Academic Journal
Bofutsushosan (Fangfengtongshengsan) improves early stages of NASH via the gut–liver axis in diabetes-induced NASH model mice
Title: | Bofutsushosan (Fangfengtongshengsan) improves early stages of NASH via the gut–liver axis in diabetes-induced NASH model mice |
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Authors: | Mitsue Nishiyama, Shiori Ishizawa, Akinori Nishi, Akinobu Taketomi, Toru Kono |
Source: | Pharmacological Research - Modern Chinese Medicine, Vol 11, Iss , Pp 100440- (2024) |
Publisher Information: | Elsevier, 2024. |
Publication Year: | 2024 |
Collection: | LCC:Other systems of medicine LCC:Therapeutics. Pharmacology |
Subject Terms: | Non-alcoholic fatty liver disease, Diabetes mellitus, Gastrointestinal microbiome, Kampo, Bofutsushosan, Gut–liver axis, Other systems of medicine, RZ201-999, Therapeutics. Pharmacology, RM1-950 |
More Details: | Background: The mechanisms underlying non-alcoholic fatty liver disease (NAFLD) are not fully understood, but the gut microbiota is deeply involved. Because the Japanese traditional medicine bofutsushosan (BTS; Fangfengtongshengsan in Chinese) is known to improve obesity-induced liver injury and increase gut Akkermansia muciniphila, we evaluated its effects in a mouse model of diabetes-induced nonalcoholic steatohepatitis (NASH). Methods: Two-day-old male C57BL/6J mice were injected subcutaneously with streptozotocin and fed a high-fat diet (HFD) from 4 weeks. Between 5 and 8 weeks, HFD was supplemented with 5% BTS (BTS) or not supplemented (CONT), and plasma, liver, and stool samples were collected and analyzed. Results: The NAFLD activity score (NAS), which was consistent with early steatohepatitis in CONT mice, was significantly lower in BTS mice (P = 0.018). Improvement of steatosis contributed most to decreasing NAS. Relative abundances of probiotic Akkermansia muciniphila and Bifidobacterium pseudolongum were significantly higher in BTS mice (both P < 0.05). Positive correlations were observed among NAS, steatosis, ballooning, and body weight change. Liver macrophage markers correlated with some microbes in BTS mice. Conclusions: BTS administration suppressed liver steatosis and improved the gut microbiome, which correlated with some liver factors. BTS may be a promising treatment for NAFLD by maintaining the gut–liver axis. |
Document Type: | article |
File Description: | electronic resource |
Language: | English |
ISSN: | 2667-1425 |
Relation: | http://www.sciencedirect.com/science/article/pii/S2667142524000836; https://doaj.org/toc/2667-1425 |
DOI: | 10.1016/j.prmcm.2024.100440 |
Access URL: | https://doaj.org/article/1f4dd0445daf4d9f9500eca658100bac |
Accession Number: | edsdoj.1f4dd0445daf4d9f9500eca658100bac |
Database: | Directory of Open Access Journals |
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Items | – Name: Title Label: Title Group: Ti Data: Bofutsushosan (Fangfengtongshengsan) improves early stages of NASH via the gut–liver axis in diabetes-induced NASH model mice – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Mitsue+Nishiyama%22">Mitsue Nishiyama</searchLink><br /><searchLink fieldCode="AR" term="%22Shiori+Ishizawa%22">Shiori Ishizawa</searchLink><br /><searchLink fieldCode="AR" term="%22Akinori+Nishi%22">Akinori Nishi</searchLink><br /><searchLink fieldCode="AR" term="%22Akinobu+Taketomi%22">Akinobu Taketomi</searchLink><br /><searchLink fieldCode="AR" term="%22Toru+Kono%22">Toru Kono</searchLink> – Name: TitleSource Label: Source Group: Src Data: Pharmacological Research - Modern Chinese Medicine, Vol 11, Iss , Pp 100440- (2024) – Name: Publisher Label: Publisher Information Group: PubInfo Data: Elsevier, 2024. – Name: DatePubCY Label: Publication Year Group: Date Data: 2024 – Name: Subset Label: Collection Group: HoldingsInfo Data: LCC:Other systems of medicine<br />LCC:Therapeutics. Pharmacology – Name: Subject Label: Subject Terms Group: Su Data: <searchLink fieldCode="DE" term="%22Non-alcoholic+fatty+liver+disease%22">Non-alcoholic fatty liver disease</searchLink><br /><searchLink fieldCode="DE" term="%22Diabetes+mellitus%22">Diabetes mellitus</searchLink><br /><searchLink fieldCode="DE" term="%22Gastrointestinal+microbiome%22">Gastrointestinal