Evidence map›Paper›PMID 23052352›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2012

Euterpe oleracea Mart.-derived polyphenols prevent endothelial dysfunction and vascular structural changes in renovascular hypertensive rats: role of oxidative stress.

Cristiane Aguiar da Costa, Paola Raquel Braz de Oliveira, Graziele Freitas de Bem, Lenize Costa Reis Marins de Cavalho, Dayane Teixeira Ognibene, Andréa Fernandes Emiliano da Silva, Samuel Dos Santos Valença, Karla Maria Pereira Pires, Pergentino José da Cunha Sousa, Roberto Soares de Moura and 1 more

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Alpinia zerumbet leaf extract reverses hypertension and improves adverse remodeling in the left ventricle and aorta in spontaneously hypertensive rats.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  6. Article
  7. Article
  8. International journal of molecular sciences · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Effects of Lyophilized Açaí (Animals : an open access journal from MDPI · 2023
    Article
  13. Article
  14. Açaí (Nutrients · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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.

Cristiane Aguiar da CostaDepartment of Pharmacology, Institute of Biology, Rio de Janeiro State University, Av. 28 de Setembro, 87, Rio de Janeiro, 20 551-030, Brazil.
Paola Raquel Braz de Oliveira
Graziele Freitas de Bem
Lenize Costa Reis Marins de Cavalho
Dayane Teixeira Ognibene
Andréa Fernandes Emiliano da Silva
Samuel Dos Santos Valença
Karla Maria Pereira Pires
Pergentino José da Cunha Sousa
Roberto Soares de Moura
Angela Castro Resende

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The consumption of polyphenol-rich foods is associated with a decreased risk of mortality from cardiovascular diseases. Previously, we have demonstrated that the stone of Euterpe oleracea Mart. (açaí) from the Amazon region exerts vasodilator and antioxidant actions. This study examined the effect of açaí stone extract (ASE) on the vascular functional and structural changes and oxidative stress associated with the two-kidney, one-clip (2K-1C) renovascular hypertension. 2K-1C and sham-operated rats were treated with ASE 200 mg/kg/day (or vehicle) for 40 days. Blood pressure was measured by tail plethysmography, and the vascular reactivity was evaluated in the rat isolated mesenteric arterial bed. Mesenteric protein expression of endothelial nitric oxide synthase (eNOS), superoxide dismutase 1 and 2 (SOD1 and SOD2), metalloproteinase 2 (MMP-2), and tissue inhibitor of MMPs (TIMP)-1 was assessed by Western blot; oxidative damage and antioxidant activity by spectrophotometry; MMP-2 levels by gelatin zymography; and structural changes by histological analysis. ASE prevented 2K-1C hypertension and the reduction of acetylcholine-induced vasodilation. The increased levels of malondialdehyde and carbonyl protein were reduced by ASE. SOD, catalase, and glutathione peroxidase activities and the expressions of SOD1 and SOD2, eNOS, and TIMP-1 were decreased in 2K-1C rats and recovered by ASE. In 2K-1C rats, ASE prevented vascular remodeling and the increased expression/levels of MMP-2. These findings indicate that ASE produces antihypertensive effect and prevents the endothelial dysfunction and vascular structural changes in 2K-1C hypertension, probably through mechanisms involving antioxidant effects, NOS activation, and inhibition of MMP-2 activation.

Indexed as

AnimalsAntioxidantsArecaceaeBlood PressureBlotting, WesternDisease Models, AnimalEndothelium, VascularGene Expression RegulationHypertension, RenovascularMaleMatrix Metalloproteinase 2Nitric Oxide Synthase Type IIIOxidative StressPlant ExtractsPlethysmographyPolyphenolsAntioxidantsMatrix Metalloproteinase 2Nitric Oxide Synthase Type IIIPlant ExtractsPolyphenols

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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.