Evidence map›Paper›PMID 33145109›Full record

ArticleInternational journal of hypertension2020

Aliskiren Reduces the Adrenal Zona Glomerulosa Apoptosis and Autophagy in Wistar Rats with 2K1C Hypertension.

Veronica S de Matos, Ana L R do Nascimento, Priscila G Pereira, Kíssila Rabelo, Cherley B V Andrade, Alan C N Moraes, Camila Salata, Victor H V de O Araújo, Bianca Torres Ciambarella, Aline Bonfim Vieira and 3 more

Abstract read
In one paragraph

Article in International journal of hypertension, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Veronica S de MatosLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-9954-1007
Ana L R do NascimentoLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Priscila G PereiraLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Kíssila RabeloLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Cherley B V AndradeTranslational Endocrinology Laboratory, Institute of Biophysics Carlos Chagas Filho, Health Sciences Center, UFRJ, Rio de Janeiro, Brazil.
Alan C N MoraesInstitute of Biology, UFF, Rio de Janeiro, RJ, Brazil.
Camila SalataLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Victor H V de O AraújoLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Bianca Torres CiambarellaLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Aline Bonfim VieiraRoss University School of Veterinary Medicine, Biomedical Department, Basseterre, Saint Kitts and Nevis.ORCID https://orcid.org/0000-0002-2479-6774
Luciana Lontro AlvesLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Jemima F R da SilvaLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-7867-3131
Jorge J de CarvalhoLaboratory of Ultrastructure and Tecidual Biology, Institute of Biology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-9426-6381

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertension is a disease classified as primary or secondary, manifested not only by elevation of blood pressure but also involved in structural and functional changes of target organs. Renal artery stenosis is a leading factor of secondary hypertension, and its progress is associated with overactivation of the renin-angiotensin-aldosterone system (RAAS). Aliskiren is a renin inhibiting drug that suppresses RAAS and culminates in decreased renin release, plasma angiotensin II concentration, and inhibition of aldosterone secretion. In this sense, the aim of the present study was to analyze the structural and ultrastructural morphophysiology of the adrenal glomerular zone, after treatment with aliskiren in Wistar rats with 2K1C hypertension. Parameters as structure and ultrastructure of the adrenal glomerular zone, cellular apoptosis, nuclear cell proliferation, and AT1 receptor expression were analyzed by immunostaining and electron microscopy. Our results showed that the hypertensive animals treated with aliskiren presented a reestablishment of AT1 receptor expression and decrease in apoptosis and autophagy. In addition, treatment with aliskiren improves the cell aspects in the adrenal glomerular zone, evidenced by ultrastructural analysis through preserved nuclei and well-developed mitochondria. Therefore, our evidence suggests that aliskiren has a beneficial effect on the adrenal glomerular zone remodeling in animals with renovascular hypertension.

Identifiers

PMID33145109
PMCPMC7596424

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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.