Evidence map›Paper›PMID 28164209›Full record

ArticleAmerican journal of hypertension2017

High-Salt Intake Augments the Activity of the RhoA/ROCK Pathway and Reduces Intracellular Calcium in Arteries From Rats.

Sandra Crestani, Robert Clinton Webb, José Eduardo da Silva-Santos

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hypertension, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Regulation of myosin light-chain phosphorylation and its roles in cardiovascular physiology and pathophysiology.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Review
  3. Article
  4. Article
  5. Review
  6. Role of Rho in Salt-Sensitive Hypertension.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Role of smooth muscle cells in Cardiovascular Disease.International journal of biological sciences · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. The Protective Effect of Total Flavones fromEvidence-based complementary and alternative medicine : eCAM · 2018
    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

3 authors at 2 institutions in 2 countries.

Sandra CrestaniDepartment of Pharmacology, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.
Robert Clinton WebbDepartment of Physiology, Augusta University, Augusta, Georgia, USA.
José Eduardo da Silva-SantosLaboratory of Cardiovascular Biology, Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Santa Catarina, Brazil.
Augusta University · USUniversidade Federal do Paraná · BR

Funding

Toll-like receptor 9 activation by mitochondrial DNA causes vascular injury in hypertensionP01HL134604 · NHLBI · AUGUSTA UNIVERSITY · PI O'CONNOR, PAUL MICHAEL · 2017 to 2021
$9.4M
Nitric Oxide Inhibits RhoA/Rho-kinase in Penile ErectionR01HL071138 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI WEBB, R CLINTON · 2003 to 2011
$2.9M
NHLBI NIH HHS P01 HL134604NHLBI NIH HHS R01 HL071138
6 · The paper itself

Abstract

backgroundWe investigated the influence of salt overconsumption on the functionality of the RhoA/Rho-associated kinase (ROCK) pathway and calcium regulation in arteries.

methodsThe aorta and small mesenteric arteries from rats fed a chow containing 2%, 4%, or 8% NaCl were evaluated in organ baths for the activity of the RhoA/ROCK pathway and intracellular calcium mobilization. Components of these pathways and intracellular calcium levels were also assessed in samples from 4% NaCl group.

resultsIn arteries from animals fed regular chow, the ROCK inhibitor Y-27632 reduced the responses to phenylephrine, even when the smallest concentrations (1 and 3 μM) were tested. However, only higher concentrations of Y-27632 (10 and 50 μM) reduced phenylephrine-induced contraction in vessels from high-salt groups. Immunoblotting revealed augmented phosphorylation of the myosin phosphatase targeting subunit 1 and increased amounts of RhoA in the membrane fraction of aorta homogenates from the 4% NaCl group. Under calcium-free solution, vessels from NaCl groups presented reduced contractile responses to phenylephrine and caffeine, compared with the regular chow group. Moreover, decreased intracellular calcium at rest and after stimulation with ATP were found in aortic smooth muscle cells from 4% NaCl-fed rats, which also showed diminished levels of SERCA2 and SERCA3, but not of IP3 and ryanodine receptors, or STIM1 and Orai1 proteins.

conclusionsArteries from rats subjected to high-salt intake are unable to properly regulate intracellular calcium levels and present augmented activity of the calcium sensitization pathway RhoA/ROCK. These changes may precede the development of vascular diseases induced by high-salt intake.

Indexed as

AmidesAnimalsAortaCalciumEnzyme InhibitorsInositol 1,4,5-Trisphosphate ReceptorsMaleMesenteric ArteriesMyocytes, Smooth MuscleORAI1 ProteinPhenylephrinePhosphorylationProtein Phosphatase 1PyridinesRatsRats, WistarAmidesAtp2a2 protein, ratAtp2a3 protein, ratCalciumEnzyme InhibitorsInositol 1,4,5-Trisphosphate ReceptorsORAI1 ProteinOrai1 protein, ratPhenylephrinePpp1r12a protein, ratProtein Phosphatase 1PyridinesRhoA protein, ratrho-Associated Kinasesrho GTP-Binding ProteinsRyanodine Receptor Calcium Release ChannelSarcoplasmic Reticulum Calcium-Transporting ATPasesSodium Chloride, DietaryStim1 protein, ratStromal Interaction Molecule 1Vasoconstrictor AgentsY 27632blood pressurecalcium sensitizationcalcium signalinghigh-salthypertensionvascular dysfunctionvascular smooth muscle cell.

Identifiers

PMID28164209
PMCPMC5861573
OpenAlexW2586304446

What OpenQuestion 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 OpenQuestion graph.