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Ginsenoside Rg1 augments oxidative metabolism and anabolic response of skeletal muscle in mice
The ginsenoside Rg1 has been shown to exert various pharmacological activities with health benefits. Previously, we have reported that Rg1 promoted myogenic differentiation and myotube growth in C2C12 myoblasts. In this study, the in vivo effect of Rg1 on fiber-type composition and oxidative metabol...
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Published in: | Journal of ginseng research 2019, 43(3), , pp.475-481 |
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description | The ginsenoside Rg1 has been shown to exert various pharmacological activities with health benefits. Previously, we have reported that Rg1 promoted myogenic differentiation and myotube growth in C2C12 myoblasts. In this study, the in vivo effect of Rg1 on fiber-type composition and oxidative metabolism in skeletal muscle was examined.
To examine the effect of Rg1 on skeletal muscle, 3-month-old mice were treated with Rg1 for 5 weeks. To assess muscle strength, grip strength tests were performed, and the lower hind limb muscles were harvested, followed by various detailed analysis, such as histological staining, immunoblotting, immunostaining, and real-time quantitative reverse transcription polymerase chain reaction. In addition, to verify the in vivo data, primary myoblasts isolated from mice were treated with Rg1, and the Rg1 effect on myotube growth was examined by immunoblotting and immunostaining analysis.
Rg1 treatment increased the expression of myosin heavy chain isoforms characteristic for both oxidative and glycolytic muscle fibers; increased myofiber sizes were accompanied by enhanced muscle strength. Rg1 treatment also enhanced oxidative muscle metabolism with elevated oxidative phosphorylation proteins. Furthermore, Rg1-treated muscles exhibited increased levels of anabolic S6 kinase signaling.
Rg1 improves muscle functionality via enhancing muscle gene expression and oxidative muscle metabolism in mice. |
doi_str_mv | 10.1016/j.jgr.2018.04.005 |
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To examine the effect of Rg1 on skeletal muscle, 3-month-old mice were treated with Rg1 for 5 weeks. To assess muscle strength, grip strength tests were performed, and the lower hind limb muscles were harvested, followed by various detailed analysis, such as histological staining, immunoblotting, immunostaining, and real-time quantitative reverse transcription polymerase chain reaction. In addition, to verify the in vivo data, primary myoblasts isolated from mice were treated with Rg1, and the Rg1 effect on myotube growth was examined by immunoblotting and immunostaining analysis.
Rg1 treatment increased the expression of myosin heavy chain isoforms characteristic for both oxidative and glycolytic muscle fibers; increased myofiber sizes were accompanied by enhanced muscle strength. Rg1 treatment also enhanced oxidative muscle metabolism with elevated oxidative phosphorylation proteins. Furthermore, Rg1-treated muscles exhibited increased levels of anabolic S6 kinase signaling.
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To examine the effect of Rg1 on skeletal muscle, 3-month-old mice were treated with Rg1 for 5 weeks. To assess muscle strength, grip strength tests were performed, and the lower hind limb muscles were harvested, followed by various detailed analysis, such as histological staining, immunoblotting, immunostaining, and real-time quantitative reverse transcription polymerase chain reaction. In addition, to verify the in vivo data, primary myoblasts isolated from mice were treated with Rg1, and the Rg1 effect on myotube growth was examined by immunoblotting and immunostaining analysis.
Rg1 treatment increased the expression of myosin heavy chain isoforms characteristic for both oxidative and glycolytic muscle fibers; increased myofiber sizes were accompanied by enhanced muscle strength. Rg1 treatment also enhanced oxidative muscle metabolism with elevated oxidative phosphorylation proteins. Furthermore, Rg1-treated muscles exhibited increased levels of anabolic S6 kinase signaling.
