Information processing at a central synapse suggests a noise filter in the auditory pathway of the noctuid moth
1. The central projections of the A1 afferent were confirmed via intracellular recording and staining with Lucifer Yellow in the pterothoracic ganglion of the noctuid moths, Agrotis infusa and Apamea amputatrix (Fig. 1). Simultaneous recordings of the A1 afferent in the tympanal nerve (extracellular...
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description | 1. The central projections of the A1 afferent were confirmed via intracellular recording and staining with Lucifer Yellow in the pterothoracic ganglion of the noctuid moths, Agrotis infusa and Apamea amputatrix (Fig. 1). Simultaneous recordings of the A1 afferent in the tympanal nerve (extracellularly) and in the pterothoracic ganglion (intracellularly) confirm the identity of the stained receptor as being the A1 cell. 2. The major postsynaptic arborizations of interneurone 501 in the pterothoracic ganglion were also demonstrated via intracellular recording and staining (Fig. 2). Simultaneous recordings of the A1 afferent (extracellularly) and neurone 501 (intracellularly) revealed that each A1 spike evokes a constant short latency EPSP in the interneurone (Fig. 2Bi). Neurone 501 receives only monaural input from the A1 afferent on its soma side as demonstrated by electrical stimulation of each afferent nerve (Fig. 2Bii). EPSPs evoked in neurone 501 by high frequency (100 Hz) electrical stimulation of the afferent nerve did not decrement (Fig. 2Biii). These data are consistent with a monosynaptic input to neurone 501 from the A1 afferent. 3. The response of neurone 501 to a sound stimulus presented at an intensity near the upper limit of its linear response range (30 ms, 16 kHz, 80 dB SPL) was a plateau-like depolarization, with tonic spiking activity which continued beyond the end of the tone. The instantaneous spike frequency of the response was as high as 800 Hz, and was maintained at above 600 Hz for the duration of the tone (Fig. 3). 4. The relationship between the instantaneous spike frequency in the A1 afferent and that recorded simultaneously in neurone 501 is linear over the entire range of A1 spike frequencies evoked by white noise sound stimuli (Fig. 4). Similarly, the relationship between instantaneous spike frequency in the A1 afferent and the mean depolarization evoked in neurone 501 is also linear for all A1 spike frequencies tested (Fig. 5). No summation of EPSPs occurred for A1 spike frequencies below 100 Hz. |
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The central projections of the A1 afferent were confirmed via intracellular recording and staining with Lucifer Yellow in the pterothoracic ganglion of the noctuid moths, Agrotis infusa and Apamea amputatrix (Fig. 1). Simultaneous recordings of the A1 afferent in the tympanal nerve (extracellularly) and in the pterothoracic ganglion (intracellularly) confirm the identity of the stained receptor as being the A1 cell. 2. The major postsynaptic arborizations of interneurone 501 in the pterothoracic ganglion were also demonstrated via intracellular recording and staining (Fig. 2). Simultaneous recordings of the A1 afferent (extracellularly) and neurone 501 (intracellularly) revealed that each A1 spike evokes a constant short latency EPSP in the interneurone (Fig. 2Bi). Neurone 501 receives only monaural input from the A1 afferent on its soma side as demonstrated by electrical stimulation of each afferent nerve (Fig. 2Bii). EPSPs evoked in neurone 501 by high frequency (100 Hz) electrical stimulation of the afferent nerve did not decrement (Fig. 2Biii). These data are consistent with a monosynaptic input to neurone 501 from the A1 afferent. 3. The response of neurone 501 to a sound stimulus presented at an intensity near the upper limit of its linear response range (30 ms, 16 kHz, 80 dB SPL) was a plateau-like depolarization, with tonic spiking activity which continued beyond the end of the tone. The instantaneous spike frequency of the response was as high as 800 Hz, and was maintained at above 600 Hz for the duration of the tone (Fig. 3). 4. The relationship between the instantaneous spike frequency in the A1 afferent and that recorded simultaneously in neurone 501 is linear over the entire range of A1 spike frequencies evoked by white noise sound stimuli (Fig. 4). Similarly, the relationship between instantaneous spike frequency in the A1 afferent and the mean depolarization evoked in neurone 501 is also linear for all A1 spike frequencies tested (Fig. 5). No summation of EPSPs occurred for A1 spike frequencies below 100 Hz.