Development of a mouse nerve-transfer model for brachial plexus injury

Nerve transfer involves the use of a portion of a healthy nerve to repair an injured nerve, and the process has been used to alleviate traumatic brachial plexus injuries in humans. Study of the neural mechanisms that occur during nerve transfer, however, requires the establishment of reliable experi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biomedical Research 2019/06/01, Vol.40(3), pp.115-123
Hauptverfasser: WAKATSUKI, Hanako, SHIBATA, Minoru, MATSUDA, Ken, SATO, Noboru
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 123
container_issue 3
container_start_page 115
container_title Biomedical Research
container_volume 40
creator WAKATSUKI, Hanako
SHIBATA, Minoru
MATSUDA, Ken
SATO, Noboru
description Nerve transfer involves the use of a portion of a healthy nerve to repair an injured nerve, and the process has been used to alleviate traumatic brachial plexus injuries in humans. Study of the neural mechanisms that occur during nerve transfer, however, requires the establishment of reliable experimental models. In this study, we developed an ulnar-musculocutaneous nerve-transfer model wherein the biceps muscle of a mouse was re-innervated using a donor ulnar nerve. Similar muscle action potentials were detected in both the end-to-end suture of the transected nerve (correctrepair) group and the ulnar-musculocutaneous nerve-transfer group. Also, re-innervated acetylcholine receptor (AChR) clusters and muscle spindles were observed in both procedures. There were fewer re-innervated AChR clusters in the nerve transfer group than in the correct repair group at 4 weeks, but the numbers were equal at 24 weeks following surgery. Thus, our ulnar-musculocutaneous nerve-transfer model allowed physiological and morphological evaluation for re-innervation process in mice and revealed the delay of this process during nerve transfer procedure. This model will provide great opportunities to study regeneration, re-innervation, and functional recovery induced via nerve transfer procedures.
doi_str_mv 10.2220/biomedres.40.115
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2246243431</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2251083215</sourcerecordid><originalsourceid>FETCH-LOGICAL-c660t-19a946c7e2331eb8d4b92b28d1675cc7a7cbca285929a7a206b2ca08f943d9503</originalsourceid><addsrcrecordid>eNpdkM1Lw0AQxRdRbK3ePUnAi5fU_UqyOUq1KgheFLwtu5uJTdgkdTcp9r93tTWgp2Hm_ebxeAidEzynlOJrXXUNFA78nOM5IckBmhIhcMwIeztEU8yEiFOCswk68b7GYSeCHaMJI5QRnPMpWt7CBmy3bqDto66MVNR0g4eoBbeBuHeq9SW4cCzARmXnIu2UWVXKRmsLn4OPqrYe3PYUHZXKejjbzxl6Xd69LB7ip-f7x8XNU2zSFPcxyVXOU5MBZYyAFgXXOdVUFCTNEmMylRltFBVJTnOVKYpTTY3Cosw5K_IEsxm62vmuXfcxgO9lU3kD1qoWQm5JKU8pZzwUMEOX_9C6G1wb0gUqIVgwSpJA4R1lXOe9g1KuXdUot5UEy--O5dix5FiSn5eLvfGggzI-_JYagMUOqH2v3mEElOsrY-GvI9vbjqpZKSehZV_N_JG-</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2251083215</pqid></control><display><type>article</type><title>Development of a mouse nerve-transfer model for brachial plexus injury</title><source>J-STAGE Free</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>WAKATSUKI, Hanako ; SHIBATA, Minoru ; MATSUDA, Ken ; SATO, Noboru</creator><creatorcontrib>WAKATSUKI, Hanako ; SHIBATA, Minoru ; MATSUDA, Ken ; SATO, Noboru</creatorcontrib><description>Nerve transfer involves the use of a portion of a healthy nerve to repair an injured nerve, and the process has been used to alleviate traumatic brachial plexus injuries in humans. Study of the neural mechanisms that occur during nerve transfer, however, requires the establishment of reliable experimental models. In this study, we developed an ulnar-musculocutaneous nerve-transfer model wherein the biceps muscle of a mouse was re-innervated using a donor ulnar nerve. Similar muscle action potentials were detected in both the end-to-end suture of the transected nerve (correctrepair) group and the ulnar-musculocutaneous nerve-transfer group. Also, re-innervated acetylcholine receptor (AChR) clusters and muscle spindles were observed in both procedures. There were fewer re-innervated AChR clusters in the nerve transfer group than in the correct repair group at 4 weeks, but the numbers were equal at 24 weeks following surgery. Thus, our ulnar-musculocutaneous nerve-transfer model allowed physiological and morphological evaluation for re-innervation process in mice and revealed the delay of this process during nerve transfer procedure. This model will provide great opportunities to study regeneration, re-innervation, and functional recovery induced via nerve transfer procedures.