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Nucleoprotein supplementation enhances the recovery of rat soleus mass with reloading after hindlimb unloading-induced atrophy via myonuclei accretion and increased protein synthesis
Abstract Hindlimb unloading results in muscle atrophy and a period of reloading has been shown to partially recover the lost muscle mass. Two of the mechanisms involved in this recovery of muscle mass are the activation of protein synthesis pathways and an increase in myonuclei number. The additiona...
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Published in: | Nutrition research (New York, N.Y.) N.Y.), 2016-12, Vol.36 (12), p.1335-1344 |
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creator | Nakanishi, Ryosuke Hirayama, Yusuke Tanaka, Minoru Maeshige, Noriaki Kondo, Hiroyo Ishihara, Akihiko Roy, Roland R Fujino, Hidemi |
description | Abstract Hindlimb unloading results in muscle atrophy and a period of reloading has been shown to partially recover the lost muscle mass. Two of the mechanisms involved in this recovery of muscle mass are the activation of protein synthesis pathways and an increase in myonuclei number. The additional myonuclei are provided by satellite cells that are activated by the mechanical stress associated with the reloading of the muscles and eventually incorporated into the muscle fibers. Amino acid supplementation with exercise also can increase skeletal muscle mass through enhancement of protein synthesis and nucleotide supplements can promote cell cycle activity. Therefore, we hypothesized that nucleoprotein supplementation, a combination of amino acids and nucleotides, would enhance the recovery of muscle mass to a greater extent than reloading alone after a period of unloading. Adult rats were assigned to four groups: control, hindlimb unloaded (14 days) (HU), reloaded (5 days) after hindlimb unloading (HUR), and reloaded after hindlimb unloading with nucleoprotein supplementation (HUR+NP). Compared to the HUR group, the HUR+NP group had larger soleus muscles and fiber cross-sectional areas, higher levels of phosphorylated-rpS6, and higher numbers of myonuclei and myogenin-positive cells. These results suggest that nucleoprotein supplementation has a synergistic effect with reloading in recovering skeletal muscle properties after a period of unloading via rpS6 activation and satellite cell differentiation and incorporation into the muscle fibers. Therefore, this supplement may be an effective therapeutic regimen to include in rehabilitative strategies for a variety of muscle wasting conditions such as aging, cancer cachexia, muscular dystrophy, bed rest, and cast immobilization. |
doi_str_mv | 10.1016/j.nutres.2016.10.007 |
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Two of the mechanisms involved in this recovery of muscle mass are the activation of protein synthesis pathways and an increase in myonuclei number. The additional myonuclei are provided by satellite cells that are activated by the mechanical stress associated with the reloading of the muscles and eventually incorporated into the muscle fibers. Amino acid supplementation with exercise also can increase skeletal muscle mass through enhancement of protein synthesis and nucleotide supplements can promote cell cycle activity. Therefore, we hypothesized that nucleoprotein supplementation, a combination of amino acids and nucleotides, would enhance the recovery of muscle mass to a greater extent than reloading alone after a period of unloading. Adult rats were assigned to four groups: control, hindlimb unloaded (14 days) (HU), reloaded (5 days) after hindlimb unloading (HUR), and reloaded after hindlimb unloading with nucleoprotein supplementation (HUR+NP). Compared to the HUR group, the HUR+NP group had larger soleus muscles and fiber cross-sectional areas, higher levels of phosphorylated-rpS6, and higher numbers of myonuclei and myogenin-positive cells. These results suggest that nucleoprotein supplementation has a synergistic effect with reloading in recovering skeletal muscle properties after a period of unloading via rpS6 activation and satellite cell differentiation and incorporation into the muscle fibers. Therefore, this supplement may be an effective therapeutic regimen to include in rehabilitative strategies for a variety of muscle wasting conditions such as aging, cancer cachexia, muscular dystrophy, bed rest, and cast immobilization.