The Randle cycle revisited: a new head for an old hat.
By L. Hue, H. Taegtmeyer. American Journal of Physiology. Endocrinology and Metabolism, 2009
727 citations recorded by the source corpus.
Subfields: Molecular Biology, Physiology
View Paper: https://www.semanticscholar.org/paper/01a171f32bbe221d09090ca571823a6242608f8e
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Citations in the corpus
- Pathological Ventricular Remodeling: Mechanisms: Part 1 of 2 (2013, background): “bolic demands of the heart are met by metabolism of fatty acids and glucose and, to a lesser extent, lactate and ketone bodies.(134)”
- Diabetic cardiomyopathy: an update of mechanisms contributing to this clinical entity (2018, background): “In this regard, activation of lipolysis provides FFAs as the preferred fuel source leading to ketogenesis during fasting whereas inhibition of glucose oxidation contributes to a glucose-sparing effect that is an essential survival mechanism during times of starvation.(67) In the fed state or during ”
- Lipolysis – A highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores (2011, background): “This mechanism adapts substrate utilization to substrate availability in coordination with hormones controlling energy metabolism [160].”
- Pathophysiology of cardiac hypertrophy and heart failure: signaling pathways and novel therapeutic targets (2015, background): “As conditions such as cardiac workload, oxygen supply and nutritional supply are altered, the heart is able to adapt and rely on varying proportions of substrates as a source of ATP to ensure that a constant supply of energy can be generated (Hue and Taegtmeyer 2009).”