Evidence map›Paper›PMID 29142252›Full record

ArticleScientific reports2017

Gallic Acid Reduces Blood Pressure and Attenuates Oxidative Stress and Cardiac Hypertrophy in Spontaneously Hypertensive Rats.

Li Jin, Zhe Hao Piao, Simei Sun, Bin Liu, Gwi Ran Kim, Young Mi Seok, Ming Quan Lin, Yuhee Ryu, Sin Young Choi, Hae Jin Kee and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 101 citations in OpenAlex.

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  16. Life (Basel, Switzerland) · 2022
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  18. ACS omega · 2022
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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

11 authors at 5 institutions in 2 countries.

Li JinHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea.
Zhe Hao PiaoDepartment of Cardiology, The Second Hospital of Jilin University, Changchun, Jilin, 130041, China.
Simei SunHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea.
Bin LiuDepartment of Cardiology, The Second Hospital of Jilin University, Changchun, Jilin, 130041, China.
Gwi Ran KimHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea.
Young Mi SeokNational Development Institute of Korean Medicine, Hwarang-ro, Gyeongsan-si, Gyeongsangbuk-do, Republic of Korea.
Ming Quan LinYanbian University Hospital, 1327, Juzi road, Jilin Yanbian, China.
Yuhee RyuHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea.
Sin Young ChoiHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea.
Hae Jin KeeHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea. sshjkee@empas.com.
Myung Ho JeongHeart Research Center of Chonnam National University Hospital, Gwangju, 61469, Republic of Korea. myungho@chollian.net.
Chonnam National University Hospital · KRSecond Affiliated Hospital of Jilin University · CNJilin Medical University · CNNational Development Institute of Korean Medicine · KRYanbian University Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gallic acid (GA) has been reported to have beneficial effects on cancer, vascular calcification, and diabetes-induced myocardial dysfunction. We hypothesized that GA controls hypertension via oxidative stress response regulation in an animal model for essential hypertension. Spontaneously hypertensive rats (SHRs) were administered GA for 16 weeks. GA treatment lowered elevated systolic blood pressure in SHRs through the inhibition of vascular contractility and components of the renin-angiotensin II system. In addition, GA administration reduced aortic wall thickness and body weight in SHRs. In SHRs, GA attenuated left ventricular hypertrophy and reduced the expression of cardiac-specific transcription factors. NADPH oxidase 2 (Nox2) and GATA4 mRNA expression was induced in SHR hearts and angiotensin II-treated H9c2 cells; this expression was downregulated by GA treatment. Nox2 promoter activity was increased by the synergistic action of GATA4 and Nkx2-5. GA seems to regulate oxidative stress by inhibiting the DNA binding activity of GATA4 in the rat Nox2 promoter. GA reduced the GATA4-induced Nox activity in SHRs and angiotensin II-treated H9c2 cells. GA administration reduced the elevation of malondialdehyde levels in heart tissue obtained from SHRs. These findings suggest that GA is a potential therapeutic agent for treating cardiac hypertrophy and oxidative stress in SHRs.

Indexed as

Angiotensin IIAnimalsBlood PressureBlood Pressure DeterminationCardiomegalyGallic AcidGATA4 Transcription FactorGene Expression RegulationHeartHomeobox Protein Nkx-2.5HumansHypertensionMaleNADPH Oxidase 2Oxidative StressRatsAngiotensin IIGallic AcidGata4 protein, ratGATA4 Transcription FactorHomeobox Protein Nkx-2.5NADPH Oxidase 2Nkx2-5 protein, rat

Identifiers

PMID29142252
PMCPMC5688141
OpenAlexW2767557912

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.