Neural control of swimming in Aplysia brasiliana. III. Serotonergic modulatory neurons
D. R. McPherson and J. E. Blankenship Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77550. 1. We describe a group of serotonergic neurons in the pedal ganglia of Aplysia brasiliana and characterize their modulatory effects on the motoneuron input to swimming muscles of t...
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creator | McPherson, D. R Blankenship, J. E |
description | D. R. McPherson and J. E. Blankenship
Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77550.
1. We describe a group of serotonergic neurons in the pedal ganglia of
Aplysia brasiliana and characterize their modulatory effects on the
motoneuron input to swimming muscles of the parapodia. Each pedal ganglion
contains one cluster of large neurons near its dorsomedial surface that
fires in phase with opening (downstroke) of the parapodia; these have been
designated parapodial opener-phase (POP) cells. 2. POP cells are large,
number 15-20 per ganglion, have peripheral axons in parapodial nerves, have
distinctively shaped action potentials, and fire in bursts phasically with
motoneurons during the opening, or downstroke portion, of parapodial
movement during fictive swimming. Firing individual POP cells with
intracellular current indicates that they have no direct detectable effect
on muscle, causing neither junction potentials nor contractions. 3.
5,7-Dihydroxytryptamine (5,7-DHT) staining, immunocytochemistry using
serotonin (5-HT) antibodies, and direct biochemical measurements revealed
that POP cells are serotonergic. Serotonergic nerve endings were also seen
in parapodial muscle. 4. Simultaneous intracellular recordings and use of
altered divalent concentrations revealed that no detectable direct synaptic
interactions exist between POP cells and motor neurons. 5. When POP cells
and motoneurons were simultaneously recorded while measuring muscle
contractions, it was found that POP cell activity enhances
motoneuron-induced tension by 120-900%, averaging around 300%. Variability
in the efficacy of individual POP cells suggests that they may influence
specific regions or groups of muscle fibers. 6. POP cell activity also
significantly increased the rate of relaxation of parapodial muscle
contractions, averaging about a 40% reduction in the time required to relax
to one-half peak tension. Increased relaxation rate implies a postsynaptic
change in muscle behavior. 7. The effectiveness of POP cells to increase
contraction tension and relaxation rate was positively correlated with POP
cell spike frequency. These effects were slow (seconds) in onset and could
persist for a minute or more after cessation of POP firing. Concurrent
motoneuron activity is not required for modulation by POP cells. 8.
Simultaneous intracellular recording from a POP cell, motoneuron, and
muscle fiber revealed that POP cell activity enhanced the amplitude of
motone |
doi_str_mv | 10.1152/jn.1991.66.4.1366 |
format | Article |
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Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77550.
1. We describe a group of serotonergic neurons in the pedal ganglia of
Aplysia brasiliana and characterize their modulatory effects on the
motoneuron input to swimming muscles of the parapodia. Each pedal ganglion
contains one cluster of large neurons near its dorsomedial surface that
fires in phase with opening (downstroke) of the parapodia; these have been
designated parapodial opener-phase (POP) cells. 2. POP cells are large,
number 15-20 per ganglion, have peripheral axons in parapodial nerves, have
distinctively shaped action potentials, and fire in bursts phasically with
motoneurons during the opening, or downstroke portion, of parapodial
movement during fictive swimming. Firing individual POP cells with
intracellular current indicates that they have no direct detectable effect
on muscle, causing neither junction potentials nor contractions. 3.
