Evidence map›Paper›PMID 26557089›Full record

ArticleFrontiers in pharmacology2015

Mechanical stretch-induced vascular hypertrophy occurs through modulation of leptin synthesis-mediated ROS formation and GATA-4 nuclear translocation.

Crystal M Ghantous, Firas H Kobeissy, Nadia Soudani, Farah A Rahman, Mustafa Al-Hariri, Hana A Itani, Ramzi Sabra, Asad Zeidan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  11. Effects of RSC96 Schwann Cell-Derived Exosomes on Proliferation, Senescence, and Apoptosis of Dorsal Root Ganglion Cells In Vitro.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  12. Mechanical Strain Induced Expression of Matrix Metalloproteinase-9 via Stretch-Activated Channels in Rat Abdominal Aortic Dissection.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
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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

8 authors at 2 institutions in 2 countries.

Crystal M GhantousCardiovascular Physiology Lab, Department of Anatomy, Cell Biology and Physiology, American University of Beirut , Beirut, Lebanon.
Firas H KobeissyDepartment of Biochemistry and Molecular Genetics, American University of Beirut , Beirut, Lebanon.
Nadia SoudaniCardiovascular Physiology Lab, Department of Anatomy, Cell Biology and Physiology, American University of Beirut , Beirut, Lebanon.
Farah A RahmanCardiovascular Physiology Lab, Department of Anatomy, Cell Biology and Physiology, American University of Beirut , Beirut, Lebanon.
Mustafa Al-HaririDepartment of Biochemistry and Molecular Genetics, American University of Beirut , Beirut, Lebanon.
Hana A ItaniDivision of Clinical Pharmacology, Department of Medicine, Vanderbilt University School of Medicine , Nashville, TN, USA.
Ramzi SabraDepartment of Pharmacology and Toxicology, American University of Beirut , Beirut, Lebanon.
Asad ZeidanCardiovascular Physiology Lab, Department of Anatomy, Cell Biology and Physiology, American University of Beirut , Beirut, Lebanon.
American University of Beirut · LBVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObesity and hypertension are associated with increased leptin production contributing to cardiovascular remodeling. Mechanisms involving mechanical stretch-induced leptin production and the cross talk between signaling pathways leading to vascular remodeling have not been fully elucidated. METHODS AND

resultsRat portal vein (RPV) organ culture was used to investigate the effect of mechanical stretch on leptin protein expression in vascular smooth muscle cells (VSMCs). Moreover, the involvement of reactive oxygen species (ROS), the RhoA/ROCK pathway, actin cytoskeleton dynamics and the transcriptional factor GATA-4 activation in mechanical stretch-induced vascular remodeling were investigated. Stretching the RPV for 1 or 24 h significantly increased leptin protein level and ROS formation in VSMCs, which was prevented by 1 h pretreatment with the ROCK inhibitor Y-27632 and the actin cytoskeleton depolymerization agent cytochalasin D. Moreover, Western blotting and immunohistochemistry revealed that mechanical stretch or treatment with 3.1 nmol/L leptin for 24 h significantly increased actin polymerization, as reflected by an increase in the F-actin to G-actin ratio. Increases in blood vessels' wet weight and [(3)H]-leucine incorporation following a 24 h treatment with conditioned media from cultured stretched RPVs indicated RPV hypertrophy. This effect was prevented by 1 h pretreatment with anti-leptin antibody, indicating leptin's crucial role in promoting VSMC hypertrophy. As an index of GATA-4 activation, GATA-4 nuclear translocation was assessed by immunohistochemistry method. Pretreating VSMC with leptin for 1 h significantly activated GATA-4 nuclear translocation, which was potently attenuated by the NADPH oxidase inhibitor apocynin, Y-27632, and cytochalasin D.

conclusionOur results demonstrate that ROS formation, RhoA/ROCK pathway, and GATA-4 activation play a pivotal role in mechanical stretch-induced leptin synthesis leading to VSMC remodeling.

Indexed as

leptinmechanical stretchremodelingROSvascular smooth muscle

Identifiers

PMID26557089
PMCPMC4615939
OpenAlexW1750309467

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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.