Abstract
Ischemia and reperfusion injury commonly occurs in ischemic heart disease, resulting in apoptotic or necrotic cell death. Apoptotic cell death is highly regulated. Two mechanisms of apoptosis involve the extrinsic death receptor pathway and the intrinsic mitochondrial pathway. Both pathways lead to the activation of effector caspases, resulting in cell death. The mitochondrial pathway plays a key role in initiating apoptosis after ischemia and reperfusion. The phosphatidylinositol 3-kinase (PI3K), protein kinase C (PKC), and extracellular signal-regulated kinase (ERK) signaling pathways protect the heart against ischemia and reperfusion injury. They inhibit mitochondrial cytochrome c release into the cytosol by regulating the Bcl-2 family proteins and activating the mitoKATP channel, thereby blocking the process of apoptosis.
Original language | English (US) |
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Title of host publication | Apoptosis, Cell Signaling, and Human Diseases |
Publisher | Humana Press |
Pages | 181-195 |
Number of pages | 15 |
Volume | 2 |
ISBN (Print) | 1588296776, 9781588296771 |
DOIs | |
State | Published - Dec 1 2007 |
Keywords
- Apoptosis
- Bcl-2
- ERK
- PI3K
- PKC
- cardioprotection
- caspases
- ischemia and reperfusion injury
- mitochondria
- signal transduction
ASJC Scopus subject areas
- General Medicine
- General Biochemistry, Genetics and Molecular Biology