Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion
Abstract Cachexia is a frequent complication in patients with respiratory failure, such as lung fibrosis, and it is a determining factor for functional capacity, health status, and mortality. Reductions in body weight and skeletal muscle mass are key features of cachexia that are resistant to curren...
Gespeichert in:
Veröffentlicht in: | Nutrition research (New York, N.Y.) N.Y.), 2014-10, Vol.34 (10), p.876-885 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 885 |
---|---|
container_issue | 10 |
container_start_page | 876 |
container_title | Nutrition research (New York, N.Y.) |
container_volume | 34 |
creator | Tsubouchi, Hironobu Yanagi, Shigehisa Miura, Ayako Mogami, Sachiko Yamada, Chihiro Iizuka, Seiichi Hattori, Tomohisa Nakazato, Masamitsu |
description | Abstract Cachexia is a frequent complication in patients with respiratory failure, such as lung fibrosis, and it is a determining factor for functional capacity, health status, and mortality. Reductions in body weight and skeletal muscle mass are key features of cachexia that are resistant to current therapies. Rikkunshito (RKT), a traditional Japanese herbal medicine, is widely used for the treatment for patients with gastrointestinal symptoms and known to stimulate ghrelin secretion. By using bleomycin (BLM)-induced lung fibrosis mice in this study, we tested our hypothesis that RKT administration could ameliorate pulmonary cachexia. After BLM administration, mice were provided with either RKT or distilled water on a daily basis. Compared with the BLM-injected mice, the RKT-treated mice had smaller reductions of food intake and body weight. Skeletal muscle weights were retained in the RKT-treated mice, in conjunction with reduced expressions of MuRF-1 and atrogin-1 in the lysates of skeletal muscle found in lung fibrosis. Rikkunshito administration restored the plasma concentrations of ghrelin in BLM-injected mice. The anticachectic efficacies of RKT administration in BLM-injected mice were canceled by the concurrent treatment of a ghrelin receptor antagonist. Rikkunshito administration did not decrease the degree of loss of body weight or food intake reduction in either ghrelin-deficient mice or growth hormone secretagogue receptor–deficient mice. Our results indicate that RKT administration exerts protective effects on pulmonary cachexia by ameliorating skeletal muscle wasting and food intake reduction as mediated by the ghrelin system and, thus, highlight RKT as a potential therapeutic agent for the management of lung fibrosis. |
doi_str_mv | 10.1016/j.nutres.2014.08.014 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1629969547</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0271531714001651</els_id><sourcerecordid>1629969547</sourcerecordid><originalsourceid>FETCH-LOGICAL-c517t-29369ed0a5725feddcab8bce92f5e4bebc14cbe425e6a0ef75bb4d07575eaabc3</originalsourceid><addsrcrecordid>eNqFkt2L1DAQwIso3t7pfyCSF8GXrknbNM2LIIeewoHgx3NI0unt7LbpmUnV_vdm2VXBF58GJr_5yI8pimeCbwUX7av9NiwpAm0rLpot77Y5PCg2olO65KrWD4sNr5QoZS3URXFJtOdcKFHXj4uLSlaKa603xfoJD4cl0A7TzOwEI87RJiDmrd_BT7TMEs0ec65nPzDtmBthnlaPocTQLz6nxyXcsQFdnAmJYWATemBuZZRwWkabML_f7WJuHhiBj5BwDk-KR4MdCZ6e41Xx9d3bL9fvy9uPNx-u39yWXgqVykrXrYaeW6kqOUDfe-s650FXg4TGgfOi8Q6aSkJrOQxKOtf0XEklwVrn66vi5anvfZy_LUDJTEgextEGmBcyoq20brVsVEabE-rzVyjCYO4jTjauRnBzlG725iTdHKUb3pkcctnz84TFTdD_KfptOQMvzoAlb8ch2uCR_nKd7tq6lZl7feIg-_iOEA15hJAdYwSfTD_j_zb5t4HPzjHPPMAKtJ-XGLJrIwxVhpvPxwM53odo8m20UtS_AA65u6c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1629969547</pqid></control><display><type>article</type><title>Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Tsubouchi, Hironobu ; Yanagi, Shigehisa ; Miura, Ayako ; Mogami, Sachiko ; Yamada, Chihiro ; Iizuka, Seiichi ; Hattori, Tomohisa ; Nakazato, Masamitsu</creator><creatorcontrib>Tsubouchi, Hironobu ; Yanagi, Shigehisa ; Miura, Ayako ; Mogami, Sachiko ; Yamada, Chihiro ; Iizuka, Seiichi ; Hattori, Tomohisa ; Nakazato, Masamitsu</creatorcontrib><description>Abstract Cachexia is a frequent complication in patients with respiratory failure, such as lung fibrosis, and it is a determining factor for functional capacity, health status, and mortality. Reductions in body weight and skeletal muscle mass are key features of cachexia that are resistant to current therapies. Rikkunshito (RKT), a traditional Japanese herbal medicine, is widely used for the treatment for patients with gastrointestinal symptoms and known to stimulate ghrelin secretion. By using bleomycin (BLM)-induced lung fibrosis mice in this study, we tested our hypothesis that RKT administration could ameliorate pulmonary cachexia. After BLM administration, mice were provided with either RKT or distilled water on a daily basis. Compared with the BLM-injected mice, the RKT-treated mice had smaller reductions of food intake and body weight. Skeletal muscle weights were retained in the RKT-treated mice, in conjunction with reduced expressions of MuRF-1 and atrogin-1 in the lysates of skeletal muscle found in lung fibrosis. Rikkunshito administration restored the plasma concentrations of ghrelin in BLM-injected mice. The anticachectic efficacies of RKT administration in BLM-injected mice were canceled by the concurrent treatment of a ghrelin receptor antagonist. Rikkunshito administration did not decrease the degree of loss of body weight or food intake reduction in either ghrelin-deficient mice or growth hormone secretagogue receptor–deficient mice. Our results indicate that RKT administration exerts protective effects on pulmonary cachexia by ameliorating skeletal muscle wasting and food intake reduction as mediated by the ghrelin system and, thus, highlight RKT as a potential therapeutic agent for the management of lung fibrosis.</description><identifier>ISSN: 0271-5317</identifier><identifier>EISSN: 1879-0739</identifier><identifier>DOI: 10.1016/j.nutres.2014.08.014</identifier><identifier>PMID: 25270999</identifier><identifier>CODEN: NTRSDC</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Bleomycin ; Cachexia ; Cachexia - etiology ; Cachexia - metabolism ; Cachexia - prevention & control ; Drugs, Chinese Herbal - pharmacology ; Drugs, Chinese Herbal - therapeutic use ; Eating - drug effects ; Energy Intake - drug effects ; Feeding. Feeding behavior ; Fundamental and applied biological sciences. Psychology ; Gastroenterology and Hepatology ; Ghrelin ; Ghrelin - secretion ; Lung fibrosis ; Male ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Muscle Proteins - metabolism ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - pathology ; Muscular Atrophy - metabolism ; Muscular Atrophy - prevention & control ; Phytotherapy ; Pneumology ; Pulmonary Fibrosis - chemically induced ; Pulmonary Fibrosis - complications ; Receptors, Ghrelin - metabolism ; Respiratory system : syndromes and miscellaneous diseases ; Rikkunshito ; SKP Cullin F-Box Protein Ligases - metabolism ; Tripartite Motif Proteins ; Ubiquitin-Protein Ligases - metabolism ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Weight Loss - drug effects</subject><ispartof>Nutrition research (New York, N.Y.), 2014-10, Vol.34 (10), p.876-885</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-29369ed0a5725feddcab8bce92f5e4bebc14cbe425e6a0ef75bb4d07575eaabc3</citedby><cites>FETCH-LOGICAL-c517t-29369ed0a5725feddcab8bce92f5e4bebc14cbe425e6a0ef75bb4d07575eaabc3</cites><orcidid>0000-0001-5486-884X ; 0000-0001-7914-4928</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.nutres.2014.08.014$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28986365$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25270999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsubouchi, Hironobu</creatorcontrib><creatorcontrib>Yanagi, Shigehisa</creatorcontrib><creatorcontrib>Miura, Ayako</creatorcontrib><creatorcontrib>Mogami, Sachiko</creatorcontrib><creatorcontrib>Yamada, Chihiro</creatorcontrib><creatorcontrib>Iizuka, Seiichi</creatorcontrib><creatorcontrib>Hattori, Tomohisa</creatorcontrib><creatorcontrib>Nakazato, Masamitsu</creatorcontrib><title>Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion</title><title>Nutrition research (New York, N.Y.)