Evidence map›Paper›PMID 15064952›Full record

ArticlePflugers Archiv : European journal of physiology2004

Cell signalling-mediating insulin increase of mRNA expression for cationic amino acid transporters-1 and -2 and membrane hyperpolarization in human umbilical vein endothelial cells.

Marcelo González, Carlos Flores, Jeremy D Pearson, Paola Casanello, Luis Sobrevia

Abstract read
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 49 citations in OpenAlex.

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  10. Liver aging and pseudocapillarization in a Werner syndrome mouse model.The journals of gerontology. Series A, Biological sciences and medical sciences · 2014
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  17. Cellular ADMA: regulation and action.Pharmacological research · 2009
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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

5 authors at 3 institutions in 2 countries.

Marcelo GonzálezCellular and Molecular Physiology Laboratory (CMPL), Department of Obstetrics and Gynaecology, Medical Research Centre (CIM), School of Medicine, Faculty of Medicine, Pontificia Universidad Católica de Chile, P.O. Box 114-D, Santiago, Chile.
Carlos Flores
Jeremy D Pearson
Paola Casanello
Luis Sobrevia
Pontificia Universidad Católica de Chile · CLAustral University of Chile · CLKing's College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin induces vasodilatation in human subjects and increases L-arginine transport and NO synthesis in human umbilical vein endothelial cells (HUVEC). Cell signalling events associated with insulin effects on activity and mRNA expression of the human cationic amino acid transporters 1 (hCAT-1) and 2B (hCAT-2B) are unknown. L-arginine transport and eNOS activity were determined in HUVEC exposed to insulin. mRNA levels for hCAT-1, hCAT-2B and eNOS were quantitated by real time RT-PCR and endothelial NO synthase (eNOS) protein was identified by Western blot analysis. Intracellular Ca2+, L-arginine and L-citrulline levels, L-[3H]citrulline formation from L-[(3)H]arginine, cGMP formation, nitrite level, ATP release and membrane potential were determined. Insulin increased L-arginine transport and the mRNA levels for hCAT-1 and hCAT-2B and eNOS expression and activity. Insulin also induced membrane hyperpolarization and increased intracellular Ca2+, L-[3H]citrulline, cGMP and nitrite formation. Insulin-mediated stimulation of the L-arginine/NO pathway is thus associated with increased hCAT-1 and hCAT-2B mRNA, and eNOS expression, via mechanisms involving membrane hyperpolarization, mitogen-activated protein kinases p42 and p44, phosphatidylinositol 3-kinase, NO and protein kinase C. We have characterized a cell signalling pathway by which hyperinsulinaemia could lead to vasodilatation in human subjects, and which could have implications in patients in whom plasma insulin levels are altered, such as in diabetes mellitus.

Indexed as

Adenosine TriphosphateAmino Acid Transport Systems, BasicArginineCalciumCationic Amino Acid Transporter 1Cationic Amino Acid Transporter 2Cells, CulturedEndothelium, VascularHumansInsulinMAP Kinase Signaling SystemMembrane PotentialsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Nitric OxideNitric Oxide SynthaseAdenosine TriphosphateAmino Acid Transport Systems, BasicArginineCalciumCationic Amino Acid Transporter 1Cationic Amino Acid Transporter 2InsulinMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Nitric OxideNitric Oxide SynthaseNitric Oxide Synthase Type IIINOS3 protein, humanOnium CompoundsOrganophosphorus CompoundsPhosphatidylinositol 3-KinasesProtein Kinase CRNA, MessengerSLC7A1 protein, humanSLC7A2 protein, humantetraphenylphosphoniumTritium

Identifiers

PMID15064952
OpenAlexW1970808263

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.