Evidence map›Paper›PMID 31253938›Full record

ArticleActa pharmacologica Sinica2019

Cardioprotective mechanisms of salvianic acid A sodium in rats with myocardial infarction based on proteome and transcriptome analysis.

Dan Jia, Cheng-Zhong Zhang, Yan Qiu, Xiao-Fei Chen, Lin Jia, Alex F Chen, Yi-Feng Chai, Zhen-Yu Zhu, Jin Huang, Chuan Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 5 institutions in 1 country.

Dan Jia *School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.
Cheng-Zhong Zhang *School of Pharmacy, Second Military Medical University, Shanghai, 200433, China.
Yan Qiu *Department of Pharmacy, Pudong New Area People's Hospital Affiliated to Shanghai University of Medicine & Health Sciences, Shanghai, 201200, China.
Xiao-Fei ChenSchool of Pharmacy, Second Military Medical University, Shanghai, 200433, China.
Lin JiaDepartment of Endodontics, Panyu Stomatological Hospital (Guangdong Provincial Stomatological Hospital) Affiliated to Southern Medical University, Guangzhou, 511400, China.
Alex F ChenSchool of Pharmacy, Second Military Medical University, Shanghai, 200433, China.
Yi-Feng ChaiSchool of Pharmacy, Second Military Medical University, Shanghai, 200433, China.
Zhen-Yu ZhuSchool of Pharmacy, Second Military Medical University, Shanghai, 200433, China.
Jin HuangDepartment of Pharmacy, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 200437, China. john70550@aliyun.com.
Chuan ZhangSchool of Pharmacy, Second Military Medical University, Shanghai, 200433, China. zhangchuan@smmu.edu.cn.
Second Military Medical University · CNGuangdong Province Stomatological Hospital · CNPudong New Area People's Hospital · CNShanghai University · CNYueyang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic heart diseases (IHDs) cause great morbidity and mortality worldwide, necessitating effective treatment. Salvianic acid A sodium (SAAS) is an active compound derived from the well-known herbal medicine Danshen, which has been widely used for clinical treatment of cardiovascular diseases in China. This study aimed to confirm the cardioprotective effects of SAAS in rats with myocardial infarction and to investigate the underlying molecular mechanisms based on proteome and transcriptome profiling of myocardial tissue. The results showed that SAAS effectively protected against myocardial injury and improved cardiac function. The differentially expressed proteins and genes included important structural molecules, receptors, transcription factors, and cofactors. Functional enrichment analysis indicated that SAAS participated in the regulation of actin cytoskeleton, phagosome, focal adhesion, tight junction, apoptosis, MAPK signaling, and Wnt signaling pathways, which are closely related to cardiovascular diseases. SAAS may exert its cardioprotective effect by targeting multiple pathways at both the proteome and transcriptome levels. This study has provided not only new insights into the pathogenesis of myocardial infarction but also a road map of the cardioprotective molecular mechanisms of SAAS, which may provide pharmacological evidence to aid in its clinical application.

Indexed as

AnimalsBiomarkersCardiotonic AgentsGene Expression ProfilingHeartLactatesMaleMyocardial InfarctionMyocardiumProtein Interaction MappingProteomeProteomicsRats, Sprague-DawleySignal TransductionTranscriptome3,4-dihydroxyphenyllactic acidBiomarkersCardiotonic AgentsLactatesProteomecardioprotectivemyocardial infarctionproteomesalvianic acid A sodiumTraditional Chinese medicinetranscriptome

Identifiers

PMID31253938
PMCPMC7468552
OpenAlexW2954526190

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.