Evidence map›Paper›PMID 30213138›Full record

ArticleNutrients2018

Dose-Related Antihypertensive Properties and the Corresponding Mechanisms of a Chicken Foot Hydrolysate in Hypertensive Rats.

Anna Mas-Capdevila, Zara Pons, Amaya Aleixandre, Francisca I Bravo, Begoña Muguerza

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Alcalase-Based Chickpea (Foods (Basel, Switzerland) · 2024
    Article
  5. Review
  6. Review
  7. Article
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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 3 institutions in 1 country.

Anna Mas-CapdevilaNutrigenomics Research Group, Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, 43007 Tarragona, Spain. anna.mas@urv.cat.
Zara PonsNutrigenomics Research Group, Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, 43007 Tarragona, Spain. zara.pons@urv.cat.
Amaya AleixandreDepartment of Pharmacology, School of Medicine, Universidad Complutense de Madrid, 28040 Madrid, Spain. amaya@med.ucm.es.
Francisca I BravoNutrigenomics Research Group, Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, 43007 Tarragona, Spain. franciscaisabel.bravo@urv.cat.ORCID 0000-0002-6468-3088
Begoña MuguerzaNutrigenomics Research Group, Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, 43007 Tarragona, Spain. begona.muguerza@urv.cat.ORCID 0000-0001-7384-8588
Universitat Rovira i Virgili · ESTechnological Center of Nutrition and Health · ESUniversidad Complutense de Madrid · ES

Funding

Ministerio de Economía, Industria y Competitividad, Gobierno de España AGL-2013-40707-RMinisterio de Economía, Industria y Competitividad, Gobierno de España AGL-2016-77105-R
6 · The paper itself

Abstract

The antihypertensive properties of different doses of a chicken foot hydrolysate, Hpp11 and the mechanisms involved in this effect were investigated. Spontaneously hypertensive rats (SHR) were administered water, Captopril (50 mg/kg) or Hpp11 at different doses (25, 55 and 85 mg/kg), and the systolic blood pressure (SBP) was recorded. The SBP of normotensive Wistar-Kyoto (WKY) rats administered water or Hpp11 was also recorded. Additionally, plasmatic angiotensin-converting enzyme (ACE) activity was determined in the SHR administered Hpp11. Moreover, the relaxation caused by Hpp11 in isolated aortic rings from Sprague-Dawley rats was evaluated. Hpp11 exhibited antihypertensive activity at doses of 55 and 85 mg/kg, with maximum activity 6 h post-administration. At this time, no differences were found between these doses and Captopril. Initial SBP values of 55 and 85 mg/kg were recovered 24 or 8 h post-administration, respectively, 55 mg/kg being the most effective dose. At this dose, a reduction in the plasmatic ACE activity in the SHR was found. However, Hpp11 did not relax the aortic ring preparations. Therefore, ACE inhibition could be the mechanism underlying Hpp11 antihypertensive effect. Remarkably, Hpp11 did not modify SBP in WKY rats, showing that the decreased SBP effect is specific to the hypertensive state.

Indexed as

Angiotensin-Converting Enzyme InhibitorsAnimalsAntihypertensive AgentsBlood PressureChickensDisease Models, AnimalDose-Response Relationship, DrugFootHypertensionMaleProtein HydrolysatesRats, Inbred SHRRats, Inbred WKYTissue ExtractsVasodilationVasodilator AgentsAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsProtein HydrolysatesTissue ExtractsVasodilator AgentsACE-inhibitory activityangiotensin-converting enzymebioactive peptidesendothelial dysfunctionhypertensionprotein hydrolysate

Identifiers

PMID30213138
PMCPMC6164708
OpenAlexW2892040976

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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.