Evidence map›Paper›PMID 37991543›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2024

Tanshinone IIA is superior to paricalcitol in ameliorating tubulointerstitial fibrosis through regulation of VDR/Wnt/β-catenin pathway in rats with diabetic nephropathy.

Jing-Yi Zeng, Yu Wang, Fu-Yuan Hong, Miao Miao, Yu-Ying Jiang, Zi-Xuan Qiao, Yun-Tao Wang, Xiao-Rong Bao

Open access · hybridAbstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Wnt/β-Catenin Signaling in Diabetic Complications: Mechanisms and Therapeutic Potential.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

8 authors at 2 institutions in 1 country.

Jing-Yi ZengDepartment of Nephrology, Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Yu WangDepartment of Nephrology, Jinshan Hospital of Fudan University, Shanghai, China.
Fu-Yuan HongDepartment of Nephrology, Fujian Provincial Hospital, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Miao MiaoDepartment of Nephrology, Jinshan Hospital of Fudan University, Shanghai, China.
Yu-Ying JiangDepartment of Nephrology, Jinshan Hospital of Fudan University, Shanghai, China.
Zi-Xuan QiaoDepartment of Nephrology, Jinshan Hospital of Fudan University, Shanghai, China.
Yun-Tao WangDepartment of Nephrology, Jinshan Hospital of Fudan University, Shanghai, China.
Xiao-Rong BaoDepartment of Nephrology, Jinshan Hospital of Fudan University, Shanghai, China. xrbao19660108@163.com.
Jinshan Hospital of Fudan University · CNFujian Provincial Hospital · CN

Funding

talent introduction project 2022YJ07
6 · The paper itself

Abstract

Glomerulosclerosis and tubulointerstitial fibrosis (TIF) are closely involved in the development of diabetic nephropathy (DN). Moreover, the development of TIF is closely related to epithelial-to-mesenchymal transition (EMT). Tanshinone IIA (Tan) has various pharmacological effects, especially the anti-fibrotic effect. And it is mainly used in the clinical treatment of cardiovascular diseases. Currently, the protective effect of Tan on DN and its possible mechanism have not been clearly elucidated. Our previous studies illustrated that Tan could improve the EMT of HK-2 cells induced by high glucose by regulating the vitamin D receptor (VDR)/Wnt/β-catenin pathway. Here, we collected demographic information and laboratory results from the National Health and Nutrition Examination Survey (NHANES) database in order to investigate the relationship between VD and DN. Then, we established a DN model and treated DN rats with Tan and paricalcitol (Par) for 6 weeks. We subsequently compared the changes in general condition, renal function, pathological changes, and TIF-related protein expression levels of control rats, DN rats induced by STZ, DN rats with Tan at 5.4 mg/kg, DN rats with Tan at 10.8 mg/kg, and DN rats with Par at 0.054 µg/kg, to explore the effect and mechanism of Tan and Par on DN rats. The results showed that VD had a protective effect against DN in diabetic patients. And we found that Tan had a protective effect on renal fibrosis in DN rats, which was superior to Par in improving the symptoms of "three more and one less," reducing fasting blood glucose level, improving renal index, BUN/SCr, and UACR, reducing histopathological damage of kidney, and improving the expression of fibrosis-related proteins in kidney tissue by regulating VDR/Wnt/β-catenin pathway. Tan was superior to Par in ameliorating tubulointerstitial fibrosis by regulating VDR/Wnt/β-catenin pathway in rats with diabetic nephropathy.

Indexed as

AbietanesDiabetes Mellitus, ExperimentalDiabetic NephropathiesErgocalciferolsFibrosisRats, Sprague-DawleyReceptors, CalcitriolWnt Signaling PathwayAnimalsbeta CateninKidneyMaleRatsAbietanesbeta CateninErgocalciferolsparicalcitolReceptors, CalcitrioltanshinoneDiabetic nephropathyParicalcitolTanshinone IIATubulointerstitial fibrosisVDR/Wnt/β-catenin pathway

Identifiers

PMID37991543
PMCPMC11111530
OpenAlexW4388904150

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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.