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Published on: June 3, 2016
Lateral excitation within the olfactory bulb
Jason M Christie1, Gary L Westbrook
1Vollum Institute, Oregon Health and Science University, Portland, Oregon 97239, USA. christij@ohsu.edu
Insights
Lateral excitation in the olfactory bulb enhances coordinated activity. Electrical coupling and glutamate spillover amplify sensory input sensitivity within glomeruli.
Area of Science:
- Neuroscience
- Olfactory system research
Background:
- Lateral inhibition is common in cortical networks for contrast enhancement.
- In the olfactory bulb, inhibition occurs via mitral cell and interneuron synapses.
- Lateral excitatory interactions between mitral cells are less recognized but enhance coordinated activity.
Purpose of the Study:
- To investigate lateral excitation between mitral cells in the olfactory bulb.
- To understand the mechanisms underlying lateral excitation in olfactory glomeruli.
Main Methods:
- Paired recordings between mitral cells projecting to the same glomerulus.
- Experiments using connexin36 knockout mice lacking mitral-mitral cell gap junctions.
- Investigating the role of glutamate spillover and uptake blockade.
Main Results:
- Trains of action potentials in one mitral cell induced autoexcitation and depolarization in a second cell.
- Lateral excitation was absent in mice lacking mitral-mitral cell gap junctions.
- Glutamate spillover contributed to lateral excitation, especially during high activity or blocked uptake.
Conclusions:
- Electrical coupling via gap junctions and glutamate spillover form a lateral excitatory network in olfactory glomeruli.
- This network significantly amplifies the sensitivity of glomeruli to sensory input.
- Lateral excitation plays a crucial role in olfactory processing and sensory information amplification.
Abstract:
Lateral inhibition is a common feature of cortical networks, serving such functions as contrast enhancement. In the olfactory bulb, inhibition is imbedded in the local connectivity at dendrodendritic synapses between mitral cells and interneurons. However, there is also evidence for excitatory interactions between mitral cells despite the lack of direct synaptic connections. This lateral excitation, although a less well recognized feature of the circuit, provides a potentially powerful mechanism to enhance coordinated activity. We examined lateral excitation in paired recordings between mitral cells projecting to the same glomerulus. Trains of action potentials in one mitral cell evoked autoexcitation in the stimulated cell and a prolonged depolarization in the second cell. This lateral excitation was absent in connexin36(-/-) mice, which lack mitral-mitral cell gap junctions. However, spillover of dendritically released glutamate contributed to lateral excitation during concerted mitral cell excitation or by single-cell activity if glutamate uptake was blocked. Our results suggest that electrical coupling and spillover create a lateral excitatory network within the glomerulus, thus markedly amplifying the sensitivity of each glomerulus to incoming sensory input.
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