Targeting perivascular and epicardial adipose tissue inflammation: Therapeutic opportunities for cardiovascular disease

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Portland Press Ltd

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Major shifts in human lifestyle and dietary habits toward sedentary behavior and refined food intake triggered steep increase in the incidence of metabolic disorders including obesity and Type 2 diabetes. Patients with metabolic disease are at a high risk of cardiovascular complications ranging from microvascular dysfunction to cardiometabolic syndromes including heart failure. Despite significant advances in the standards of care for obese and diabetic patients, current therapeutic approaches are not always successful in averting the accompanying cardiovascular deterioration. There is a strong relationship between adipose inflammation seen in metabolic disorders and detrimental changes in cardiovascular structure and function. The particular importance of epicardial and perivascular adipose pools emerged as main modulators of the physiology or pathology of heart and blood vessels. Here, we review the peculiarities of these two fat depots in terms of their origin, function, and pathological changes during metabolic deterioration. We highlight the rationale for pharmacological targeting of the perivascular and epicardial adipose tissue or associated signaling pathways as potential disease modifying approaches in cardiometabolic syndromes. © 2020 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.

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Adipogenesis, Adipokines, Adipose tissue, Adiposity, Animals, Anti-inflammatory agents, Blood vessels, Cardiovascular diseases, Energy metabolism, Humans, Inflammation, Inflammation mediators, Molecular targeted therapy, Pericardium, Signal transduction, Adipocytokine receptor, Adiponectin, Angiotensin converting enzyme 2, Angiotensin ii, Angiotensin[1-7], Chemerin, Hydroxymethylglutaryl coenzyme a reductase inhibitor, Leptin, Mas receptor, Metformin, Mineralocorticoid antagonist, Renin, Resistin, Sodium glucose cotransporter 2 inhibitor, Unclassified drug, Uncoupling protein 1, Adipocytokine, Antiinflammatory agent, Autacoid, Cardiovascular disease, Cell aging, Diabetes mellitus, Diet, Drug mechanism, Epicardial fat, Heart failure with preserved ejection fraction, Human, Immunomodulation, Lifestyle, Metabolic disorder, Nonhuman, Obesity, Pericardial fat, Perivascular adipose tissue, Priority journal, Protein function, Renin angiotensin aldosterone system, Review, Thromboembolism, Tissue structure, Vascular disease, Animal, Blood vessel, Drug effect, Metabolism, Molecularly targeted therapy, Pathology, Pathophysiology, Cytokine release, Diet therapy, Heart tissue, Lifestyle modification

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