Characterization of a radula opener neuromuscular system in Aplysia
C. G. Evans, S. Rosen, I. Kupfermann, K. R. Weiss and E. C. Cropper Department of Physiology and Biophysics, Mt. Sinai Medical Center, New York 10029, USA. 1. Several lines of evidence suggest that the I7-I10 muscle group contributes to the radula opening phase of behavior in Aplysia; 1) extracellul...
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creator | Evans, C. G Rosen, S Kupfermann, I Weiss, K. R Cropper, E. C |
description | C. G. Evans, S. Rosen, I. Kupfermann, K. R. Weiss and E. C. Cropper
Department of Physiology and Biophysics, Mt. Sinai Medical Center, New York 10029, USA.
1. Several lines of evidence suggest that the I7-I10 muscle group
contributes to the radula opening phase of behavior in Aplysia; 1)
extracellular stimulation of these muscles in reduced preparations causes
the halves of the radula to separate, 2) synaptic activity can be recorded
from muscles I7-I10 in intact animals when the radula is opening, and 3)
motor neurons innervating I7-I10 are activated out of phase with
retractor/closer motor neurons during cycles of buccal activity driven by
the cerebral-to-buccal interneuron 2 (CBI-2). 2. All of the opener muscles
are innervated by the B48 neurons, a bilaterally symmetrical pair of
cholinergic motor neurons. B48 neurons produce excitatory junction
potentials (EJPs) in opener muscle fibers that summate to produce muscle
contractions. Contraction size is determined by the size of depolarization
in muscle fibers and/or by action potentials that are triggered by
summation of B48-evoked EJPs. 3. In addition to input from B48 neurons,
opener muscles also receive excitatory input from the cholinergic
multiaction neurons B4/B5. EJPs evoked by stimulation of neurons B4/B5 are
1/10 the size of B48-evoked EJPs. Consequently, changes in muscle tension
produced by B4/B5 activity are relatively small. In contrast to B48
neurons, neurons B4/B5 are likely to be active during the
closing/retraction phase of behavior. During cycles of buccal activity
driven by neuron CBI-2, neurons B4/B5 fire in phase with closer/retractor
motor neurons. Thus opener muscles may develop a modest amount of tension
during the closing/retraction phase of behavior as a result of synaptic
input from neurons B4/B5. 4. Opener muscles may also develop tension during
closing/retraction simply by virtue of the fact that they have been
stretched. When isolated opener muscles are lengthened, depolarizations are
recorded from individual muscle fibers, and muscle tension increases. With
sufficient changes in fiber length, action potentials are elicited. These
action potentials produce twitchlike muscle contractions that become
rhythmic with maintained stretch. Stretch-activated depolarizations are
generally first apparent when muscle length is increased by 1 mm. Length
changes of 4-5 mm are generally necessary to elicit twitchlike muscle
contractions. Changes of 1-2 mm in muscle length are observed when |
doi_str_mv | 10.1152/jn.1996.76.2.1267 |
format | Article |
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Department of Physiology and Biophysics, Mt. Sinai Medical Center, New York 10029, USA.
1. Several lines of evidence suggest that the I7-I10 muscle group
contributes to the radula opening phase of behavior in Aplysia; 1)
extracellular stimulation of these muscles in reduced preparations causes
the halves of the radula to separate, 2) synaptic activity can be recorded
from muscles I7-I10 in intact animals when the radula is opening, and 3)
motor neurons innervating I7-I10 are activated out of phase with
retractor/closer motor neurons during cycles of buccal activity driven by
the cerebral-to-buccal interneuron 2 (CBI-2). 2. All of the opener muscles
are innervated by the B48 neurons, a bilaterally symmetrical pair of
cholinergic motor neurons. B48 neurons produce excitatory junction
potentials (EJPs) in opener muscle fibers that summate to produce muscle
contractions. Contraction size is determined by the size of depolarization