</description><identifier>ISSN: 0340-7594</identifier><identifier>EISSN: 1432-1351</identifier><identifier>DOI: 10.1007/BF00603955</identifier><identifier>PMID: 3244131</identifier><identifier>CODEN: JCPADN</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Action Potentials ; Agrotis ; Animals ; Apamea ; Apamea amputatrix ; Auditory Pathways - physiology ; Biochemistry. Physiology. Immunology ; Biological and medical sciences ; Central Nervous System - cytology ; Central Nervous System - physiology ; Female ; Fluorescent Dyes ; Fundamental and applied biological sciences. Psychology ; hearing ; information processing ; Insecta ; Invertebrates ; Isoquinolines ; Lepidoptera - physiology ; Male ; Moths - physiology ; Neurons, Afferent - cytology ; Neurons, Afferent - physiology ; Noctuidae ; Noise ; Physiology. Development ; sounds</subject><ispartof>Journal of Comparative Physiology A, 1988-01, Vol.164 (2), p.251-258</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-653eefaf1496be8dd02821f54d3c13b8292ad022f0290e480273e479d1e86c6d3</citedby><cites>FETCH-LOGICAL-c335t-653eefaf1496be8dd02821f54d3c13b8292ad022f0290e480273e479d1e86c6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7303596$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3244131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boyan, G.S</creatorcontrib><creatorcontrib>Fullard, J.H</creatorcontrib><title>Information processing at a central synapse suggests a noise filter in the auditory pathway of the noctuid moth</title><title>Journal of Comparative Physiology A</title><addtitle>J Comp Physiol A</addtitle><description>1. The central projections of the A1 afferent were confirmed via intracellular recording and staining with Lucifer Yellow in the pterothoracic ganglion of the noctuid moths, Agrotis infusa and Apamea amputatrix (Fig. 1). Simultaneous recordings of the A1 afferent in the tympanal nerve (extracellularly) and in the pterothoracic ganglion (intracellularly) confirm the identity of the stained receptor as being the A1 cell. 2. The major postsynaptic arborizations of interneurone 501 in the pterothoracic ganglion were also demonstrated via intracellular recording and staining (Fig. 2). Simultaneous recordings of the A1 afferent (extracellularly) and neurone 501 (intracellularly) revealed that each A1 spike evokes a constant short latency EPSP in the interneurone (Fig. 2Bi). Neurone 501 receives only monaural input from the A1 afferent on its soma side as demonstrated by electrical stimulation of each afferent nerve (Fig. 2Bii). EPSPs evoked in neurone 501 by high frequency (100 Hz) electrical stimulation of the afferent nerve did not decrement (Fig. 2Biii). These data are consistent with a monosynaptic input to neurone 501 from the A1 afferent. 3. The response of neurone 501 to a sound stimulus presented at an intensity near the upper limit of its linear response range (30 ms, 16 kHz, 80 dB SPL) was a plateau-like depolarization, with tonic spiking activity which continued beyond the end of the tone. The instantaneous spike frequency of the response was as high as 800 Hz, and was maintained at above 600 Hz for the duration of the tone (Fig. 3). 4. The relationship between the instantaneous spike frequency in the A1 afferent and that recorded simultaneously in neurone 501 is linear over the entire range of A1 spike frequencies evoked by white noise sound stimuli (Fig. 4). Similarly, the relationship between instantaneous spike frequency in the A1 afferent and the mean depolarization evoked in neurone 501 is also linear for all A1 spike frequencies tested (Fig. 5). No summation of EPSPs occurred for A1 spike frequencies below 100 Hz.</description><subject>Action Potentials</subject><subject>Agrotis</subject><subject>Animals</subject><subject>Apamea</subject><subject>Apamea amputatrix</subject><subject>Auditory Pathways - physiology</subject><subject>Biochemistry. Physiology. Immunology</subject><subject>Biological and medical sciences</subject><subject>Central Nervous System - cytology</subject><subject>Central Nervous System - physiology</subject><subject>Female</subject><subject>Fluorescent Dyes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hearing</subject><subject>information processing</subject><subject>Insecta</subject><subject>Invertebrates</subject><subject>Isoquinolines</subject><subject>Lepidoptera - physiology</subject><subject>Male</subject><subject>Moths - physiology</subject><subject>Neurons, Afferent - cytology</subject><subject>Neurons, Afferent - physiology</subject><subject>Noctuidae</subject><subject>Noise</subject><subject>Physiology. Development</subject><subject>sounds</subject><issn>0340-7594</issn><issn>1432-1351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM2LFDEQxYMo6-zqxbuYg3gQWiuppD-OurjrwoIH3XNTk05mIt3JmKSR-e-NzrCeCt778Xj1GHsl4IMA6D5-vgFoAQetn7CNUCgbgVo8ZRtABU2nB_WcXeb8EwCkkOKCXaBUSqDYsHgXXEwLFR8DP6RobM4-7DgVTtzYUBLNPB8DHbLled3tbC65WiH6Kjg_F5u4D7zsLad18iWmIz9Q2f-mI4_unx6iKauf-BLL_gV75mjO9uX5XrGHmy8_rr82999u764_3TcGUZem1WitIyfU0G5tP00geymcVhMagdteDpKqJh3IAazqQXZoVTdMwvataSe8Yu9OufWnX2stPS4-GzvPFGxc8yi0lKA7VcH3J9CkmHOybjwkv1A6jgLGv-uO_9et8Otz6rpd7PSInues_tuzT9nQ7BIF4_Mj1iGgHtqKvTlhjuJIu1SRh-8SBIJs-wF1i38AHzeKxg</recordid><startdate>19880101</startdate><enddate>19880101</enddate><creator>Boyan, G.S</creator><creator>Fullard, J.H</creator><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope><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>7SS</scope><scope>7TK</scope></search><sort><creationdate>19880101</creationdate><title>Information