Evidence map›Paper›PMID 35707274›Full record

ReviewOxidative medicine and cellular longevity2022

SS-31, a Mitochondria-Targeting Peptide, Ameliorates Kidney Disease.

Yuexin Zhu, Manyu Luo, Xue Bai, Jicui Li, Ping Nie, Bing Li, Ping Luo

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  10. Mitochondria as a Therapeutic Target in Metabolic Disorders.Mini reviews in medicinal chemistry · 2026
    Review
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  13. Article
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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

7 authors at 1 institution in 1 country.

Yuexin ZhuDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0001-8367-0277
Manyu LuoDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0002-3081-2793
Xue BaiDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0002-9158-1087
Jicui LiDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0002-8052-4060
Ping NieDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0003-2029-4432
Bing LiDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0001-7640-9468
Ping LuoDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, China.ORCID https://orcid.org/0000-0003-0029-0872
Second Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria are essential for eukaryotic cell activity and function, and their dysfunction is associated with the development and progression of renal diseases. In recent years, there has been a rapid development in mitochondria-targeting pharmacological strategies as mitochondrial biogenesis, morphology, and function, as well as dynamic changes in mitochondria, have been studied in disease states. Mitochondria-targeting drugs include nicotinamide mononucleotide, which supplements the NAD+ pool; mitochondria-targeted protective compounds, such as MitoQ; the antioxidant coenzyme, Q10; and cyclosporin A, an inhibitor of the mitochondrial permeability transition pore. However, traditional drugs targeting mitochondria have limited clinical applications due to their inability to be effectively absorbed by mitochondria

Indexed as

Kidney DiseasesMitochondrial Permeability Transition PoreAnimalsAntioxidantsMitochondriaPeptidesReactive Oxygen SpeciesAntioxidantsMitochondrial Permeability Transition PorePeptidesReactive Oxygen Species

Identifiers

PMID35707274
PMCPMC9192202
OpenAlexW4282002355

What OpenQuestion 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 OpenQuestion graph.