Relationships Between Odor-Elicited Oscillations in the Salamander Olfactory Epithelium and Olfactory Bulb
Department of Neuroscience, Tufts University School of Medicine, Boston, Massachusetts 02111 Dorries, Kathleen M. and John S. Kauer. Relationships Between Odor-Elicited Oscillations in the Salamander Olfactory Epithelium and Olfactory Bulb. J. Neurophysiol. 83: 754-765, 2000. Oscillations in neurona...
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description | Department of Neuroscience, Tufts University School of Medicine,
Boston, Massachusetts 02111
Dorries, Kathleen M. and
John S. Kauer.
Relationships Between Odor-Elicited Oscillations in the
Salamander Olfactory Epithelium and Olfactory Bulb. J. Neurophysiol. 83: 754-765, 2000. Oscillations in
neuronal population activity, or the synchronous neuronal spiking that
underlies them, are thought to play a functional role in sensory
processing in the CNS. In the olfactory system, stimulus-induced
oscillations are observed both in central processing areas and in the
peripheral receptor epithelium. To examine the relationship between
these peripheral and central oscillations, we recorded local field
potentials simultaneously from the olfactory epithelium and olfactory
bulb in tiger salamanders ( Ambystoma tigrinum ).
Stimulus-induced oscillations recorded at these two sites were matched
in frequency and slowed concurrently over the time course of the
response, suggesting that the oscillations share a common source or are
modulated together. Both the power and duration of oscillations
increased over a range of amyl acetate concentrations from 2.5 × 10 2 to 1 × 10 1 dilution of saturated
vapor, but peak frequency was not affected. The frequency of the
oscillation did vary with different odorant compounds in both olfactory
epithelium and bulb (OE and OB): amyl acetate, ethyl fenchol and
d -carvone elicited oscillations of significantly
different frequencies, and there was no difference in OE and OB
oscillation frequencies. No change in the power or frequency of OE
oscillations was observed after sectioning the olfactory nerve,
indicating that the OE oscillations have a peripheral source. Finally,
application of 1.0 and 10 µM tetrodotoxin to the epithelium blocked
OE oscillations in a dose-dependent and reversible manner, suggesting
that peripheral olfactory oscillations are related to receptor neuron spiking. |
doi_str_mv | 10.1152/jn.2000.83.2.754 |
format | Article |
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Boston, Massachusetts 02111
Dorries, Kathleen M. and
John S. Kauer.
Relationships Between Odor-Elicited Oscillations in the
Salamander Olfactory Epithelium and Olfactory Bulb. J. Neurophysiol. 83: 754-765, 2000. Oscillations in
neuronal population activity, or the synchronous neuronal spiking that
underlies them, are thought to play a functional role in sensory
processing in the CNS. In the olfactory system, stimulus-induced
oscillations are observed both in central processing areas and in the
peripheral receptor epithelium. To examine the relationship between
these peripheral and central oscillations, we recorded local field
potentials simultaneously from the olfactory epithelium and olfactory
bulb in tiger salamanders ( Ambystoma tigrinum ).
Stimulus-induced oscillations recorded at these two sites were matched
in frequency and slowed concurrently over the time course of the
response, suggesting that the oscillations share a common source or are
modulated together. Both the power and duration of oscillations
increased over a range of amyl acetate concentrations from 2.5 × 10 2 to 1 × 10 1 dilution of saturated
vapor, but peak frequency was not affected. The frequency of the
oscillation did vary with different odorant compounds in both olfactory
epithelium and bulb (OE and OB): amyl acetate, ethyl fenchol and
d -carvone elicited oscillations of significantly
different frequencies, and there was no difference in OE and OB
oscillation frequencies. No change in the power or frequency of OE
oscillations was observed after sectioning the olfactory nerve,
indicating that the OE oscillations have a peripheral source. Finally,
application of 1.0 and 10 µM tetrodotoxin to the epithelium blocked
OE oscillations in a dose-dependent and reversible manner, suggesting
that peripheral olfactory oscillations are related to receptor neuron spiking.</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.2000.83.2.754</identifier><identifier>PMID: 10669491</identifier><language>eng</language><publisher>United States: Am Phys Soc</publisher><subject>Ambystoma ; Ambystoma tigrinum ; Animals ; Electrophysiology ; Freshwater ; Odorants ; Olfactory Bulb - chemistry ; Olfactory Bulb - drug effects ; Olfactory Bulb - physiology ; Olfactory Mucosa - chemistry ; Olfactory Mucosa - drug effects ; Olfactory Mucosa - physiology ; Olfactory Nerve - chemistry ; Olfactory Nerve - drug effects ; Olfactory Nerve - physiology ; Periodicity ; Reaction Time - drug effects ; Reaction Time - physiology ; Receptors, Odorant - physiology ; Smell - physiology ; Tetrodotoxin - pharmacology</subject><ispartof>Journal of neurophysiology, 2000-02, Vol.83 (2), p.754-765</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-f9b34a4f69456e6bd3670dcdde9fe62dbf19212aa83d38be34193f2e1c062a5d3</citedby><cites>FETCH-LOGICAL-c466t-f9b34a4f69456e6bd3670dcdde9fe62dbf19212aa83d38be34193f2e1c062a5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10669491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dorries, Kathleen M</creatorcontrib><creatorcontrib>Kauer, John S</creatorcontrib><title>Relationships Between Odor-Elicited Oscillations in the Salamander Olfactory Epithelium and Olfactory Bulb</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>Department of Neuroscience, Tufts University School of Medicine,
Boston, Massachusetts 02111
Dorries, Kathleen M. and
John S. Kauer.