in muscle fibers and/or by action potentials that are triggered by
summation of B48-evoked EJPs. 3. In addition to input from B48 neurons,
opener muscles also receive excitatory input from the cholinergic
multiaction neurons B4/B5. EJPs evoked by stimulation of neurons B4/B5 are
1/10 the size of B48-evoked EJPs. Consequently, changes in muscle tension
produced by B4/B5 activity are relatively small. In contrast to B48
neurons, neurons B4/B5 are likely to be active during the
closing/retraction phase of behavior. During cycles of buccal activity
driven by neuron CBI-2, neurons B4/B5 fire in phase with closer/retractor
motor neurons. Thus opener muscles may develop a modest amount of tension
during the closing/retraction phase of behavior as a result of synaptic
input from neurons B4/B5. 4. Opener muscles may also develop tension during
closing/retraction simply by virtue of the fact that they have been
stretched. When isolated opener muscles are lengthened, depolarizations are
recorded from individual muscle fibers, and muscle tension increases. With
sufficient changes in fiber length, action potentials are elicited. These
action potentials produce twitchlike muscle contractions that become
rhythmic with maintained stretch. Stretch-activated depolarizations are
generally first apparent when muscle length is increased by 1 mm. Length
changes of 4-5 mm are generally necessary to elicit twitchlike muscle
contractions. Changes of 1-2 mm in muscle length are observed when the
opener muscle's antagonist, the accessory radula closer, is activated in
reduced preparations. 5. Stretch may also modulate B48-induced contractions
of the opener muscles. When muscle length is increased, B48-elicited
contractions of the I7 muscle are larger. These increases in contraction
amplitude are accompanied by decreases in contraction latency. 6. We
conclude that muscles I7-I10 contract vigorously in response to strong
excitatory input from neuron B48 and contribute to radula opening. Stretch
may potentiate this activity. Thus, if radula closer muscles contract
vigorously and pull on the opener muscles, the opener muscles will respond
by contracting more vigorously themselves. This may be a mechanism for
maintaining amplitude relationships between antagonistic muscles.
Additionally, it is likely that the opener muscles will develop at least a
modest amount of tension during closure/retraction of the radula. Part of
this activation may derive from the weak excitatory input that the muscles
receive from neurons B4/B5. Another part may derive from the stretch. One
function of this co-contraction may be to act as a brake on closure,
bringing this phase of feeding behavior to a smooth halt.</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.1996.76.2.1267</identifier><identifier>PMID: 8871235</identifier><language>eng</language><publisher>United States: Am Phys Soc</publisher><subject>Action Potentials - physiology ; Animals ; Aplysia ; Aplysia - physiology ; In Vitro Techniques ; Marine ; Motor Neurons - physiology ; Muscle Contraction - physiology ; Muscle Fibers, Skeletal - physiology ; Muscles - innervation ; Muscles - physiology ; Neuromuscular Junction - physiology ; Stress, Mechanical</subject><ispartof>Journal of neurophysiology, 1996-08, Vol.76 (2), p.1267-1281</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-eb09b63dc3a4a0f42e58073d5e3134fd42f84764fb92cd93cb8cb999d30831b13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8871235$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Evans, C. G</creatorcontrib><creatorcontrib>Rosen, S</creatorcontrib><creatorcontrib>Kupfermann, I</creatorcontrib><creatorcontrib>Weiss, K. R</creatorcontrib><creatorcontrib>Cropper, E. C</creatorcontrib><title>Characterization of a radula opener neuromuscular system in Aplysia</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>C. G. Evans, S. Rosen, I. Kupfermann, K. R. Weiss and E. C. Cropper
Department of Physiology and Biophysics, Mt. Sinai Medical Center, New York 10029, USA.
