| Literature DB >> 35156138 |
Gianluca Iacobellis1, Sara Basilico2, Alexis Elias Malavazos2.
Abstract
Epicardial adipose tissue surrounds and infiltrates the heart. Epicardial fat displays unique anatomic, genetic, and biomolecular properties. People with obesity and in particular, those with abdominal obesity and associated type 2 diabetes mellitus, have an increased amount of epicardial adipose tissue (EAT). Epicardial fat works well as therapeutic target due to its fast-responding metabolism, organ fat specificity, and easy measurability. Epicardial fat responds to thiazolidinediones (TZD), glucagon-like peptide 1-receptor agonists (GLP1A), sodium-glucose cotransporter 2 inhibitors (SGLT2i), dipeptidyl peptidase-4 inhibitors (DPP4i), and statins. Modulating epicardial fat morphology and genetic profile with targeted pharmacological agents suggests novel strategies in the pharmacotherapy of diabetes and obesity.Entities:
Keywords: Dipeptidyl peptidase-4 inhibitors; Epicardial adipose tissue: pharmaceutical target; Epicardial fat; Glucagon-like peptide 1-receptor agonists; Sodium glucose co-transporter 2 inhibitors; Statins; Thiazolidinediones
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Year: 2022 PMID: 35156138 DOI: 10.1007/164_2021_577
Source DB: PubMed Journal: Handb Exp Pharmacol ISSN: 0171-2004