Evidence map›Paper›PMID 31803758›Full record

ArticleFrontiers in cardiovascular medicine2019

Activation of the Human Angiotensin-(1-12)-Chymase Pathway in Rats With Human Angiotensinogen Gene Transcripts.

Carlos M Ferrario, Jessica VonCannon, Sarfaraz Ahmad, Kendra N Wright, Drew J Roberts, Hao Wang, Tomohisa Yamashita, Leanne Groban, Che Ping Cheng, James F Collawn and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 12% 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, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  4. Internalization of Angiotensin-(1-12) in Adult Retinal Pigment Epithelial-19 Cells.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2023
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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

12 authors at 2 institutions in 1 country.

Carlos M FerrarioDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Jessica VonCannonDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Sarfaraz AhmadDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Kendra N WrightDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Drew J RobertsDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Hao WangDepartment of Anesthesia, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Tomohisa YamashitaDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Leanne GrobanDepartment of Anesthesia, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Che Ping ChengSection on Cardiovascular Center, Wake Forest School of Medicine, Winston-Salem, NC, United States.
James F CollawnDepartment of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham School of Medicine, Birmingham, AL, United States.
Louis J Dell'ItaliaDivision of Cardiovascular Disease, University of Alabama at Birmingham School of Medicine, Birmingham, AL, United States.
Jasmina VaragicDepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Wake Forest University · USUniversity of Alabama at Birmingham · US

Funding

Vaso-Hormonal Mechanisms in HypertensionP01HL051952 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI GROBAN, LEANNE · 1994 to 2019
$34.8M
Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
NCATS NIH HHS UL1 TR001420NHLBI NIH HHS P01 HL051952NIDDK NIH HHS P30 DK079626
6 · The paper itself

Abstract

Angiotensin-(1-12) [Ang-(1-12)], an alternate substrate for tissue angiotensin II (Ang II) formation, underscores the importance of alternative renin-independent pathway(s) for the generation of angiotensins. Since renin enzymatic activity is species-specific, a transgenic model of hypertension due to insertion of the human angiotensinogen (AGT) gene in Sprague Dawley rats allowed for characterizing the contribution of a non-renin dependent mechanism for Ang II actions in their blood and heart tissue. With this in mind, we investigated whether TGR(hAGT)L1623 transgenic rats express the human sequence of Ang-(1-12) before and following a 2-week oral therapy with the type I Ang II receptor (AT1-R) antagonist valsartan. Plasma and cardiac expression of angiotensins, plasma renin activity, cardiac angiotensinogen, and chymase protein and the enzymatic activities of chymase, angiotensin converting enzyme (ACE) and ACE2 were determined in TGR(hAGT)L1623 rats given vehicle or valsartan. The antihypertensive effect of valsartan after 14-day treatment was associated with reduced left ventricular wall thickness and augmented plasma concentrations of angiotensin I (Ang I) and Ang II; rat and human concentrations of angiotensinogen or Ang-(1-12) did not change. On the other hand, AT

Indexed as

cardiac hypertrophychymasehypertensionrenin angiotensin systemtransgenic rats

Identifiers

PMID31803758
PMCPMC6872498
OpenAlexW2987739296

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.