Evidence map›Paper›PMID 29862242›Full record

ArticleAnnals of translational medicine2018

Traditional Chinese medicine Qiliqiangxin attenuates phenylephrine-induced cardiac hypertrophy via upregulating PPARγ and PGC-1α.

Rong-Rong Gao, Xiao-Dong Wu, Hui-Min Jiang, Yu-Jiao Zhu, Yan-Li Zhou, Hai-Feng Zhang, Wen-Ming Yao, Yong-Qin Li, Xin-Li Li

Open access · hybridAbstract read
In one paragraph

Article in Annals of translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

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  13. Annals of translational medicine · 2020
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  16. Novel PGC-1Oxidative medicine and cellular longevity · 2020
    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

9 authors at 4 institutions in 1 country.

Rong-Rong GaoDepartment of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Xiao-Dong WuDepartment of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Hui-Min JiangClinical Laboratory Center, Beijing Hospital of Traditional Chinese Medicine, Beijing 100010, China.
Yu-Jiao ZhuCardiac Regeneration and Ageing Lab, Institute of Cardiovascular Sciences, Experimental Center of Life Sciences, School of Life Science, Shanghai University, Shanghai 200444, China.
Yan-Li ZhouDepartment of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Hai-Feng ZhangDepartment of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Wen-Ming YaoDepartment of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Yong-Qin LiCardiac Regeneration and Ageing Lab, Institute of Cardiovascular Sciences, Experimental Center of Life Sciences, School of Life Science, Shanghai University, Shanghai 200444, China.
Xin-Li LiDepartment of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Nanjing Medical University · CNJiangsu Province Hospital · CNShanghai University · CNBeijing Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical study has demonstrated that the traditional Chinese medicine Qiliqiangxin (QLQX) has protective effects on heart failure. Phenylephrine (PE) is an important inducing factor for cardiac hypertrophy and our previous studies have showed that QLQX attenuates PE-induced cardiac hypertrophy. Besides, QLQX protects against cardiac remodeling after myocardial infarction via activating PPARγ. However, whether QLQX prevents PE-induced cardiac hypertrophy through PPARγ and its coactivator PGC-1α is still unknown.

methodsThe effects of QLQX were investigated based on PE induced cardiac hypertrophy mouse models. Echocardiography and hematoxylin-eosin (HE) staining were used to determine cardiac function and cross-sectional area, respectively. Quantitative real time PCR (qRT-PCR) was used to determine ANP and BNP expressions. Based on primary neonatal rat ventricular cardiomyocytes (NRVMs) treated with PE, the cell size and expressions of ANP and BNP were determined by immunofluorescent staining and qRT-PCR, respectively. In addition, western blot was used to determine PPARγ and PGC-1α expressions.

resultsIn present study, we confirmed that QLQX could significantly attenuate cardiac hypertrophy in mice treated with PE. Then we showed that PPARγ and PGC-1α were downregulated in PE-induced cardiac hypertrophy, and QLQX could block the decrease of PPARγ and PGC-1α both

conclusionsOur study suggested that QLQX prevents from PE-induced cardiac hypertrophy by activating PPARγ and its coactivator PGC-1α.

Indexed as

Cardiac hypertrophyPGC-1αPPARγQiliqiangxin (QLQX)

Identifiers

PMID29862242
PMCPMC5952020
OpenAlexW2799333949

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.