</title><addtitle>Nutr Res</addtitle><description>Abstract Cachexia is a frequent complication in patients with respiratory failure, such as lung fibrosis, and it is a determining factor for functional capacity, health status, and mortality. Reductions in body weight and skeletal muscle mass are key features of cachexia that are resistant to current therapies. Rikkunshito (RKT), a traditional Japanese herbal medicine, is widely used for the treatment for patients with gastrointestinal symptoms and known to stimulate ghrelin secretion. By using bleomycin (BLM)-induced lung fibrosis mice in this study, we tested our hypothesis that RKT administration could ameliorate pulmonary cachexia. After BLM administration, mice were provided with either RKT or distilled water on a daily basis. Compared with the BLM-injected mice, the RKT-treated mice had smaller reductions of food intake and body weight. Skeletal muscle weights were retained in the RKT-treated mice, in conjunction with reduced expressions of MuRF-1 and atrogin-1 in the lysates of skeletal muscle found in lung fibrosis. Rikkunshito administration restored the plasma concentrations of ghrelin in BLM-injected mice. The anticachectic efficacies of RKT administration in BLM-injected mice were canceled by the concurrent treatment of a ghrelin receptor antagonist. Rikkunshito administration did not decrease the degree of loss of body weight or food intake reduction in either ghrelin-deficient mice or growth hormone secretagogue receptor–deficient mice. Our results indicate that RKT administration exerts protective effects on pulmonary cachexia by ameliorating skeletal muscle wasting and food intake reduction as mediated by the ghrelin system and, thus, highlight RKT as a potential therapeutic agent for the management of lung fibrosis.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bleomycin</subject><subject>Cachexia</subject><subject>Cachexia - etiology</subject><subject>Cachexia - metabolism</subject><subject>Cachexia - prevention & control</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Eating - drug effects</subject><subject>Energy Intake - drug effects</subject><subject>Feeding. Feeding behavior</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology and Hepatology</subject><subject>Ghrelin</subject><subject>Ghrelin - secretion</subject><subject>Lung fibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Muscle Proteins - metabolism</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - pathology</subject><subject>Muscular Atrophy - metabolism</subject><subject>Muscular Atrophy - prevention & control</subject><subject>Phytotherapy</subject><subject>Pneumology</subject><subject>Pulmonary Fibrosis - chemically induced</subject><subject>Pulmonary Fibrosis - complications</subject><subject>Receptors, Ghrelin - metabolism</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Rikkunshito</subject><subject>SKP Cullin F-Box Protein Ligases - metabolism</subject><subject>Tripartite Motif Proteins</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Weight Loss - drug