Evidence map›Paper›PMID 29982808›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2018

Exacerbation of Type 1 Diabetes in Perinatally Genistein Exposed Female Non-Obese Diabetic (NOD) Mouse Is Associated With Alterations of Gut Microbiota and Immune Homeostasis.

Guannan Huang, Joella Xu, Dunpeng Cai, Shi-You Chen, Tamas Nagy, Tai L Guo

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
  7. Xenoestrogen Effects on the Gut Microbiome.Current opinion in endocrine and metabolic research · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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 1 institution in 1 country.

Guannan HuangDepartment of Environmental Health Sciences, College of Public Health.
Joella XuDepartment of Veterinary Biosciences and Diagnostic Imaging, College of Veterinary Medicine.
Dunpeng CaiDepartment of Physiology and Pharmacology, College of Veterinary Medicine.
Shi-You ChenDepartment of Physiology and Pharmacology, College of Veterinary Medicine.
Tamas NagyDepartment of Pathology, College of Veterinary Medicine, University of Georgia, Athens, Georgia 30602.
Tai L GuoDepartment of Veterinary Biosciences and Diagnostic Imaging, College of Veterinary Medicine.
University of Georgia · US

Funding

Exacerbation of type 1 diabetes in mice by bisphenol A and genisteinR21ES024487 · NIEHS · UNIVERSITY OF GEORGIA · PI GUO, TAI L · 2014 to 2015
$411k
Engineering probiotics to biosynthesize natural substances for microbiome-brain researchR41AT009523 · NCCIH · HGG RESEARCH, LLC · PI GUO, TAI L, WU, SHENG-CHENG · 2017 to 2017
$225k
NCCIH NIH HHS R41 AT009523NIEHS NIH HHS R21 ES024487
6 · The paper itself

Abstract

Despite various hypothesized benefits of dietary isoflavone genistein (GEN) from soy-based products, many questions surrounding GEN's immunotoxic effects, especially during perinatal exposure, have yet to be answered. The objective of the study was to determine if there existed a sex-specific effect of GEN on type 1 diabetes (T1D) following perinatal exposure. We exposed offspring of non-obese diabetic (NOD) mice to GEN per oral at a physiological dose (20 mg/kg body weight) from embryonic day 7 to postnatal day (PND) 21. In female offspring, perinatal GEN dosing significantly increased the incidence of T1D at early time points, and the exacerbation was associated with decreased serum levels of interleukin (IL)-10, IgG2a, and IgM. In male offspring dosed with GEN, a decrease in serum IgG1 was also observed. Flow cytometric analysis in females suggested an increased pro-inflammatory splenic CD5+CD24- and CD4-CD8+ cell counts, while both %T cells and %CD4+ T cells were significantly decreased in males, suggesting an anti-inflammatory effect. Gut microbiota (GMB) analysis indicated that fecal microbiota from PND 90 female offspring exhibited an increased level of Enterobacteriales (suggesting a pro-inflammatory response), while the similar changes were not found in PND 30 females. Moreover, RNA sequencing showed that intestinal α-defensin expression was down-regulated in GEN-treated females, supporting a pro-inflammatory response. However, perinatal GEN administration perturbed GMB toward an anti-inflammatory response in PND 90 males. Taken together, a strong sex-specific effect was found in the perinatal GEN exposure window, and the T1D exacerbation in NOD females was associated with GMB-related immunomodulatory mechanisms.

Indexed as

HomeostasisAnimalsAnimals, NewbornBlood GlucoseCytokinesDiabetes Mellitus, Type 1FemaleGastrointestinal MicrobiomeGenisteinMice, Inbred NODPregnancyPrenatal Exposure Delayed EffectsSex FactorsBlood GlucoseCytokinesGenistein

Identifiers

PMID29982808
PMCPMC6154270
OpenAlexW2883566830

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.