Evidence map›Paper›PMID 35448529›Full record

ReviewMetabolites2022

Effects of Arachidonic Acid and Its Metabolites on Functional Beta-Cell Mass.

Karin J Bosma, Cecilia E Kaiser, Michelle E Kimple, Maureen Gannon

Open access · goldAbstract readReview
In one paragraph

Review in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Effect ofPlants (Basel, Switzerland) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. The prostaglandin EAmerican journal of physiology. Endocrinology and metabolism · 2024
    Article
  9. Article
  10. Review
  11. Review
  12. Observational
  13. Article
  14. Article
  15. Targeting metabolic pathways: a novel therapeutic direction for type 2 diabetes.Frontiers in cellular and infection microbiology · 2023
    Article
  16. Review
  17. Journal of diabetes research · 2023
    Article
  18. Article
  19. Plasma Prostaglandin EMetabolites · 2022
    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

4 authors at 2 institutions in 1 country.

Karin J BosmaDepartment of Veterans Affairs, Tennessee Valley Authority, Nashville, TN 37212, USA.ORCID 0000-0002-1221-1169
Cecilia E KaiserDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA.
Michelle E KimpleDepartment of Medicine, University of Wisconsin-Madison, Madison, WI 53705, USA.
Maureen GannonDepartment of Veterans Affairs, Tennessee Valley Authority, Nashville, TN 37212, USA.ORCID 0000-0003-3287-8101
Tennessee Valley Authority · USUniversity of Wisconsin–Madison · US

Funding

Manipulating islet GPCR activity to promote beta cell proliferation and survivalR01DK120626 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GANNON, MAUREEN A · 2019 to 2022
$1.7M
G Protein Mediated Mechanisms of Beta Cell Death Dysfunction and Decompensation in DiabetesI01BX003700 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI KIMPLE, MICHELLE E · 2018 to 2021
–
Pathways regulating adult pancreatic beta cell replicationI01BX003744 · VA · VETERANS HEALTH ADMINISTRATION · PI GANNON, MAUREEN A · 2017 to 2020
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Modulating prostaglandin E2 receptor activity to improve pancreatic islet functionI01BX005399 · VA · VETERANS HEALTH ADMINISTRATION · PI GANNON, MAUREEN A · 2022 to 2025
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BLRD VA I01 BX003700BLRD VA I01 BX003744BLRD VA I01 BX005399NIDDK NIH HHS R01 DK120626
6 · The paper itself

Abstract

Arachidonic acid (AA) is a polyunsaturated 20-carbon fatty acid present in phospholipids in the plasma membrane. The three primary pathways by which AA is metabolized are mediated by cyclooxygenase (COX) enzymes, lipoxygenase (LOX) enzymes, and cytochrome P450 (CYP) enzymes. These three pathways produce eicosanoids, lipid signaling molecules that play roles in biological processes such as inflammation, pain, and immune function. Eicosanoids have been demonstrated to play a role in inflammatory, renal, and cardiovascular diseases as well type 1 and type 2 diabetes. Alterations in AA release or AA concentrations have been shown to affect insulin secretion from the pancreatic beta cell, leading to interest in the role of AA and its metabolites in the regulation of beta-cell function and maintenance of beta-cell mass. In this review, we discuss the metabolism of AA by COX, LOX, and CYP, the roles of these enzymes and their metabolites in beta-cell mass and function, and the possibility of targeting these pathways as novel therapies for treating diabetes.

Indexed as

arachidonic acidbeta-cell masseicosanoidsprostaglandins

Identifiers

PMID35448529
PMCPMC9031745
OpenAlexW4223541734

What OpenQuestion 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 OpenQuestion graph.