</description><identifier>ISSN: 0388-6107</identifier><identifier>EISSN: 1880-313X</identifier><identifier>DOI: 10.2220/biomedres.40.115</identifier><identifier>PMID: 31231094</identifier><language>eng</language><publisher>Japan: Biomedical Research Press</publisher><subject>Acetylcholine receptors ; Brachial plexus ; Clusters ; Injuries ; Innervation ; Muscle spindles ; Muscles ; Receptor density ; Recovery of function ; Regeneration ; Repair ; Surgery</subject><ispartof>Biomedical Research, 2019/06/01, Vol.40(3), pp.115-123</ispartof><rights>2019 Biomedical Research Press</rights><rights>Copyright Japan Science and Technology Agency 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c660t-19a946c7e2331eb8d4b92b28d1675cc7a7cbca285929a7a206b2ca08f943d9503</citedby><cites>FETCH-LOGICAL-c660t-19a946c7e2331eb8d4b92b28d1675cc7a7cbca285929a7a206b2ca08f943d9503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31231094$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WAKATSUKI, Hanako</creatorcontrib><creatorcontrib>SHIBATA, Minoru</creatorcontrib><creatorcontrib>MATSUDA, Ken</creatorcontrib><creatorcontrib>SATO, Noboru</creatorcontrib><title>Development of a mouse nerve-transfer model for brachial plexus injury</title><title>Biomedical Research</title><addtitle>Biomed. Res.</addtitle><description>Nerve transfer involves the use of a portion of a healthy nerve to repair an injured nerve, and the process has been used to alleviate traumatic brachial plexus injuries in humans. Study of the neural mechanisms that occur during nerve transfer, however, requires the establishment of reliable experimental models. In this study, we developed an ulnar-musculocutaneous nerve-transfer model wherein the biceps muscle of a mouse was re-innervated using a donor ulnar nerve. Similar muscle action potentials were detected in both the end-to-end suture of the transected nerve (correctrepair) group and the ulnar-musculocutaneous nerve-transfer group. Also, re-innervated acetylcholine receptor (AChR) clusters and muscle spindles were observed in both procedures. There were fewer re-innervated AChR clusters in the nerve transfer group than in the correct repair group at 4 weeks, but the numbers were equal at 24 weeks following surgery. Thus, our ulnar-musculocutaneous nerve-transfer model allowed physiological and morphological evaluation for re-innervation process in mice and revealed the delay of this process during nerve transfer procedure. This model will provide great opportunities to study regeneration, re-innervation, and functional recovery induced via nerve transfer procedures.</description><subject>Acetylcholine receptors</subject><subject>Brachial plexus</subject><subject>Clusters</subject><subject>Injuries</subject><subject>Innervation</subject><subject>Muscle spindles</subject><subject>Muscles</subject><subject>Receptor density</subject><subject>Recovery of function</subject><subject>Regeneration</subject><subject>Repair</subject><subject>Surgery</subject><issn>0388-6107</issn><issn>1880-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkM1Lw0AQxRdRbK3ePUnAi5fU_UqyOUq1KgheFLwtu5uJTdgkdTcp9r93tTWgp2Hm_ebxeAidEzynlOJrXXUNFA78nOM5IckBmhIhcMwIeztEU8yEiFOCswk68b7GYSeCHaMJI5QRnPMpWt7CBmy3bqDto66MVNR0g4eoBbeBuHeq9SW4cCzARmXnIu2UWVXKRmsLn4OPqrYe3PYUHZXKejjbzxl6Xd69LB7ip-f7x8XNU2zSFPcxyVXOU5MBZYyAFgXXOdVUFCTNEmMylRltFBVJTnOVKYpTTY3Cosw5K_IEsxm62vmuXfcxgO9lU3kD1qoWQm5JKU8pZzwUMEOX_9C6G1wb0gUqIVgwSpJA4R1lXOe9g1KuXdUot5UEy--O5dix5FiSn5eLvfGggzI-_JYagMUOqH2v3mEElOsrY-GvI9vbjqpZKSehZV_N_JG-</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>WAKATSUKI, Hanako</creator><creator>SHIBATA, Minoru</creator><creator>MATSUDA, Ken</creator><creator>SATO, Noboru</creator><general>Biomedical