Evidence map›Paper›PMID 35501375›Full record

ArticleExperimental & molecular medicine2022

Suberoylanilide hydroxamic acid suppresses axonal damage and neurological dysfunction after subarachnoid hemorrhage via the HDAC1/HSP70/TDP-43 axis.

Kui Luo, Zhifei Wang, Kai Zhuang, Shishan Yuan, Fei Liu, Aihua Liu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. TDP-43: unveiling the hidden key to cellular fate decisions.Cell communication and signaling : CCS · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. A Novel Drosophila-based Drug Repurposing Platform Identified Fingolimod As a Potential Therapeutic for TDP-43 Proteinopathy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  8. Review
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Kui LuoDepartment of Neurosurgery, The Third Xiangya Hospital, Central South University, 410013, Changsha, China.
Zhifei WangDepartment of Neurosurgery, The Third Xiangya Hospital, Central South University, 410013, Changsha, China.
Kai ZhuangDepartment of Neurosurgery, The Third Xiangya Hospital, Central South University, 410013, Changsha, China.
Shishan YuanMedical College, Hunan Normal University, 410000, Changsha, China.
Fei LiuDepartment of Neurosurgery, The Third Xiangya Hospital, Central South University, 410013, Changsha, China. doctorlf@126.com.
Aihua LiuDepartment of Neurosurgery, The Third Xiangya Hospital, Central South University, 410013, Changsha, China. liuaihuadoctor@163.com.
Third Xiangya Hospital · CNBeijing Institute of Neurosurgery · CNCentral South University · CNHunan Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased focus has been placed on the role of histone deacetylase inhibitors as crucial players in subarachnoid hemorrhage (SAH) progression. Therefore, this study was designed to expand the understanding of SAH by exploring the downstream mechanism of the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) in SAH. The expression of TDP-43 in patients with SAH and rat models of SAH was measured. Then, western blot analysis, immunofluorescence staining, and transmission electron microscope were used to investigate the in vitro effect of TDP-43 on a neuronal cell model of SAH established by oxyhemoglobin treatment. Immunofluorescence staining and coimmunoprecipitation assays were conducted to explore the relationship among histone deacetylase 1 (HDAC1), heat shock protein 70 (HSP70), and TDP-43. Furthermore, the in vivo effect of HDAC1 on SAH was investigated in rat models of SAH established by endovascular perforation. High expression of TDP-43 in the cerebrospinal fluid of patients with SAH and brain tissues of rat models of SAH was observed, and TDP-43 accumulation in the cytoplasm and the formation of inclusion bodies were responsible for axonal damage, abnormal nuclear membrane morphology, and apoptosis in neurons. TDP-43 degradation was promoted by the HDAC1 inhibitor SAHA via the acetylation of HSP70, alleviating SAH, and this effect was verified in vivo in rat models. In conclusion, SAHA relieved axonal damage and neurological dysfunction after SAH via the HSP70 acetylation-induced degradation of TDP-43, highlighting a novel therapeutic target for SAH.

Indexed as

Subarachnoid HemorrhageAnimalsApoptosisDNA-Binding ProteinsHistone Deacetylase 1Histone Deacetylase InhibitorsHSP70 Heat-Shock ProteinsHydroxamic AcidsOxyhemoglobinsRatsRats, Sprague-DawleyVorinostatDNA-Binding ProteinsHdac1 protein, ratHistone Deacetylase 1Histone Deacetylase InhibitorsHSP70 Heat-Shock ProteinsHydroxamic AcidsOxyhemoglobinsVorinostat

Identifiers

PMID35501375
PMCPMC9535006
OpenAlexW4225272243

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LicenceCC BY
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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.