Evidence mapPaperPMID 42589441Full record

ArticleInternational journal of molecular sciences2026

Dopamine D1-like and Angiotensin II Type 1 Receptors Counter-Regulate Autophagy and Cell Proliferation in Rat Embryonic Thoracic Vascular Smooth Muscle Cells.

Hewang Lee, Amy Lu, Waleed N Qaddumi, Bibhas Amatya, Jacob Polzin, Maithri Verma, Raisha C Cadme, Robin A Felder, Ines Armando, Jeffrey B Kopp and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. 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

11 authors.

Hewang LeeDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.ORCID 0000-0003-1338-2573
Amy LuDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.
Waleed N QaddumiDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.ORCID 0000-0003-3480-5088
Bibhas AmatyaDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.
Jacob PolzinDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.ORCID 0009-0000-8202-0432
Maithri VermaDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.
Raisha C CadmeDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.
Robin A FelderDepartment of Pathology, University of Virginia Health Sciences Center, Charlottesville, VA 22908, USA.ORCID 0000-0003-2797-4289
Ines ArmandoDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.
Jeffrey B KoppIndependent Researcher, 2324 North Apple Lane, Pocatello, ID 83204, USA.ORCID 0000-0001-9052-186X
Pedro A JoseDepartment of Medicine, Division of Kidney Disease & Hypertension, The George Washington University School of Medicine & Health Sciences, Washington, DC 20052, USA.

Funding

FOCAL SEGMENTAL GLOMERULOSCLEROSIS--PATHOGENESIS AND TREATMENTZ01DK043308 · DIABETES, DIGESTIVE, KIDNEY DISEASES · 1997 to 2005
National Natural Science Foundation of China 81670406National Natural Science Foundation of China 81670698National Natural Science Foundation of China 91739119NIDDK NIH HHS Z01DK043308NIH HHS 5R01DK134574-04
6 · The paper itself

Abstract

Vascular smooth muscle cells (VSMCs), the contractile cells in the tunica media of blood vessels, maintain vascular tone. The proliferation of VSMCs is an important feature of vascular remodeling that contributes to the regulation of blood pressure. Autophagy, an intracellular self-degrading process that delivers cytoplasmic constituents to lysosomes, plays a vital role in VSMC proliferation. This is regulated by the dopaminergic and renin-angiotensin systems but their interplay in their regulation of autophagy in VSMCs is not well-understood. In rat VSMCs, fenoldopam (Fen), a dopamine D1-like receptor agonist, increased autophagy, as determined by the increase in the protein expressions of microtubule-associated protein 1 light chain (LC)3-II and beclin-1 (BECN1), in a time- and concentration-dependent manner. Conversely, angiotensin II (Ang II), the endogenous Ang II type 1 receptor (AT

Indexed as

AutophagyCell ProliferationMuscle, Smooth, VascularMyocytes, Smooth MuscleReceptor, Angiotensin, Type 1Receptors, Dopamine D1Angiotensin IIAnimalsCells, CulturedCyclic AMPFenoldopamMicrotubule-Associated ProteinsRatsSignal TransductionTOR Serine-Threonine KinasesAngiotensin IICyclic AMPFenoldopamMicrotubule-Associated ProteinsReceptor, Angiotensin, Type 1Receptors, Dopamine D1TOR Serine-Threonine KinasesAng II type 1 receptorautophagycyclic AMPD1-like receptorsmTORproliferationVSMC

Identifiers

PMID42589441
PMCPMC13467237

What Socratic 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 Socratic graph.