Mechanical actions of heterogenic reflexes among ankle stabilizers and their interactions with plantarflexors of the cat hindlimb
S. J. Bonasera and T. R. Nichols Department of Physiology, Emory University, Atlanta, Georgia 30322, USA. 1. The stretch-evoked reflex organization of muscles whose major action is to abduct [peroneus brevis (PB); peroneus longus (PL)] and adduct [tibialis posterior (TP); flexor digitorum longus (FD...
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description | S. J. Bonasera and T. R. Nichols
Department of Physiology, Emory University, Atlanta, Georgia 30322, USA.
1. The stretch-evoked reflex organization of muscles whose major action is
to abduct [peroneus brevis (PB); peroneus longus (PL)] and adduct [tibialis
posterior (TP); flexor digitorum longus (FDL); flexor hallucis longus
(FHL)] the ankle, and their interactions with the hindlimb extensors
gastrocnemius (G) and soleus (S), were studied in 27 unanesthetized
decerebrate cats. Ramp-hold-release stretches of physiological amplitudes
were applied to muscle tendons detached from their bony insertion, and
muscle force output was measured in response to these perturbations.
Flexion and crossed-extension reflexes were used to modulate baseline
force. 2. PB and TP shared strong, length-dependent, short-latency
inhibitory reflexes prominent when the muscles were either actively
generating force or quiescent. The mechanical characteristics of this
reflex suggest Ia reciprocal inhibition as the underlying mechanism. Just
as reciprocal inhibition between S and tibialis anterior stiffens the ankle
joint against sagittal perturbations, we propose that reciprocal inhibition
between PB and TP stiffens the ankle joint against nonsagittal
perturbations. 3. In all preparations (n = 7) and under all conditions
examined, PB and PL shared well-demonstrated mutual excitation. The reflex
responses were asymmetric (favoring excitation of PL), length dependent,
and occurred simultaneously with the stretch reflex at a latency of 16-18
ms. Mutual monosynaptic projections previously described between these two
muscles explain all of the above findings. Our data further demonstrate
that, under certain conditions, the ensemble activity of this reflex
interaction has a powerful effect on the mechanical behavior of the muscle.
4. The heterogenic reflex organization of the ankle adductors was as
follows: FDL evoked a modest excitation on TP, whereas FHL evoked weak
inhibition. Latency of the excitation from FDL onto TP (24 ms) was greater
than expected if the reflex were mediated by heteronymous Ia afferents. In
all preparations examined (n = 3), TP contributed no significant reflexes
onto either FDL or FHL. 5. Mutual, asymmetric inhibition characterized
interactions between PB and the plantarflexors S and G. Most remarkable was
a novel, long-latency (72-74 ms) reflex inhibition evoked on both S and G
by stretch of PB. When this inhibition occurred, it dramatically decreased
the S (or G) |
doi_str_mv | 10.1152/jn.1996.75.5.2050 |
format | Article |
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Department of Physiology, Emory University, Atlanta, Georgia 30322, USA.
1. The stretch-evoked reflex organization of muscles whose major action is
to abduct [peroneus brevis (PB); peroneus longus (PL)] and adduct [tibialis
posterior (TP); flexor digitorum longus (FDL); flexor hallucis longus
(FHL)] the ankle, and their interactions with the hindlimb extensors
gastrocnemius (G) and soleus (S), were studied in 27 unanesthetized
decerebrate cats. Ramp-hold-release stretches of physiological amplitudes
were applied to muscle tendons detached from their bony insertion, and
muscle force output was measured in response to these perturbations.
Flexion and crossed-extension reflexes were used to modulate baseline
force. 2. PB and TP shared strong, length-dependent, short-latency
inhibitory reflexes prominent when the muscles were either actively
generating force or quiescent. The mechanical characteristics of this
reflex suggest Ia reciprocal inhibition as the underlying mechanism. Just
as reciprocal inhibition between S and tibialis anterior stiffens the ankle
joint against sagittal perturbations, we propose that reciprocal inhibition
between PB and TP stiffens the ankle joint against nonsagittal
perturbations. 3. In all preparations (n = 7) and under all conditions
examined, PB and PL shared well-demonstrated mutual excitation. The reflex
responses were asymmetric (favoring excitation of PL), length dependent,
and occurred simultaneously with the stretch reflex at a latency of 16-18
ms. Mutual monosynaptic projections previously described between these two
muscles explain all of the above findings. Our data further demonstrate
that, under certain conditions, the ensemble activity of this reflex
interaction has a powerful effect on the mechanical behavior of the muscle.
4. The heterogenic reflex organization of the ankle adductors was as
follows: FDL evoked a modest excitation on TP, whereas FHL evoked weak
inhibition. Latency of the excitation from FDL onto TP (24 ms) was greater
than expected if the reflex were mediated by heteronymous Ia afferents. In
all preparations examined (n = 3), TP contributed no significant reflexes
onto either FDL or FHL. 5. Mutual, asymmetric inhibition characterized
interactions between PB and the plantarflexors S and G. Most remarkable was
a novel, long-latency (72-74 ms) reflex inhibition evoked on both S and G
by stretch of PB. When this inhibition occurred, it dramatically decreased
the S (or G) stretch response. Longer PB lengths evoked greater inhibition
of isometric S; regression analysis indicated that the model best
predicting this inhibition contained muscle force and stiffness terms. No
long-latency reflexes were noted from either G or S onto PB. The mechanism
underlying long-latency inhibition is presently unknown; however, features
of this interaction suggest interneurons receive either group II or group
III afferent input. 6. G and TP shared short latency, mutually inhibitory,
asymmetric reflexes favoring inhibition of TP. No long-latency interactions
were noted, nor were there any mechanically significant interactions
between S and TP. 7. Reflex interactions across the abduction/adduction
axis thus favored inhibition of plantarflexion and adduction torques while
emphasizing abduction torques: PB/S (or PB/G) interactions were mutual,
asymmetric, and favored inhibition of G and S; TP/G interactions were
mutual, asymmetric, and favored inhibition of TP; TP/PB interactions were
approximately balanced. The overall mechanical outcome of these inhibitory
interactions may partly underlie the global corrective strategy seen in
intact cats subjected to linear perturbations. 8. No significant reflex
interactions were demonstrated between PL and TP, G, or S, nor were any
long-latency reflexes noted. Thus, whereas reflex interactions between the
stereotypically activated PB and other stereotypically activated muscles
(including TP, G, and S) were strong and well-demonstrated, interactions
between the variably activated PL and these same muscles were far weaker.</description><identifier>ISSN: 0022-3077</identifier><identifier>EISSN: 1522-1598</identifier><identifier>DOI: 10.1152/jn.1996.75.5.2050</identifier><identifier>PMID: 8734603</identifier><language>eng</language><publisher>United States: Am Phys Soc</publisher><subject>Animals ; Biomechanical Phenomena ; Cats ; Female ; Hindlimb - anatomy & histology ; Hindlimb - innervation ; Hindlimb - physiology ; Isometric Contraction - physiology ; Male ; Muscle Contraction - physiology ; Muscle, Skeletal - anatomy & histology ; Muscle, Skeletal - innervation ; Muscle, Skeletal - physiology ; Neurons, Afferent - physiology ; Reflex, Monosynaptic - physiology</subject><ispartof>Journal of neurophysiology, 1996-05, Vol.75 (5), p.2050-2070</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-30540eb433de5916821277c48dd886a2d9012b01d0c5e8d78b27d599e2130fda3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8734603$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonasera, S. J</creatorcontrib><creatorcontrib>Nichols, T. R</creatorcontrib><title>Mechanical actions of heterogenic reflexes among ankle stabilizers and their interactions with plantarflexors of the cat hindlimb</title><title>Journal of neurophysiology</title><addtitle>J Neurophysiol</addtitle><description>S. J. Bonasera and T. R. Nichols
Department of Physiology, Emory University, Atlanta, Georgia 30322, USA.
1. The stretch-evoked reflex organization of muscles whose major action is
to abduct [peroneus brevis (PB); peroneus longus (PL)] and adduct [tibialis
posterior (TP); flexor digitorum longus (FDL); flexor hallucis longus
(FHL)] the ankle, and their interactions with the hindlimb extensors
gastrocnemius (G) and soleus (S), were studied in 27 unanesthetized
decerebrate cats. Ramp-hold-release stretches of physiological amplitudes
were applied to muscle tendons detached from their bony insertion, and
muscle force output was measured in response to these perturbations.
Flexion and crossed-extension reflexes were used to modulate baseline
force. 2. PB and TP shared strong, length-dependent, short-latency
inhibitory reflexes prominent when the muscles were either actively
generating force or quiescent. The mechanical characteristics of this
reflex suggest Ia reciprocal inhibition as the underlying mechanism. Just
as reciprocal inhibition between S and tibialis anterior stiffens the ankle
joint against sagittal perturbations, we propose that reciprocal inhibition
between PB and TP stiffens the ankle joint against nonsagittal
perturbations. 3. In all preparations (n = 7) and under all conditions
examined, PB and PL shared well-demonstrated mutual excitation. The reflex
responses were asymmetric (favoring excitation of PL), length dependent,
and occurred simultaneously with the stretch reflex at a latency of 16-18
ms. Mutual monosynaptic projections previously described between these two
muscles explain all of the above findings. Our data further demonstrate
that, under certain conditions, the ensemble activity of this reflex
interaction has a powerful effect on the mechanical behavior of the muscle.
4. The heterogenic reflex organization of the ankle adductors was as
follows: FDL evoked a modest excitation on TP, whereas FHL evoked weak
inhibition. Latency of the excitation from FDL onto TP (24 ms) was greater
than expected if the reflex were mediated by heteronymous Ia afferents. In
all preparations examined (n = 3), TP contributed no significant reflexes
onto either FDL or FHL. 5. Mutual, asymmetric inhibition characterized
interactions between PB and the plantarflexors S and G. Most remarkable was
a novel, long-latency (72-74 ms) reflex inhibition evoked on both S and G
by stretch of PB. When this inhibition occurred, it dramatically decreased
the S (or G) stretch response. Longer PB lengths evoked greater inhibition
of isometric S; regression analysis indicated that the model best
predicting this inhibition contained muscle force and stiffness terms. No
long-latency reflexes were noted from either G or S onto PB. The mechanism
underlying long-latency inhibition is presently unknown; however, features
of this interaction suggest interneurons receive either group II or group
III afferent input. 6. G and TP shared short latency, mutually inhibitory,
asymmetric reflexes favoring inhibition of TP. No long-latency interactions
were noted, nor were there any mechanically significant interactions
between S and TP. 7. Reflex interactions across the abduction/adduction
axis thus favored inhibition of plantarflexion and adduction torques while
emphasizing abduction torques: PB/S (or PB/G) interactions were mutual,
asymmetric, and favored inhibition of G and S; TP/G interactions were
mutual, asymmetric, and favored inhibition of TP; TP/PB interactions were
approximately balanced. The overall mechanical outcome of these inhibitory
interactions may partly underlie the global corrective strategy seen in
intact cats subjected to linear perturbations. 8. No significant reflex
interactions were demonstrated between PL and TP, G, or S, nor were any
long-latency reflexes noted. Thus, whereas reflex interactions between the
stereotypically activated PB and other stereotypically activated muscles
(including TP, G, and S) were strong and well-demonstrated, interactions
between the variably activated PL and these same muscles were far weaker.</description><subject>Animals</subject><subject>Biomechanical Phenomena</subject><subject>Cats</subject><subject>Female</subject><subject>Hindlimb - anatomy & histology</subject><subject>Hindlimb - innervation</subject><subject>Hindlimb - physiology</subject><subject>Isometric Contraction - physiology</subject><subject>Male</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle, Skeletal - anatomy & histology</subject><subject>Muscle, Skeletal - innervation</subject><subject>Muscle, Skeletal - physiology</subject><subject>Neurons, Afferent - physiology</subject><subject>Reflex, Monosynaptic - physiology</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>eNqFkUuPFCEUhYnRjO3oD3BhwkpXXfJoCmppJuMjGeNG14SC2120FLRAZ2x3_nMpu9WlK8g953yBexB6TklHqWCv97Gjw9B3UnSiY0SQB2jV5mxNxaAeohUh7c6JlI_Rk1L2hBApCLtCV0ryTU_4Cv38CHYy0VsTsLHVp1hw2uIJKuS0gybgDNsA36FgM6e4wyZ-DYBLNaMP_gfkNo8O1wl8xj622B_Mva8TPgQTq8kLIeXf6ObE1lQ8-eiCn8en6NHWhALPLuc1-vL29vPN-_Xdp3cfbt7crS0XQ22_EBsC44ZzB2KgvWKUSWk3yjmlesPcQCgbCXXEClBOqpFJJ4YBGOVk6wy_Ri_P3ENO345Qqp59sRDaAyEdi5aqrZJw-V8jFUIy1i9GejbanEppa9KH7GeTT5oSvfSj91Ev_WgptNBLPy3z4gI_jjO4v4lLIU1_ddYnv5vufQZ9mE7Fp5B2pwX3j_QLiwubmQ</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>Bonasera, S. J</creator><creator>Nichols, T. R</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>7X8</scope></search><sort><creationdate>19960501</creationdate><title>Mechanical actions of heterogenic reflexes among ankle stabilizers and their interactions with plantarflexors of the cat hindlimb</title><author>Bonasera, S. J ; Nichols, T. R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-30540eb433de5916821277c48dd886a2d9012b01d0c5e8d78b27d599e2130fda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Biomechanical Phenomena</topic><topic>Cats</topic><topic>Female</topic><topic>Hindlimb - anatomy & histology</topic><topic>Hindlimb - innervation</topic><topic>Hindlimb - physiology</topic><topic>Isometric Contraction - physiology</topic><topic>Male</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle, Skeletal - anatomy & histology</topic><topic>Muscle, Skeletal - innervation</topic><topic>Muscle, Skeletal - physiology</topic><topic>Neurons, Afferent - physiology</topic><topic>Reflex, Monosynaptic - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonasera, S. J</creatorcontrib><creatorcontrib>Nichols, T. R</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>MEDLINE - Academic</collection><jtitle>Journal of neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonasera, S. J</au><au>Nichols, T. R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanical actions of heterogenic reflexes among ankle stabilizers and their interactions with plantarflexors of the cat hindlimb</atitle><jtitle>Journal of neurophysiology</jtitle><addtitle>J Neurophysiol</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>75</volume><issue>5</issue><spage>2050</spage><epage>2070</epage><pages>2050-2070</pages><issn>0022-3077</issn><eissn>1522-1598</eissn><abstract>S. J. Bonasera and T. R. Nichols
Department of Physiology, Emory University, Atlanta, Georgia 30322, USA.
1. The stretch-evoked reflex organization of muscles whose major action is
to abduct [peroneus brevis (PB); peroneus longus (PL)] and adduct [tibialis
posterior (TP); flexor digitorum longus (FDL); flexor hallucis longus
(FHL)] the ankle, and their interactions with the hindlimb extensors
gastrocnemius (G) and soleus (S), were studied in 27 unanesthetized
decerebrate cats. Ramp-hold-release stretches of physiological amplitudes
were applied to muscle tendons detached from their bony insertion, and
muscle force output was measured in response to these perturbations.
Flexion and crossed-extension reflexes were used to modulate baseline
force. 2. PB and TP shared strong, length-dependent, short-latency
inhibitory reflexes prominent when the muscles were either actively
generating force or quiescent. The mechanical characteristics of this
reflex suggest Ia reciprocal inhibition as the underlying mechanism. Just
as reciprocal inhibition between S and tibialis anterior stiffens the ankle
joint against sagittal perturbations, we propose that reciprocal inhibition
between PB and TP stiffens the ankle joint against nonsagittal
perturbations. 3. In all preparations (n = 7) and under all conditions
examined, PB and PL shared well-demonstrated mutual excitation. The reflex
responses were asymmetric (favoring excitation of PL), length dependent,
and occurred simultaneously with the stretch reflex at a latency of 16-18
ms. Mutual monosynaptic projections previously described between these two
muscles explain all of the above findings. Our data further demonstrate
that, under certain conditions, the ensemble activity of this reflex
interaction has a powerful effect on the mechanical behavior of the muscle.
4. The heterogenic reflex organization of the ankle adductors was as
follows: FDL evoked a modest excitation on TP, whereas FHL evoked weak
inhibition. Latency of the excitation from FDL onto TP (24 ms) was greater
than expected if the reflex were mediated by heteronymous Ia afferents. In
all preparations examined (n = 3), TP contributed no significant reflexes
onto either FDL or FHL. 5. Mutual, asymmetric inhibition characterized
interactions between PB and the plantarflexors S and G. Most remarkable was
a novel, long-latency (72-74 ms) reflex inhibition evoked on both S and G
by stretch of PB. When this inhibition occurred, it dramatically decreased
the S (or G) stretch response. Longer PB lengths evoked greater inhibition
of isometric S; regression analysis indicated that the model best
predicting this inhibition contained muscle force and stiffness terms. No
long-latency reflexes were noted from either G or S onto PB. The mechanism
underlying long-latency inhibition is presently unknown; however, features
of this interaction suggest interneurons receive either group II or group
III afferent input. 6. G and TP shared short latency, mutually inhibitory,
asymmetric reflexes favoring inhibition of TP. No long-latency interactions
were noted, nor were there any mechanically significant interactions
between S and TP. 7. Reflex interactions across the abduction/adduction
axis thus favored inhibition of plantarflexion and adduction torques while
emphasizing abduction torques: PB/S (or PB/G) interactions were mutual,
asymmetric, and favored inhibition of G and S; TP/G interactions were
mutual, asymmetric, and favored inhibition of TP; TP/PB interactions were
approximately balanced. The overall mechanical outcome of these inhibitory
interactions may partly underlie the global corrective strategy seen in
intact cats subjected to linear perturbations. 8. No significant reflex
interactions were demonstrated between PL and TP, G, or S, nor were any
long-latency reflexes noted. Thus, whereas reflex interactions between the
stereotypically activated PB and other stereotypically activated muscles
(including TP, G, and S) were strong and well-demonstrated, interactions
between the variably activated PL and these same muscles were far weaker.</abstract><cop>United States</cop><pub>Am Phys Soc</pub><pmid>8734603</pmid><doi>10.1152/jn.1996.75.5.2050</doi><tpages>21</tpages></addata></record> |
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source | MEDLINE; Alma/SFX Local Collection |
subjects | Animals Biomechanical Phenomena Cats Female Hindlimb - anatomy & histology Hindlimb - innervation Hindlimb - physiology Isometric Contraction - physiology Male Muscle Contraction - physiology Muscle, Skeletal - anatomy & histology Muscle, Skeletal - innervation Muscle, Skeletal - physiology Neurons, Afferent - physiology Reflex, Monosynaptic - physiology |
title | Mechanical actions of heterogenic reflexes among ankle stabilizers and their interactions with plantarflexors of the cat hindlimb |
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