Research Press</general><general>Japan Science and Technology Agency</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20190601</creationdate><title>Development of a mouse nerve-transfer model for brachial plexus injury</title><author>WAKATSUKI, Hanako ; SHIBATA, Minoru ; MATSUDA, Ken ; SATO, Noboru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c660t-19a946c7e2331eb8d4b92b28d1675cc7a7cbca285929a7a206b2ca08f943d9503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acetylcholine receptors</topic><topic>Brachial plexus</topic><topic>Clusters</topic><topic>Injuries</topic><topic>Innervation</topic><topic>Muscle spindles</topic><topic>Muscles</topic><topic>Receptor density</topic><topic>Recovery of function</topic><topic>Regeneration</topic><topic>Repair</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WAKATSUKI, Hanako</creatorcontrib><creatorcontrib>SHIBATA, Minoru</creatorcontrib><creatorcontrib>MATSUDA, Ken</creatorcontrib><creatorcontrib>SATO, Noboru</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedical Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WAKATSUKI, Hanako</au><au>SHIBATA, Minoru</au><au>MATSUDA, Ken</au><au>SATO, Noboru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a mouse nerve-transfer model for brachial plexus injury</atitle><jtitle>Biomedical Research</jtitle><addtitle>Biomed. Res.</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>40</volume><issue>3</issue><spage>115</spage><epage>123</epage><pages>115-123</pages><issn>0388-6107</issn><eissn>1880-313X</eissn><abstract>Nerve transfer involves the use of a portion of a healthy nerve to repair an injured nerve, and the process has been used to alleviate traumatic brachial plexus injuries in humans. Study of the neural mechanisms that occur during nerve transfer, however, requires the establishment of reliable experimental models. In this study, we developed an ulnar-musculocutaneous nerve-transfer model wherein the biceps muscle of a mouse was re-innervated using a donor ulnar nerve. Similar muscle action potentials were detected in both the end-to-end suture of the transected nerve (correctrepair) group and the ulnar-musculocutaneous nerve-transfer group. Also, re-innervated acetylcholine receptor (AChR) clusters and muscle spindles were observed in both procedures. There were fewer re-innervated AChR clusters in the nerve transfer group than in the correct repair group at 4 weeks, but the numbers were equal at 24 weeks following surgery. Thus, our ulnar-musculocutaneous nerve-transfer model allowed physiological and morphological evaluation for re-innervation process in mice and revealed the delay of this process during nerve transfer procedure. This model will provide great opportunities to study regeneration, re-innervation, and functional recovery induced via nerve transfer procedures.</abstract><cop>Japan</cop><pub>Biomedical Research Press</pub><pmid>31231094</pmid><doi>10.2220/biomedres.40.115</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0388-6107
ispartof Biomedical Research, 2019/06/01, Vol.40(3), pp.115-123
issn 0388-6107
1880-313X
language eng
recordid cdi_proquest_miscellaneous_2246243431
source J-STAGE Free; EZB-FREE-00999 freely available EZB journals
subjects Acetylcholine receptors
Brachial plexus
Clusters
Injuries
Innervation
Muscle spindles
Muscles
Receptor density
Recovery of function
Regeneration
Repair
Surgery
title Development of a mouse nerve-transfer model for brachial plexus injury
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T20%3A37%3A09IST&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=Development%20of%20a%20mouse%20nerve-transfer%20model%20for%20brachial%20plexus%20injury&rft.jtitle=Biomedical%20Research&rft.au=WAKATSUKI,%20Hanako&rft.date=2019-06-01&rft.volume=40&rft.issue=3&rft.spage=115&rft.epage=123&rft.pages=115-123&rft.issn=0388-6107&rft.eissn=1880-313X&rft_id=info:doi/10.2220/biomedres.40.115&rft_dat=%3Cproquest_cross%3E2251083215%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2251083215&rft_id=info:pmid/31231094&rfr_iscdi=true