Evidence map›Paper›PMID 41201767›Full record

ArticleArchives of pharmacal research2025

Salvianolic acid A enhances T

Jiayang Wu, Kui Liu, Jinqian Song, Lihua Huang, Jiahong Gao, Fei Li, Tao Pang

Abstract read
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In one paragraph

Article in Archives of pharmacal research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jiayang WuState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Kui LiuState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Jinqian SongState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Lihua HuangState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Jiahong GaoState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Fei LiState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China. lifei@cpu.edu.cn.ORCID http://orcid.org/0000-0001-8721-5183
Tao PangState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, People's Republic of China. tpang@cpu.edu.cn.ORCID http://orcid.org/0000-0001-5420-2060

Funding

National Natural Science Foundation of China 81973512National Natural Science Foundation of China 82174010National Natural Science Foundation of China 82322072
6 · The paper itself

Abstract

Salvianolic acid A (SAA), a major water-soluble bioactive compound extracted from Salvia miltiorrhiza, has been extensively studied for its diverse pharmacological properties in cerebrovascular diseases. However, its immunomodulatory effects on lymphocytes in stroke remain incompletely understood. This study systematically investigated the therapeutic efficacy and underlying mechanisms of SAA in a murine model of transient middle cerebral artery occlusion (tMCAO). Early administration of SAA (20 mg/kg) to ischemic stroke (IS) mice demonstrated neuroprotective effects, characterized by reduced infarct volume and improved behavioral outcomes, alongside creating a T

Indexed as

Caffeic AcidsImmunologic FactorsIschemic StrokeLactatesNeuroprotective AgentsT-Lymphocytes, RegulatoryAnimalsCore Binding Factor Alpha 2 SubunitDisease Models, AnimalForkhead Transcription FactorsInfarction, Middle Cerebral ArteryMaleMiceMice, Inbred C57BLCaffeic AcidsCore Binding Factor Alpha 2 SubunitForkhead Transcription FactorsFoxp3 protein, mouseImmunologic FactorsLactatesNeuroprotective Agentssalvianolic acid AImmunomodulatorIschemic strokeRUNX1/CBFβ complexSalvianolic acid ATreg cells

Identifiers

What OpenQuestion holds

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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.