Evidence map›Paper›PMID 26097534›Full record

ArticleInternational journal of clinical and experimental pathology2015

Protective effects of calcitriol on diabetic nephropathy are mediated by down regulation of TGF-β1 and CIP4 in diabetic nephropathy rat.

Rui Yu, Jiangfeng Mao, Ye Yang, Yuanyuan Zhang, Yanyan Tian, Jun Zhu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. A broad look into the future of systemic sclerosis.Therapeutic advances in musculoskeletal disease · 2022
    Review
  4. Article
  5. Review
  6. Article
  7. Shared and distinct mechanisms of fibrosis.Nature reviews. Rheumatology · 2019
    Review
  8. Article
  9. Veterinary world · 2019
    Article
  10. Review
  11. Regulatory Effect of 1,25(OH)2D3 on TGF-International journal of endocrinology · 2019
    Article
  12. Article
  13. 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

6 authors at 2 institutions in 1 country.

Rui YuDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University Urumqi 830054, China.
Jiangfeng MaoDepartment of Endocrinology, Peking Union Medical College Hospital Beijing 100730, China.
Ye YangDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University Urumqi 830054, China.
Yuanyuan ZhangDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University Urumqi 830054, China.
Yanyan TianDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University Urumqi 830054, China.
Jun ZhuDepartment of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University Urumqi 830054, China.
Xinjiang Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the protective effects of calcitriol on diabetic nephropathy by modulating the expressions of transforming growth factor-beta 1 (TGF-β1) and Cdc42 interacting protein-4 (CIP4).

methodsStreptozotocin-induced diabetic nephropathy rats (n=36) were randomly divided into control group (control-H, control-M, control-L) and calcitriol group (calcitriol-H, calcitriol-M, calcitriol-L). The expression of TGF-β1 gradually decreased in control-H, control-M and control-L subgroups by injection of different virus vectors. Peanut oil and calcitriol were given to control and calcitriol group, respectively. The expressions of TGF-β1 and CIP4 in kidney, the pathology, and the renal function and lipid profiles were compared between control and calcitriol treatment groups.

resultsIn the control group, the higher level of TGF-β1 was associated with more severe glomerular pathology (P<0.05). There is a positive correlation between the expression of CIP4 and TGF-β1. Control-H subgroup had significant more severe kidney disease, higher levels of cholesterol, triglyceride, blood glucose, blood urea nitrogen (BUN) and creatinine (Cr) than control-M and control-L subgroups. After calcitriol treatment, the expression of TGF-β1 and CIP4 were significantly decreased compared to the corresponding control subgroups (all P<0.05). Renal fibrosis and pathological changes were markedly improved. The levels of cholesterol, triglyceride, blood glucose, BUN and Cr were significantly reduced (P<0.05).

conclusionCalcitriol may protect diabetic nephropathy from fibrosis via inhibition of TGF-β1 and CIP4.

Indexed as

AnimalsBiomarkersBlood Urea NitrogenCalcitriolDiabetes Mellitus, ExperimentalDiabetic NephropathiesDown-RegulationFibrosisHumansKidneyMaleMicrotubule-Associated ProteinsMinor Histocompatibility AntigensProtective AgentsRandom AllocationRatsBiomarkersCalcitriolMicrotubule-Associated ProteinsMinor Histocompatibility AntigensProtective AgentsTransforming Growth Factor beta1Trip10 protein, ratcalcitriolCdc42 interacting protein-4 (CIP4)Diabetic nephropathytransforming growth factor beta 1 (TGF-β1)

Identifiers

PMID26097534
PMCPMC4466921
OpenAlexW2394966378

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.