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Background

In 1991, Linda Buck and Richard Axel reported the discovery of odorant receptor genes and began a series of studies that clarified the foundation of odor perception (Buck and Axel, 1991). In rats, there appear to be about 1000 different receptors. Most olfactory sensory neurons in the nose appear to express only one of these genes, and while homologous sensory neurons expressing the same odorant receptor gene are distributed in fairly broad zones stretching from anterior to posterior within the main olfactory epithelium (Ressler et al., 1993, Vassar et al., 1993), they converge in their projections to the brain and connect to only a very few glomeruli in the main olfactory bulb (Ressler et al., 1994, Vassar et al., 1994, Mombaerts et al., 1996). Glomeruli are roughly spherical masses of neuropil containing the synapses between sensory neuron axons and the dendrites of bulbar projection neurons and interneurons. The typical projection from homologous sensory neurons involves one glomerulus on the lateral aspect and one on the medial aspect of the bulb (Mombaerts et al., 1996), and all synapses within a glomerulus appear to be from sensory neurons expressing a single receptor (Treloar et al., 2002). The topography of the epithelium-to-bulb connection is such that sensory neurons located in the central channel of the olfactory epithelium project to dorsal parts of the bulb, whereas peripheral and ventral parts of the epithelium project more ventrally (Schoenfeld et al., 1994). There are also atypical sensory neurons that cluster in the epithelium and that make an unpaired projection to the extreme ventral part of the bulb (Strotmann et al., 1992, 2000).

Projection pattern of homologous sensory neurons.

This orderly pattern of projection, which is consistent across different animals, suggests that one can get a read-out of odorant receptor activation by studying the pattern of odorant-evoked neural activity across the glomerular layer of the rat olfactory bulb.  We have investigated these patterns of activity using uptake of radiolabeled 2-deoxyglucose (2DG) as a metabolic marker, and this website is intended to share these patterns as well as the insights that we have gained from them.

 
 
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Our Research
Background
Combinatorial Coding
Molecular Features
Glomerular Modules
Chemotopic Progressions
Global Chemotopy
Feature Interactions
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Odorant Concentration
Odorant Contaminants
Effects of Experience
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2-DG Technique
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Histology, etc.
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UC Irvine HBP NIDCD NIMH
 
This Human Brain Project/Neuroinformatics project is funded by the National Institute on Deafness and Other Communication Disorders and the National Institute of Mental Health