Abstract
3[H]-(-)-Sulpiride and 3[H]-spiperone binding was compared in rat amygdala, nucleus accumbens and striatum, using (+/-)-sulpiride to define specific binding. 3[H]-(-)-Sulpiride bound to twice as many sites in amygdala and nucleus accumbens as 3[H]-spiperone. 3[H]-(-)-Sulpiride binding was directed to these additional sites by using 1 μM spiperone to mask dopaminergic binding. The binding of 3[H]-(-)-sulpiride to these sites was high affinity, reversible, Na+-dependent, but not stereospecific. Metoclopramide, tiapride and antidepressant medications, but not other neuroleptics, ADTN, or serotonin displaced 3[H]-(-)-sulpiride binding to these sites. These data suggest that 3[H]-(-)-sulpiride labels mesolimbic sites other than dopamine receptors which may mediate antidepressant effects.
Original language | English (US) |
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Pages (from-to) | 1419-1421 |
Number of pages | 3 |
Journal | Experientia |
Volume | 41 |
Issue number | 11 |
DOIs | |
State | Published - Nov 1985 |
Keywords
- Sulpiride
- alprazolam
- antidepressants
- spiperone
- substituted benzamide
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology