Loading…
Patterns of muscle activation in human hopping
In the present study, we examined the electromyogram (EMG) patterns of the soleus and medial gastrocnemius (MG) muscles during rhythmical, two-legged hopping to investigate the contributions of the monosynaptic short- and long-latency stretch reflexes during such a natural movement in human. During...
Saved in:
Published in: | European journal of applied physiology 2001-06, Vol.84 (6), p.503-509 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c316t-f5732ca79e6834dac846cf97883e04314db18c2e375a274f2034afc33752e7563 |
---|---|
cites | |
container_end_page | 509 |
container_issue | 6 |
container_start_page | 503 |
container_title | European journal of applied physiology |
container_volume | 84 |
creator | Funase, K Higashi, T Sakakibara, A Imanaka, K Nishihira, Y Miles, T S |
description | In the present study, we examined the electromyogram (EMG) patterns of the soleus and medial gastrocnemius (MG) muscles during rhythmical, two-legged hopping to investigate the contributions of the monosynaptic short- and long-latency stretch reflexes during such a natural movement in human. During rhythmical hopping, soleus muscle is activated reflexly at near-monosynaptic latency by stretch resulting from passive ankle flexion upon landing. Soleus muscle also contracts voluntarily in order to launch the body into the next hop. This is part of the rhythmical bursts of activity producing the hops. Depending on the hopping interval, this phase of activation can follow the short-latency phase or precede landing at very short hopping intervals. In MG, there is an initial phase of activity that stiffens the muscle in preparation for landing, and continues through the contact phase. The monosynaptic reflex response to landing is usually superimposed on this activity. Depending on the hopping interval, both of these responses may be overlaid with activity that is time-locked to the take-off into the next hop, and serves to launch the body into the next hop. However, no evidence for a long-latency stretch reflex was found. In addition, the preferred hopping frequency for all subjects was about 2 Hz. This frequency is associated with a pattern of EMG activity the timing of which indicates that it balances the requirement for a comfortable landing from a hop with the optimal muscle activation required for launching the following hop. |
doi_str_mv | 10.1007/s004210100414 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71061450</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2466287601</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-f5732ca79e6834dac846cf97883e04314db18c2e375a274f2034afc33752e7563</originalsourceid><addsrcrecordid>eNpdkM1LAzEUxIMotlaPXmXx4G1rXl52kxyl1A8o6EHPIU0T3bJfJruC_72RFkUv783Aj2EYQs6BzoFScR0p5Qxo0hz4AZkCR5WXyMThjwY1IScxbimlkoE8JhMALlnB-ZTMn8wwuNDGrPNZM0Zbu8zYofowQ9W1WdVmb2Nj0u36vmpfT8mRN3V0Z_s_Iy-3y-fFfb56vHtY3Kxyi1AOuS8EMmuEcqVEvjFW8tJ6JaRERzkC36xBWuZQFIYJ7hlFbrzF5JkTRYkzcrXL7UP3Pro46KaK1tW1aV03Ri2AlsALmsDLf-C2G0ObummpMLVQChOU7yAbuhiD87oPVWPCpwaqv1fUf1ZM_MU-dFw3bvNL72fDL72Nab4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>893732993</pqid></control><display><type>article</type><title>Patterns of muscle activation in human hopping</title><source>Springer Link</source><creator>Funase, K ; Higashi, T ; Sakakibara, A ; Imanaka, K ; Nishihira, Y ; Miles, T S</creator><creatorcontrib>Funase, K ; Higashi, T ; Sakakibara, A ; Imanaka, K ; Nishihira, Y ; Miles, T S</creatorcontrib><description>In the present study, we examined the electromyogram (EMG) patterns of the soleus and medial gastrocnemius (MG) muscles during rhythmical, two-legged hopping to investigate the contributions of the monosynaptic short- and long-latency stretch reflexes during such a natural movement in human. During rhythmical hopping, soleus muscle is activated reflexly at near-monosynaptic latency by stretch resulting from passive ankle flexion upon landing. Soleus muscle also contracts voluntarily in order to launch the body into the next hop. This is part of the rhythmical bursts of activity producing the hops. Depending on the hopping interval, this phase of activation can follow the short-latency phase or precede landing at very short hopping intervals. In MG, there is an initial phase of activity that stiffens the muscle in preparation for landing, and continues through the contact phase. The monosynaptic reflex response to landing is usually superimposed on this activity. Depending on the hopping interval, both of these responses may be overlaid with activity that is time-locked to the take-off into the next hop, and serves to launch the body into the next hop. However, no evidence for a long-latency stretch reflex was found. In addition, the preferred hopping frequency for all subjects was about 2 Hz. This frequency is associated with a pattern of EMG activity the timing of which indicates that it balances the requirement for a comfortable landing from a hop with the optimal muscle activation required for launching the following hop.