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

被引:0
作者
Yamada, Shinichiro [1 ,5 ]
Morine, Yuji [1 ]
Imura, Satoru [1 ]
Ikemoto, Tetsuya [1 ]
Saito, Yu [1 ]
Shimizu, Mayuko [2 ,3 ]
Tsuneyama, Koichi [2 ,3 ]
Nishiyama, Mitsue [4 ]
Ishizawa, Shiori [4 ]
Shimada, Mitsuo [1 ]
机构
[1] Tokushima Univ, Dept Surg, Tokushima, Japan
[2] Tokushima Univ, Dept Pathol, Tokushima, Japan
[3] Tokushima Univ, Lab Med, Tokushima, Japan
[4] Tsumura & Co, Tsumura Res Labs, Ami, Ibaraki, Japan
[5] Tokushima Univ, Dept Surg, 3-18-15 Kuramoto Cho, Tokushima 7708503, Japan
关键词
NASH; HCC; hepatocarcinogenesis; TU-100; microbiome; FATTY LIVER-DISEASE; DAI-KENCHU-TO; PREVENTS BACTERIAL TRANSLOCATION; HEPATOCELLULAR-CARCINOMA; MOUSE MODEL; COLONIC TRANSIT; MEDICINE; CANCER; PROGRESSION; INTERLEUKIN-6;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
: 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. Meth-ods : 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 : 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 ami- notransferase. 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 : TU-100 regulates the intestinal microbiome and may suppress subsequent hepatocarcinogenesis in the NASH model. J. Med. Invest. 70 : 66-73, February, 2023
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页码:66 / 73
页数:8
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共 51 条
  • [1] Mouse models in non-alcoholic fatty liver disease and steatohepatitis research
    Anstee, QM
    Goldin, RD
    [J]. INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2006, 87 (01) : 1 - 16
  • [2] Utility and Appropriateness of the Fatty Liver Inhibition of Progression (FLIP) Algorithm and Steatosis, Activity, and Fibrosis (SAF) Score in the Evaluation of Biopsies of Nonalcoholic Fatty Liver Disease
    Bedossa, Pierre
    [J]. HEPATOLOGY, 2014, 60 (02) : 565 - 575
  • [3] IL-17 and TNF-α co-operation contributes to the proinflammatory response of hepatic stellate cells
    Beringer, A.
    Miossec, P.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2019, 198 (01) : 111 - 120
  • [4] Specific gut microbiota features and metabolic markers in postmenopausal women with obesity
    Brahe, L. K.
    Le Chatelier, E.
    Prifti, E.
    Pons, N.
    Kennedy, S.
    Hansen, T.
    Pedersen, O.
    Astrup, A.
    Ehrlich, S. D.
    Larsen, L. H.
    [J]. NUTRITION & DIABETES, 2015, 5 : e159 - e159
  • [5] Microbiota, NASH, HCC and the potential role of probiotics
    Brandi, Giovanni
    De Lorenzo, Stefania
    Candela, Marco
    Pantaleo, Maria Abbondanza
    Bellentani, Stefano
    Tovoli, Francesco
    Saccoccio, Gioconda
    Biasco, Guido
    [J]. CARCINOGENESIS, 2017, 38 (03) : 231 - 240
  • [6] Kampo medicine "Dai-kenchu-to" prevents CPT-11-induced small-intestinal injury in rats
    Chikakiyo, Motoya
    Shimada, Mitsuo
    Nakao, Toshihiro
    Higashijima, Jun
    Yoshikawa, Kozo
    Nishioka, Masanori
    Iwata, Takashi
    Kurita, Nobuhiro
    [J]. SURGERY TODAY, 2012, 42 (01) : 60 - 67
  • [7] Senescence-Associated Secretory Phenotypes Reveal Cell-Nonautonomous Functions of Oncogenic RAS and the p53 Tumor Suppressor
    Coppe, Jean-Philippe
    Patil, Christopher K.
    Rodier, Francis
    Sun, Yu
    Munoz, Denise P.
    Goldstein, Joshua
    Nelson, Peter S.
    Desprez, Pierre-Yves
    Campisi, Judith
    [J]. PLOS BIOLOGY, 2008, 6 (12) : 2853 - 2868
  • [8] Gut Microbiota Profiling of Pediatric Nonalcoholic Fatty Liver Disease and Obese Patients Unveiled by an Integrated Meta-omics-Based Approach
    Del Chierico, Federica
    Nobili, Valerio
    Vernocchi, Pamela
    Russo, Alessandra
    De Stefanis, Cristiano
    Gnani, Daniela
    Furlanello, Cesare
    Alessandro, Zandon A.
    Paci, Paola
    Capuani, Giorgio
    Dallapiccola, Bruno
    Miccheli, Alfredo
    Alisi, Anna
    Putignani, Lorenza
    [J]. HEPATOLOGY, 2017, 65 (02) : 451 - 464
  • [9] Steatohepatitis induced by intragastric overfeeding in mice
    Deng, QG
    She, HY
    Cheng, JH
    French, SW
    Koop, DR
    Xiong, SG
    Tsukamoto, H
    [J]. HEPATOLOGY, 2005, 42 (04) : 905 - 914
  • [10] Progression and Regression of Hepatic Lesions in a Mouse Model of NASH Induced by Dietary Intervention and Its Implications in Pharmacotherapy
    Ding, Zhi-Ming
    Xiao, Yue
    Wu, Xikun
    Zou, Haixia
    Yang, Shurong
    Shen, Yiyun
    Xu, Juehua
    Workman, Heather C.
    Usborne, Amy L.
    Hua, Haiqing
    [J]. FRONTIERS IN PHARMACOLOGY, 2018, 9