsin, Milwaukee 53226.
Synapse (New York, N.Y.)
|January 1, 1993
Summary
Intracranial self-stimulation (ICS) activates brain opioid systems. Opioid peptide release varies with stimulation conditions, suggesting their role in mediating rewarding brain stimulation effects.
Area of Science:
- Neuroscience
- Behavioral Neuroscience
- Neuropharmacology
Background:
- Intracranial self-stimulation (ICS) activates neural systems for reward.
- Opiates are known to enhance ICS, indicating a potential role for opioid peptides.
Purpose of the Study:
- To investigate the role of opioid peptides as mediators of ICS.
- To determine how opioid peptide release is affected by stimulation contingency and reinforcement schedules.
Main Methods:
- Rats underwent training on fixed ratio (FR) schedules of ICS.
- Opioid peptide release was assessed using in vivo receptor occupancy and autoradiography.
- Rats were assigned to active stimulation, yoked stimulation, or control groups.
Main Results:
- Specific brain structures showed altered opioid peptide release based on stimulation contingency and schedule.
- Inhibition of peptide release was observed in the habenula and preinsular cortex.
- Widespread increases in receptor binding were noted, potentially due to stimulation-induced blood flow changes.
Conclusions:
- Rewarding brain stimulation activates discrete neuronal opioid systems.
- Opioid system activation is contingent on specific behavioral and stimulus conditions.
- These findings elucidate the neurobiological mechanisms underlying reward processing.