Evidence map›Paper›PMID 37198412›Full record

ArticleActa pharmacologica Sinica2023

A novel small-molecular CCR5 antagonist promotes neural repair after stroke.

Qing-Lin Wu, Li-Yuan Cui, Wen-Yu Ma, Sha-Sha Wang, Zhao Zhang, Zhong-Ping Feng, Hong-Shuo Sun, Shi-Feng Chu, Wen-Bin He, Nai-Hong Chen

Open access · greenAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  10. Targeting angiogenesis and white matter repair for enhanced functional recovery after acute ischemic stroke: A focus on the roles of glial cells.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
  11. Article
  12. Review
  13. Article
  14. Astrocytic BEST1 can serve as a target for functional recovery after ischemic stroke.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
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  20. Observational
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 5 institutions in 2 countries.

Qing-Lin WuClinical Pharmacology Institute, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Li-Yuan CuiState Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia Medica, Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China.
Wen-Yu MaClinical Pharmacology Institute, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Sha-Sha WangClinical Pharmacology Institute, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Zhao ZhangState Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia Medica, Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China.
Zhong-Ping FengDepartment of Physiology, Temerty Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada.
Hong-Shuo SunDepartment of Physiology, Temerty Faculty of Medicine, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada.
Shi-Feng ChuState Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia Medica, Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China. chushifeng@imm.ac.cn.
Wen-Bin HeShanxi Key Laboratory of Chinese Medicine Encephalopathy, Shanxi University of Chinese Medicine, Taiyuan, 030024, China. hewb@sxtcm.edu.cn.
Nai-Hong ChenClinical Pharmacology Institute, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China. chennh@imm.ac.cn.
Guangzhou University of Chinese Medicine · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNCanada Research Chairs · CAShanxi University of Traditional Chinese Medicine · CNUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokine receptor 5 (CCR5) is one of the main co-receptors of HIV-1, and has been found to be a potential therapeutic target for stroke. Maraviroc is a classic CCR5 antagonist, which is undergoing clinical trials against stroke. As maraviroc shows poor blood-brain barrier (BBB) permeability, it is of interest to find novel CCR5 antagonists suitable for neurological medication. In this study we characterized the therapeutic potential of a novel CCR5 antagonist A14 in treating ischemic stroke mice. A14 was discovered in screening millions compounds in the Chemdiv library based on the molecular docking diagram of CCR5 and maraviroc. We found that A14 dose-dependently inhibited the CCR5 activity with an IC

Indexed as

CCR5 Receptor AntagonistsIschemic StrokeNeuroblastomaStrokeAnimalsHumansMaravirocMiceMolecular Docking SimulationReceptors, CCR5CCR5 protein, humanCCR5 Receptor AntagonistsMaravirocReceptors, CCR5CCR5 antagonistchemokine receptor 5CKLF1CREB signalingischemic strokeneural repair

Identifiers

PMID37198412
PMCPMC10545720
OpenAlexW4376876901

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.