Chronic heart failure: Ca(2+), catabolism, and catastrophic cell death. Review uri icon

Overview

abstract

  • Robust successes have been achieved in recent years in conquering the acutely lethal manifestations of heart disease. Many patients who previously would have died now survive to enjoy happy and productive lives. Nevertheless, the devastating impact of heart disease continues unabated, as the spectrum of disease has evolved with new manifestations. In light of this ever-evolving challenge, insights that culminate in novel therapeutic targets are urgently needed. Here, we review fundamental mechanisms of heart failure, both with reduced (HFrEF) and preserved (HFpEF) ejection fraction. We discuss pathways that regulate cardiomyocyte remodeling and turnover, focusing on Ca(2+) signaling, autophagy, and apoptosis. In particular, we highlight recent insights pointing to novel connections among these events. We also explore mechanisms whereby potential therapeutic approaches targeting these processes may improve morbidity and mortality in the devastating syndrome of heart failure.

publication date

  • January 13, 2016

Research

keywords

  • Calcium
  • Calcium Signaling
  • Heart Failure
  • Myocytes, Cardiac

Identity

PubMed Central ID

  • PMC4791054

Scopus Document Identifier

  • 84958817706

Digital Object Identifier (DOI)

  • 10.1016/j.bbadis.2016.01.011

PubMed ID

  • 26775029

Additional Document Info

volume

  • 1862

issue

  • 4