Literature DB >> 35218041

Bioactive lipids and metabolic syndrome-a symposium report.

Loren M DeVito1, Edward A Dennis2, Barbara B Kahn3, Gerald I Shulman4, Joseph L Witztum2, Sudeshna Sadhu5, Joseph Nickels6, Matthew Spite3, Susan Smyth7, Sarah Spiegel8.   

Abstract

Recent research has shed light on the cellular and molecular functions of bioactive lipids that go far beyond what was known about their role as dietary lipids. Bioactive lipids regulate inflammation and its resolution as signaling molecules. Genetic studies have identified key factors that can increase the risk of cardiovascular diseases and metabolic syndrome through their effects on lipogenesis. Lipid scientists have explored how these signaling pathways affect lipid metabolism in the liver, adipose tissue, and macrophages by utilizing a variety of techniques in both humans and animal models, including novel lipidomics approaches and molecular dynamics models. Dissecting out these lipid pathways can help identify mechanisms that can be targeted to prevent or treat cardiometabolic conditions. Continued investigation of the multitude of functions mediated by bioactive lipids may reveal additional components of these pathways that can provide a greater understanding of metabolic homeostasis.
© 2022 New York Academy of Sciences.

Entities:  

Keywords:  bioactive lipids; cardiometabolic disease; inflammation; lipid mediators; lipid metabolism

Mesh:

Substances:

Year:  2022        PMID: 35218041      PMCID: PMC9219555          DOI: 10.1111/nyas.14752

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   6.499


  163 in total

1.  SphK1 mediates hepatic inflammation in a mouse model of NASH induced by high saturated fat feeding and initiates proinflammatory signaling in hepatocytes.

Authors:  Tuoyu Geng; Alton Sutter; Michael D Harland; Brittany A Law; Jessica S Ross; David Lewin; Arun Palanisamy; Sarah B Russo; Kenneth D Chavin; L Ashley Cowart
Journal:  J Lipid Res       Date:  2015-10-19       Impact factor: 5.922

2.  Senescent intimal foam cells are deleterious at all stages of atherosclerosis.

Authors:  Bennett G Childs; Darren J Baker; Tobias Wijshake; Cheryl A Conover; Judith Campisi; Jan M van Deursen
Journal:  Science       Date:  2016-10-27       Impact factor: 47.728

3.  Techniques to Induce and Quantify Cellular Senescence.

Authors:  Nicole Noren Hooten; Michele K Evans
Journal:  J Vis Exp       Date:  2017-05-01       Impact factor: 1.355

4.  Intestine-specific expression of MOGAT2 partially restores metabolic efficiency in Mogat2-deficient mice.

Authors:  Yu Gao; David W Nelson; Taylor Banh; Mei-I Yen; Chi-Liang Eric Yen
Journal:  J Lipid Res       Date:  2013-03-27       Impact factor: 5.922

Review 5.  Using hydrogen/deuterium exchange mass spectrometry to define the specific interactions of the phospholipase A2 superfamily with lipid substrates, inhibitors, and membranes.

Authors:  Jian Cao; John E Burke; Edward A Dennis
Journal:  J Biol Chem       Date:  2012-12-03       Impact factor: 5.157

Review 6.  Bioactive lipids in metabolic syndrome.

Authors:  Koji Nagao; Teruyoshi Yanagita
Journal:  Prog Lipid Res       Date:  2007-12-15       Impact factor: 16.195

Review 7.  Pro-resolving lipid mediators are leads for resolution physiology.

Authors:  Charles N Serhan
Journal:  Nature       Date:  2014-06-05       Impact factor: 49.962

Review 8.  Sphingolipid metabolites in inflammatory disease.

Authors:  Michael Maceyka; Sarah Spiegel
Journal:  Nature       Date:  2014-06-05       Impact factor: 49.962

9.  PKCε contributes to lipid-induced insulin resistance through cross talk with p70S6K and through previously unknown regulators of insulin signaling.

Authors:  Brandon M Gassaway; Max C Petersen; Yulia V Surovtseva; Karl W Barber; Joshua B Sheetz; Hans R Aerni; Jane S Merkel; Varman T Samuel; Gerald I Shulman; Jesse Rinehart
Journal:  Proc Natl Acad Sci U S A       Date:  2018-09-04       Impact factor: 11.205

10.  Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.

Authors:  Hong-Hee Won; Pradeep Natarajan; Amanda Dobbyn; Daniel M Jordan; Panos Roussos; Kasper Lage; Soumya Raychaudhuri; Eli Stahl; Ron Do
Journal:  PLoS Genet       Date:  2015-10-28       Impact factor: 5.917

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