Evidence map›Paper›PMID 33955513›Full record

ArticleMolecular medicine reports2021

Rapamycin protects against aristolochic acid nephropathy in mice by potentiating mammalian target of rapamycin‑mediated autophagy.

Fan Lin, Yunqi Liu, Lili Tang, Xiaohui Xu, Xueli Zhang, Yifan Song, Bicheng Chen, Yeping Ren, Xiangdong Yang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. The Ginsenoside RgLife (Basel, Switzerland) · 2021
    Article
  5. 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

9 authors at 4 institutions in 1 country.

Fan Lin *Department of Nephrology, Qilu Hospital, Shandong University, Jinan, Shandong 250015, P.R. China.
Yunqi Liu *Department of Nephrology, Qilu Hospital, Shandong University, Jinan, Shandong 250015, P.R. China.
Lili TangClinical Laboratory, Chinese Medical Hospital of Jining, Jining, Shandong 272037, P.R. China.
Xiaohui XuDepartment of Nephrology, Shenzhen University General Hospital, Shenzhen, Guangdong 518055, P.R. China.
Xueli ZhangDepartment of Nephrology, Shenzhen University General Hospital, Shenzhen, Guangdong 518055, P.R. China.
Yifan SongDepartment of Nephrology, Shenzhen University General Hospital, Shenzhen, Guangdong 518055, P.R. China.
Bicheng ChenKey Laboratory of Diagnosis and Treatment of Severe Hepato‑Pancreatic Diseases of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, P.R. China.
Yeping RenDepartment of Nephrology, Shenzhen University General Hospital, Shenzhen, Guangdong 518055, P.R. China.
Xiangdong YangDepartment of Nephrology, Qilu Hospital, Shandong University, Jinan, Shandong 250015, P.R. China.
Shenzhen University · CNQilu Hospital of Shandong University · CNJining Traditional Chinese Medicine Hospital · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy serves a crucial role in the etiology of kidney diseases, including drug‑induced renal impairment, inherited kidney disease, diabetic nephropathy and aristolochic acid nephropathy (AAN) and is, therefore, a potential target for treatment. We previously demonstrated that rapamycin could attenuate AAN in mice; however, the underlying mechanism remains to be elucidated. Therefore, whether the renal protective effect of rapamycin (an autophagy activator) is related to autophagy in aristolochic acid (AA)‑treated mice was of particular interest. The pathophysiological roles of rapamycin were investigated in AA‑induced nephrotoxicity in mice and the mechanisms of rapamycin action were explored by evaluating the modulation of autophagy in rapamycin‑treated mice and cultured renal tubular epithelial cells. Supplementation with rapamycin reversed AA‑induced kidney injury in mice and improved AA‑induced autophagy damage

Indexed as

AnimalsApoptosisAristolochic AcidsAutophagyCell LineDisease Models, AnimalHumansKidney DiseasesMaleMiceMice, Inbred C57BLProtective AgentsSirolimusTOR Serine-Threonine Kinasesaristolochic acid IAristolochic AcidsMTOR protein, humanmTOR protein, mouseProtective AgentsSirolimusTOR Serine-Threonine Kinasesapoptosisaristolochic acid nephropathyautophagymTORrapamycin

Identifiers

PMID33955513
PMCPMC8127069
OpenAlexW3158023810

What OpenQuestion holds

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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.