Effect of daikenchuto (TU-100) on carcinogenesis in non-alcoholic steatohepatitis.


Journal

The journal of medical investigation : JMI
ISSN: 1349-6867
Titre abrégé: J Med Invest
Pays: Japan
ID NLM: 9716841

Informations de publication

Date de publication:
2023
Historique:
medline: 12 5 2023
pubmed: 11 5 2023
entrez: 10 5 2023
Statut: ppublish

Résumé

Non-alcoholic steatohepatitis (NASH) is associated with a higher risk of hepatocellular carcinoma (HCC), and the importance of the gut?liver axis has been recognized in NASH-associated HCC. We investigated the effect of TU-100 on the intestinal microbiome and hepatocarcinogenesis in a NASH model. Seven-week-old Tsumura Suzuki obese diabetes mice, a model that shows the spontaneous onset of NASH and HCC, were used. They were divided into a TU-100 treated group and a control group. Mice were sacrificed at 24 and 48 weeks to evaluate hepatic steatosis, fibrosis, carcinogenesis, cytokine expression, and microbiome abundance. At 24 weeks, the TU-100 group showed significantly lower expression of IL6, IL1B, and ACTA2 mRNA in the liver (P?<?0.05). At 48 weeks, the TU-100 group showed significantly lower levels of serum alanine aminotransferase. The TU-100 group also showed a lower rate of NASH than the control group (28% vs 72%?;?P?=?0.1). Tumor diameter was significantly smaller in the TU-100 group compared with that in the control group (P?<?0.05). Regarding the intestinal microbiome, the genera Blautia and Ruminococcus were increased in the TU-100 group (P?<?0.05), whereas Dorea and Erysipelotrichaceae were decreased in the TU-100 group (P?<?0.05). TU-100 regulates the intestinal microbiome and may suppress subsequent hepatocarcinogenesis in the NASH model. J. Med. Invest. 70 : 66-73, February, 2023.

Sections du résumé

BACKGROUND BACKGROUND
Non-alcoholic steatohepatitis (NASH) is associated with a higher risk of hepatocellular carcinoma (HCC), and the importance of the gut?liver axis has been recognized in NASH-associated HCC. We investigated the effect of TU-100 on the intestinal microbiome and hepatocarcinogenesis in a NASH model.
METHODS METHODS
Seven-week-old Tsumura Suzuki obese diabetes mice, a model that shows the spontaneous onset of NASH and HCC, were used. They were divided into a TU-100 treated group and a control group. Mice were sacrificed at 24 and 48 weeks to evaluate hepatic steatosis, fibrosis, carcinogenesis, cytokine expression, and microbiome abundance.
RESULTS RESULTS
At 24 weeks, the TU-100 group showed significantly lower expression of IL6, IL1B, and ACTA2 mRNA in the liver (P?<?0.05). At 48 weeks, the TU-100 group showed significantly lower levels of serum alanine aminotransferase. The TU-100 group also showed a lower rate of NASH than the control group (28% vs 72%?;?P?=?0.1). Tumor diameter was significantly smaller in the TU-100 group compared with that in the control group (P?<?0.05). Regarding the intestinal microbiome, the genera Blautia and Ruminococcus were increased in the TU-100 group (P?<?0.05), whereas Dorea and Erysipelotrichaceae were decreased in the TU-100 group (P?<?0.05).
CONCLUSIONS CONCLUSIONS
TU-100 regulates the intestinal microbiome and may suppress subsequent hepatocarcinogenesis in the NASH model. J. Med. Invest. 70 : 66-73, February, 2023.

Identifiants

pubmed: 37164745
doi: 10.2152/jmi.70.66
doi:

Substances chimiques

dai-kenchu-to 0
12,13-dihydro-N-methyl-6,11,13-trioxo-5H-benzo(4,5)cyclohepta(1,2-b)naphthalen-5,12-imine 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

66-73

Auteurs

Shinichiro Yamada (S)

Department of Surgery, Tokushima University, Tokushima, Japan.

Yuji Morine (Y)

Department of Surgery, Tokushima University, Tokushima, Japan.

Satoru Imura (S)

Department of Surgery, Tokushima University, Tokushima, Japan.

Tetsuya Ikemoto (T)

Department of Surgery, Tokushima University, Tokushima, Japan.

Yu Saito (Y)

Department of Surgery, Tokushima University, Tokushima, Japan.

Mayuko Shimizu (M)

Department of Pathology and Laboratory Medicine, Tokushima University, Tokushima, Japan.

Koichi Tsuneyama (K)

Department of Pathology and Laboratory Medicine, Tokushima University, Tokushima, Japan.

Mitsue Nishiyama (M)

Tsumura Research Laboratories, Tsumura & Co., Ami, Ibaraki, Japan.

Shiori Ishizawa (S)

Tsumura Research Laboratories, Tsumura & Co., Ami, Ibaraki, Japan.

Mitsuo Shimada (M)

Department of Surgery, Tokushima University, Tokushima, Japan.

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