Evidence map›Paper›PMID 25759521›Full record

ArticleJournal of clinical biochemistry and nutrition2015

Bacterial cell wall components regulate adipokine secretion from visceral adipocytes.

Risa Taira, Sayori Yamaguchi, Kyoko Shimizu, Kiminori Nakamura, Tokiyoshi Ayabe, Toshio Taira

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical biochemistry and nutrition, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Glucocorticosteroids and the Risk of NAFLD in Inflammatory Bowel Disease.Canadian journal of gastroenterology & hepatology · 2022
    Review
  7. Review
  8. Review
  9. Nutrients · 2020
    Article
  10. Article
  11. Connection between gut microbiome and the development of obesity.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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

6 authors at 2 institutions in 1 country.

Risa TairaDivision of Biology, Department of Biological Sciences, School of Science, Hokkaido University, Kita10 Nishi 8, Kita-ku, Sapporo 060-0810, Japan.
Sayori YamaguchiCosmo Bio Co., Ltd., Primary Cell Division, YS Bldg, 1-12 12 Nishimachi-kita, Sapporo 063-0061, Japan.
Kyoko ShimizuCosmo Bio Co., Ltd., Primary Cell Division, YS Bldg, 1-12 12 Nishimachi-kita, Sapporo 063-0061, Japan.
Kiminori NakamuraDepartment of Cell Biological Science, Faculty of Advanced Life Science, Graduate School of Life Science, Hokkaido University, North 21 West 11, Kita-ku, Sapporo 001-0021, Japan.
Tokiyoshi AyabeDepartment of Cell Biological Science, Faculty of Advanced Life Science, Graduate School of Life Science, Hokkaido University, North 21 West 11, Kita-ku, Sapporo 001-0021, Japan.
Toshio TairaCosmo Bio Co., Ltd., Primary Cell Division, YS Bldg, 1-12 12 Nishimachi-kita, Sapporo 063-0061, Japan.
Cosmo Bio (Japan) · JPHokkaido University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies suggest a relationship between intestinal microbiota and metabolic syndromes; however, the underlying mechanism remains unclear. To clarify this issue, we assessed the effects of bacterial cell wall components on adiponectin, leptin and resistin secretion from rat visceral adipocytes in vitro. We also measured the relative population of Firmicutes and Bacteroidetes in fecal microbiota and the amount of fecal mucin as an intestinal barrier function, when mice were fed a high-fat diet. In the present study, we demonstrated that bacterial cell wall components affect the secretion of adipokines, depending on the presence of antigens from gram-positive or gram-negative bacteria. Lipopolysaccharide markedly inhibited adiponectin, leptin, and resistin secretion, whereas peptidoglycan increased adiponectin secretion and decreased resistin secretion in vitro. In vivo experiments showed that the high-fat diet increased the population of Firmicutes and decreased that of Bacteroidetes. In contrast, the high-fat diet downregulated the stool output and fecal mucin content. These results demonstrate that bacterial cell wall components affect the onset of metabolic syndromes by mediating the secretion of adipokines from visceral adipose tissue. Furthermore, we believe that metabolic endotoxemia is not due to the increasing dominance of gram-negative bacteria, Bacteroidetes, but due to the depression of intestinal barrier function.

Indexed as

adipokine secretiongut microbiotalipopolysaccharidepeptidoglycanvisceral adipocyte

Identifiers

PMID25759521
PMCPMC4345181
OpenAlexW1970847772

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.