E
Eva Tomas
Researcher at Boston University
Publications - 9
Citations - 2917
Eva Tomas is an academic researcher from Boston University. The author has contributed to research in topics: AMPK & AMP-activated protein kinase. The author has an hindex of 8, co-authored 9 publications receiving 2804 citations. Previous affiliations of Eva Tomas include University of Barcelona & Boston Medical Center.
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Enhanced muscle fat oxidation and glucose transport by ACRP30 globular domain: Acetyl–CoA carboxylase inhibition and AMP-activated protein kinase activation
Eva Tomas,Tsu-Shuen Tsao,Asish K. Saha,Heather E. Murrey,Cheng Cheng Zhang,Samar I. Itani,Harvey F. Lodish,Neil B. Ruderman,Neil B. Ruderman +8 more
TL;DR: Both in vivo and in vitro, activation of AMPK was the first effect of gACRP30 and was transient, whereas alterations in malonyl CoA and ACC occurred later and were more sustained, indicating that gAC RP30 most likely exerts its actions on muscle fatty acid oxidation by inactivating ACC via activation ofAMPK and perhaps other signal transduction proteins.
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Mice Lacking Adiponectin Show Decreased Hepatic Insulin Sensitivity and Reduced Responsiveness to Peroxisome Proliferator-activated Receptor γ Agonists
Andrea R. Nawrocki,Michael W. Rajala,Eva Tomas,Utpal B. Pajvani,Asish K. Saha,Myrna E. Trumbauer,Zhen Pang,Airu S. Chen,Neil B. Ruderman,Howard Y. Chen,Luciano Rossetti,Philipp E. Scherer +11 more
TL;DR: Adiponectin is an important contributor to PPARγ-mediated improvements in glucose tolerance through mechanisms that involve the activation of the AMPK pathway.
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Role of disulfide bonds in Acrp30/adiponectin structure and signaling specificity. Different oligomers activate different signal transduction pathways.
Tsu-Shuen Tsao,Eva Tomas,Heather E. Murrey,Christopher Hug,Christopher Hug,David H. Lee,Neil B. Ruderman,John E. Heuser,Harvey F. Lodish +8 more
TL;DR: T trimeric and HMW/hexameric Acrp30 activate different signal transduction pathways, and Acr p30 represents a novel example of the control of ligand signaling via changes in its oligomerization state.
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AICAR Administration Causes an Apparent Enhancement of Muscle and Liver Insulin Action in Insulin-Resistant High-Fat-Fed Rats
Miguel A. Iglesias,Ji-Ming Ye,Georgia Frangioudakis,Asish K. Saha,Eva Tomas,Neil B. Ruderman,Gregory J. Cooney,Edward W. Kraegen +7 more
TL;DR: A single dose of AICAR leads to an apparent enhancement in whole-body, muscle, and liver insulin action in HF rats that extends beyond the expected time of AM PK activation, and the results suggest that pharmacological activation of AMPK may have potential in treating insulin-resistant states and type 2 diabetes.
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Thiazolidinediones can rapidly activate AMP-activated protein kinase in mammalian tissues.
Nathan K. LeBrasseur,Meghan Kelly,Tsu Shuen Tsao,Stephen R. Farmer,Asish K. Saha,Neil B. Ruderman,Eva Tomas +6 more
TL;DR: The results indicate that TZDs can act within minutes to activate AMPK in mammalian tissues and suggest that this effect is associated with a change in cellular energy state and that it is not dependent on PPARgamma-mediated gene transcription.