effects</subject><issn>0271-5317</issn><issn>1879-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkt2L1DAQwIso3t7pfyCSF8GXrknbNM2LIIeewoHgx3NI0unt7LbpmUnV_vdm2VXBF58GJr_5yI8pimeCbwUX7av9NiwpAm0rLpot77Y5PCg2olO65KrWD4sNr5QoZS3URXFJtOdcKFHXj4uLSlaKa603xfoJD4cl0A7TzOwEI87RJiDmrd_BT7TMEs0ec65nPzDtmBthnlaPocTQLz6nxyXcsQFdnAmJYWATemBuZZRwWkabML_f7WJuHhiBj5BwDk-KR4MdCZ6e41Xx9d3bL9fvy9uPNx-u39yWXgqVykrXrYaeW6kqOUDfe-s650FXg4TGgfOi8Q6aSkJrOQxKOtf0XEklwVrn66vi5anvfZy_LUDJTEgextEGmBcyoq20brVsVEabE-rzVyjCYO4jTjauRnBzlG725iTdHKUb3pkcctnz84TFTdD_KfptOQMvzoAlb8ch2uCR_nKd7tq6lZl7feIg-_iOEA15hJAdYwSfTD_j_zb5t4HPzjHPPMAKtJ-XGLJrIwxVhpvPxwM53odo8m20UtS_AA65u6c</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Tsubouchi, Hironobu</creator><creator>Yanagi, Shigehisa</creator><creator>Miura, Ayako</creator><creator>Mogami, Sachiko</creator><creator>Yamada, Chihiro</creator><creator>Iizuka, Seiichi</creator><creator>Hattori, Tomohisa</creator><creator>Nakazato, Masamitsu</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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><orcidid>https://orcid.org/0000-0001-5486-884X</orcidid><orcidid>https://orcid.org/0000-0001-7914-4928</orcidid></search><sort><creationdate>20141001</creationdate><title>Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion</title><author>Tsubouchi, Hironobu ; Yanagi, Shigehisa ; Miura, Ayako ; Mogami, Sachiko ; Yamada, Chihiro ; Iizuka, Seiichi ; Hattori, Tomohisa ; Nakazato, Masamitsu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-29369ed0a5725feddcab8bce92f5e4bebc14cbe425e6a0ef75bb4d07575eaabc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bleomycin</topic><topic>Cachexia</topic><topic>Cachexia - etiology</topic><topic>Cachexia - metabolism</topic><topic>Cachexia - prevention & control</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Drugs, Chinese Herbal - therapeutic use</topic><topic>Eating - drug effects</topic><topic>Energy Intake - drug effects</topic><topic>Feeding. Feeding behavior</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology and Hepatology</topic><topic>Ghrelin</topic><topic>Ghrelin - secretion</topic><topic>Lung fibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Muscle Proteins - metabolism</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - pathology</topic><topic>Muscular Atrophy - metabolism</topic><topic>Muscular Atrophy - prevention & control</topic><topic>Phytotherapy</topic><topic>Pneumology</topic><topic>Pulmonary Fibrosis - chemically induced</topic><topic>Pulmonary Fibrosis - complications</topic><topic>Receptors, Ghrelin - metabolism</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Rikkunshito</topic><topic>SKP Cullin F-Box Protein Ligases - metabolism</topic><topic>Tripartite Motif Proteins</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Weight Loss - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsubouchi, Hironobu</creatorcontrib><creatorcontrib>Yanagi, Shigehisa</creatorcontrib><creatorcontrib>Miura, Ayako</creatorcontrib><creatorcontrib>Mogami, Sachiko</creatorcontrib><creatorcontrib>Yamada, Chihiro</creatorcontrib><creatorcontrib>Iizuka, Seiichi</creatorcontrib><creatorcontrib>Hattori, Tomohisa</creatorcontrib><creatorcontrib>Nakazato, Masamitsu</creatorcontrib><collection>Pascal-Francis</collection><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>Tsubouchi, Hironobu</au><au>Yanagi, Shigehisa</au><au>Miura, Ayako</au><au>Mogami, Sachiko</au><au>Yamada, Chihiro</au><au>Iizuka, Seiichi</au><au>Hattori, Tomohisa</au><au>Nakazato, Masamitsu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion</atitle><jtitle>Nutrition research (New York, N.Y.)