Evidence map›Paper›PMID 37248536›Full record

ArticleStem cell research & therapy2023

Intravenous injection of human umbilical cord-derived mesenchymal stem cells ameliorates not only blood glucose but also nephrotic complication of diabetic rats through autophagy-mediated anti-senescent mechanism.

Xinyue Li, Le Guo, Jingan Chen, Haowei Liang, Yi Liu, Wei Chen, Li Zhou, Letian Shan, Hui Wang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
10.8field-weighted citation impact, top 1% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  10. Multidimensional mechanisms of quercetin in diabetic kidney disease.Frontiers in cell and developmental biology · 2025
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  18. The therapeutic effect of mesenchymal stem cells in diabetic kidney disease.Journal of molecular medicine (Berlin, Germany) · 2024
    Review
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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

9 authors at 2 institutions in 1 country.

Xinyue Li *School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Le Guo *School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Jingan Chen *School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Haowei LiangSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Yi LiuSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Wei ChenCancer Institute of Integrated Traditional Chinese and Western Medicine, Key Laboratory of Cancer Prevention and Therapy Combining Traditional Chinese and Western Medicine of Zhejiang Province, Zhejiang Academy of Traditional Chinese Medicine, Tongde Hospital of Zhejiang Province, 234 Gucui Road, Hangzhou, 310012, Zhejiang, China.
Li ZhouThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China. zhouli@zcmu.edu.cn.
Letian ShanThe First Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, China. letian.shan@zcmu.edu.cn.
Hui WangSchool of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China. wh@zcmu.edu.cn.ORCID 0000-0003-0108-8254
Zhejiang Chinese Medical University · CNTongde Hospital of Zhejiang Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic nephropathy (DN) is one of the most severe complications of diabetes mellitus, which is characterized by early occurrence of albuminuria and end-stage glomerulosclerosis. Senescence and autophagy of podocytes play an important role in DN development. Human umbilical cord-derived mesenchymal stem cells (hucMSCs) have potential in the treatment of diabetes and its complications. However, the role of hucMSCs in the treatment of DN and the underlying mechanism remain unclear.

methodsIn vivo, a streptozotocin-induced diabetic male Sprague Dawley rat model was established to determine the renoprotective effect of hucMSCs on DN by biochemical analysis, histopathology, and immunohistochemical staining of renal tissues. And the distribution of hucMSCs in various organs in rats within 168 h was analyzed. In vitro, CCK8 assay, wound healing assay, and β-galactosidase staining were conducted to detect the beneficial effects of hucMSCs on high glucose-induced rat podocytes. Real-time PCR and western blot assays were applied to explore the mechanism of action of hucMSCs.

resultsThe in vivo data revealed that hucMSCs were distributed into kidneys and significantly protected kidneys from diabetic damage. The in vitro data indicated that hucMSCs improved cell viability, wound healing, senescence of the high glucose-damaged rat podocytes through a paracrine action mode. Besides, the altered expressions of senescence-associated genes (p16, p53, and p21) and autophagy-associated genes (Beclin-1, p62, and LC3) were improved by hucMSCs. Mechanistically, hucMSCs protected high glucose-induced injury in rat podocytes by activating autophagy and attenuating senescence through the AMPK/mTOR pathway.

conclusionsIn conclusion, hucMSCs might be a promising therapeutic strategy for the clinical treatment of DN-induced renal damages.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic NephropathiesMesenchymal Stem CellsAnimalsAutophagyBlood GlucoseHumansInjections, IntravenousMaleRatsRats, Sprague-DawleyUmbilical CordBlood GlucoseAMPK/mTOR signalingDiabetic nephropathyHuman umbilical cord-derived mesenchymal stem cellsParacrine effectPodocytes

Identifiers

PMID37248536
PMCPMC10228071
OpenAlexW4378650404

What Socratic 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 Socratic graph.