</description><identifier>ISSN: 0271-5317</identifier><identifier>EISSN: 1879-0739</identifier><identifier>DOI: 10.1016/j.nutres.2016.10.007</identifier><identifier>PMID: 27866827</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Differentiation ; Cell Nucleus ; Dietary Supplements ; Female ; Gastroenterology and Hepatology ; Hindlimb ; Hindlimb suspension ; Muscle Fibers, Skeletal - drug effects ; Muscle Fibers, Skeletal - metabolism ; Muscle Fibers, Skeletal - physiology ; Muscle Proteins - metabolism ; Muscle, Skeletal - cytology ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - pathology ; Muscular Atrophy - drug therapy ; Muscular Atrophy - rehabilitation ; Myogenin - metabolism ; Nucleoproteins ; Nucleoproteins - pharmacology ; Nucleoproteins - therapeutic use ; Organ Size - drug effects ; Physical Conditioning, Animal ; Protein Biosynthesis - drug effects ; Rat ; Rats, Wistar ; rpS6 ; Satellite Cells, Skeletal Muscle - drug effects ; Satellite Cells, Skeletal Muscle - physiology ; Stress, Mechanical</subject><ispartof>Nutrition research (New York, N.Y.), 2016-12, Vol.36 (12), p.1335-1344</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-56b5bdac9d9ad9cf5adfc0069da5c11da53d768432598bfd8a4ff6da3cbd16833</citedby><cites>FETCH-LOGICAL-c501t-56b5bdac9d9ad9cf5adfc0069da5c11da53d768432598bfd8a4ff6da3cbd16833</cites></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/27866827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakanishi, Ryosuke</creatorcontrib><creatorcontrib>Hirayama, Yusuke</creatorcontrib><creatorcontrib>Tanaka, Minoru</creatorcontrib><creatorcontrib>Maeshige, Noriaki</creatorcontrib><creatorcontrib>Kondo, Hiroyo</creatorcontrib><creatorcontrib>Ishihara, Akihiko</creatorcontrib><creatorcontrib>Roy, Roland R</creatorcontrib><creatorcontrib>Fujino, Hidemi</creatorcontrib><title>Nucleoprotein supplementation enhances the recovery of rat soleus mass with reloading after hindlimb unloading-induced atrophy via myonuclei accretion and increased protein synthesis</title><title>Nutrition research (New York, N.Y.)</title><addtitle>Nutr Res</addtitle><description>Abstract Hindlimb unloading results in muscle atrophy and a period of reloading has been shown to partially recover the lost muscle mass. Two of the mechanisms involved in this recovery of muscle mass are the activation of protein synthesis pathways and an increase in myonuclei number. The additional myonuclei are provided by satellite cells that are activated by the mechanical stress associated with the reloading of the muscles and eventually incorporated into the muscle fibers. Amino acid supplementation with exercise also can increase skeletal muscle mass through enhancement of protein synthesis and nucleotide supplements can promote cell cycle activity. Therefore, we hypothesized that nucleoprotein supplementation, a combination of amino acids and nucleotides, would enhance the recovery of muscle mass to a greater extent than reloading alone after a period of unloading. Adult rats were assigned to four groups: control, hindlimb unloaded (14 days) (HU), reloaded (5 days) after hindlimb unloading (HUR), and reloaded after hindlimb unloading with nucleoprotein supplementation (HUR+NP). Compared to the HUR group, the HUR+NP group had larger soleus muscles and fiber cross-sectional areas, higher levels of phosphorylated-rpS6, and higher numbers of myonuclei and myogenin-positive cells. These results suggest that nucleoprotein supplementation has a synergistic effect with reloading in recovering skeletal muscle properties after a period of unloading via rpS6 activation and satellite cell differentiation and incorporation into the muscle fibers. Therefore, this supplement may be an effective therapeutic regimen to include in rehabilitative strategies for a variety of muscle wasting conditions such as aging, cancer cachexia, muscular dystrophy, bed rest, and cast immobilization.