1. Several lines of evidence suggest that the I7-I10 muscle group
contributes to the radula opening phase of behavior in Aplysia; 1)
extracellular stimulation of these muscles in reduced preparations causes
the halves of the radula to separate, 2) synaptic activity can be recorded
from muscles I7-I10 in intact animals when the radula is opening, and 3)
motor neurons innervating I7-I10 are activated out of phase with
retractor/closer motor neurons during cycles of buccal activity driven by
the cerebral-to-buccal interneuron 2 (CBI-2). 2. All of the opener muscles
are innervated by the B48 neurons, a bilaterally symmetrical pair of
cholinergic motor neurons. B48 neurons produce excitatory junction
potentials (EJPs) in opener muscle fibers that summate to produce muscle
contractions. Contraction size is determined by the size of depolarization
in muscle fibers and/or by action potentials that are triggered by
summation of B48-evoked EJPs. 3. In addition to input from B48 neurons,
opener muscles also receive excitatory input from the cholinergic
multiaction neurons B4/B5. EJPs evoked by stimulation of neurons B4/B5 are
1/10 the size of B48-evoked EJPs. Consequently, changes in muscle tension
produced by B4/B5 activity are relatively small. In contrast to B48
neurons, neurons B4/B5 are likely to be active during the
closing/retraction phase of behavior. During cycles of buccal activity
driven by neuron CBI-2, neurons B4/B5 fire in phase with closer/retractor
motor neurons. Thus opener muscles may develop a modest amount of tension
during the closing/retraction phase of behavior as a result of synaptic
input from neurons B4/B5. 4. Opener muscles may also develop tension during
closing/retraction simply by virtue of the fact that they have been
stretched. When isolated opener muscles are lengthened, depolarizations are
recorded from individual muscle fibers, and muscle tension increases. With
sufficient changes in fiber length, action potentials are elicited. These
action potentials produce twitchlike muscle contractions that become
rhythmic with maintained stretch. Stretch-activated depolarizations are
generally first apparent when muscle length is increased by 1 mm. Length
changes of 4-5 mm are generally necessary to elicit twitchlike muscle
contractions. Changes of 1-2 mm in muscle length are observed when the
opener muscle's antagonist, the accessory radula closer, is activated in
reduced preparations. 5. Stretch may also modulate B48-induced contractions
of the opener muscles. When muscle length is increased, B48-elicited
contractions of the I7 muscle are larger. These increases in contraction
amplitude are accompanied by decreases in contraction latency. 6. We
conclude that muscles I7-I10 contract vigorously in response to strong
excitatory input from neuron B48 and contribute to radula opening. Stretch
may potentiate this activity. Thus, if radula closer muscles contract
vigorously and pull on the opener muscles, the opener muscles will respond
by contracting more vigorously themselves. This may be a mechanism for
maintaining amplitude relationships between antagonistic muscles.
Additionally, it is likely that the opener muscles will develop at least a
modest amount of tension during closure/retraction of the radula. Part of
this activation may derive from the weak excitatory input that the muscles
receive from neurons B4/B5. Another part may derive from the stretch. One
function of this co-contraction may be to act as a brake on closure,
bringing this phase of feeding behavior to a smooth halt.</description><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>Aplysia</subject><subject>Aplysia - physiology</subject><subject>In Vitro Techniques</subject><subject>Marine</subject><subject>Motor Neurons - physiology</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle Fibers, Skeletal - physiology</subject><subject>Muscles - innervation</subject><subject>Muscles - physiology</subject><subject>Neuromuscular Junction - physiology</subject><subject>Stress, Mechanical</subject><issn>0022-3077</issn><issn>1522-1598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOhDAUhhujGcfRB3BhwkpXYO-lS0O8JZO40XVTShmYAMUWYvDphcxEl67OyX9bfABcI5ggxPD9vkuQlDwRPMEJwlycgPWs4xgxmZ6CNYTzT6AQ5-AihD2EUDCIV2CVpgJhwtYgyyrttRmsr7_1ULsucmWkI6-LsdGR621nfdTZ0bt2DGbWfBSmMNg2qrvooW-mUOtLcFbqJtir492Aj6fH9-wl3r49v2YP29gQJofY5lDmnBSGaKphSbFlKRSkYJYgQsuC4jKlgtMyl9gUkpg8NbmUsiAwJShHZANuD7u9d5-jDYNq62Bs0-jOujEokVJKOCf_BhGHTGAq5iA6BI13IXhbqt7XrfaTQlAthNW-UwthJbjCaiE8d26O42Pe2uK3cUQ6-3cHv6p31VftreqrmZJr3G5a5v6WfgAv9ITX</recordid><startdate>19960801</startdate><enddate>19960801</enddate><creator>Evans, C. G</creator><creator>Rosen, S</creator><creator>Kupfermann, I</creator><creator>Weiss, K. R</creator><creator>Cropper, E. C</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>7TK</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>19960801</creationdate><title>Characterization of a radula opener neuromuscular system in Aplysia</title><author>Evans, C. G ; Rosen, S ; Kupfermann, I ; Weiss, K. R ; Cropper, E. C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-eb09b63dc3a4a0f42e58073d5e3134fd42f84764fb92cd93cb8cb999d30831b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Aplysia</topic><topic>Aplysia - physiology</topic><topic>In Vitro Techniques</topic><topic>Marine</topic><topic>Motor Neurons - physiology</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle Fibers, Skeletal - physiology</topic><topic>Muscles - innervation</topic><topic>Muscles - physiology</topic><topic>Neuromuscular Junction - physiology</topic><topic>Stress, Mechanical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Evans, C. G</creatorcontrib><creatorcontrib>Rosen, S</creatorcontrib><creatorcontrib>Kupfermann, I</creatorcontrib><creatorcontrib>Weiss, K. R</creatorcontrib><creatorcontrib>Cropper, E. C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Evans, C. G</au><au>Rosen, S</au><au>Kupfermann, I</au><au>Weiss, K. R</au><au>Cropper, E. C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of a radula opener neuromuscular system in Aplysia</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>1996-08-01</date><risdate>1996</risdate><volume>76</volume><issue>2</issue><spage>1267</spage><epage>1281</epage><pages>1267-1281</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><abstract>C. G. Evans, S. Rosen, I. Kupfermann, K. R. Weiss and E. C. Cropper
Department of Physiology and Biophysics, Mt. Sinai Medical Center, New York 10029, USA.