5,7-Dihydroxytryptamine (5,7-DHT) staining, immunocytochemistry using
serotonin (5-HT) antibodies, and direct biochemical measurements revealed
that POP cells are serotonergic. Serotonergic nerve endings were also seen
in parapodial muscle. 4. Simultaneous intracellular recordings and use of
altered divalent concentrations revealed that no detectable direct synaptic
interactions exist between POP cells and motor neurons. 5. When POP cells
and motoneurons were simultaneously recorded while measuring muscle
contractions, it was found that POP cell activity enhances
motoneuron-induced tension by 120-900%, averaging around 300%. Variability
in the efficacy of individual POP cells suggests that they may influence
specific regions or groups of muscle fibers. 6. POP cell activity also
significantly increased the rate of relaxation of parapodial muscle
contractions, averaging about a 40% reduction in the time required to relax
to one-half peak tension. Increased relaxation rate implies a postsynaptic
change in muscle behavior. 7. The effectiveness of POP cells to increase
contraction tension and relaxation rate was positively correlated with POP
cell spike frequency. These effects were slow (seconds) in onset and could
persist for a minute or more after cessation of POP firing. Concurrent
motoneuron activity is not required for modulation by POP cells. 8.
Simultaneous intracellular recording from a POP cell, motoneuron, and
muscle fiber revealed that POP cell activity enhanced the amplitude of
motoneuron-induced excitatory junction potentials (EJPs). Activity of POP
cells did not alter muscle fiber membrane potential, but the experiments
left open the possibility that EJP enhancement is presynaptic,
postsynaptic, or a combination.</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.1991.66.4.1366</identifier><identifier>PMID: 1662263</identifier><identifier>CODEN: JONEA4</identifier><language>eng</language><publisher>Bethesda, MD: Am Phys Soc</publisher><subject>5,7-Dihydroxytryptamine - metabolism ; Animals ; Aplysia - physiology ; Axons - physiology ; Biochemistry. Physiology. Immunology ; Biological and medical sciences ; Evoked Potentials - physiology ; Extremities - innervation ; Fundamental and applied biological sciences. Psychology ; Ganglia - cytology ; Ganglia - physiology ; Immunohistochemistry ; Invertebrates ; Mollusca ; Motor Neurons - physiology ; Muscle Contraction - physiology ; Muscle Relaxation - physiology ; Muscles - innervation ; Neuromuscular Junction - physiology ; Physiology. Development ; Serotonin - metabolism ; Serotonin - physiology ; Swimming ; Synaptic Transmission - physiology</subject><ispartof>Journal of neurophysiology, 1991-10, Vol.66 (4), p.1366-1379</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c272t-a53af851ad621ab17c8ccc4bd6c4b3e444b135dafe65d026ac424f434ca931283</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5023029$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1662263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McPherson, D. R</creatorcontrib><creatorcontrib>Blankenship, J. E</creatorcontrib><title>Neural control of swimming in Aplysia brasiliana. III. Serotonergic modulatory neurons</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>D. R. McPherson and J. E. Blankenship
Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77550.
1. We describe a group of serotonergic neurons in the pedal ganglia of
Aplysia brasiliana and characterize their modulatory effects on the
motoneuron input to swimming muscles of the parapodia. Each pedal ganglion
contains one cluster of large neurons near its dorsomedial surface that
fires in phase with opening (downstroke) of the parapodia; these have been
designated parapodial opener-phase (POP) cells. 2. POP cells are large,
number 15-20 per ganglion, have peripheral axons in parapodial nerves, have
distinctively shaped action potentials, and fire in bursts phasically with
motoneurons during the opening, or downstroke portion, of parapodial
movement during fictive swimming. Firing individual POP cells with
intracellular current indicates that they have no direct detectable effect
on muscle, causing neither junction potentials nor contractions. 3.
5,7-Dihydroxytryptamine (5,7-DHT) staining, immunocytochemistry using
serotonin (5-HT) antibodies, and direct biochemical measurements revealed
that POP cells are serotonergic. Serotonergic nerve endings were also seen
in parapodial muscle. 4. Simultaneous intracellular recordings and use of
altered divalent concentrations revealed that no detectable direct synaptic
interactions exist between POP cells and motor neurons. 5. When POP cells
and motoneurons were simultaneously recorded while measuring muscle
contractions, it was found that POP cell activity enhances
motoneuron-induced tension by 120-900%, averaging around 300%. Variability
in the efficacy of individual POP cells suggests that they may influence
specific regions or groups of muscle fibers. 6. POP cell activity also
significantly increased the rate of relaxation of parapodial muscle
contractions, averaging about a 40% reduction in the time required to relax
to one-half peak tension. Increased relaxation rate implies a postsynaptic
change in muscle behavior. 7. The effectiveness of POP cells to increase
contraction tension and relaxation rate was positively correlated with POP
cell spike frequency. These effects were slow (seconds) in onset and could
persist for a minute or more after cessation of POP firing. Concurrent
motoneuron activity is not required for modulation by POP cells. 8.
