The purpose of the proposal is to investigate the ability of dopamine, adenosine and 5-hydroxytryptamine to regulate GABA release from striatal nerve terminals in the globus pallidus and substantia nigra pars reticulate. Experiments will use patch pipettes in voltage clamp to record whole cell membrane currents in GP and SNR neurons in rat brain slices. Biopolar stimulation electrodes will be placed in the brain slice to evoke currents produced by release of GABA from afferent nerve terminals. The hypothesis is that dopamine acts at presynaptic D1 receptors to increase the release of GABA from nerve terminals in the SNR, whereas stimulation of adenosine A1 and 5-HT1B receptors reduce GABA release. In contrast, the potentially opposing influences of presynaptic dopamine D1 and adenosine A2A receptor-stimulation on GABA release from nerve terminals in the GP will be investigated. In addition, the hypothesis that the straitonigral pathway selectively releases GABA onto GABAB receptors on dopamine neurons in the sustantia nigra zona compacta will be tested.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS035437-01A1
Application #
2038402
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Program Officer
Oliver, Eugene J
Project Start
1997-08-15
Project End
2000-05-31
Budget Start
1997-08-15
Budget End
1998-05-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Physiology
Type
Schools of Medicine
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239