Evidence map›Paper›PMID 30534570›Full record

ArticleJournal of diabetes research2018

Artificially Cultivated

Chao Wang, Xiao-Xia Hou, Hong-Liang Rui, Li-Jing Li, Jing Zhao, Min Yang, Li-Jun Sun, Hong-Rui Dong, Hong Cheng, Yi-Pu Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

33 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Research Progress of Pyroptosis in Diabetic Kidney Disease.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Research Progress ofJournal of inflammation research · 2023
    Review
  17. Review
  18. Review
  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

10 authors at 1 institution in 1 country.

Chao WangDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Xiao-Xia HouDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Hong-Liang RuiDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Li-Jing LiDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Jing ZhaoDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Min YangDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Li-Jun SunDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Hong-Rui DongDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Hong ChengDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.ORCID 0000-0002-7908-3333
Yi-Pu ChenDivision of Nephrology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.ORCID 0000-0002-5079-4334
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsIt is known that chronic low-grade inflammation contributes to the initiation and development of both diabetes and diabetic nephropathy (DN), so we designed this study to investigate the role of P2X7R and NLRP3 inflammasome in DN pathogenesis and the antagonistic effects of artificially cultivated

methodsA rat model of DN caused by high-fat-diet feeding and low-dose streptozotocin injection and a mouse podocyte injury model induced by high-glucose (HG) stimulation were established, and the intervention effects of ACOS on them were observed. The biological parameters of serum and urine and the pathological manifestations of kidney tissue were examined. The expression of mRNA and protein of P2X7R and NLRP3 inflammasome (NLRP3, ASC, and caspase-1) and downstream effectors (IL-1

resultsThe DN rats showed to have developed insulin resistance, elevated fasting blood glucose, increased urinary protein excretion, and serum creatinine level as well as corresponding glomerular pathological alterations including podocyte damages. ACOS significantly antagonized the above changes. The experiments

conclusionOur research work suggests that P2X7R and NLRP3 inflammasome are involved in the pathogenesis of DN, and ACOS can effectively inhibit the high expression of P2X7R and the activation of NLRP3 inflammasome, which may contribute to the therapeutic effects of

Indexed as

CordycepsMedicine, Chinese TraditionalAnimalsApoptosisDiabetic NephropathiesInflammasomesInsulin ResistanceMaleMiceNLR Family, Pyrin Domain-Containing 3 ProteinPodocytesRatsRats, Sprague-DawleyReactive Oxygen SpeciesReceptors, Purinergic P2X7InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinReactive Oxygen SpeciesReceptors, Purinergic P2X7

Identifiers

PMID30534570
PMCPMC6252193
OpenAlexW2899668023

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.