Literature DB >> 25270999

Rikkunshito ameliorates cachexia associated with bleomycin-induced lung fibrosis in mice by stimulating ghrelin secretion.

Hironobu Tsubouchi1, Shigehisa Yanagi1, Ayako Miura1, Sachiko Mogami2, Chihiro Yamada2, Seiichi Iizuka2, Tomohisa Hattori2, Masamitsu Nakazato3.   

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.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bleomycin; Cachexia; Ghrelin; Lung fibrosis; Mice; Rikkunshito

Mesh:

Substances:

Year:  2014        PMID: 25270999     DOI: 10.1016/j.nutres.2014.08.014

Source DB:  PubMed          Journal:  Nutr Res        ISSN: 0271-5317            Impact factor:   3.315


  6 in total

1.  Tumor cell anabolism and host tissue catabolism-energetic inefficiency during cancer cachexia.

Authors:  Mangala Hegde; Uzini Devi Daimary; Sosmitha Girisa; Aviral Kumar; Ajaikumar B Kunnumakkara
Journal:  Exp Biol Med (Maywood)       Date:  2022-05-06

Review 2.  Antifibrotic activity of acylated and unacylated ghrelin.

Authors:  Elia Angelino; Simone Reano; Michele Ferrara; Emanuela Agosti; Andrea Graziani; Nicoletta Filigheddu
Journal:  Int J Endocrinol       Date:  2015-04-16       Impact factor: 3.257

Review 3.  Rikkunshito, a ghrelin potentiator, ameliorates anorexia-cachexia syndrome.

Authors:  Naoki Fujitsuka; Yasuhito Uezono
Journal:  Front Pharmacol       Date:  2014-12-10       Impact factor: 5.810

4.  CRF receptor 1 antagonism and brain distribution of active components contribute to the ameliorative effect of rikkunshito on stress-induced anorexia.

Authors:  Sachiko Mogami; Chiharu Sadakane; Miwa Nahata; Yasuharu Mizuhara; Chihiro Yamada; Tomohisa Hattori; Hiroshi Takeda
Journal:  Sci Rep       Date:  2016-06-08       Impact factor: 4.379

5.  Rikkunshito Ameliorates Cancer Cachexia Partly through Elevation of Glucarate in Plasma.

Authors:  Katsuya Ohbuchi; Shin Nishiumi; Naoki Fujitsuka; Tomohisa Hattori; Masahiro Yamamoto; Akio Inui; Takeshi Azuma; Masaru Yoshida
Journal:  Evid Based Complement Alternat Med       Date:  2015-09-15       Impact factor: 2.629

6.  Increased ghrelin signaling prolongs survival in mouse models of human aging through activation of sirtuin1.

Authors:  N Fujitsuka; A Asakawa; A Morinaga; M S Amitani; H Amitani; G Katsuura; Y Sawada; Y Sudo; Y Uezono; E Mochiki; I Sakata; T Sakai; K Hanazaki; T Yada; K Yakabi; E Sakuma; T Ueki; A Niijima; K Nakagawa; N Okubo; H Takeda; M Asaka; A Inui
Journal:  Mol Psychiatry       Date:  2016-02-02       Impact factor: 15.992

  6 in total

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