Literature DB >> 25031407

Long-term plasticity in the regulation of olfactory bulb activity by centrifugal fibers from piriform cortex.

Joy L Cauthron1, Jeffrey S Stripling2.   

Abstract

Olfactory bulb granule cells are activated synaptically via two main pathways. Mitral/tufted (M/T) cells form dendrodendritic synapses on granule cells that can be activated by antidromic stimulation of the lateral olfactory tract (LOT). Centrifugal fibers originating from the association fiber (AF) system in piriform cortex (PC) make axodendritic synapses on granule cells within the granule cell layer (GCL) that can be activated by orthodromic stimulation of AF axons in the PC. We explored functional plasticity in the AF pathway by recording extracellularly from individual M/T cells and presumed granule cells in male Long-Evans rats under urethane anesthesia while testing their response to LOT and AF stimulation. Presumed granule cells driven synaptically by LOT stimulation (type L cells) were concentrated in the superficial half of the GCL and were activated at short latencies, whereas those driven synaptically by AF stimulation (type A cells) were concentrated in the deep half of the GCL and were activated at longer latencies. Type A cells were readily detected only in animals in which the AF input to the GCL had been previously potentiated by repeated high-frequency stimulation. An additional bout of high-frequency stimulation administered under urethane caused an immediate increase in the number of action potentials evoked in type A cells by AF test stimulation and a concomitant increase in inhibition of M/T cells. These results underscore the importance of the role played in olfactory processing by PC regulation of OB activity and document the long-lasting potentiation of that regulation by repeated high-frequency AF activation.
Copyright © 2014 the authors 0270-6474/14/349677-11$15.00/0.

Entities:  

Keywords:  granule cell; mitral cell; olfactory bulb; piriform cortex; potentiation; tufted cell

Mesh:

Year:  2014        PMID: 25031407      PMCID: PMC4099545          DOI: 10.1523/JNEUROSCI.1314-14.2014

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  56 in total

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