Evidence map›Paper›PMID 38200148›Full record

ArticleActa pharmacologica Sinica2024

DsbA-L ameliorates renal aging and renal fibrosis by maintaining mitochondrial homeostasis.

Ming Yang, Yan Liu, Shi-Lu Luo, Chong-Bin Liu, Na Jiang, Chen-Rui Li, Hao Zhao, Ya-Chun Han, Wei Chen, Li Li and 1 more

Open access · greenAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.7field-weighted citation impact, top 6% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Gastrodin as a nephroprotective agent: Molecular docking-based modulation of oxidative stress, fibrosis, and inflammation.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2026
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  8. Review
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  10. Article
  11. High-mobility group box 1 in acute kidney injury.Frontiers in pharmacology · 2025
    Review
  12. 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

11 authors at 2 institutions in 1 country.

Ming Yang *Department of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Yan Liu *Department of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Shi-Lu LuoDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Chong-Bin LiuDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Na JiangDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Chen-Rui LiDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Hao ZhaoDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Ya-Chun HanDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Wei ChenDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Li LiDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Lin SunDepartment of Nephrology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China. sunlin@csu.edu.cn.
Central South University · CNSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal fibrosis is the final pathological change in renal disease, and aging is closely related to renal fibrosis. Mitochondrial dysfunction has been reported to play an important role in aging, but the exact mechanism remains unclear. Disulfide-bond A oxidoreductase-like protein (DsbA-L) is mainly located in mitochondria and plays an important role in regulating mitochondrial function and endoplasmic reticulum (ER) stress. However, the role of DsbA-L in renal aging has not been reported. In this study, we showed a reduction in DsbA-L expression, the disruption of mitochondrial function and an increase in fibrosis in the kidneys of 12- and 24-month-old mice compared to young mice. Furthermore, the deterioration of mitochondrial dysfunction and fibrosis were observed in DsbA-L

Indexed as

Glutathione TransferaseKidneyKidney DiseasesMitochondriaAgingAnimalsFibrosisHomeostasisMiceMitochondrial DiseasesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktdisulfide-bond A oxidoreductase-like protein DsbA-L, mouseGlutathione TransferasePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktagingDsbA-LFlt4kidneymitochondria

Identifiers

PMID38200148
PMCPMC10943083
OpenAlexW4390701479

What OpenQuestion holds

Textmetadata
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.