Protein kinases and kinase-modulated effectors in the late phase of ischemic preconditioning

Basic Res Cardiol. May-Jun 2001;96(3):207-18. doi: 10.1007/s003950170051.

Abstract

In the 15 years since the first publication on ischemic preconditioning (PC), our knowledge of this phenomenon has increased exponentially. While the original studies described the early phase of ischemic PC, we now know that a second or late phase of ischemic PC also exists. In particular, the late phase of PC is triggered by factors such as adenosine, opioids, radicals, and nitric oxide. These factors in turn initiate a molecular chain reaction, which includes activation of serine/threonine kinases, tyrosine kinases, and mitogen-activated protein kinases. Subsequently, this cascade of reactions modulates a plethora of cardioprotective proteins including heat shock proteins, KATP channels, nitric oxide synthase, cyclooxygenase-2, and antioxidants. However, despite this phenomenal amount of information, the construction of a unifying hypothesis describing the signaling mechanism of late PC has proved challenging. The purpose of this article, therefore, is to review the current literature and hypothesis regarding the signaling system in the late phase of ischemic PC, to tackle areas of controversy within this model, and to address potential future directions of investigation that will hopefully promote the generation of a unifying paradigm.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Forecasting
  • Heat-Shock Proteins / pharmacology
  • Heat-Shock Proteins / physiology
  • Humans
  • Ischemic Preconditioning, Myocardial*
  • Myocardial Infarction / metabolism
  • Myocardial Infarction / physiopathology*
  • Myocardial Infarction / prevention & control*
  • Protein Kinase C / pharmacology
  • Protein Kinase C / physiology
  • Protein Kinases / pharmacology
  • Protein Kinases / physiology*
  • Protein-Tyrosine Kinases / pharmacology
  • Protein-Tyrosine Kinases / physiology
  • Signal Transduction / physiology

Substances

  • Heat-Shock Proteins
  • Protein Kinases
  • Protein-Tyrosine Kinases
  • Protein Kinase C