</description><subject>Animals</subject><subject>Cell Differentiation</subject><subject>Cell Nucleus</subject><subject>Dietary Supplements</subject><subject>Female</subject><subject>Gastroenterology and Hepatology</subject><subject>Hindlimb</subject><subject>Hindlimb suspension</subject><subject>Muscle Fibers, Skeletal - drug effects</subject><subject>Muscle Fibers, Skeletal - metabolism</subject><subject>Muscle Fibers, Skeletal - physiology</subject><subject>Muscle Proteins - metabolism</subject><subject>Muscle, Skeletal - cytology</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - pathology</subject><subject>Muscular Atrophy - drug therapy</subject><subject>Muscular Atrophy - rehabilitation</subject><subject>Myogenin - metabolism</subject><subject>Nucleoproteins</subject><subject>Nucleoproteins - pharmacology</subject><subject>Nucleoproteins - therapeutic use</subject><subject>Organ Size - drug effects</subject><subject>Physical Conditioning, Animal</subject><subject>Protein Biosynthesis - drug effects</subject><subject>Rat</subject><subject>Rats, Wistar</subject><subject>rpS6</subject><subject>Satellite Cells, Skeletal Muscle - drug effects</subject><subject>Satellite Cells, Skeletal Muscle - physiology</subject><subject>Stress, Mechanical</subject><issn>0271-5317</issn><issn>1879-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFks-O0zAQxiMEYsvCGyDkI5cUO26c5IKEVssfaQUH4GxN7Al1SezicYryYjwfDi174MLF1oy_mfnsn4viueBbwYV6ddj6OUWkbZWjnNpy3jwoNqJtupI3sntYbHjViLKWorkqnhAdOBeNkPJxcVU1rVJt1WyKXx9nM2I4xpDQeUbz8TjihD5BcsEz9HvwBomlPbKIJpwwLiwMLEJiFEaciU1AxH66tM-CMYB1_huDIWFke-ft6Kaezf5yUObMbNAySDEc9ws7OWDTEvzqwjEwJuKfweAtcz5HQFl9b2_x2Qg5elo8GmAkfHbZr4uvb2-_3Lwv7z69-3Dz5q40NReprFVf9xZMZzuwnRlqsIPhXHUWaiNEXqVtVLuTVd21_WBb2A2DsiBNb4VqpbwuXp77Zgc_ZqSkJ0cGxxE8hpm0aHdVvatVp7J0d5aaGIgiDvoY3QRx0YLrlZg-6DMxvRJbs5lYLntxmTD3E9r7or-IsuD1WYD5nieHUZNxmKFYl4EkbYP734R_G5jReWdg_I4L0iHM0ec31EJTpbn-vP6a9dMIJXmtWiF_Awk6xiE</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Nakanishi, Ryosuke</creator><creator>Hirayama, Yusuke</creator><creator>Tanaka, Minoru</creator><creator>Maeshige, Noriaki</creator><creator>Kondo, Hiroyo</creator><creator>Ishihara, Akihiko</creator><creator>Roy, Roland R</creator><creator>Fujino, Hidemi</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20161201</creationdate><title>Nucleoprotein supplementation enhances the recovery of rat soleus mass with reloading after hindlimb unloading-induced atrophy via myonuclei accretion and increased protein synthesis</title><author>Nakanishi, Ryosuke ; Hirayama, Yusuke ; Tanaka, Minoru ; Maeshige, Noriaki ; Kondo, Hiroyo ; Ishihara, Akihiko ; Roy, Roland R ; Fujino, Hidemi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-56b5bdac9d9ad9cf5adfc0069da5c11da53d768432598bfd8a4ff6da3cbd16833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cell Differentiation</topic><topic>Cell Nucleus</topic><topic>Dietary Supplements</topic><topic>Female</topic><topic>Gastroenterology and Hepatology</topic><topic>Hindlimb</topic><topic>Hindlimb suspension</topic><topic>Muscle Fibers, Skeletal - drug effects</topic><topic>Muscle Fibers, Skeletal - metabolism</topic><topic>Muscle Fibers, Skeletal - physiology</topic><topic>Muscle Proteins - metabolism</topic><topic>Muscle, Skeletal - cytology</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - pathology</topic><topic>Muscular Atrophy - drug therapy</topic><topic>Muscular Atrophy - rehabilitation</topic><topic>Myogenin - metabolism</topic><topic>Nucleoproteins</topic><topic>Nucleoproteins - pharmacology</topic><topic>Nucleoproteins - therapeutic use</topic><topic>Organ Size - drug effects</topic><topic>Physical Conditioning, Animal</topic><topic>Protein Biosynthesis - drug effects</topic><topic>Rat</topic><topic>Rats, Wistar</topic><topic>rpS6</topic><topic>Satellite Cells, Skeletal Muscle - drug effects</topic><topic>Satellite Cells, Skeletal Muscle - physiology</topic><topic>Stress, Mechanical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakanishi, Ryosuke</creatorcontrib><creatorcontrib>Hirayama, Yusuke</creatorcontrib><creatorcontrib>Tanaka, Minoru</creatorcontrib><creatorcontrib>Maeshige, Noriaki</creatorcontrib><creatorcontrib>Kondo, Hiroyo</creatorcontrib><creatorcontrib>Ishihara, Akihiko</creatorcontrib><creatorcontrib>Roy, Roland R</creatorcontrib><creatorcontrib>Fujino, Hidemi</creatorcontrib><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>Nutrition research (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakanishi, Ryosuke</au><au>Hirayama, Yusuke</au><au>Tanaka, Minoru</au><au>Maeshige, Noriaki</au><au>Kondo, Hiroyo</au><au>Ishihara, Akihiko</au><au>Roy, Roland R</au><au>Fujino, Hidemi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nucleoprotein supplementation enhances the recovery of rat soleus mass with reloading after hindlimb unloading-induced atrophy via myonuclei accretion and increased protein synthesis</atitle><jtitle>Nutrition research (New York, N.Y.)</jtitle><addtitle>Nutr Res</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>36</volume><issue>12</issue><spage>1335</spage><epage>1344</epage><pages>1335-1344</pages><issn>0271-5317</issn><eissn>1879-0739</eissn><abstract>Abstract Hindlimb unloading results in muscle atrophy and a period of reloading has been shown to partially recover the lost muscle mass. Two of the mechanisms involved in this recovery of muscle mass are the activation of protein synthesis pathways and an increase in myonuclei number. The additional myonuclei are provided by satellite cells that are activated by the mechanical stress associated with the reloading of the muscles and eventually incorporated into the muscle fibers. Amino acid supplementation with exercise also can increase skeletal muscle mass through enhancement of protein synthesis and nucleotide supplements can promote cell cycle activity. Therefore, we hypothesized that nucleoprotein supplementation, a combination of amino acids and nucleotides, would enhance the recovery of muscle mass to a greater extent than reloading alone after a period of unloading. Adult rats were assigned to four groups: control, hindlimb unloaded (14 days) (HU), reloaded (5 days) after hindlimb unloading (HUR), and reloaded after hindlimb unloading with nucleoprotein supplementation (HUR+NP). Compared to the HUR group, the HUR+NP group had larger soleus muscles and fiber cross-sectional areas, higher levels of phosphorylated-rpS6, and higher numbers of myonuclei and myogenin-positive cells. These results suggest that nucleoprotein supplementation has a synergistic effect with reloading in recovering skeletal muscle properties after a period of unloading via rpS6 activation and satellite cell differentiation and incorporation into the muscle fibers. Therefore, this supplement may be an effective therapeutic regimen to include in rehabilitative strategies for a variety of muscle wasting conditions such as aging, cancer cachexia, muscular dystrophy, bed rest, and cast immobilization.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27866827</pmid><doi>10.1016/j.nutres.2016.10.007</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Cell Differentiation Cell Nucleus Dietary Supplements Female Gastroenterology and Hepatology Hindlimb Hindlimb suspension Muscle Fibers, Skeletal - drug effects Muscle Fibers, Skeletal - metabolism Muscle Fibers, Skeletal - physiology Muscle Proteins - metabolism Muscle, Skeletal - cytology Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscular Atrophy - drug therapy Muscular Atrophy - rehabilitation Myogenin - metabolism Nucleoproteins Nucleoproteins - pharmacology Nucleoproteins - therapeutic use Organ Size - drug effects Physical Conditioning, Animal Protein Biosynthesis - drug effects Rat Rats, Wistar rpS6 Satellite Cells, Skeletal Muscle - drug effects Satellite Cells, Skeletal Muscle - physiology Stress, Mechanical |
title | Nucleoprotein supplementation enhances the recovery of rat soleus mass with reloading after hindlimb unloading-induced atrophy via myonuclei accretion and increased protein synthesis |
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