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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

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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AICAR Administration Causes an Apparent Enhancement of Muscle and Liver Insulin Action in Insulin-Resistant High-Fat-Fed Rats

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.

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.