Evidence map›Paper›PMID 35682723›Full record

ArticleInternational journal of molecular sciences2022

Angiotensin II Inhibits Insulin Receptor Signaling in Adipose Cells.

Citlaly Gutierrez-Rodelo, Araceli Arellano-Plancarte, Judith Hernandez-Aranda, Huguet V Landa-Galvan, G Karina Parra-Mercado, Nicole J Moreno-Licona, Karla D Hernandez-Gonzalez, Kevin J Catt, Rafael Villalobos-Molina, J Alberto Olivares-Reyes

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 31 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Citlaly Gutierrez-RodeloLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
Araceli Arellano-PlancarteLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
Judith Hernandez-ArandaLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
Huguet V Landa-GalvanLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
G Karina Parra-MercadoLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
Nicole J Moreno-LiconaLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
Karla D Hernandez-GonzalezLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.
Kevin J CattSection on Hormonal Regulation, PDEGEN, National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892, USA.
Rafael Villalobos-MolinaBiomedicine Research Unit, Faculty of Higher Studies, FES-Iztacala, National Autonomous University of Mexico, UNAM, Edo. Mex., Tlalnepantla 54090, Mexico.
J Alberto Olivares-ReyesLaboratory of Signal Transduction, Department of Biochemistry, Center for Research and Advanced Studies of the National Polytechnic Institute, Cinvestav-IPN, Mexico City 07360, Mexico.ORCID 0000-0001-8389-9274
Instituto Politécnico Nacional · MXEunice Kennedy Shriver National Institute of Child Health and Human Development · USUniversidad Nacional Autónoma de México · MX

Funding

Consejo Nacional de Ciencia y Tecnología 169944-AA-PConsejo Nacional de Ciencia y Tecnología 261975-CG-RConsejo Nacional de Ciencia y Tecnología 278067-HL-GConsejo Nacional de Ciencia y Tecnología 296029-KGP-MConsejo Nacional de Ciencia y Tecnología 48777 and 167673Consejo Nacional de Ciencia y Tecnología 632503-NJM-LConsejo Nacional de Ciencia y Tecnología 925174-KDH-GMiguel Aleman Valdes Estímulo a la investigacion Medica-2018
6 · The paper itself

Abstract

Angiotensin II (Ang II) is a critical regulator of insulin signaling in the cardiovascular system and metabolic tissues. However, in adipose cells, the regulatory role of Ang II on insulin actions remains to be elucidated. The effect of Ang II on insulin-induced insulin receptor (IR) phosphorylation, Akt activation, and glucose uptake was examined in 3T3-L1 adipocytes. In these cells, Ang II specifically inhibited insulin-stimulated IR and insulin receptor substrate-1 (IRS-1) tyrosine-phosphorylation, Akt activation, and glucose uptake in a time-dependent manner. These inhibitory actions were associated with increased phosphorylation of the IR at serine residues. Interestingly, Ang II-induced serine-phosphorylation of IRS was not detected, suggesting that Ang II-induced desensitization begins from IR regulation itself. PKC inhibition by BIM I restored the inhibitory effect of Ang II on insulin actions. We also found that Ang II promoted activation of several PKC isoforms, including PKCα/βI/βII/δ, and its association with the IR, particularly PKCβII, showed the highest interaction. Finally, we also found a similar regulatory effect of Ang II in isolated adipocytes, where insulin-induced Akt phosphorylation was inhibited by Ang II, an effect that was prevented by PKC inhibitors. These results suggest that Ang II may lead to insulin resistance through PKC activation in adipocytes.

Indexed as

Angiotensin IIReceptor, InsulinAdipocytesGlucoseInsulinInsulin Receptor Substrate ProteinsPhosphorylationProto-Oncogene Proteins c-aktSerineAngiotensin IIGlucoseInsulinInsulin Receptor Substrate ProteinsProto-Oncogene Proteins c-aktReceptor, InsulinSerineadipose cellsangiotensin IIinsulin receptorinsulin resistanceprotein kinase Cserine-phosphorylation

Identifiers

PMID35682723
PMCPMC9181642
OpenAlexW4281754532

What OpenQuestion holds

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LicenceCC BY
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.