Evidence map›Paper›PMID 20211684›Full record

ArticleMolecular and cellular endocrinology2010

AGI-1067, a novel antioxidant and anti-inflammatory agent, enhances insulin release and protects mouse islets.

William S Crim, Runpei Wu, Jeffrey D Carter, Banumathi K Cole, Anthony P Trace, Raghavendra G Mirmira, Charles Kunsch, Jerry L Nadler, Craig S Nunemaker

Abstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Mouse and human islets survive and function after coating by biosilicification.American journal of physiology. Endocrinology and metabolism · 2013
    Article
  11. Article
  12. Article
  13. 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

9 authors at 4 institutions in 1 country.

William S CrimDepartment of Medicine, University of Virginia, VA 22908, USA.
Runpei Wu
Jeffrey D Carter
Banumathi K Cole
Anthony P Trace
Raghavendra G Mirmira
Charles Kunsch
Jerry L Nadler
Craig S Nunemaker
University of Virginia · USEastern Virginia Medical School · USCryogenic Industries (United States) · USIndiana University School of Medicine

Funding

PILOT--PILOT/FEASIBILITY PROGRAMP30DK063609 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BARRETT, EUGENE JOSEPH · 2003 to 2007
$5.7M
Lipid Mediators in Pancreatic Islet DysfunctionR01DK055240 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI NADLER, JERRY L. · 1998 to 2010
$1.6M
Assessing and Improving Pancreatic Islet Viability and FunctionK01DK081621 · NIDDK · UNIVERSITY OF VIRGINIA · PI NUNEMAKER, CRAIG S · 2008 to 2010
$324k
NIDDK NIH HHS 1K01 DK081621NIDDK NIH HHS DK063609NIDDK NIH HHS K01 DK081621NIDDK NIH HHS P30 DK063609NIDDK NIH HHS R01 DK055240NIDDK NIH HHS R01 DK 55240
6 · The paper itself

Abstract

The antioxidant and anti-inflammatory compound AGI-1067 (succinobucol) has potential as an oral anti-diabetic agent. AGI-1067 reduces H(b)A1c, improves fasting plasma glucose, and reduces new-onset diabetes. We investigated AGI-1067 for possible effects on mouse pancreatic islets in vitro. Pretreatment with 10 microM AGI-1067 increased glucose-stimulated insulin secretion (11 mM) without affecting secretion in basal (3 mM) glucose. AGI-1067 enhanced the intracellular calcium response to glucose stimulation in 7 mM and 11 mM glucose, but had no effect in 28 mM or basal glucose. AGI-1067-pretreated islets also showed enhanced calcium responses to methyl pyruvate and alpha-ketoisocaproate at low doses, but not high doses. The AGI-1067-mediated effects on glucose-stimulated calcium were maintained during continuous diazoxide exposure, suggesting effects on the K(ATP)-channel-independent pathway. AGI-1067 also reduced cytokine-induced islet cell death and expression of iNOS, a key component in cytokine signaling. This is the first report of direct stimulatory and protective effects of a first-in-class potential anti-diabetic agent on pancreatic islets.

Indexed as

AnimalsAntihypertensive AgentsAnti-Inflammatory AgentsAntioxidantsCalciumCell DeathCytokinesDiazoxideGene ExpressionGlucoseHumansHypoglycemic AgentsInsulinInsulin SecretionIslets of LangerhansKeto Acidsalpha-ketoisocaproic acidAntihypertensive AgentsAnti-Inflammatory AgentsAntioxidantsCalciumCytokinesDiazoxideGlucoseHypoglycemic AgentsInsulinKeto AcidsNitric Oxide Synthase Type IIPotassium ChannelsProbucolsuccinobucolTolbutamide

Identifiers

PMID20211684
PMCPMC2875300
OpenAlexW2015749069

What OpenQuestion holds

Textmetadata
LicenceTDM
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.