</description><identifier>ISSN: 1439-6319</identifier><identifier>EISSN: 1439-6327</identifier><identifier>DOI: 10.1007/s004210100414</identifier><identifier>PMID: 11482544</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Adult ; Ankle ; Ankle Joint - physiology ; Electromyography ; Experiments ; Humans ; Male ; Middle Aged ; Motor Activity - physiology ; Muscle function ; Muscle, Skeletal - physiology ; Reflex, Stretch - physiology ; Volition - physiology</subject><ispartof>European journal of applied physiology, 2001-06, Vol.84 (6), p.503-509</ispartof><rights>Springer-Verlag 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-f5732ca79e6834dac846cf97883e04314db18c2e375a274f2034afc33752e7563</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/11482544$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Funase, K</creatorcontrib><creatorcontrib>Higashi, T</creatorcontrib><creatorcontrib>Sakakibara, A</creatorcontrib><creatorcontrib>Imanaka, K</creatorcontrib><creatorcontrib>Nishihira, Y</creatorcontrib><creatorcontrib>Miles, T S</creatorcontrib><title>Patterns of muscle activation in human hopping</title><title>European journal of applied physiology</title><addtitle>Eur J Appl Physiol</addtitle><description>In the present study, we examined the electromyogram (EMG) patterns of the soleus and medial gastrocnemius (MG) muscles during rhythmical, two-legged hopping to investigate the contributions of the monosynaptic short- and long-latency stretch reflexes during such a natural movement in human. During rhythmical hopping, soleus muscle is activated reflexly at near-monosynaptic latency by stretch resulting from passive ankle flexion upon landing. Soleus muscle also contracts voluntarily in order to launch the body into the next hop. This is part of the rhythmical bursts of activity producing the hops. Depending on the hopping interval, this phase of activation can follow the short-latency phase or precede landing at very short hopping intervals. In MG, there is an initial phase of activity that stiffens the muscle in preparation for landing, and continues through the contact phase. The monosynaptic reflex response to landing is usually superimposed on this activity. Depending on the hopping interval, both of these responses may be overlaid with activity that is time-locked to the take-off into the next hop, and serves to launch the body into the next hop. However, no evidence for a long-latency stretch reflex was found. In addition, the preferred hopping frequency for all subjects was about 2 Hz. This frequency is associated with a pattern of EMG activity the timing of which indicates that it balances the requirement for a comfortable landing from a hop with the optimal muscle activation required for launching the following hop.</description><subject>Adult</subject><subject>Ankle</subject><subject>Ankle Joint - physiology</subject><subject>Electromyography</subject><subject>Experiments</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Motor Activity - physiology</subject><subject>Muscle function</subject><subject>Muscle, Skeletal - physiology</subject><subject>Reflex, Stretch - physiology</subject><subject>Volition - physiology</subject><issn>1439-6319</issn><issn>1439-6327</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpdkM1LAzEUxIMotlaPXmXx4G1rXl52kxyl1A8o6EHPIU0T3bJfJruC_72RFkUv783Aj2EYQs6BzoFScR0p5Qxo0hz4AZkCR5WXyMThjwY1IScxbimlkoE8JhMALlnB-ZTMn8wwuNDGrPNZM0Zbu8zYofowQ9W1WdVmb2Nj0u36vmpfT8mRN3V0Z_s_Iy-3y-fFfb56vHtY3Kxyi1AOuS8EMmuEcqVEvjFW8tJ6JaRERzkC36xBWuZQFIYJ7hlFbrzF5JkTRYkzcrXL7UP3Pro46KaK1tW1aV03Ri2AlsALmsDLf-C2G0ObummpMLVQChOU7yAbuhiD87oPVWPCpwaqv1fUf1ZM_MU-dFw3bvNL72fDL72Nab4</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Funase, K</creator><creator>Higashi, T</creator><creator>Sakakibara, A</creator><creator>Imanaka, K</creator><creator>Nishihira, Y</creator><creator>Miles, T S</creator><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20010601</creationdate><title>Patterns