</jtitle><addtitle>Nutr Res</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>34</volume><issue>10</issue><spage>876</spage><epage>885</epage><pages>876-885</pages><issn>0271-5317</issn><eissn>1879-0739</eissn><coden>NTRSDC</coden><abstract>Abstract Cachexia is a frequent complication in patients with respiratory failure, such as lung fibrosis, and it is a determining factor for functional capacity, health status, and mortality. Reductions in body weight and skeletal muscle mass are key features of cachexia that are resistant to current therapies. Rikkunshito (RKT), a traditional Japanese herbal medicine, is widely used for the treatment for patients with gastrointestinal symptoms and known to stimulate ghrelin secretion. By using bleomycin (BLM)-induced lung fibrosis mice in this study, we tested our hypothesis that RKT administration could ameliorate pulmonary cachexia. After BLM administration, mice were provided with either RKT or distilled water on a daily basis. Compared with the BLM-injected mice, the RKT-treated mice had smaller reductions of food intake and body weight. Skeletal muscle weights were retained in the RKT-treated mice, in conjunction with reduced expressions of MuRF-1 and atrogin-1 in the lysates of skeletal muscle found in lung fibrosis. Rikkunshito administration restored the plasma concentrations of ghrelin in BLM-injected mice. The anticachectic efficacies of RKT administration in BLM-injected mice were canceled by the concurrent treatment of a ghrelin receptor antagonist. Rikkunshito administration did not decrease the degree of loss of body weight or food intake reduction in either ghrelin-deficient mice or growth hormone secretagogue receptor–deficient mice. Our results indicate that RKT administration exerts protective effects on pulmonary cachexia by ameliorating skeletal muscle wasting and food intake reduction as mediated by the ghrelin system and, thus, highlight RKT as a potential therapeutic agent for the management of lung fibrosis.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>25270999</pmid><doi>10.1016/j.nutres.2014.08.014</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5486-884X</orcidid><orcidid>https://orcid.org/0000-0001-7914-4928</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0271-5317 |
ispartof | Nutrition research (New York, N.Y.), 2014-10, Vol.34 (10), p.876-885 |
issn | 0271-5317 1879-0739 |
language | eng |
recordid | cdi_proquest_miscellaneous_1629969547 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Animals Biological and medical sciences Bleomycin Cachexia Cachexia - etiology Cachexia - metabolism Cachexia - prevention & control Drugs, Chinese Herbal - pharmacology Drugs, Chinese Herbal - therapeutic use Eating - drug effects Energy Intake - drug effects Feeding. Feeding behavior Fundamental and applied biological sciences. Psychology Gastroenterology and Hepatology Ghrelin Ghrelin - secretion Lung fibrosis Male Medical sciences Mice Mice, Inbred C57BL Muscle Proteins - metabolism Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscular Atrophy - metabolism Muscular Atrophy - prevention & control Phytotherapy Pneumology Pulmonary Fibrosis - chemically induced Pulmonary Fibrosis - complications Receptors, Ghrelin - metabolism Respiratory system : syndromes and miscellaneous diseases Rikkunshito SKP Cullin F-Box Protein Ligases - metabolism Tripartite Motif Proteins Ubiquitin-Protein Ligases - metabolism Vertebrates: anatomy and physiology, studies on body, several organs or systems Weight Loss - drug effects |
title | Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T23%3A47%3A33IST&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=Rikkunshito%20ameliorates%20cachexia%20associated%20with%20bleomycin-induced%20lung%20fibrosis%20in%20mice%20by%20stimulating%20ghrelin%20secretion&rft.jtitle=Nutrition%20research%20(New%20York,%20N.Y.)&rft.au=Tsubouchi,%20Hironobu&rft.date=2014-10-01&rft.volume=34&rft.issue=10&rft.spage=876&rft.epage=885&rft.pages=876-885&rft.issn=0271-5317&rft.eissn=1879-0739&rft.coden=NTRSDC&rft_id=info:doi/10.1016/j.nutres.2014.08.014&rft_dat=%3Cproquest_cross%3E1629969547%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=1629969547&rft_id=info:pmid/25270999&rft_els_id=1_s2_0_S0271531714001651&rfr_iscdi=true |