Rg1 improves muscle functionality via enhancing muscle gene expression and oxidative muscle metabolism in mice.</description><subject>Atrophy</subject><subject>Exercise-specific signaling</subject><subject>Ginsenoside</subject><subject>Rg1</subject><subject>Skeletal muscle</subject><subject>기타의약학</subject><issn>1226-8453</issn><issn>2093-4947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kktv1DAUhSMEokPhB7BB2SDBIsP1M46QkKpSykgVlaqyxXL8GDyTxFM7GcG_x_NgRDcsLMv2d46vr09RvEYwR4D4h9V8tYxzDEjMgc4B2JNihqEhFW1o_bSYIYx5JSgjZ8WLlFYAvMY1fV6cEURACNTMih_Xfkh2CMkbW94tUammZW-HMZXhlzdq9Ftb9nZUbeh86ks1mDz2K11GmzYhq8vgyrS2Xca6sp-S7mzph7L32r4snjnVJfvqOJ8X379c3V9-rW5urxeXFzeVZgKNlWVOONQIx7nQQAlipKGUmPwAqo1DGgGnzoJoMdSICUagYaRueUNxyw0n58X7g-8QnVxrL4Py-3kZ5DrKi7v7hWQi6zBkdnFgTVAruYm-V_H3XrDfCHEpVRx9foV0ILRmjoB1LXVCtaBqYRoOCoEzrclenw5em6ntrdG5c1F1j0wfnwz-Z65pKzkHLjDJBu-OBjE8TDaNsvdJ265Tgw1TkhgzURMqWJ1RdEB1DClF607XIJC7PMiVzHmQuzxIoDLnIWve_FvfSfE3ABl4e2zclI-s8erEfLv9fAWiZg2mO6OPB87mX9x6G2XS3g46K6LVY26d_08ZfwDw4dKC</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Jeong, Hyeon-Ju</creator><creator>So, Hyun-Kyung</creator><creator>Jo, Ayoung</creator><creator>Kim, Hye-Been</creator><creator>Lee, Sang-Jin</creator><creator>Bae, Gyu-Un</creator><creator>Kang, Jong-Sun</creator><general>Elsevier B.V</general><general>고려인삼학회</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>DBRKI</scope><scope>TDB</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0002-1527-0412</orcidid></search><sort><creationdate>20190701</creationdate><title>Ginsenoside Rg1 augments oxidative metabolism and anabolic response of skeletal muscle in mice</title><author>Jeong, Hyeon-Ju ; So, Hyun-Kyung ; Jo, Ayoung ; Kim, Hye-Been ; Lee, Sang-Jin ; Bae, Gyu-Un ; Kang, Jong-Sun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-e5f8f198f668c0431539443d1224cdf1c1064fe08b2071585309537b6942b6d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Atrophy</topic><topic>Exercise-specific signaling</topic><topic>Ginsenoside</topic><topic>Rg1</topic><topic>Skeletal muscle</topic><topic>기타의약학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeong, Hyeon-Ju</creatorcontrib><creatorcontrib>So, Hyun-Kyung</creatorcontrib><creatorcontrib>Jo, Ayoung</creatorcontrib><creatorcontrib>Kim, Hye-Been</creatorcontrib><creatorcontrib>Lee, Sang-Jin</creatorcontrib><creatorcontrib>Bae, Gyu-Un</creatorcontrib><creatorcontrib>Kang, Jong-Sun</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>DBPIA - 디비피아</collection><collection>DBpia 人文社会系パッケージ</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><collection>Korean Citation Index (Open Access)</collection><jtitle>Journal of ginseng research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeong, Hyeon-Ju</au><au>So, Hyun-Kyung</au><au>Jo, Ayoung</au><au>Kim, Hye-Been</au><au>Lee, Sang-Jin</au><au>Bae, Gyu-Un</au><au>Kang, Jong-Sun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ginsenoside Rg1 augments oxidative metabolism and anabolic response of skeletal muscle in mice</atitle><jtitle>Journal of ginseng research</jtitle><addtitle>J Ginseng Res</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>43</volume><issue>3</issue><spage>475</spage><epage>481</epage><pages>475-481</pages><issn>1226-8453</issn><eissn>2093-4947</eissn><abstract>The ginsenoside Rg1 has been shown to exert various pharmacological activities with health benefits. Previously, we have reported that Rg1 promoted myogenic differentiation and myotube growth in C2C12 myoblasts. In this study, the in vivo effect of Rg1 on fiber-type composition and oxidative metabolism in skeletal muscle was examined.
To examine the effect of Rg1 on skeletal muscle, 3-month-old mice were treated with Rg1 for 5 weeks. To assess muscle strength, grip strength tests were performed, and the lower hind limb muscles were harvested, followed by various detailed analysis, such as histological staining, immunoblotting, immunostaining, and real-time quantitative reverse transcription polymerase chain reaction. In addition, to verify the in vivo data, primary myoblasts isolated from mice were treated with Rg1, and the Rg1 effect on myotube growth was examined by immunoblotting and immunostaining analysis.
Rg1 treatment increased the expression of myosin heavy chain isoforms characteristic for both oxidative and glycolytic muscle fibers; increased myofiber sizes were accompanied by enhanced muscle strength. Rg1 treatment also enhanced oxidative muscle metabolism with elevated oxidative phosphorylation proteins. Furthermore, Rg1-treated muscles exhibited increased levels of anabolic S6 kinase signaling.
Rg1 improves muscle functionality via enhancing muscle gene expression and oxidative muscle metabolism in mice.</abstract><cop>Korea (South)</cop><pub>Elsevier B.V</pub><pmid>31308819</pmid><doi>10.1016/j.jgr.2018.04.005</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1527-0412</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Atrophy Exercise-specific signaling Ginsenoside Rg1 Skeletal muscle 기타의약학 |
title | Ginsenoside Rg1 augments oxidative metabolism and anabolic response of skeletal muscle in mice |
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