Evidence map›Paper›PMID 32884732›Full record

ArticleFood science & nutrition2020

Effects of a ready-to-eat cereal formula powder on glucose metabolism, inflammation, and gut microbiota in diabetic db/db mice.

Caina Li, Xing Wang, Sujuan Sun, Shuainan Liu, Yi Huan, Rongcui Li, Quan Liu, Hui Cao, Tian Zhou, Lei Lei and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Food science & nutrition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

12 authors at 1 institution in 1 country.

Caina LiState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Xing WangState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Sujuan SunState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Shuainan LiuState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Yi HuanState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Rongcui LiState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Quan LiuState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Hui CaoState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Tian ZhouState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Lei LeiState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Minzhi LiuState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.
Zhufang ShenState Key Laboratory of Bioactive Substances and Functions of Natural Medicines Key Laboratory of Polymorphic Drugs of Beijing Institute of Materia Medica Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China.ORCID https://orcid.org/0000-0003-0690-015X
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cereal formula powder, Zhengda Jingshan (ZDJS), comprises dietary fiber, multivitamins, fine protein, and various cereal ingredients. The present study evaluated the effects of ZDJS on glucose metabolism and explored the corresponding mechanisms in terms of modulating gut microbiota and the fecal metabolome. Type 2 diabetic db/db mice were given ZDJS (1 g/kg) orally twice daily for 55 days, after which glucose metabolism, inflammation, gut microbiota, and fecal metabolomics were assayed. Repeated administration of ZDJS was associated with a trend toward decreasing fasting blood glucose and a 0.12% decrease in hemoglobin A1c (HbA1c), as well as statistically significant increases in the insulin sensitivity index and decreases in serum levels of tumor necrosis factor (TNF-α) and ileum expression of mucin-2. ZDJS also ameliorated the compensatory enlargement of islets and decreased the ratio of the α-cell area to total islet area; however, this amelioration of impaired oral glucose tolerance became less pronounced as treatment continued. In addition, ZDJS remarkably decreased the abundance of phylum Proteobacteria and the phylum ratio of Firmicutes to Bacteroidetes, as well as altered the fecal metabolic profile. Taken together, our findings demonstrate that ZDJS improved glucose metabolism and reduced inflammation in type 2 diabetic db/db mice, which may be associated with a reshaping of the gut microbiome and fecal metabolome in db/db mice. Thus, our study suggests that ZDJS may represent a complementary therapy for patients with type 2 diabetes.

Indexed as

cereal formula powderfecal metabolomeglucose metabolismgut microbiotainflammation

Identifiers

PMID32884732
PMCPMC7455957
OpenAlexW3038488427

What OpenQuestion holds

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Registered trials

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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.