Evidence map›Paper›PMID 36750199›Full record

ArticlePhysiological reports2023

COVID-19: Understanding the impact of anti-hypertensive drugs and hydroxychloroquine on the ACE1 and ACE2 in lung and adipose tissue in SHR and WKY rats.

Beatriz Santos Geoffroy Corrêa, Silvana de Barros, Julia Braga Vaz, Maria Angelica Peres, Mayara Klimuk Uchiyama, Alexandre Alves da Silva, Luzia Naoko Shinohara Furukawa

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 2 institutions in 2 countries.

Beatriz Santos Geoffroy CorrêaLaboratory of Renal Pathophysiology, Department of Internal Medicine, School of Medicine, University of São Paulo, São Paulo, Brazil.ORCID 0000-0002-0663-9134
Silvana de BarrosHypertension Unit, Renal Division, General Hospital of School of Medicine, University of São Paulo, São Paulo, Brazil.ORCID 0000-0003-0069-8464
Julia Braga VazLaboratory of Renal Pathophysiology, Department of Internal Medicine, School of Medicine, University of São Paulo, São Paulo, Brazil.ORCID 0000-0001-6782-3325
Maria Angelica PeresLaboratory of Renal Pathophysiology, Department of Internal Medicine, School of Medicine, University of São Paulo, São Paulo, Brazil.ORCID 0000-0002-0368-188X
Mayara Klimuk UchiyamaLaboratory of Supramolecular Chemistry & Nanotechnology, Department of Fundamental Chemistry, Institute of Chemistry, University of São Paulo, São Paulo, Brazil.ORCID 0000-0002-6623-9765
Alexandre Alves da SilvaDepartment of Physiology and Biophysics, University of Mississippi Medical Center Jackson, Jackson, Mississippi, USA.ORCID 0000-0003-4504-0607
Luzia Naoko Shinohara FurukawaLaboratory of Renal Pathophysiology, Department of Internal Medicine, School of Medicine, University of São Paulo, São Paulo, Brazil.ORCID 0000-0002-0457-6651
Universidade de São Paulo · BRJackson Memorial Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertensive individuals taking anti-hypertensive drugs from renin-angiotensin system inhibitors may exhibit a more severe evolution of the disease when contracting the SARS-CoV-2 virus (COVID-19 disease) due to potential increases in ACE2 expression. The study investigated ACE1 and ACE2 axes and hydroxychloroquine in the lungs and adipose tissue of male and female normotensive Wistar Kyoto (WKY) and spontaneously hypertensive rats (SHRs). SHRs were treated with losartan (10 mg/kg/day) or captopril (10 mg/kg/day) for 14 days or 7 days with hydroxychloroquine (200 mg/kg/day) in drinking water. WKY rats were also treated for 7 days with hydroxychloroquine. Blood pressure (BP), protein, and mRNA expression of ACE1 and ACE2 were analyzed in serum, adipose, and lung tissues. Losartan and captopril reduced BP in both sexes in SHR, whereas hydroxychloroquine increased BP in WKY rats. Losartan reduced ACE2 in serum and lungs in both sexes and in adipose tissue of male SHRs. Captopril decreased ACE2 protein in the lung of females and in adipose tissue in both sexes of SHRs. Hydroxychloroquine decreased ACE1 and ACE2 proteins in the lungs in both sexes and adipose tissue in male SHRs. In female WKY rats, ACE2 protein was lower only in the lungs and adipose tissue. Losartan effectively inhibited ACE2 in male and captopril in female SHRs. Hydroxychloroquine inhibited ACE2 in male SHRs and female WKY rats. These results further our understanding of the ACE2 mechanism in patients under renin-angiotensin anti-hypertensive therapy and in many trials using hydroxychloroquine for COVID-19 treatment and potential sex differences in response to drug treatment.

Indexed as

COVID-19HypertensionAdipose TissueAngiotensin-Converting Enzyme 2AnimalsAntihypertensive AgentsBlood PressureCaptoprilCOVID-19 Drug TreatmentFemaleHumansHydroxychloroquineLosartanLungMalePeptidyl-Dipeptidase AAngiotensin-Converting Enzyme 2Antihypertensive AgentsCaptoprilHydroxychloroquineLosartanPeptidyl-Dipeptidase AACE2COVID-19hydroxychloroquinelung tissuespontaneously hypertensive rat

Identifiers

PMID36750199
PMCPMC9904959
OpenAlexW4319335944

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.