Relationships Between Odor-Elicited Oscillations in the
Salamander Olfactory Epithelium and Olfactory Bulb. J. Neurophysiol. 83: 754-765, 2000. Oscillations in
neuronal population activity, or the synchronous neuronal spiking that
underlies them, are thought to play a functional role in sensory
processing in the CNS. In the olfactory system, stimulus-induced
oscillations are observed both in central processing areas and in the
peripheral receptor epithelium. To examine the relationship between
these peripheral and central oscillations, we recorded local field
potentials simultaneously from the olfactory epithelium and olfactory
bulb in tiger salamanders ( Ambystoma tigrinum ).
Stimulus-induced oscillations recorded at these two sites were matched
in frequency and slowed concurrently over the time course of the
response, suggesting that the oscillations share a common source or are
modulated together. Both the power and duration of oscillations
increased over a range of amyl acetate concentrations from 2.5 × 10 2 to 1 × 10 1 dilution of saturated
vapor, but peak frequency was not affected. The frequency of the
oscillation did vary with different odorant compounds in both olfactory
epithelium and bulb (OE and OB): amyl acetate, ethyl fenchol and
d -carvone elicited oscillations of significantly
different frequencies, and there was no difference in OE and OB
oscillation frequencies. No change in the power or frequency of OE
oscillations was observed after sectioning the olfactory nerve,
indicating that the OE oscillations have a peripheral source. Finally,
application of 1.0 and 10 µM tetrodotoxin to the epithelium blocked
OE oscillations in a dose-dependent and reversible manner, suggesting
that peripheral olfactory oscillations are related to receptor neuron spiking.</description><subject>Ambystoma</subject><subject>Ambystoma tigrinum</subject><subject>Animals</subject><subject>Electrophysiology</subject><subject>Freshwater</subject><subject>Odorants</subject><subject>Olfactory Bulb - chemistry</subject><subject>Olfactory Bulb - drug effects</subject><subject>Olfactory Bulb - physiology</subject><subject>Olfactory Mucosa - chemistry</subject><subject>Olfactory Mucosa - drug effects</subject><subject>Olfactory Mucosa - physiology</subject><subject>Olfactory Nerve - chemistry</subject><subject>Olfactory Nerve - drug effects</subject><subject>Olfactory Nerve - physiology</subject><subject>Periodicity</subject><subject>Reaction Time - drug effects</subject><subject>Reaction Time - physiology</subject><subject>Receptors, Odorant - physiology</subject><subject>Smell - physiology</subject><subject>Tetrodotoxin - pharmacology</subject><issn>0022-3077</issn><issn>1522-1598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkDtv2zAUhYkgReK63TsVnLJJ5UOipLE2nDZAAAOtOxOUeGnRoB4lJST-96Vh5zF0IsHz3XMPD0JfKEkpzdm3Q58yQkha8pSlRZ5doUV8ZgnNq_IaLQiJd06K4hZ9DOEQySIn7AbdUiJElVV0gQ6_wKnJDn1o7RjwCqYngB5v9eCTjbONnUDjbWisu2DY9nhqAf9WTnWq1-Dx1hnVTIM_4s1oo-bs3OEovRNWs6s_oQ9GuQCfL-cS_bnf7NY_k8ftj4f198ekyYSYElPVPFOZiQFzAaLWXBREN1pDZUAwXRtaMcqUKrnmZQ08oxU3DGhDBFO55kt0d_Yd_fB3hjDJzoYG4gd6GOYgaZGVBctZBMkZbPwQggcjR2875Y-SEnnqVx56eepXllwyGfuNI18v3nPdgX43cC40AuwMtHbfPlkPcmyPwQ5u2B_l_ezcDp6n6PviKEdt3hL_byhmeF3_Dzi0mFA</recordid><startdate>20000201</startdate><enddate>20000201</enddate><creator>Dorries, Kathleen M</creator><creator>Kauer, John S</creator><general>Am Phys Soc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>P64</scope></search><sort><creationdate>20000201</creationdate><title>Relationships Between Odor-Elicited Oscillations in the Salamander Olfactory Epithelium and Olfactory Bulb</title><author>Dorries, Kathleen M ; Kauer, John S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-f9b34a4f69456e6bd3670dcdde9fe62dbf19212aa83d38be34193f2e1c062a5d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Ambystoma</topic><topic>Ambystoma tigrinum</topic><topic>Animals</topic><topic>Electrophysiology</topic><topic>Freshwater</topic><topic>Odorants</topic><topic>Olfactory Bulb - chemistry</topic><topic>Olfactory