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Behavioral sensitization following a single apomorphine pretreatment--selective effects on the dopamine release
R E Wilcox1, J A Severson, J J Woodward
1Department of Pharmacology and Toxicology, College of Pharmacy, University of Texas, Austin.
Brain Research
|September 24, 1990
Summary
A single dose of apomorphine (APO) 24 hours before testing enhanced behavioral responses. However, dopamine (DA) synthesis, metabolism, and D2 receptor binding in the striatum remained unchanged, indicating complex adaptive mechanisms.
Area of Science:
- Neuroscience
- Pharmacology
- Biochemistry
Background:
- Repeated daily administration of the dopamine (DA) agonist apomorphine (APO) leads to adaptations in striatal DA synthesis and metabolism.
- These adaptations suggest that the effects of APO do not fully resolve within a 24-hour period.
Purpose of the Study:
- To investigate the behavioral and neurochemical effects of a single APO treatment administered 24 hours prior to assessment.
- To determine the impact of this pretreatment on striatal DA synthesis, metabolism, release, and receptor binding.
Main Methods:
- Rats were administered a single dose of APO.
- 24 hours later, behavioral responses to a subsequent APO challenge were evaluated.
- Striatal synaptosomes were isolated to measure DA release.
- Striatal tissue was analyzed for DA synthesis, metabolism, and D2 receptor binding.
Main Results:
- A single APO pretreatment 24 hours before testing reduced DA release from striatal synaptosomes.
- Striatal DA synthesis, metabolism, and high-affinity D2 receptor binding were not significantly altered at this time point.
- The stereotypic behavioral response to a subsequent APO challenge was enhanced.
Conclusions:
- A single APO pretreatment induces specific adaptive changes that persist for at least 24 hours.
- These adaptations differ from those observed after acute (60 min) or subchronic APO administration.
- The findings highlight the complex temporal dynamics of dopamine agonist-induced neuroadaptations.