Benefits of GLP-1 Mimetics on Epicardial Adiposity

Author:

Yaribeygi Habib1,Maleki Mina2,Nasimi Fatemeh1,Jamialahmadi Tannaz34,Stanford Fatima C.5,Sahebkar Amirhossein467

Affiliation:

1. Research Center of Physiology, Semnan University of Medical Sciences, Semnan, Iran

2. Urology and Nephrology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

3. Surgical Oncology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

4. Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

5. Massachusetts General Hospital, MGH Weight Center, Department of Medicine-Division of Endocrinology-Neuroendocrine, Department of Pediatrics-Division of Endocrinology, Nutrition Obesity Research Center at Harvard (NORCH), Harvard Medical School, Boston, MA, USA

6. Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran

7. Department of Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Abstract

Abstract: The epicardial adipose tissue, which is referred to as fats surrounding the myocardium, is an active organ able to induce cardiovascular problems in pathophysiologic conditions through several pathways, such as inflammation, fibrosis, fat infiltration, and electrophysiologic problems. So, control of its volume and thickness, especially in patients with diabetes, is highly important. Incretin-based pharmacologic agents are newly developed antidiabetics that could provide further cardiovascular benefits through control and modulating epicardial adiposity. They can reduce cardiovascular risks by rapidly reducing epicardial adipose tissues, improving cardiac efficiency. We are at the first steps of a long way, but current evidence demonstrates the sum of possible mechanisms. In this study, we evaluate epicardial adiposity in physiologic and pathologic states and the impact of incretin-based drugs.

Funder

National Institutes of Health

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry

Reference69 articles.

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