Evidence map›Paper›PMID 24946790›Full record

ReviewExperimental & molecular medicine2014

Inhibitory G proteins and their receptors: emerging therapeutic targets for obesity and diabetes.

Michelle E Kimple, Joshua C Neuman, Amelia K Linnemann, Patrick J Casey

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The prostaglandin EAmerican journal of physiology. Endocrinology and metabolism · 2024
    Article
  6. Article
  7. Review
  8. Plasma Prostaglandin EMetabolites · 2022
    Article
  9. Article
  10. Article
  11. Human Islet Expression Levels of Prostaglandin EACS pharmacology & translational science · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Free fatty acid receptor 3 differentially contributes to β-cell compensation under high-fat diet and streptozotocin stress.American journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Article
  16. Article
  17. Review
  18. Regulator of G-protein signaling Gβ5-R7 is a crucial activator of muscarinic M3 receptor-stimulated insulin secretion.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  19. The EP3 Receptor/GThe AAPS journal · 2017
    Review
  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

4 authors at 2 institutions in 1 country.

Michelle E KimpleDepartment of Medicine-Division of Endocrinology, Diabetes, and Metabolism, University of Wisconsin-Madison, Madison, WI, USA.
Joshua C NeumanDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Amelia K LinnemannDepartment of Medicine-Division of Endocrinology, Diabetes, and Metabolism, University of Wisconsin-Madison, Madison, WI, USA.
Patrick J CaseyDuke University Medical Center Department of Pharmacology and Cancer Biology, Durham, NC, USA.
University of Wisconsin–Madison · USDuke University · US

Funding

Biology of Aging and Age-Related Diseases Training GrantT32AG000213 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Rozalyn M. Anderson, Sanjay Asthana · 1991 to 2026
$9.9M
Molecular Mechanisms of Dysfunctional Prostaglandin Signaling in the Beta-CellR01DK102598 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI KIMPLE, MICHELLE E · 2014 to 2018
$1.7M
Regulation of G-Protein SignalingR01DK076488 · NIDDK · DUKE UNIVERSITY · PI CASEY, PATRICK J. · 2006 to 2009
$1.1M
G(alpha)Z signaling in insulin secretion and glucose toleranceK01DK080845 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI KIMPLE, MICHELLE E · 2008 to 2010
$301k
Role of G(alpha)Z in pancreatic islet beta-cell biologyF32DK067799 · NIDDK · DUKE UNIVERSITY · PI KIMPLE, MICHELLE E · 2004 to 2005
$97k
NIA NIH HHS T32 AG000213NIDDK NIH HHS F32 DK067799NIDDK NIH HHS K01 DK080845NIDDK NIH HHS R01 DK076488NIDDK NIH HHS R01 DK102598
6 · The paper itself

Abstract

The worldwide prevalence of obesity is steadily increasing, nearly doubling between 1980 and 2008. Obesity is often associated with insulin resistance, a major risk factor for type 2 diabetes mellitus (T2DM): a costly chronic disease and serious public health problem. The underlying cause of T2DM is a failure of the beta cells of the pancreas to continue to produce enough insulin to counteract insulin resistance. Most current T2DM therapeutics do not prevent continued loss of insulin secretion capacity, and those that do have the potential to preserve beta cell mass and function are not effective in all patients. Therefore, developing new methods for preventing and treating obesity and T2DM is very timely and of great significance. There is now considerable literature demonstrating a link between inhibitory guanine nucleotide-binding protein (G protein) and G protein-coupled receptor (GPCR) signaling in insulin-responsive tissues and the pathogenesis of obesity and T2DM. These studies are suggesting new and emerging therapeutic targets for these conditions. In this review, we will discuss inhibitory G proteins and GPCRs that have primary actions in the beta cell and other peripheral sites as therapeutic targets for obesity and T2DM, improving satiety, insulin resistance and/or beta cell biology.

Indexed as

AnimalsDiabetes Mellitus, Type 2GTP-Binding Protein alpha SubunitsHumansInsulin-Secreting CellsObesityReceptor, Melatonin, MT2Receptors, Adrenergic, alpha-1Receptors, ProstaglandinGTP-Binding Protein alpha SubunitsReceptor, Melatonin, MT2Receptors, Adrenergic, alpha-1Receptors, Prostaglandin

Identifiers

PMID24946790
PMCPMC4081554
OpenAlexW1967031212

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.