Evidence map›Paper›PMID 30013094›Full record

ArticleScientific reports2018

Amelioratory Effects of Testosterone Propionate on Age-related Renal Fibrosis via Suppression of TGF-β1/Smad Signaling and Activation of Nrf2-ARE Signaling.

Guoliang Zhang, Yunxiao Kang, Chenming Zhou, Rui Cui, Min Jia, Shen Hu, Xiaoming Ji, Jiayu Yuan, Huixian Cui, Geming Shi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
  4. Article
  5. NRF2 Dysregulation and Therapeutic Insights Across Chronic Kidney Diseases.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Male reproductive ageing: a radical road to ruin.Human reproduction (Oxford, England) · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Hormonal Regulation of Renal Fibrosis.Life (Basel, Switzerland) · 2022
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

10 authors at 3 institutions in 1 country.

Guoliang ZhangDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, PR China.
Yunxiao KangDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, PR China.
Chenming ZhouDepartment of electron microscopy center, Hebei Medical University, Shijiazhuang, 050017, PR China.
Rui CuiDepartment of Human Anatomy, Hebei Medical University, Shijiazhuang, 050017, PR China.
Min JiaDepartment of urology, Hebei Civil Affairs General Hospital, Xingtai, 054000, PR China.
Shen HuDepartment of urology, Handan Second hospital, Handan, 056001, PR China.
Xiaoming JiDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, PR China.
Jiayu YuanDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, PR China.
Huixian CuiDepartment of electron microscopy center, Hebei Medical University, Shijiazhuang, 050017, PR China.
Geming ShiDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, PR China. shigeming@163.com.
Hebei Medical University · CNHandan College · CNHebei General Hospital · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81200252National Natural Science Foundation of China (National Science Foundation of China) 82100252
6 · The paper itself

Abstract

Androgen plays a pivotal role in the progression of renal fibrosis. However, whether exogenous androgen treatment to aged male rats can improve the age-related renal fibrosis was not explored. In our study, the changes of morphological structure, renal fibrosis, ultrastructure and renal function, the expressions of extracellular matrix (ECM), matrix metalloproteinases (MMPs) and its tissue inhibitors of metalloproteinases (TIMPs), the expressions of tumor growth factor β1 (TGF-β1)/Smad signaling and oxidative stress parameters as well as nuclear factor erythroid 2-related factor 2-antioxidant response element (Nrf2-ARE) signaling were tested in kidney of aged male Wistar rats after subcutaneous testosterone propionate (TP, 2 mg/kg/d, 84-day) injection. Aged rats showed significantly renal histopathological changes, increased renal fibrosis, increased thickening of the glomerular basement membrane and the Bowman's capsule basement membrane, declined renal functional, increased ECM, lower expressions of MMP-2 and MMP-9 and higher expressions of TIMP-1 and TIMP-2 in renal tissues and higher expressions of TGF-β1/Smad signaling, as well as lower expressions of Nrf2-ARE signaling compared to young rats. TP treatment significantly improved age-related above indexes. These results suggested that TP supplement may alleviate age-related renal fibrosis via suppression of TGF-β1/Smad signaling and activation of Nrf2-ARE signaling in aged rats.

Indexed as

AgingAnimalsAntioxidant Response ElementsFibrosisGene Expression RegulationKidneyMaleMicroscopy, Electron, TransmissionModels, AnimalNF-E2-Related Factor 2RatsRats, WistarSignal TransductionSmad ProteinsTestosterone PropionateTransforming Growth Factor beta1Nfe2l2 protein, ratNF-E2-Related Factor 2Smad ProteinsTestosterone PropionateTgfb1 protein, ratTransforming Growth Factor beta1

Identifiers

PMID30013094
PMCPMC6048025
OpenAlexW2823905884

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.