Simultaneous intracellular recording from a POP cell, motoneuron, and
muscle fiber revealed that POP cell activity enhanced the amplitude of
motoneuron-induced excitatory junction potentials (EJPs). Activity of POP
cells did not alter muscle fiber membrane potential, but the experiments
left open the possibility that EJP enhancement is presynaptic,
postsynaptic, or a combination.</description><subject>5,7-Dihydroxytryptamine - metabolism</subject><subject>Animals</subject><subject>Aplysia - physiology</subject><subject>Axons - physiology</subject><subject>Biochemistry. Physiology. Immunology</subject><subject>Biological and medical sciences</subject><subject>Evoked Potentials - physiology</subject><subject>Extremities - innervation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia - cytology</subject><subject>Ganglia - physiology</subject><subject>Immunohistochemistry</subject><subject>Invertebrates</subject><subject>Mollusca</subject><subject>Motor Neurons - physiology</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle Relaxation - physiology</subject><subject>Muscles - innervation</subject><subject>Neuromuscular Junction - physiology</subject><subject>Physiology. Development</subject><subject>Serotonin - metabolism</subject><subject>Serotonin - physiology</subject><subject>Swimming</subject><subject>Synaptic Transmission - physiology</subject><issn>0022-3077</issn><issn>1522-1598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMFu1DAQhi0EKkvLA3BA8gHBaYPHdpzkWFW0rFTBAejVmjjOrleOvdiJqn17vNoVvYxHnm_-kT5CPgCrAGr-dR8q6DqolKpkBUKpV2RV_vka6q59TVaMlV6wpnlL3uW8Z4w1NeNX5AqU4lyJFXn6YZeEnpoY5hQ9jSPNz26aXNhSF-jtwR-zQ9onzM47DFjRzWZT0V82xTkGm7bO0CkOi8c5piMNJS6GfEPejOizfX95r8mf-2-_776vH38-bO5uH9eGN3xeYy1wbGvAQXHAHhrTGmNkP6hShJVS9iDqAUer6oFxhUZyOUohDXYCeCuuyedz7iHFv4vNs55cNtZ7DDYuWTe8bhkHKCCcQZNizsmO-pDchOmogemTS70P-uRSK6WlPrksOx8v4Us_2eFl4yyvzD9d5pgN-jFhMC7_x4ppwXhXsC9nbOe2u2eXrD7sitTo4_Z4uvpy8B8VPora</recordid><startdate>199110</startdate><enddate>199110</enddate><creator>McPherson, D. R</creator><creator>Blankenship, J. E</creator><general>Am Phys Soc</general><general>American Physiological Society</general><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>7X8</scope></search><sort><creationdate>199110</creationdate><title>Neural control of swimming in Aplysia brasiliana. III. Serotonergic modulatory neurons</title><author>McPherson, D. R ; Blankenship, J. E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c272t-a53af851ad621ab17c8ccc4bd6c4b3e444b135dafe65d026ac424f434ca931283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>5,7-Dihydroxytryptamine - metabolism</topic><topic>Animals</topic><topic>Aplysia - physiology</topic><topic>Axons - physiology</topic><topic>Biochemistry. Physiology. Immunology</topic><topic>Biological and medical sciences</topic><topic>Evoked Potentials - physiology</topic><topic>Extremities - innervation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia - cytology</topic><topic>Ganglia - physiology</topic><topic>Immunohistochemistry</topic><topic>Invertebrates</topic><topic>Mollusca</topic><topic>Motor Neurons - physiology</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle Relaxation - physiology</topic><topic>Muscles - innervation</topic><topic>Neuromuscular Junction - physiology</topic><topic>Physiology. Development</topic><topic>Serotonin - metabolism</topic><topic>Serotonin - physiology</topic><topic>Swimming</topic><topic>Synaptic Transmission - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McPherson, D. R</creatorcontrib><creatorcontrib>Blankenship, J. E</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McPherson, D. R</au><au>Blankenship, J. E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neural control of swimming in Aplysia brasiliana. III. Serotonergic modulatory neurons</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>1991-10</date><risdate>1991</risdate><volume>66</volume><issue>4</issue><spage>1366</spage><epage>1379</epage><pages>1366-1379</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><coden>JONEA4</coden><abstract>D. R. McPherson and J. E. Blankenship
Marine Biomedical Institute, University of Texas Medical Branch, Galveston 77550.
