Evidence map›Paper›PMID 30825261›Full record

ArticleJournal of diabetes investigation2019

Glycine increases glyoxalase-1 function by promoting nuclear factor erythroid 2-related factor 2 translocation into the nucleus of kidney cells of streptozotocin-induced diabetic rats.

Ziwei Wang, Dan Zhao, Lei Chen, Jingjing Li, Geheng Yuan, Guosheng Yang, Hong Zhang, Xiaohui Guo, Junqing Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 28% 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, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Glycine Alleviates HMolecular neurobiology · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. PARK7/DJ-1 as a Therapeutic Target in Gut-Brain Axis Diseases.International journal of molecular sciences · 2022
    Review
  13. Review
  14. 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

9 authors at 1 institution in 1 country.

Ziwei WangEndocrinology, Peking University First Hospital, Beijing, China.
Dan ZhaoEndocrinology, Peking University First Hospital, Beijing, China.
Lei ChenEndocrinology, Peking University First Hospital, Beijing, China.
Jingjing LiEndocrinology, Peking University First Hospital, Beijing, China.
Geheng YuanEndocrinology, Peking University First Hospital, Beijing, China.
Guosheng YangAnimal Center, Peking University First Hospital, Beijing, China.
Hong ZhangEndocrinology, Peking University First Hospital, Beijing, China.
Xiaohui GuoEndocrinology, Peking University First Hospital, Beijing, China.
Junqing ZhangEndocrinology, Peking University First Hospital, Beijing, China.ORCID http://orcid.org/0000-0002-8574-1945
Peking University · CN

Funding

Beijing Municipal Science and Technology Project D17110000281701China National Key R&D Program during the 13th Five-year Plan 2016YFC1305401China National Key R&D Program during the 13th Five-year Plan 2016YFC1305405Clinical Medical Research of Chinese Medical Association 13040700455
6 · The paper itself

Abstract

AIMS/

introductionWe have previously reported that glycine suppresses the advanced glycation end-products signaling pathway and mitigates subsequent oxidative stress in the kidneys of diabetic rats. In the present study, we investigated whether this beneficial effect was associated with upregulation of glyoxalase-1 (Glo1) and activation of the nuclear factor erythroid 2-related factor 2 (Nrf2). MATERIALS AND

methodsBoth healthy rats and streptozotocin-induced diabetic rats were administrated with glycine (1% added to the drinking water) for 12 weeks. The function of Glo1, messenger ribonucleic acid (mRNA) and protein expressions of Nrf2, and markers of oxidative status were measured in the kidneys. The mRNA expressions of other downstream signaling molecules of the Nrf2 pathway were also determined.

resultsThe mRNA and protein expressions, as well as the activity of Glo1, were decreased in the kidneys of diabetic rats, accompanied by diminished glutathione levels. After glycine treatment, these parameters of Glo1 function were markedly increased. Compared with the control group, the levels of Nrf2 mRNA and protein in the total kidney lysis were both markedly elevated in the diabetic group and glycine-treated group. However, the nuclear translocation of Nrf2 was significantly increased in the glycine-treated group than in the diabetic group. In addition, the anti-oxidant capacity and the expressions of other downstream molecules of the Nrf2 signaling pathway were significantly increased after glycine treatment.

conclusionsThe present study shows that glycine might enhance the function of Glo1 and restore anti-oxidant defense by promoting the nuclear translocation of Nrf2, thus inhibiting advanced glycation end-products formation and protecting against renal oxidative stress.

Indexed as

AnimalsCell NucleusDiabetes Mellitus, ExperimentalGene Expression RegulationGlycineKidneyLactoylglutathione LyaseMaleNF-E2-Related Factor 2Protein TransportRatsRats, WistarGlycineLactoylglutathione LyaseNfe2l2 protein, ratNF-E2-Related Factor 2GlycineGlyoxalase-1Nuclear factor erythroid 2-related factor 2

Identifiers

PMID30825261
PMCPMC6717822
OpenAlexW2918344977

What OpenQuestion holds

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LicenceCC BY-NC
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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.