Evidence map›Paper›PMID 40055063›Full record

ArticleAmerican journal of physiology. Cell physiology2025

Transient angiotensin-converting enzyme inhibition confers sex-specific protection against angiotensin II-induced cardiac remodeling.

Alexandra M Garvin, Dana B Floyd, Alexis C Bailey, Merry L Lindsey, Chad C Carroll, Taben M Hale

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2025. 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

6 authors.

Alexandra M GarvinDepartment of Basic Medical Sciences, University of Arizona College of Medicine, Phoenix, Arizona, United States.ORCID 0000-0002-5784-5587
Dana B FloydDepartment of Basic Medical Sciences, University of Arizona College of Medicine, Phoenix, Arizona, United States.
Alexis C BaileyDepartment of Basic Medical Sciences, University of Arizona College of Medicine, Phoenix, Arizona, United States.
Merry L LindseySchool of Graduate Studies, Meharry Medical College, Nashville, Tennessee, United States.ORCID 0000-0002-4090-0391
Chad C CarrollDepartment of Health and Kinesiology, Purdue University, West Lafayette, Indiana, United States.ORCID 0000-0003-0152-5821
Taben M HaleDepartment of Basic Medical Sciences, University of Arizona College of Medicine, Phoenix, Arizona, United States.ORCID 0000-0002-5066-1216

Funding

PHYSIOLOGYT32HL007249 · NHLBI · UNIVERSITY OF ARIZONA · PI Brett A Colson, JOHN P KONHILAS · 1985 to 2026
$12.5M
Short Course In Transferable Skills Training (SHIFT) ProgramR25GM151274 · NIGMS · MEHARRY MEDICAL COLLEGE · PI MERRY L. LINDSEY, Pius N Nde · 2023 to 2026
$1.9M
Targeting Resident Cardiac Fibroblast Subpopulations for Protection Against FibrosisR01HL153112 · NHLBI · UNIVERSITY OF ARIZONA · PI HALE, TABEN M. · 2022 to 2025
$1.9M
BLRD VA I01 BX000505HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL153112HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) T32HL007249-44HHS | NIH | National Institute of General Medical Sciences (NIGMS) GM151274NHLBI NIH HHS R01 HL153112NHLBI NIH HHS T32 HL007249NIGMS NIH HHS R25 GM151274U.S. Department of Veterans Affairs (VA) I01BX000505
6 · The paper itself

Abstract

Hypertension increases the prevalence of heart failure to a greater extent in women than men. The fibrotic remodeling of the left ventricle (LV) is a major contributor to increased myocardial stiffness and eventual decrease in cardiac function. Cardiac fibrosis can be prevented in the spontaneously hypertensive rat (SHR) by transient angiotensin-converting enzyme inhibitors (ACEi) in males. Whether transient ACEi also protects against fibrosis in females is not known. In the present study, we evaluated angiotensin II (Ang II)-induced cardiac fibrosis and related signaling in male and female SHR to determine how these responses are altered by prior transient ACEi treatment. Relative changes in blood pressure response to both ACEi and Ang II were similar between sexes, whereas Ang II-induced cardiac hypertrophy was attenuated by prior ACEi in males only. Ang II-induced changes in gene expression for collagens I, III, and IV were attenuated by prior ACEi in males but not females. Despite these sex-specific differences, prior ACEi-attenuated Ang II-induced increases in fibrogenic proteins [phosphorylated SMAD3/SMAD3, periostin, and lysyl oxidase (LOX)] and pro-oxidative proteins (NOX2 and NOX4), as well as hydroxyproline (HYP) content similarly in both sexes. Interestingly, a positive correlation between angiotensin II type 1 (AT1) receptor gene expression and

Indexed as

Angiotensin-Converting Enzyme InhibitorsAngiotensin IIHypertensionVentricular RemodelingAnimalsBlood PressureFemaleFibrosisMaleMyocardiumRatsRats, Inbred SHRSex CharacteristicsSex FactorsSignal TransductionAngiotensin-Converting Enzyme InhibitorsAngiotensin IIangiotensincardiacfibrosishypertensionsex differences

Identifiers

PMID40055063
PMCPMC12272740

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.