Evidence map›Paper›PMID 34026879›Full record

ArticleFrontiers in cardiovascular medicine2021

UPLC-MS-Based Serum Metabolomics Reveals Potential Biomarkers of Ang II-Induced Hypertension in Mice.

Shaying Yang, Zhiwei Wang, Mengting Guo, Mengfan Du, Xin Wen, Li Geng, Fan Yu, Liangliang Liu, Yanting Li, Lei Feng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2021. 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
0.2field-weighted citation impact, top 48% 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, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. ProbioticsmSystems · 2023
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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 1 institution in 1 country.

Shaying YangLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Zhiwei WangLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Mengting GuoLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Mengfan DuLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Xin WenLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Li GengLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Fan YuLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Liangliang LiuLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Yanting LiLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Lei FengLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Tingting ZhouLaboratory of Cardiovascular Research, School of Medicine, Jiangnan University, Wuxi, China.
Jiangnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertension is caused by polygenic inheritance and the interaction of various environmental factors. Abnormal function of the renin-angiotensin-aldosterone system (RAAS) is closely associated with changes in blood pressure. As an essential factor in the RAAS, angiotensin II (Ang II) contributes to vasoconstriction and inflammatory responses. However, the effects of overproduction of Ang II on the whole body-metabolism have been unclear. In this study, we established a hypertensive mouse model by micro-osmotic pump perfusion of Ang II, and the maximum systolic blood pressure reached 140 mmHg after 2 weeks. By ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry, the metabolites in the serum of hypertensive model and control mice were analyzed. Partial least squares discriminant analysis (PLS-DA) in both positive and negative ionization modes showed clear separation of the two groups. Perfusion of Ang II induced perturbations of multiple metabolic pathways in mice, such as steroid hormone biosynthesis and galactose metabolism. Tandem mass spectrometry revealed 40 metabolite markers with potential diagnostic value for hypertension. Our data indicate that non-targeted metabolomics can reveal biochemical pathways associated with Ang II-induced hypertension. Although researches about the clinical use of these metabolites as potential biomarkers in hypertension is still needed, the current study improves the understanding of systemic metabolic response to sustained release of Ang II in hypertensive mice, providing a new panel of biomarkers that may be used to predict blood pressure fluctuations in the early stages of hypertension.

Indexed as

angiotensin IIbiomarkershypertensionLC-MSmetabolomicsmiceserum metabolites

Identifiers

PMID34026879
PMCPMC8131677
OpenAlexW3157210092

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.