1. Several lines of evidence suggest that the I7-I10 muscle group
contributes to the radula opening phase of behavior in Aplysia; 1)
extracellular stimulation of these muscles in reduced preparations causes
the halves of the radula to separate, 2) synaptic activity can be recorded
from muscles I7-I10 in intact animals when the radula is opening, and 3)
motor neurons innervating I7-I10 are activated out of phase with
retractor/closer motor neurons during cycles of buccal activity driven by
the cerebral-to-buccal interneuron 2 (CBI-2). 2. All of the opener muscles
are innervated by the B48 neurons, a bilaterally symmetrical pair of
cholinergic motor neurons. B48 neurons produce excitatory junction
potentials (EJPs) in opener muscle fibers that summate to produce muscle
contractions. Contraction size is determined by the size of depolarization
in muscle fibers and/or by action potentials that are triggered by
summation of B48-evoked EJPs. 3. In addition to input from B48 neurons,
opener muscles also receive excitatory input from the cholinergic
multiaction neurons B4/B5. EJPs evoked by stimulation of neurons B4/B5 are
1/10 the size of B48-evoked EJPs. Consequently, changes in muscle tension
produced by B4/B5 activity are relatively small. In contrast to B48
neurons, neurons B4/B5 are likely to be active during the
closing/retraction phase of behavior. During cycles of buccal activity
driven by neuron CBI-2, neurons B4/B5 fire in phase with closer/retractor
motor neurons. Thus opener muscles may develop a modest amount of tension
during the closing/retraction phase of behavior as a result of synaptic
input from neurons B4/B5. 4. Opener muscles may also develop tension during
closing/retraction simply by virtue of the fact that they have been
stretched. When isolated opener muscles are lengthened, depolarizations are
recorded from individual muscle fibers, and muscle tension increases. With
sufficient changes in fiber length, action potentials are elicited. These
action potentials produce twitchlike muscle contractions that become
rhythmic with maintained stretch. Stretch-activated depolarizations are
generally first apparent when muscle length is increased by 1 mm. Length
changes of 4-5 mm are generally necessary to elicit twitchlike muscle
contractions. Changes of 1-2 mm in muscle length are observed when the
opener muscle's antagonist, the accessory radula closer, is activated in
reduced preparations. 5. Stretch may also modulate B48-induced contractions
of the opener muscles. When muscle length is increased, B48-elicited
contractions of the I7 muscle are larger. These increases in contraction
amplitude are accompanied by decreases in contraction latency. 6. We
conclude that muscles I7-I10 contract vigorously in response to strong
excitatory input from neuron B48 and contribute to radula opening. Stretch
may potentiate this activity. Thus, if radula closer muscles contract
vigorously and pull on the opener muscles, the opener muscles will respond
by contracting more vigorously themselves. This may be a mechanism for
maintaining amplitude relationships between antagonistic muscles.
Additionally, it is likely that the opener muscles will develop at least a
modest amount of tension during closure/retraction of the radula. Part of
this activation may derive from the weak excitatory input that the muscles
receive from neurons B4/B5. Another part may derive from the stretch. One
function of this co-contraction may be to act as a brake on closure,
bringing this phase of feeding behavior to a smooth halt.</abstract><cop>United States</cop><pub>Am Phys Soc</pub><pmid>8871235</pmid><doi>10.1152/jn.1996.76.2.1267</doi><tpages>15</tpages></addata></record> |
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subjects | Action Potentials - physiology Animals Aplysia Aplysia - physiology In Vitro Techniques Marine Motor Neurons - physiology Muscle Contraction - physiology Muscle Fibers, Skeletal - physiology Muscles - innervation Muscles - physiology Neuromuscular Junction - physiology Stress, Mechanical |
title | Characterization of a radula opener neuromuscular system in Aplysia |
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