Evidence map›Paper›PMID 30816496›Full record

ArticleMolecular medicine reports2019

Astaxanthin ameliorates renal interstitial fibrosis and peritubular capillary rarefaction in unilateral ureteral obstruction.

Jin Zhao, Meixia Meng, Jinhua Zhang, Lili Li, Xiaojing Zhu, Li Zhang, Chang Wang, Ming Gao

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Uremic Myopathy and Mitochondrial Dysfunction in Kidney Disease.International journal of molecular sciences · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

8 authors at 1 institution in 1 country.

Jin ZhaoDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Meixia MengDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Jinhua ZhangDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Lili LiDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Xiaojing ZhuDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Li ZhangDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Chang WangDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Ming GaoDepartment of Nephrology, Xi'an No. 4 Hospital, Xi'an, Shaanxi 710004, P.R. China.
Wuhan No. 7 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loss of peritubular capillaries is a notable feature of progressive renal interstitial fibrosis. Astaxanthin (ASX) is a natural carotenoid with various biological activities. The present study aimed to evaluate the effect of ASX on unilateral ureteral obstruction (UUO)‑induced renal fibrosis in mice. For that purpose, mice were randomly divided into five treatment groups: Sham, ASX 100 mg/kg, UUO, UUO + ASX 50 mg/kg and UUO + ASX 100 mg/kg. ASX was administered to the mice for 7 or 14 days following UUO. The results demonstrated that UUO‑induced histopathological changes in the kidney tissue were prevented by ASX. Renal function was improved by ASX treatment, as evidenced by decreased blood urea nitrogen and serum creatinine levels. Furthermore, the extent of renal fibrosis and collagen deposition induced by UUO was suppressed by ASX. The levels of collagen I, fibronectin and α‑smooth muscle actin were increased by UUO in mice or by transforming growth factor (TGF)‑β1 treatment in NRK‑52E cells, and were reduced by ASX administration. In addition, ASX inhibited the UUO‑induced decrease in peritubular capillary density by upregulating vascular endothelial growth factor and downregulating thrombospondin 1 levels. Inactivation of the TGF‑β1/Smad signaling pathway was involved in the anti‑fibrotic mechanism of ASX in UUO mice and TGF‑β1‑treated NRK‑52E cells. In conclusion, ASX attenuated renal interstitial fibrosis and peritubular capillary rarefaction via inactivation of the TGF‑β1/Smad signaling pathway.

Indexed as

AnimalsBiomarkersBiopsyCell LineDisease Models, AnimalFibrinolytic AgentsFibrosisKidney DiseasesMaleMiceMicrovascular RarefactionRatsSignal TransductionSmad ProteinsTransforming Growth Factor beta1Ureteral ObstructionastaxanthineBiomarkersFibrinolytic AgentsSmad ProteinsTransforming Growth Factor beta1Vascular Endothelial Growth Factor AXanthophylls

Identifiers

PMID30816496
PMCPMC6423568
OpenAlexW2916253731

What OpenQuestion holds

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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.