Evidence map›Paper›PMID 25845661›Full record

ArticleDiabetes2015

Metabolic Syndrome Abolishes Glucagon-Like Peptide 1 Receptor Agonist Stimulation of SERCA in Coronary Smooth Muscle.

Stacey L Dineen, Mikaela L McKenney, Lauren N Bell, Allison M Fullenkamp, Kyle A Schultz, Mouhamad Alloosh, Naga Chalasani, Michael Sturek

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Review
  3. Insulin resistance, CaFrontiers in physiology · 2025
    Review
  4. Intracellular CaJournal of cardiovascular translational research · 2022
    Article
  5. Review
  6. Roles of sarcoplasmic reticulum CaScientific reports · 2020
    Article
  7. Article
  8. Article
  9. Effect of metabolic syndrome and aging on CaExperimental gerontology · 2018
    Article
  10. Intracellular calcium increases in vascular smooth muscle cells with progression of chronic kidney disease in a rat model.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Stacey L DineenDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN.
Mikaela L McKenneyDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN.
Lauren N BellDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Allison M FullenkampDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Kyle A SchultzDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN.
Mouhamad AllooshDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN.
Naga ChalasaniDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Michael SturekDepartment of Cellular & Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN msturek@iu.edu.
Indiana University – Purdue University Indianapolis · US

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
EXERCISE, DIABETES, &CORONARY SMOOTH MUSCLE Ca2+R01HL062552 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI STUREK, MICHAEL · 1999 to 2013
$4.5M
NHLBI NIH HHS HL-062552NHLBI NIH HHS R01 HL062552NIDDK NIH HHS P30 DK097512
6 · The paper itself

Abstract

Metabolic syndrome (MetS) doubles the risk of adverse cardiovascular events. Glucagon-like peptide 1 (GLP-1) receptor agonists induce weight loss, increase insulin secretion, and improve glucose tolerance. Studies in healthy animals suggest cardioprotective properties of GLP-1 receptor agonists, perhaps partially mediated by improved sarco-endoplasmic reticulum Ca(2+) ATPase (SERCA) activity. We examined the acute effect of GLP-1 receptor agonists on coronary smooth muscle cells (CSM) enzymatically isolated from lean, healthy Ossabaw miniature swine. Intracellular Ca(2+) handling was interrogated with fura-2. The GLP-1 receptor agonist exenatide activated SERCA but did not alter other Ca(2+) transporters. Further, we tested the hypothesis that chronic, in vivo treatment with GLP-1 receptor agonist AC3174 would attenuate coronary artery disease (CAD) in swine with MetS. MetS was induced in 20 swine by 6 months' feeding of a hypercaloric, atherogenic diet. Swine were then randomized (n = 10/group) into placebo or AC3174 treatment groups and continued the diet for an additional 6 months. AC3174 treatment attenuated weight gain, increased insulin secretion, and improved glucose tolerance. Intravascular ultrasound and histology showed no effect of AC3174 on CAD. MetS abolished SERCA activation by GLP-1 receptor agonists. We conclude that MetS confers vascular resistance to GLP-1 receptor agonists, partially through impaired cellular signaling steps involving SERCA.

Indexed as

AnimalsBlood GlucoseCalciumCoronary Artery DiseaseCoronary VesselsDiet, AtherogenicExenatideGlucagon-Like Peptide-1 ReceptorInsulinInsulin SecretionMetabolic SyndromeMuscle, Smooth, VascularMyocytes, Smooth MusclePeptidesRandom AllocationReceptors, GlucagonAC3174Blood GlucoseCalciumExenatideGlucagon-Like Peptide-1 ReceptorInsulinPeptidesReceptors, GlucagonSarcoplasmic Reticulum Calcium-Transporting ATPasesVenoms

Identifiers

PMID25845661
PMCPMC4542436
OpenAlexW2104338804

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.