Evidence map›Paper›PMID 31196042›Full record

ArticleBMC complementary and alternative medicine2019

The protective effects of polysaccharide extract from Xin-Ji-Er-Kang formula on Ang II-induced HUVECs injury, L-NAME-induced hypertension and cardiovascular remodeling in mice.

Ling Ding, Pan Cheng, Li Wang, Juan Hu, Yong-Xue Zhang, Guo-Wei Cai, Guang-Yao Huang, Shan Gao

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 13 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

8 authors at 1 institution in 1 country.

Ling DingDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Pan ChengDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Li WangDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Juan HuDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Yong-Xue ZhangDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Guo-Wei CaiDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Guang-Yao HuangDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China.
Shan GaoDepartment of Pharmacology, Basic Medical College, Anhui Medical University, Hefei, China. gaoshan@ahmu.edu.cn.
Anhui Medical University · CN

Funding

Anhui Medical University Foundation for Middle-aged and Young Scientist Leaders of Disciplines in Science 201324National Natural Science Foundation of China 81373774National Natural Science Foundation of China 81873126National Science and Technology Major Projects for Major New Drugs Innovation and Development 2017ZX09301012
6 · The paper itself

Abstract

backgroundXin-Ji-Er-Kang (XJEK) is a Chinese herbal formula, which has been reported to exert effective protection against cardiovascular diseases, including hypertension and myocarditis.

methodsCultured human umbilical vascular endothelial cells (HUVECs) were treated with angiotensin II (Ang II) and different concentrations of aqueous layer extracts (AqE). Subsequently nitric oxide (NO) and endothelial nitric oxide synthase (eNOS) expression levels were detected. In addition, fifty Kunming mice were randomized into control, Nω-nitro-L-arginine methyl ester (L-NAME), L-NAME+AqE, L-NAME+XJEK and L-NAME+fosinopril treatment groups. Following 8 weeks of treatment, the cardiac hemodynamic index was measured, relaxation of the aorta was examined and pathological changes were observed. Colorimetric analysis and enzyme linked immunosorbent assay (ELISA) were applied to determine the relevant indicators in plasma and cardiac tissues.

resultsThe in vitro study results demonstrated that AqE could preserve endothelial function (NO, 21.05 ± 2.03 vs. 8.64 ± 0.59; eNOS, 1.08 ± 0.17 vs.0.73 ± 0.06). In addition, the in vivo results demonstrated that compared with the control group, treatment with AqE could enhance a high hemodynamic state (left ventricular systolic pressure, 116.76 ± 9.96 vs.114.5 ± 15.16), improve endothelial function (NO, 7.98 ± 9.64 vs. 1.66 ± 3.11; eNOS, 19.78 ± 3.18 vs.19.38 ± 3.85), suppress oxidative stress (OS) (superoxide dismutase, 178.17 ± 13.78 vs. 159.38 ± 18.86; malondialdehyde, 0.77 ± 0.13 vs.1.25 ± 0.36) and reverse cardiovascular remodeling.

conclusionPolysaccharide from XJEK exerts protective effects against Ang II-induced injury in HUVECs and L-NAME-induced hypertension in mice and the underlying mechanism may be attributed to improving endothelial dysfunction, OS and the inflammation status in mice.

Indexed as

Angiotensin IIAnimalsAortaArginineBlood PressureCytokinesDrug Evaluation, PreclinicalDrugs, Chinese HerbalEndothelial CellsEndothelium, VascularHumansHuman Umbilical Vein Endothelial CellsHypertensionInflammationMaleMalondialdehydeAngiotensin IIArginineCytokinesDrugs, Chinese HerbalMalondialdehydeNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide Synthase Type IIIN,N-dimethylarginineNOS3 protein, humanSuperoxide Dismutasexin-ji-er-kangCardiac remodelingEndothelial dysfunctionHypertensionInflammationOxidative stress

Identifiers

PMID31196042
PMCPMC6567637
OpenAlexW2951116710

What OpenQuestion holds

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LicenceCC BY
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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.