Macromolecular Degradation Systems and Cardiovascular Aging.

Abstract

Aging-related cardiovascular diseases are a rapidly increasing problem worldwide. Cardiac aging demonstrates progressive decline of diastolic dysfunction of ventricle and increase in ventricular and arterial stiffness accompanied by increased fibrosis stimulated by angiotensin II and proinflammatory cytokines. Reactive oxygen species and multiple signaling pathways on cellular senescence play major roles in the process. Aging is also associated with an alteration in steady state of macromolecular dynamics including a dysfunction of protein synthesis and degradation. Currently, impaired macromolecular degradation is considered to be closely related to enhanced inflammation and be involved in the process and mechanism of cardiac aging. Herein, we review the role and mechanisms of the degradation system of intracellular macromolecules in the process and pathophysiology of cardiovascular aging.

• Authors: Hiroyuki Nakayama, Kazuhiko Nishida, Kinya Otsu
• Journal: Circulation research (Circ Res) Vol. 118 Issue 10 Pg. 1577-92 (05 13 2016) ISSN: 1524-4571 [Electronic] United States
• PMID: 27174951 (Publication Type: Journal Article, Review, Research Support, Non-U.S. Gov't)
• Copyright: © 2016 American Heart Association, Inc.

Chemical References

• Proteasome Endopeptidase Complex

Topics

• Aging (metabolism, pathology)
• Animals
• Autophagy
• Coronary Vessels (growth & development, metabolism)
• Humans
• Myocardium (metabolism)
• Proteasome Endopeptidase Complex (metabolism)
• Proteolysis