processing at a central synapse suggests a noise filter in the auditory pathway of the noctuid moth</title><author>Boyan, G.S ; Fullard, J.H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-653eefaf1496be8dd02821f54d3c13b8292ad022f0290e480273e479d1e86c6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Action Potentials</topic><topic>Agrotis</topic><topic>Animals</topic><topic>Apamea</topic><topic>Apamea amputatrix</topic><topic>Auditory Pathways - physiology</topic><topic>Biochemistry. Physiology. Immunology</topic><topic>Biological and medical sciences</topic><topic>Central Nervous System - cytology</topic><topic>Central Nervous System - physiology</topic><topic>Female</topic><topic>Fluorescent Dyes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hearing</topic><topic>information processing</topic><topic>Insecta</topic><topic>Invertebrates</topic><topic>Isoquinolines</topic><topic>Lepidoptera - physiology</topic><topic>Male</topic><topic>Moths - physiology</topic><topic>Neurons, Afferent - cytology</topic><topic>Neurons, Afferent - physiology</topic><topic>Noctuidae</topic><topic>Noise</topic><topic>Physiology. Development</topic><topic>sounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boyan, G.S</creatorcontrib><creatorcontrib>Fullard, J.H</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of Comparative Physiology A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boyan, G.S</au><au>Fullard, J.H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Information processing at a central synapse suggests a noise filter in the auditory pathway of the noctuid moth</atitle><jtitle>Journal of Comparative Physiology A</jtitle><addtitle>J Comp Physiol A</addtitle><date>1988-01-01</date><risdate>1988</risdate><volume>164</volume><issue>2</issue><spage>251</spage><epage>258</epage><pages>251-258</pages><issn>0340-7594</issn><eissn>1432-1351</eissn><coden>JCPADN</coden><abstract>1. The central projections of the A1 afferent were confirmed via intracellular recording and staining with Lucifer Yellow in the pterothoracic ganglion of the noctuid moths, Agrotis infusa and Apamea amputatrix (Fig. 1). Simultaneous recordings of the A1 afferent in the tympanal nerve (extracellularly) and in the pterothoracic ganglion (intracellularly) confirm the identity of the stained receptor as being the A1 cell. 2. The major postsynaptic arborizations of interneurone 501 in the pterothoracic ganglion were also demonstrated via intracellular recording and staining (Fig. 2). Simultaneous recordings of the A1 afferent (extracellularly) and neurone 501 (intracellularly) revealed that each A1 spike evokes a constant short latency EPSP in the interneurone (Fig. 2Bi). Neurone 501 receives only monaural input from the A1 afferent on its soma side as demonstrated by electrical stimulation of each afferent nerve (Fig. 2Bii). EPSPs evoked in neurone 501 by high frequency (100 Hz) electrical stimulation of the afferent nerve did not decrement (Fig. 2Biii). These data are consistent with a monosynaptic input to neurone 501 from the A1 afferent. 3. The response of neurone 501 to a sound stimulus presented at an intensity near the upper limit of its linear response range (30 ms, 16 kHz, 80 dB SPL) was a plateau-like depolarization, with tonic spiking activity which continued beyond the end of the tone. The instantaneous spike frequency of the response was as high as 800 Hz, and was maintained at above 600 Hz for the duration of the tone (Fig. 3). 4. The relationship between the instantaneous spike frequency in the A1 afferent and that recorded simultaneously in neurone 501 is linear over the entire range of A1 spike frequencies evoked by white noise sound stimuli (Fig. 4). Similarly, the relationship between instantaneous spike frequency in the A1 afferent and the mean depolarization evoked in neurone 501 is also linear for all A1 spike frequencies tested (Fig. 5). No summation of EPSPs occurred for A1 spike frequencies below 100 Hz.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>3244131</pmid><doi>10.1007/BF00603955</doi><tpages>8</tpages></addata></record> |
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subjects | Action Potentials Agrotis Animals Apamea Apamea amputatrix Auditory Pathways - physiology Biochemistry. Physiology. Immunology Biological and medical sciences Central Nervous System - cytology Central Nervous System - physiology Female Fluorescent Dyes Fundamental and applied biological sciences. Psychology hearing information processing Insecta Invertebrates Isoquinolines Lepidoptera - physiology Male Moths - physiology Neurons, Afferent - cytology Neurons, Afferent - physiology Noctuidae Noise Physiology. Development sounds |
title | Information processing at a central synapse suggests a noise filter in the auditory pathway of the noctuid moth |
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