Evidence map›Paper›PMID 32765804›Full record

ArticleOxidative medicine and cellular longevity2020

Sinapic Acid Attenuates Cardiovascular Disorders in Rats by Modulating Reactive Oxygen Species and Angiotensin Receptor Expression.

Maha A Aldubayan, Amira S Ahmed, Ashraf M Emara, Ahmed A Ahmed, Rehab M Elgharabawy

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 23 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

5 authors at 1 institution in 2 countries.

Maha A AldubayanDepartment of Pharmacology & Toxicology, College of Pharmacy, Qassim University, Qassim, Saudi Arabia.ORCID https://orcid.org/0000-0002-3277-1702
Amira S AhmedDepartment of Pharmacology & Toxicology, College of Pharmacy, Qassim University, Qassim, Saudi Arabia.ORCID https://orcid.org/0000-0002-3989-1408
Ashraf M EmaraDepartment of Pharmacology & Toxicology, College of Pharmacy, Qassim University, Qassim, Saudi Arabia.ORCID https://orcid.org/0000-0002-1114-7580
Ahmed A AhmedMedical Research Center, Faculty of Medicine, Qassim University, Qassim, Saudi Arabia.ORCID https://orcid.org/0000-0002-8495-4623
Rehab M ElgharabawyDepartment of Pharmacology & Toxicology, College of Pharmacy, Qassim University, Qassim, Saudi Arabia.ORCID https://orcid.org/0000-0002-4399-8195
Qassim University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main avoidable risk factor for cardiovascular conditions is high blood pressure (hypertension). At global level, hypertension is believed to be responsible for a 54% stroke-related mortality rate and a 47% mortality rate associated with coronary heart disease. It is postulated that sinapic acid (SA) could help in hypertension management because it displays robust antioxidant, antihyperglycemic, and peroxynitrite scavenging effects. To explore this hypothesis, this work examined the effect of SA on oxidative stress and cardiovascular disease in rats with hypertension by comparison against captopril. For this purpose, 50 male rats were used and equally allocated to five groups, namely, normal control, positive control (L-NAME), L-NAME with concomitant captopril administration, L-NAME with concomitant SA administration, and L-NAME with concomitant administration of both SA and captopril. Results showed that, by contrast to control, L-NAME exhibited marked elevation in serum CK-MB, total cholesterol, triglycerides, VLDL-C, LDL-C, Ang II, AT2R, ET-1, and angiopoietin-2; on the other hand, L-NAME exhibited marked reduction in serum HDL-C, superoxide dismutase (SOD) activity, nitric oxide synthase 3 (NOS3), and glutathione (GSH). Furthermore, joint administration of SA and captopril ameliorated hypertension, enhanced cardiovascular function, hindered hyperlipidemia, and decreased oxidative stress and myocardial hypertrophy displayed by rats with hypertension. Based on such findings, better chemopreventive or therapeutic approaches can be devised to manage hypertension and cardiovascular conditions.

Indexed as

AnimalsCardiovascular DiseasesCoumaric AcidsMaleRatsRats, WistarReactive Oxygen SpeciesReceptors, AngiotensinCoumaric AcidsReactive Oxygen SpeciesReceptors, Angiotensinsinapinic acid

Identifiers

PMID32765804
PMCPMC7374234
OpenAlexW3041169115

What OpenQuestion holds

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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.