Evidence map›Paper›PMID 20609918›Full record

ArticleMethods in enzymology2010

Synthesis, quantification, characterization, and signaling properties of glutathionyl conjugates of enals.

Sanjay Srivastava, Kota V Ramana, Aruni Bhatnagar, Satish K Srivastava

Open access · greenAbstract read
In one paragraph

Article in Methods in enzymology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
10.5field-weighted citation impact, top 2% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Intra-site differential inhibition of multi-specific enzymes.Journal of enzyme inhibition and medicinal chemistry · 2020
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Aldehyde reduction by cytochrome P450.Current protocols in toxicology · 2011
    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

4 authors at 2 institutions in 1 country.

Sanjay SrivastavaDiabetes and Obesity Center, University of Louisville, Louisville, Kentucky, USA.
Kota V Ramana
Aruni Bhatnagar
Satish K Srivastava
University of Louisville · USThe University of Texas Medical Branch at Galveston · US

Funding

STEM CELLS AND DIABETIC CARDIOMYOPATHY PROJ 2 2009P20RR024489 · NCRR · UNIVERSITY OF LOUISVILLE · PI ROKOSH, GREGG · 2008 to 2011
$10.0M
Role of Platelet Activation and Vascular Pathology in Aldehyde ToxicityP01ES011860 · NIEHS · UNIVERSITY OF LOUISVILLE · PI PIERCE, WILLIAM M · 2003 to 2007
$7.0M
Role of Aldose Reductase in Diabetic ComplicationsR37DK036118 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SRIVASTAVA, SATISH K · 2003 to 2013
$4.1M
CARDIAC METABOLISM OF ENALSR01HL059378 · NHLBI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI BHATNAGAR, ARUNI · 1998 to 2011
$3.3M
Aldose Reductase: A Regulator of Inflammatory SignalsR01GM071036 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI RAMANA, KOTA VENKATA · 2005 to 2011
$1.8M
Atherogenic Mechanisms of ArsenicR01ES017260 · NIEHS · UNIVERSITY OF LOUISVILLE · PI SRIVASTAVA, SANJAY · 2009 to 2013
$1.6M
Metabolism and Detoxification of Base PropenalsR01ES011594 · NIEHS · UNIVERSITY OF LOUISVILLE · PI SRIVASTAVA, SANJAY · 2003 to 2007
$1.6M
Atherogenic mechanism of lipid peroxidation-derived aldehydesR01HL095593 · NHLBI · UNIVERSITY OF LOUISVILLE · PI SRIVASTAVA, SANJAY · 2010 to 2013
$1.5M
ALDOSE REDUCTASE AND DIABETIC COMPLICATIONSR01DK036118 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SRIVASTAVA, SATISH K · 1987 to 2002
$626k
Structural Biology /Structural Genomics of TraffickingZ01DK036118 · NIDDK · DIABETES, DIGESTIVE, KIDNEY DISEASES · PI HURLEY, JAMES H · 1994 to 2006
–
Intramural NIH HHS Z01 DK036118NCRR NIH HHS P20 RR024489NCRR NIH HHS RR 24489NHLBI NIH HHS HL59378NHLBI NIH HHS HL95593NHLBI NIH HHS R01 HL059378NHLBI NIH HHS R01 HL095593NIDDK NIH HHS R01 DK036118NIDDK NIH HHS R37 DK036118NIEHS NIH HHS ES11594NIEHS NIH HHS ES11860NIEHS NIH HHS ES17260NIEHS NIH HHS P01 ES011860NIEHS NIH HHS R01 ES011594NIEHS NIH HHS R01 ES017260NIGMS NIH HHS GM71036NIGMS NIH HHS R01 GM071036
6 · The paper itself

Abstract

Oxidation of lipids generates large quantities of highly reactive alpha,beta-unsaturated aldehydes (enals). Enals and their protein adducts accumulate in the tissues of several pathologies. In vitro, low concentrations of enals such as HNE (4-hydroxy trans-2-nonenal) affect cell signaling whereas high concentrations of enals are cytotoxic. Direct conjugation of the C2-C3 double bond of enals with the sulfhydryl group of GSH is a major route for the metabolism and detoxification of enals. Recently, we found that glutathionyl conjugate of HNE (GS-HNE) enhances the peritoneal leukocyte infiltration and stimulates the formation of proinflammatory lipid mediators. Moreover, the reduced form of the glutathione conjugate of HNE (GS-DHN) elicits strong mitogenic signaling in smooth muscle cells. In this chapter we discuss the methods to study the metabolism of enals and the redox signaling properties of glutathionyl conjugates of HNE.

Indexed as

AldehydesSignal TransductionAnimalsCells, CulturedGlutathioneHumansModels, BiologicalOxidation-ReductionPC12 CellsRats2-nonenalAldehydesGlutathione

Identifiers

PMID20609918
PMCPMC3049297
OpenAlexW1535946984

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.