Bulb - drug effects</topic><topic>Olfactory Bulb - physiology</topic><topic>Olfactory Mucosa - chemistry</topic><topic>Olfactory Mucosa - drug effects</topic><topic>Olfactory Mucosa - physiology</topic><topic>Olfactory Nerve - chemistry</topic><topic>Olfactory Nerve - drug effects</topic><topic>Olfactory Nerve - physiology</topic><topic>Periodicity</topic><topic>Reaction Time - drug effects</topic><topic>Reaction Time - physiology</topic><topic>Receptors, Odorant - physiology</topic><topic>Smell - physiology</topic><topic>Tetrodotoxin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dorries, Kathleen M</creatorcontrib><creatorcontrib>Kauer, John S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dorries, Kathleen M</au><au>Kauer, John S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationships Between Odor-Elicited Oscillations in the Salamander Olfactory Epithelium and Olfactory Bulb</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>2000-02-01</date><risdate>2000</risdate><volume>83</volume><issue>2</issue><spage>754</spage><epage>765</epage><pages>754-765</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><abstract>Department of Neuroscience, Tufts University School of Medicine,
Boston, Massachusetts 02111
Dorries, Kathleen M. and
John S. Kauer.
Relationships Between Odor-Elicited Oscillations in the
Salamander Olfactory Epithelium and Olfactory Bulb. J. Neurophysiol. 83: 754-765, 2000. Oscillations in
neuronal population activity, or the synchronous neuronal spiking that
underlies them, are thought to play a functional role in sensory
processing in the CNS. In the olfactory system, stimulus-induced
oscillations are observed both in central processing areas and in the
peripheral receptor epithelium. To examine the relationship between
these peripheral and central oscillations, we recorded local field
potentials simultaneously from the olfactory epithelium and olfactory
bulb in tiger salamanders ( Ambystoma tigrinum ).
Stimulus-induced oscillations recorded at these two sites were matched
in frequency and slowed concurrently over the time course of the
response, suggesting that the oscillations share a common source or are
modulated together. Both the power and duration of oscillations
increased over a range of amyl acetate concentrations from 2.5 × 10 2 to 1 × 10 1 dilution of saturated
vapor, but peak frequency was not affected. The frequency of the
oscillation did vary with different odorant compounds in both olfactory
epithelium and bulb (OE and OB): amyl acetate, ethyl fenchol and
d -carvone elicited oscillations of significantly
different frequencies, and there was no difference in OE and OB
oscillation frequencies. No change in the power or frequency of OE
oscillations was observed after sectioning the olfactory nerve,
indicating that the OE oscillations have a peripheral source. Finally,
application of 1.0 and 10 µM tetrodotoxin to the epithelium blocked
OE oscillations in a dose-dependent and reversible manner, suggesting
that peripheral olfactory oscillations are related to receptor neuron spiking.</abstract><cop>United States</cop><pub>Am Phys Soc</pub><pmid>10669491</pmid><doi>10.1152/jn.2000.83.2.754</doi><tpages>12</tpages></addata></record> |
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source | MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals |
subjects | Ambystoma Ambystoma tigrinum Animals Electrophysiology Freshwater Odorants Olfactory Bulb - chemistry Olfactory Bulb - drug effects Olfactory Bulb - physiology Olfactory Mucosa - chemistry Olfactory Mucosa - drug effects Olfactory Mucosa - physiology Olfactory Nerve - chemistry Olfactory Nerve - drug effects Olfactory Nerve - physiology Periodicity Reaction Time - drug effects Reaction Time - physiology Receptors, Odorant - physiology Smell - physiology Tetrodotoxin - pharmacology |
title | Relationships Between Odor-Elicited Oscillations in the Salamander Olfactory Epithelium and Olfactory Bulb |
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