JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Agneter, E.
Right arrow Articles by Cubeddu, L. X.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Agneter, E.
Right arrow Articles by Cubeddu, L. X.

Behavior of mesocortical dopamine terminals during single and repetitive stimulation: comparison with nigrostriatal neurons

E Agneter, IS Hoffmann, EA Singer and LX Cubeddu

Institute of Pharmacology, University of Vienna, Austria.

The present study reinvestigates the role of autoinhibition in dopamine (DA) release from mesoprefrontal and nigrostriatal DA neurons using improved methodology. Slices of rabbit prefrontal cortex (PFC) and striatum (STR) were labeled with [3H]DA and superfused in the presence of nomifensine (3 microM). Overflow was elicited by field stimulation with a single pulse (autoinhibition-free condition) or trains of pulses (4, 16 and 64) delivered at 0.05 to 30 Hz. One-pulse stimulation caused a measurable overflow of tritium in the PFC and STR (0.12% vs. 0.21% of tissue tritium, respectively). At increasing numbers of pulses, per- pulse over-flow decreased at all frequencies, but it was consistently more pronounced in the STR than in the PFC (e.g., 64 pulses/3 Hz: -30% PFC, -70% STR). The frequency dependence of DA release was biphasic at all numbers of pulses with overflow largest at 0.05 Hz and smallest at 3 Hz. In the PFC, however, the magnitude of the changes was considerably smaller, and the per-pulse release at higher frequencies was much larger than in the STR. The DA D2-receptor antagonist sulpiride (3 microM) enhanced pulse-train-evoked overflow from the STR at all frequencies between 0.3 and 10 Hz, whereas facilitation in the PFC was achieved at 10 Hz only. One-pulse-evoked overflow was not facilitated by sulpiride in either region. In conclusion, DA overflow from PFC terminals is not generally higher than overflow from STR terminals, as suggested in earlier studies. Larger per-pulse overflow from mesoprefrontal DA neurons occurs only under intense stimulation and is only in part a consequence of weak autoinhibition in this region.

Volume 269, Issue 2, pp. 470-476, 05/01/1994
Copyright © 1994 by American Society for Pharmacology and Experimental Therapeutics




This article has been cited by other articles:


Home page
J. Neurosci.Home page
M. Benoit-Marand, E. Borrelli, and F. Gonon
Inhibition of Dopamine Release Via Presynaptic D2 Receptors: Time Course and Functional Characteristics In Vivo
J. Neurosci., December 1, 2001; 21(23): 9134 - 9141.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1994 by the American Society for Pharmacology and Experimental Therapeutics.