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Studying the Role of AMPK in Cardiac Hypertrophy and Protein Synthesis.

Authors :
UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire
UCL - (SLuc) Service de pathologies cardiovasculaires intensives
UCL - (SLuc) Département cardiovasculaire
UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique
UCL - (SLuc) Département de médecine interne et services associés
Mailleux, Florence
Beauloye, Christophe
Balligand, Jean-Luc
Horman, Sandrine
Bertrand, Luc
UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire
UCL - (SLuc) Service de pathologies cardiovasculaires intensives
UCL - (SLuc) Département cardiovasculaire
UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique
UCL - (SLuc) Département de médecine interne et services associés
Mailleux, Florence
Beauloye, Christophe
Balligand, Jean-Luc
Horman, Sandrine
Bertrand, Luc
Source :
Methods in molecular biology (Clifton, N.J.), Vol. 1732, no.1, p. 321-342 (2018)
Publication Year :
2018

Abstract

Pathological cardiac hypertrophy, which is a compensatory mechanism established to maintain cardiac function in response to neurohormonal or mechanical stresses, becomes maladaptive with time and frequently leads to heart failure. AMP-activated protein kinase (AMPK) has been extensively described in the literature to act as a break in cardiac hypertrophy development. Its anti-hypertrophic action mostly correlates with the inhibition of several important players of cardiac hypertrophy including protein synthesis and pro-hypertrophic gene expression pathways involving the transcription factor nuclear factor of activated T cells (NFAT) and the mitogen-activated protein kinases ERK1/2. In this chapter, we describe methodologies designed to evaluate cardiomyocyte hypertrophy and its major molecular mechanisms in response to AMPK activation. Two different compounds, AICAr and the biguanide phenformin, were used to promote AMPK activation.

Details

Database :
OAIster
Journal :
Methods in molecular biology (Clifton, N.J.), Vol. 1732, no.1, p. 321-342 (2018)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372953900
Document Type :
Electronic Resource