Evidence map›Paper›PMID 33920473›Full record

ArticleInternational journal of molecular sciences2021

β Cell GHS-R Regulates Insulin Secretion and Sensitivity.

Geetali Pradhan, Chia-Shan Wu, Daniel Villarreal, Jong Han Lee, Hye Won Han, Akhilesh Gaharwar, Yanan Tian, Wenxian Fu, Shaodong Guo, Roy G Smith and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
2.9field-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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Ghrelin receptor signaling in health and disease: a biased view.Trends in endocrinology and metabolism: TEM · 2023
    Review
  7. Article
  8. Article
  9. "Sibling" battle or harmony: crosstalk between nesfatin-1 and ghrelin.Cellular and molecular life sciences : CMLS · 2022
    Review
  10. Article
  11. Article
  12. Article
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

11 authors at 6 institutions in 2 countries.

Geetali PradhanUSDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
Chia-Shan WuDepartment of Nutrition, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-6034-939X
Daniel VillarrealDepartment of Nutrition, Texas A&M University, College Station, TX 77843, USA.
Jong Han LeeUSDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
Hye Won HanDepartment of Nutrition, Texas A&M University, College Station, TX 77843, USA.
Akhilesh GaharwarDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Yanan TianDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX 77843, USA.
Wenxian FuDepartment of Pediatrics, University of California, San Diego, CA 92161, USA.
Shaodong GuoDepartment of Nutrition, Texas A&M University, College Station, TX 77843, USA.
Roy G SmithDepartment of Metabolism and Aging, The Scripps Research Institute, Jupiter, FL 33458, USA.
Yuxiang SunUSDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
Texas A&M University · USBaylor College of Medicine · USChildren's Nutrition Research Center at Baylor College of Medicine · USHanseo University · KRScripps Research Institute · USUniversity of California San Diego · US

Funding

The role of GHS-R in macrophage reprogramming during meta-inflammationR01DK118334 · NIDDK · TEXAS A&M AGRILIFE RESEARCH · PI SUN, YUXIANG · 2019 to 2022
$1.2M
Long noncoding RNA MALAT1 ablation reverses sepsis in mouse: epitranscriptomic mechanisms and therapeutic applicationR21AI152050 · NIAID · TEXAS A&M AGRILIFE RESEARCH · PI TIAN, YANAN · 2020 to 2021
$421k
NIAID NIH HHS R21 AI152050NIH HHS AG064869NIH HHS R01DK118334
6 · The paper itself

Abstract

Growth hormone secretagogue receptor (GHS-R) is widely known to regulate food intake and adiposity, but its role in glucose homeostasis is unclear. In this study, we investigated the expression of GHS-R in mouse pancreatic islets and its role in glycemic regulation. We used Ghsr-IRES-tauGFP mice, with Green Fluorescent Protein (GFP) as a surrogate for GHS-R, to demonstrate the GFP co-localization with insulin and glucagon expression in pancreatic islets, confirming GHS-R expression in β and α cells. We then generated β-cell-specific GHSR-deleted mice with MIP-Cre/ERT and validated that GHS-R suppression was restricted to the pancreatic islets. MIP-Cre/ERT;Ghsr

Indexed as

Insulin SecretionAnimalsDiabetes Mellitus, Type 2Insulin-Secreting CellsMiceMice, KnockoutReceptors, GhrelinReceptors, Ghrelinglucose-stimulated insulin secretion (GSIS)growth hormone secretagogue receptor (GHS-R)insulin secretioninsulin sensitivityMIP-Cre/ERTpancreatic isletsβ cells

Identifiers

PMID33920473
PMCPMC8069226
OpenAlexW3155920937

What Socratic holds

Textmetadata
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 Socratic graph.