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Diazepam modulates lateral hypothalamic self-stimulation but not stimulation-escape in rats
1Department of Psychology, New York University, NY 10003.
Brain Research
|April 3, 1989
Summary
Rats show dual brain systems for reward and aversion. Diazepam (DZ) enhances reward but not aversion, suggesting distinct neural pathways for these behaviors in the lateral hypothalamus.
Area of Science:
- Neuroscience
- Behavioral Neuroscience
- Neuropharmacology
Background:
- Electrical stimulation of the lateral hypothalamus (LH) can elicit feeding and self-stimulation in rats.
- The effects of drugs like diazepam (DZ) on these behaviors are not fully understood.
- Distinguishing between reward and aversion systems in the brain is crucial for understanding motivated behaviors.
Purpose of the Study:
- To investigate the neural substrates of reward and aversion in the rat hypothalamus.
- To determine the effects of diazepam (DZ) on stimulation-bound feeding (SBF) and self-stimulation (SS) versus stimulation-escape (SE).
- To differentiate between a diazepam-sensitive reward system and a drug-resistant aversion system.
Main Methods:
- Rats with chronically implanted LH electrodes were tested for SBF and bar-pressing rates for SS and SE.
- Animals were tested with and without systemic diazepam (DZ) administration.
- Histological analysis of electrode placements was performed to correlate behavior with brain regions.
Main Results:
- Pure-reward rats (exhibiting SBF) had electrode tips in the medial forebrain bundle (MFB) and zona inserta near the ventromedial nucleus of the hypothalamus (VMH).
- Reward-escape rats (not exhibiting SBF) had more anterior electrode placements in the MFB.
- Diazepam increased SS rates and decreased SBF thresholds in both groups, while SE rates remained unchanged.
Conclusions:
- The results support the existence of distinct neural substrates for reward and aversion in the LH.
- A diazepam-sensitive reward system is present in both reward and reward-escape rats.
- A drug-resistant aversion system, more strongly engaged in reward-escape rats, operates independently of the reward system.