of muscle activation in human hopping</title><author>Funase, K ; Higashi, T ; Sakakibara, A ; Imanaka, K ; Nishihira, Y ; Miles, T S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-f5732ca79e6834dac846cf97883e04314db18c2e375a274f2034afc33752e7563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Ankle</topic><topic>Ankle Joint - physiology</topic><topic>Electromyography</topic><topic>Experiments</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Motor Activity - physiology</topic><topic>Muscle function</topic><topic>Muscle, Skeletal - physiology</topic><topic>Reflex, Stretch - physiology</topic><topic>Volition - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Funase, K</creatorcontrib><creatorcontrib>Higashi, T</creatorcontrib><creatorcontrib>Sakakibara, A</creatorcontrib><creatorcontrib>Imanaka, K</creatorcontrib><creatorcontrib>Nishihira, Y</creatorcontrib><creatorcontrib>Miles, T 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>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of applied physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Funase, K</au><au>Higashi, T</au><au>Sakakibara, A</au><au>Imanaka, K</au><au>Nishihira, Y</au><au>Miles, T S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patterns of muscle activation in human hopping</atitle><jtitle>European journal of applied physiology</jtitle><addtitle>Eur J Appl Physiol</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>84</volume><issue>6</issue><spage>503</spage><epage>509</epage><pages>503-509</pages><issn>1439-6319</issn><eissn>1439-6327</eissn><abstract>In the present study, we examined the electromyogram (EMG) patterns of the soleus and medial gastrocnemius (MG) muscles during rhythmical, two-legged hopping to investigate the contributions of the monosynaptic short- and long-latency stretch reflexes during such a natural movement in human. During rhythmical hopping, soleus muscle is activated reflexly at near-monosynaptic latency by stretch resulting from passive ankle flexion upon landing. Soleus muscle also contracts voluntarily in order to launch the body into the next hop. This is part of the rhythmical bursts of activity producing the hops. Depending on the hopping interval, this phase of activation can follow the short-latency phase or precede landing at very short hopping intervals. In MG, there is an initial phase of activity that stiffens the muscle in preparation for landing, and continues through the contact phase. The monosynaptic reflex response to landing is usually superimposed on this activity. Depending on the hopping interval, both of these responses may be overlaid with activity that is time-locked to the take-off into the next hop, and serves to launch the body into the next hop. However, no evidence for a long-latency stretch reflex was found. In addition, the preferred hopping frequency for all subjects was about 2 Hz. This frequency is associated with a pattern of EMG activity the timing of which indicates that it balances the requirement for a comfortable landing from a hop with the optimal muscle activation required for launching the following hop.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>11482544</pmid><doi>10.1007/s004210100414</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1439-6319 |
ispartof | European journal of applied physiology, 2001-06, Vol.84 (6), p.503-509 |
issn | 1439-6319 1439-6327 |
language | eng |
recordid | cdi_proquest_miscellaneous_71061450 |
source | Springer Link |
subjects | Adult Ankle Ankle Joint - physiology Electromyography Experiments Humans Male Middle Aged Motor Activity - physiology Muscle function Muscle, Skeletal - physiology Reflex, Stretch - physiology Volition - physiology |
title | Patterns of muscle activation in human hopping |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T15%3A55%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Patterns%20of%20muscle%20activation%20in%20human%20hopping&rft.jtitle=European%20journal%20of%20applied%20physiology&rft.au=Funase,%20K&rft.date=2001-06-01&rft.volume=84&rft.issue=6&rft.spage=503&rft.epage=509&rft.pages=503-509&rft.issn=1439-6319&rft.eissn=1439-6327&rft_id=info:doi/10.1007/s004210100414&rft_dat=%3Cproquest_cross%3E2466287601%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c316t-f5732ca79e6834dac846cf97883e04314db18c2e375a274f2034afc33752e7563%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=893732993&rft_id=info:pmid/11482544&rfr_iscdi=true |