Evidence map›Paper›PMID 31506648›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2019

Stimulation of the ACE2/Ang-(1-7)/Mas axis in hypertensive pregnant rats attenuates cardiovascular dysfunction in adult male offspring.

Amanda S M Bessa, Érika F Jesus, Allancer D C Nunes, Carolina N R Pontes, Ismaley S Lacerda, Jaqueline M Costa, Elisângela J Souza, Ruy S Lino-Júnior, Manoel F Biancardi, Fernanda C A Dos Santos and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 63 citations in OpenAlex.

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  13. ACE2: a key modulator of the renin-angiotensin system and pregnancy.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  14. Early-Life Origins of Metabolic Syndrome: Mechanisms and Preventive Aspects.International journal of molecular sciences · 2021
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  17. Novel therapeutics for the treatment of hypertension and its associated complications: peptide- and nonpeptide-based strategies.Hypertension research : official journal of the Japanese Society of Hypertension · 2021
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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

15 authors at 1 institution in 1 country.

Amanda S M BessaDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Érika F JesusDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Allancer D C NunesDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Carolina N R PontesDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Ismaley S LacerdaDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Jaqueline M CostaDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Elisângela J SouzaDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Ruy S Lino-JúniorInstituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Manoel F BiancardiDepartamento de Histologia, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Fernanda C A Dos SantosDepartamento de Histologia, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Gustavo R PedrinoDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Diego B ColugnatiDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Renata Mazaro-CostaDepartamento de Farmacologia, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Elizabeth P MendesDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil.
Carlos H CastroDepartamento de Ciências Fisiológicas, Universidade Federal de Goiás, Goiânia, GO, 74.690-900, Brazil. castro@ufg.br.
Universidade Federal de Goiás · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate whether treatment with diminazene aceturate (DIZE), a putative ACE2 activator, or with angiotensin-(1-7) during pregnancy could attenuate the development of cardiovascular dysfunction in the adult offspring of spontaneously hypertensive rats (SHRs). For this, pregnant SHRs received DIZE or Ang-(1-7) throughout gestation. The systolic blood pressure (SBP) was measured in the male offspring from the 6th to16th weeks of age by tail-cuff plethysmography. Thereafter, the left ventricular contractile function and coronary reactivity were evaluated by the Langendorff technique. Samples of the left ventricles (LVs) and kidneys were collected for histology and western blot assay in another batch of adult rat offspring. Maternal treatment with DIZE or Ang-(1-7) during pregnancy attenuated the increase in SBP in adult offspring. In addition, both DIZE and Ang-(1-7) treatments reduced the cardiomyocyte diameter and fibrosis deposition in the LV, and treatment with Ang-(1-7) also reduced the fibrosis deposition in the kidneys. Maternal treatment with DIZE, as well as Ang-(1-7), improved the coronary vasodilation induced by bradykinin in isolated hearts from adult offspring. However, no difference was observed in the contractile function of the LVs of these animals. The expression levels of AT1 and Mas receptors, ACE, ACE2, SOD, and catalase in the LV were not modified by maternal treatment with Ang-(1-7), but this treatment elicited a reduction in AT2 expression. These data show that treatment with DIZE or Ang-(1-7) during gestation promoted beneficial effects of attenuating hypertension and cardiac remodeling in adult offspring.

Indexed as

Angiotensin-Converting Enzyme 2Angiotensin IAnimalsBlood PressureCardiovascular DiseasesDiminazeneEnzyme ActivatorsFemaleHeartHypertension, Pregnancy-InducedKidneyMaleMyocardial ContractionPeptide FragmentsPeptidyl-Dipeptidase APregnancyAce2 protein, ratAngiotensin-Converting Enzyme 2Angiotensin Iangiotensin I (1-7)Diminazenediminazene aceturateEnzyme ActivatorsPeptide FragmentsPeptidyl-Dipeptidase AACE2Angiotensin-(1–7)Cardiac fibrosisCardiac hypertrophyDiminazene aceturateHypertension

Identifiers

PMID31506648
OpenAlexW2973075551

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.