Excitatory synaptic input leads to neuronal firing if its intensity is sufficient to reach a threshold depolarization. The requisite intensity for firing, however, is adjusted by synaptic inhibition. In the olfactory system, the mitral and tufted cells of the olfactory bulb serve as the excitatory link between the olfactory receptors and the cortex. The first stage of inhibition of mitral/tufted cells is provided by periglomerular cells through both feedforward and feedback pathways. The general aim of this proposal is to determine the role of periglomerular cells in mitral/tufted cell inhibition. Patch clamp techniques will be used to record from neurons in acute slices of rat olfactory bulb. A large subpopulation of periglomerular cells release the inhibitory transmitter GABA onto mitral/tufted cells and also onto themselves, resulting in self-inhibition. The proposed research will determine the strength of this self-inhibition, whether neighboring, otherwise inactive, periglomerular cells are also inhibited by spillover, and whether GABA release from periglomerular cells is altered by endogenous transmitters. Simultaneous recordings from pairs of periglomerular cells and pairs of periglomerular and mitral/tufted cells will determine whether action potentials are necessary to evoke release from these cell types, and measure the strength and effects of transmitter spillover from release sites to extrasynaptic and neighboring synaptic receptors. The firing pattern of individual neurons is the basic unit of neuronal circuit behavior. Firing patterns are, in turn, dependent on the rules by which single neurons integrate synaptic inputs. An understanding of synaptic integration requires knowledge of the temporal and spatial properties of synaptic inhibition and excitation. Studies such as those proposed herein will determine how mechanisms of synaptic transmission through direct connections, as well as through spillover, affect integration and firing properties and will therefore provide a basis for understanding olfactory information processing.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS021419-21
Application #
6830232
Study Section
Special Emphasis Panel (ZRG1-MDCN-4 (01))
Program Officer
Talley, Edmund M
Project Start
1987-09-01
Project End
2006-11-30
Budget Start
2004-12-01
Budget End
2006-11-30
Support Year
21
Fiscal Year
2005
Total Cost
$215,175
Indirect Cost
Name
Oregon Health and Science University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Smith, T Caitlin; Jahr, Craig E (2002) Self-inhibition of olfactory bulb neurons. Nat Neurosci 5:760-6
Bergles, Dwight E; Tzingounis, Anastassios V; Jahr, Craig E (2002) Comparison of coupled and uncoupled currents during glutamate uptake by GLT-1 transporters. J Neurosci 22:10153-62
Diamond, J S; Jahr, C E (2000) Synaptically released glutamate does not overwhelm transporters on hippocampal astrocytes during high-frequency stimulation. J Neurophysiol 83:2835-43
Bergles, D E; Diamond, J S; Jahr, C E (1999) Clearance of glutamate inside the synapse and beyond. Curr Opin Neurobiol 9:293-8
Dzubay, J A; Jahr, C E (1999) The concentration of synaptically released glutamate outside of the climbing fiber-Purkinje cell synaptic cleft. J Neurosci 19:5265-74
Otis, T S; Jahr, C E (1998) Anion currents and predicted glutamate flux through a neuronal glutamate transporter. J Neurosci 18:7099-110
Diamond, J S; Bergles, D E; Jahr, C E (1998) Glutamate release monitored with astrocyte transporter currents during LTP. Neuron 21:425-33
Diamond, J S; Jahr, C E (1997) Transporters buffer synaptically released glutamate on a submillisecond time scale. J Neurosci 17:4672-87
Otis, T S; Kavanaugh, M P; Jahr, C E (1997) Postsynaptic glutamate transport at the climbing fiber-Purkinje cell synapse. Science 277:1515-8
Dzubay, J A; Jahr, C E (1996) Kinetics of NMDA channel opening. J Neurosci 16:4129-34

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