Evidence map›Paper›PMID 30953402›Full record

ArticleJournal of cellular and molecular medicine2019

Rutaecarpine prevents hypertensive cardiac hypertrophy involving the inhibition of Nox4-ROS-ADAM17 pathway.

Si-Yu Zeng, Li Yang, Hui-Qin Lu, Qiu-Jiang Yan, Ling Gao, Xu-Ping Qin

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. 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
1.6field-weighted citation impact, top 16% 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, 31 citations in OpenAlex.

  1. Article
  2. Transmembrane protein 117 knockdown protects against angiotensin-II-induced cardiac hypertrophy.Hypertension research : official journal of the Japanese Society of Hypertension · 2023
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  6. Life (Basel, Switzerland) · 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

6 authors at 4 institutions in 1 country.

Si-Yu ZengDepartment of Drug Clinical Trial, Guangdong Second Provincial General Hospital, Guangzhou, China.ORCID 0000-0003-1185-2658
Li YangLaboratory of Vascular Biology, Institute of Pharmacy and Pharmacology, University of South China, Hengyang, China.
Hui-Qin LuDepartment of Drug Clinical Trial, Guangdong Second Provincial General Hospital, Guangzhou, China.
Qiu-Jiang YanDepartment of Cardiac & Thoracic Surgery, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Ling GaoDepartment of Pharmacy, Guangdong Second Provincial General Hospital, Guangzhou, China.
Xu-Ping QinLaboratory of Vascular Biology, Institute of Pharmacy and Pharmacology, University of South China, Hengyang, China.
Guangdong Provincial Hospital of Traditional Chinese Medicine · CNUniversity of South China · CNGuangdong Provincial People's Hospital · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rutaecarpine attenuates hypertensive cardiac hypertrophy in the rats with abdominal artery constriction (AAC); however, its mechanism of action remains largely unknown. Our previous study indicated that NADPH oxidase 4 (Nox4) promotes angiotensin II (Ang II)-induced cardiac hypertrophy through the pathway between reactive oxygen species (ROS) and a disintegrin and metalloproteinase-17 (ADAM17) in primary cardiomyocytes. This research aimed to determine whether the Nox4-ROS-ADAM17 pathway is involved in the protective action of rutaecarpine against hypertensive cardiac hypertrophy. AAC-induced hypertensive rats were adopted to evaluate the role of rutaecarpine in hypertensive cardiac hypertrophy. Western blotting and real-time PCR were used to detect gene expression. Rutaecarpine inhibited hypertensive cardiac hypertrophy in AAC-induced hypertensive rats. These findings were confirmed by the results of in vitro experiments that rutaecarpine significantly inhibited Ang II-induced cardiac hypertrophy in primary cardiomyocytes. Likewise, rutaecarpine significantly suppressed the Nox4-ROS-ADAM17 pathway and over-activation of extracellular signal-regulated kinase (ERK) 1/2 pathway in the left ventricle of AAC-induced hypertensive rats and primary cardiomyocytes stimulated with Ang II. The inhibition of Nox4-ROS-ADAM17 pathway and over-activation of ERK1/2 might be associated with the beneficial role of rutaecarpine in hypertensive cardiac hypertrophy, thus providing additional evidence for preventing hypertensive cardiac hypertrophy with rutaecarpine.

Indexed as

ADAM17 ProteinAngiotensin IIAnimalsAorta, AbdominalCardiomegalyConstriction, PathologicGene Expression RegulationHumansHypertensionIndole AlkaloidsMAP Kinase Signaling SystemMyocytes, CardiacNADPH Oxidase 4QuinazolinesQuinazolinonesRatsADAM17 ProteinAngiotensin IIIndole AlkaloidsNADPH Oxidase 4QuinazolinesQuinazolinonesReactive Oxygen Speciesrutecarpinea disintegrin and metalloproteinase-17extracellular signal-regulated kinase ½hypertensive cardiac hypertrophyNADPH oxidase 4rutaecarpine

Identifiers

PMID30953402
PMCPMC6533562
OpenAlexW2934596634

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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.