Evidence map›Paper›PMID 26977303›Full record

ArticlePharmacology research & perspectives2016

Daikenchuto (TU-100) shapes gut microbiota architecture and increases the production of ginsenoside metabolite compound K.

Takumu Hasebe, Nobuhiro Ueno, Mark W Musch, Anuradha Nadimpalli, Atsushi Kaneko, Noriko Kaifuchi, Junko Watanabe, Masahiro Yamamoto, Toru Kono, Yuhei Inaba and 3 more

Abstract read
In one paragraph

Article in Pharmacology research & perspectives, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

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  14. Effect of Daikenchuto On Spontaneous Intestinal Tumors in ApcThe Kobe journal of medical sciences · 2021
    Article
  15. Review
  16. Review
  17. Microbial Metabolites Determine Host Health and the Status of Some Diseases.International journal of molecular sciences · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Takumu HasebeDepartment of Medicine Inflammatory Bowel Disease Center The University of Chicago Chicago Illinois; Division of Gastroenterology and Hematology/Oncology Department of Medicine Asahikawa Medical University Asahikawa Hokkaido Japan.
Nobuhiro UenoDepartment of Medicine Inflammatory Bowel Disease Center The University of Chicago Chicago Illinois; Division of Gastroenterology and Hematology/Oncology Department of Medicine Asahikawa Medical University Asahikawa Hokkaido Japan.
Mark W MuschDepartment of Medicine Inflammatory Bowel Disease Center The University of Chicago Chicago Illinois.
Anuradha NadimpalliDepartment of Medicine Inflammatory Bowel Disease Center The University of Chicago Chicago Illinois.
Atsushi KanekoTsumura Research Laboratories Tsumura & Co., Ami Ibaraki Japan.
Noriko KaifuchiTsumura Research Laboratories Tsumura & Co., Ami Ibaraki Japan.
Junko WatanabeTsumura Research Laboratories Tsumura & Co., Ami Ibaraki Japan.
Masahiro YamamotoTsumura Research Laboratories Tsumura & Co., Ami Ibaraki Japan.
Toru KonoFaculty of Pharmaceutical Sciences Hokkaido University Sapporo Hokkaido Japan; Center for Clinical and Biomedical Research Sapporo Higashi Tokushukai Hospital Sapporo Hokkaido Japan.
Yuhei InabaDivision of Gastroenterology and Hematology/Oncology Department of Medicine Asahikawa Medical University Asahikawa Hokkaido Japan.
Mikihiro FujiyaDivision of Gastroenterology and Hematology/Oncology Department of Medicine Asahikawa Medical University Asahikawa Hokkaido Japan.
Yutaka KohgoDivision of Gastroenterology and Hematology/Oncology Department of Medicine Asahikawa Medical University Asahikawa Hokkaido Japan.
Eugene B ChangDepartment of Medicine Inflammatory Bowel Disease Center The University of Chicago Chicago Illinois.

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI LIU, CAMBRIAN YANGSHAO · 1990 to 2025
$29.8M
Mutualistic relationship between Hsp25/27 and gut microbes as a major and essential determinant of mucosal healing and microbial fitness following intestinal injuryR01DK047722 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 1993 to 2020
$4.3M
Cytoprotective Role of Heat Shock Proteins in IBDR37DK047722 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 2008 to 2017
$3.8M
Dietary fat effects on gut microbes, host immune state and experimental colitisR01DK097268 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 2012 to 2016
$2.2M
NIDDK NIH HHS P30 DK042086NIDDK NIH HHS R01 DK047722NIDDK NIH HHS R01 DK097268NIDDK NIH HHS R37 DK047722
6 · The paper itself

Abstract

Many pharmaceutical agents not only require microbial metabolism for increased bioavailability and bioactivity, but also have direct effects on gut microbial assemblage and function. We examined the possibility that these actions are not mutually exclusive and may be mutually reinforcing in ways that enhance long-term of these agents. Daikenchuto, TU-100, is a traditional Japanese medicine containing ginseng. Conversion of the ginsenoside Rb1 (Rb1) to bioactive compound K (CK) requires bacterial metabolism. Diet-incorporated TU-100 was administered to mice over a period of several weeks. T-RFLP and 454 pyrosequencing were performed to analyze the time-dependent effects on fecal microbial membership. Fecal microbial capacity to metabolize Rb1 to CK was measured by adding TU-100 or ginseng to stool samples to assess the generation of bioactive metabolites. Levels of metabolized TU-100 components in plasma and in stool samples were measured by LC-MS/MS. Cecal and stool short-chain fatty acids were measured by GC-MS. Dietary administration of TU-100 for 28 days altered the gut microbiota, increasing several bacteria genera including members of Clostridia and Lactococcus lactis. Progressive capacity of microbiota to convert Rb1 to CK was observed over the 28 days administration of dietary TU-100. Concomitantly with these changes, increases in all SCFA were observed in cecal contents and in acetate and butyrate content of the stool. Chronic consumption of dietary TU-100 promotes changes in gut microbiota enhancing metabolic capacity of TU-100 and increased bioavailability. We believe these findings have broad implications in optimizing the efficacy of natural compounds that depend on microbial bioconversion in general.

Indexed as

Bacterial metabolismbioavailabilityDaikenchutomicrobiometraditional Japanese medicine

Identifiers

PMID26977303
PMCPMC4777267

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.