microbiome</searchLink><br /><searchLink fieldCode="DE" term="%22Kampo%22">Kampo</searchLink><br /><searchLink fieldCode="DE" term="%22Bofutsushosan%22">Bofutsushosan</searchLink><br /><searchLink fieldCode="DE" term="%22Gut–liver+axis%22">Gut–liver axis</searchLink><br /><searchLink fieldCode="DE" term="%22Other+systems+of+medicine%22">Other systems of medicine</searchLink><br /><searchLink fieldCode="DE" term="%22RZ201-999%22">RZ201-999</searchLink><br /><searchLink fieldCode="DE" term="%22Therapeutics%2E+Pharmacology%22">Therapeutics. Pharmacology</searchLink><br /><searchLink fieldCode="DE" term="%22RM1-950%22">RM1-950</searchLink> – Name: Abstract Label: Description Group: Ab Data: Background: The mechanisms underlying non-alcoholic fatty liver disease (NAFLD) are not fully understood, but the gut microbiota is deeply involved. Because the Japanese traditional medicine bofutsushosan (BTS; Fangfengtongshengsan in Chinese) is known to improve obesity-induced liver injury and increase gut Akkermansia muciniphila, we evaluated its effects in a mouse model of diabetes-induced nonalcoholic steatohepatitis (NASH). Methods: Two-day-old male C57BL/6J mice were injected subcutaneously with streptozotocin and fed a high-fat diet (HFD) from 4 weeks. Between 5 and 8 weeks, HFD was supplemented with 5% BTS (BTS) or not supplemented (CONT), and plasma, liver, and stool samples were collected and analyzed. Results: The NAFLD activity score (NAS), which was consistent with early steatohepatitis in CONT mice, was significantly lower in BTS mice (P = 0.018). Improvement of steatosis contributed most to decreasing NAS. Relative abundances of probiotic Akkermansia muciniphila and Bifidobacterium pseudolongum were significantly higher in BTS mice (both P < 0.05). Positive correlations were observed among NAS, steatosis, ballooning, and body weight change. Liver macrophage markers correlated with some microbes in BTS mice. Conclusions: BTS administration suppressed liver steatosis and improved the gut microbiome, which correlated with some liver factors. BTS may be a promising treatment for NAFLD by maintaining the gut–liver axis. – Name: TypeDocument Label: Document Type Group: TypDoc Data: article – Name: Format Label: File Description Group: SrcInfo Data: electronic resource – Name: Language Label: Language Group: Lang Data: English – Name: ISSN Label: ISSN Group: ISSN Data: 2667-1425 – Name: NoteTitleSource Label: Relation Group: SrcInfo Data: http://www.sciencedirect.com/science/article/pii/S2667142524000836; https://doaj.org/toc/2667-1425 – Name: DOI Label: DOI Group: ID Data: 10.1016/j.prmcm.2024.100440 – Name: URL Label: Access URL Group: URL Data: <link linkTarget="URL" linkTerm="https://doaj.org/article/1f4dd0445daf4d9f9500eca658100bac" linkWindow="_blank">https://doaj.org/article/1f4dd0445daf4d9f9500eca658100bac</link> – Name: AN Label: Accession Number Group: ID Data: edsdoj.1f4dd0445daf4d9f9500eca658100bac |
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RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.prmcm.2024.100440 Languages: – Text: English Subjects: – SubjectFull: Non-alcoholic fatty liver disease Type: general – SubjectFull: Diabetes mellitus Type: general – SubjectFull: Gastrointestinal microbiome Type: general – SubjectFull: Kampo Type: general – SubjectFull: Bofutsushosan Type: general – SubjectFull: Gut–liver axis Type: general – SubjectFull: Other systems of medicine Type: general – SubjectFull: RZ201-999 Type: general – SubjectFull: Therapeutics. Pharmacology Type: general – SubjectFull: RM1-950 Type: general Titles: – TitleFull: Bofutsushosan (Fangfengtongshengsan) improves early stages of NASH via the gut–liver axis in diabetes-induced NASH model mice Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mitsue Nishiyama – PersonEntity: Name: NameFull: Shiori Ishizawa – PersonEntity: Name: NameFull: Akinori Nishi – PersonEntity: Name: NameFull: Akinobu Taketomi – PersonEntity: Name: NameFull: Toru Kono IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 26671425 Numbering: – Type: volume Value: 11 – Type: issue Value: 100440- Titles: – TitleFull: Pharmacological Research - Modern Chinese Medicine Type: main |
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