Evidence map›Paper›PMID 34747570›Full record

ArticlePharmacology research & perspectives2021

Normal variation of the gut microbiota affects hepatic cytochrome P450 activity in mice.

Masao Togao, Shinnosuke Tajima, Takashi Kurakawa, Gaku Wagai, Jun Otsuka, Shoichi Kado, Koji Kawakami

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Integrating the gut microbiome and pharmacology.Science translational medicine · 2024
    Review
  6. Article
  7. Article
  8. Article
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

7 authors at 1 institution in 1 country.

Masao TogaoSafety Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.ORCID 0000-0003-1468-9075
Shinnosuke TajimaSafety Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.
Takashi KurakawaBasic Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.
Gaku WagaiSafety Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.
Jun OtsukaSafety Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.
Shoichi KadoSafety Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.
Koji KawakamiSafety Research Department, Yakult Central Institute, Kunitachi-shi, Tokyo, Japan.
Yakult Central Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies revealed that substantial artificial changes in the gut microbiota resulted in modification of hepatic cytochrome P450 3a (Cyp3a) in mice. Consequently, we hypothesized that "normal" variation of the gut microbiota might also alter hepatic Cyp activity and lead to individual differences in drug metabolism. Therefore, this study investigated the effects of normal gut microbiota variation on hepatic Cyp activity under the same genetic and environmental conditions using ex-germ-free mice. Using the feces of three breeder BALB/c mice (Jcl, Slc, and Crj), germ-free BALB/cYit mice were conventionalized (Yit-Jcl, Yit-Slc, and Yit-Crj). The gut microbiota composition and hepatic Cyp activity of these donors and recipients were evaluated. 16S rRNA sequencing revealed clear differences of the gut microbiota among donors and among recipients. Cyp3a activity was significantly higher in Slc mice than in Jcl and Crj mice. Notably, among recipients, Cyp3a activity was significantly higher in Yit-Slc and Yit-Crj mice than in Yit-Jcl mice. Cyp2b activity was significantly higher in Slc mice than in Jcl and Crj mice. Cyp2b activity was significantly higher in Yit-Slc mice than in Yit-Jcl mice. Additionally, in correlation analysis, some genera displayed significant positive or negative correlations with Cyp activity, particular the strong positive correlation between Clostridium sensu stricto 1 with Cyp3a activity. In conclusion, this study demonstrated that normal variation of the gut microbiota affected hepatic Cyp3a and Cyp2b activity, which might result in individual differences of drug metabolism.

Indexed as

AnimalsCytochrome P-450 CYP3ACytochrome P450 Family 2Gastrointestinal MicrobiomeLiverMaleMembrane ProteinsMiceMice, Inbred BALB CRNA, Ribosomal, 16SCyp3a11 protein, mouseCytochrome P-450 CYP3ACytochrome P450 Family 2Membrane ProteinsRNA, Ribosomal, 16S16S rRNA genecytochrome P450drug metabolismintestinal floranormalization

Identifiers

PMID34747570
PMCPMC8573722
OpenAlexW3213810108

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.