1. We describe a group of serotonergic neurons in the pedal ganglia of
Aplysia brasiliana and characterize their modulatory effects on the
motoneuron input to swimming muscles of the parapodia. Each pedal ganglion
contains one cluster of large neurons near its dorsomedial surface that
fires in phase with opening (downstroke) of the parapodia; these have been
designated parapodial opener-phase (POP) cells. 2. POP cells are large,
number 15-20 per ganglion, have peripheral axons in parapodial nerves, have
distinctively shaped action potentials, and fire in bursts phasically with
motoneurons during the opening, or downstroke portion, of parapodial
movement during fictive swimming. Firing individual POP cells with
intracellular current indicates that they have no direct detectable effect
on muscle, causing neither junction potentials nor contractions. 3.
5,7-Dihydroxytryptamine (5,7-DHT) staining, immunocytochemistry using
serotonin (5-HT) antibodies, and direct biochemical measurements revealed
that POP cells are serotonergic. Serotonergic nerve endings were also seen
in parapodial muscle. 4. Simultaneous intracellular recordings and use of
altered divalent concentrations revealed that no detectable direct synaptic
interactions exist between POP cells and motor neurons. 5. When POP cells
and motoneurons were simultaneously recorded while measuring muscle
contractions, it was found that POP cell activity enhances
motoneuron-induced tension by 120-900%, averaging around 300%. Variability
in the efficacy of individual POP cells suggests that they may influence
specific regions or groups of muscle fibers. 6. POP cell activity also
significantly increased the rate of relaxation of parapodial muscle
contractions, averaging about a 40% reduction in the time required to relax
to one-half peak tension. Increased relaxation rate implies a postsynaptic
change in muscle behavior. 7. The effectiveness of POP cells to increase
contraction tension and relaxation rate was positively correlated with POP
cell spike frequency. These effects were slow (seconds) in onset and could
persist for a minute or more after cessation of POP firing. Concurrent
motoneuron activity is not required for modulation by POP cells. 8.
Simultaneous intracellular recording from a POP cell, motoneuron, and
muscle fiber revealed that POP cell activity enhanced the amplitude of
motoneuron-induced excitatory junction potentials (EJPs). Activity of POP
cells did not alter muscle fiber membrane potential, but the experiments
left open the possibility that EJP enhancement is presynaptic,
postsynaptic, or a combination.</abstract><cop>Bethesda, MD</cop><pub>Am Phys Soc</pub><pmid>1662263</pmid><doi>10.1152/jn.1991.66.4.1366</doi><tpages>14</tpages></addata></record> |
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subjects | 5,7-Dihydroxytryptamine - metabolism Animals Aplysia - physiology Axons - physiology Biochemistry. Physiology. Immunology Biological and medical sciences Evoked Potentials - physiology Extremities - innervation Fundamental and applied biological sciences. Psychology Ganglia - cytology Ganglia - physiology Immunohistochemistry Invertebrates Mollusca Motor Neurons - physiology Muscle Contraction - physiology Muscle Relaxation - physiology Muscles - innervation Neuromuscular Junction - physiology Physiology. Development Serotonin - metabolism Serotonin - physiology Swimming Synaptic Transmission - physiology |
title | Neural control of swimming in Aplysia brasiliana. III. Serotonergic modulatory neurons |
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