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...

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Veröffentlicht in:Nutrition research (New York, N.Y.) N.Y.), 2014-10, Vol.34 (10), p.876-885
Hauptverfasser: Tsubouchi, Hironobu, Yanagi, Shigehisa, Miura, Ayako, Mogami, Sachiko, Yamada, Chihiro, Iizuka, Seiichi, Hattori, Tomohisa, Nakazato, Masamitsu
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container_title Nutrition research (New York, N.Y.)
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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
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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. 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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 &amp; 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. 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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. 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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 &amp; 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>
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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
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