Evidence map›Paper›PMID 23299501›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2013

Losartan increases muscle insulin delivery and rescues insulin's metabolic action during lipid infusion via microvascular recruitment.

Nasui Wang, Weidong Chai, Lina Zhao, Lijian Tao, Wenhong Cao, Zhenqi Liu

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
14.5field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. The Renin Angiotensin System as a Therapeutic Target in Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Modeling the acute effects of exercise on insulin kinetics in type 1 diabetes.Journal of pharmacokinetics and pharmacodynamics · 2018
    Article
  10. Article
  11. Article
  12. Inflammation-induced microvascular insulin resistance is an early event in diet-induced obesity.Clinical science (London, England : 1979) · 2015 · on this map
    Article
  13. Article
  14. Vascular function, insulin action, and exercise: an intricate interplay.Trends in endocrinology and metabolism: TEM · 2015
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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

6 authors at 3 institutions in 2 countries.

Nasui WangDiv. of Endocrinology and Metabolism, Dept. of Medicine, Univ. of Virginia Health System, Charlottesville, VA 22908, USA.
Weidong Chai
Lina Zhao
Lijian Tao
Wenhong Cao
Zhenqi Liu
University of Virginia Health System · USCentral South University · CNUniversity of North Carolina at Chapel Hill · US

Funding

Insulin action in human cardiac and skeletal muscle microvasculatureR01HL094722 · NHLBI · UNIVERSITY OF VIRGINIA · PI LIU, ZHENQI · 2010 to 2014
$1.9M
NHLBI NIH HHS R01 HL094722NHLBI NIH HHS R01-HL-094722
6 · The paper itself

Abstract

Insulin delivery and transendothelial insulin transport are two discrete steps that limit muscle insulin action. Angiotensin II type 1 receptor (AT1R) blockade recruits microvasculature and increases glucose use in muscle. Increased muscle microvascular perfusion is associated with increased muscle delivery and action of insulin. To examine the effect of acute AT1R blockade on muscle insulin uptake and action, rats were studied after an overnight fast to examine the effects of losartan on muscle insulin uptake (protocol 1), microvascular perfusion (protocol 2), and insulin's microvascular and metabolic actions in the state of insulin resistance (protocol 3). Endothelial cell insulin uptake was assessed, using (125)I-insulin as tracer. Systemic lipid infusion was used to induce insulin resistance. Losartan significantly increased muscle insulin uptake (∼60%, P < 0.03), which was associated with a two- to threefold increase in muscle microvascular blood volume (MBV; P = 0.002) and flow (MBF; P = 0.002). Losartan ± angiotensin II had no effect on insulin internalization in cultured endothelial cells. Lipid infusion abolished insulin-mediated increases in muscle MBV and MBF and lowered insulin-stimulated whole body glucose disposal (P = 0.0001), which were reversed by losartan administration. Inhibition of nitric oxide synthase abolished losartan-induced muscle insulin uptake and reversal of lipid-induced metabolic insulin resistance. We conclude that AT1R blockade increases muscle insulin uptake mainly via microvascular recruitment and rescues insulin's metabolic action in the insulin-resistant state. This may contribute to the clinical findings of decreased cardiovascular events and new onset of diabetes in patients receiving AT1R blockers.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsBlood PressureCapillariesCells, CulturedEndothelial CellsEnzyme InhibitorsHypoglycemic AgentsInsulinLipidsLosartanMaleMAP Kinase Signaling SystemMicrocirculationMuscle, SkeletalNG-Nitroarginine Methyl EsterAngiotensin II Type 1 Receptor BlockersEnzyme InhibitorsHypoglycemic AgentsInsulinLipidsLosartanNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide SynthaseProto-Oncogene Proteins c-akt

Identifiers

PMID23299501
PMCPMC3602659
OpenAlexW2098532941

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.