Evidence map›Paper›PMID 36558932›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

A Class I HDAC Inhibitor BG45 Alleviates Cognitive Impairment through the CaMKII/ITPKA/Ca

Jingyun Liu, Chenghong Zhang, Jiale Wang, Yufei Huang, Di Shen, Yingqiu Hu, Haiying Chu, Xuebin Yu, Liyuan Zhang, Haiying Ma

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

10 authors at 1 institution in 1 country.

Jingyun LiuDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Chenghong ZhangDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Jiale WangDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Yufei HuangDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Di ShenDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Yingqiu HuDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Haiying ChuDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Xuebin YuDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Liyuan ZhangDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Haiying MaDepartment of Histology and Embryology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.ORCID 0000-0002-1314-7816
Dalian Medical University · CN

Funding

National Natural Science Foundation of China 21974017Natural Science Foundation of Liaoning Province 20180550468
6 · The paper itself

Abstract

Alzheimer's disease (AD) seriously endangers the health and life of elderly individuals worldwide. However, despite all scientific efforts, at the moment there are no effective clinical treatment options for AD. In this work, the effect of the class I histone deacetylase inhibitor (HDACI) BG45 on synapse-related proteins was investigated in primary neurons from APP/PS1 transgenic mice. The results showed that BG45 can upregulate the expression of synaptotagmin-1 (SYT-1) and neurofilament light chain (NF-L) in primary neurons. In vivo, the APPswe/PS1dE9 (APP/PS1) transgenic mice were treated with BG45 (30 mg/kg) daily for 12 days. Behavioral testing of BG45-treated APP/PS1 mice showed improvements in learning and memory. BG45 can alleviate damage to the dendritic spine and reduce the deposition of Aβ. Similar to the in vitro results, synapse-related proteins in the prefrontal cortex were increased after BG45 treatment. Proteomic analysis results highlighted the differences in the biological processes of energy metabolism and calmodulin regulation in APP/PS1 mice with or without BG45 treatment. Further verification demonstrated that the effect of BG45 on synapses and learning and memory may involve the CaMKII/ITPKA/Ca

Indexed as

Alzheimer’s diseasehistone deacetylase inhibitorproteomicssynaptic plasticity

Identifiers

PMID36558932
PMCPMC9786203
OpenAlexW4310154838

What OpenQuestion holds

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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.