Mechanism of DNA fragmentation during hypoxia in the cerebral cortex of newborn piglets.

Abstract

We have previously shown that hypoxia results in increased activity of caspase-9, caspase-3 and fragmentation of nuclear DNA in the cerebral cortex of newborn piglets. The present study tested the hypothesis that mechanism of DNA fragmentation during hypoxia in the cerebral cortex of newborn piglets is mediated by caspase-9-dependent caspase-3 activation. Newborn piglets were randomly assigned to normoxic, hypoxic, and hypoxic pretreated with a highly selective caspase-9 inhibitor, Z-LEHD-FMK groups. The data showed that cerebral tissue hypoxia results in increased expression of caspase-activated DNase (CAD) protein in the nucleus and fragmentation of nuclear DNA. A pretreatment with Z-LEHD-FMK attenuated the expression of CAD protein in the nucleus and the fragmentation of nuclear DNA. Based on these results, we conclude that the mechanism by which the nuclear DNA was fragmented is mediated by caspase-9-dependent caspase-3 activation and the consequence of caspase-activated DNase activation in the cerebral cortex of newborn piglets.

• Authors: Ming-Chou Chiang, Qazi M Ashraf, Om P Mishra, Maria Delivoria-Papadopoulos
• Journal: Neurochemical research (Neurochem Res) Vol. 33 Issue 7 Pg. 1232-7 (Jul 2008) ISSN: 0364-3190 [Print] United States
• PMID: 18253826 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Apoptosis Regulatory Proteins
• Caspase Inhibitors
• Enzyme Inhibitors
• Nerve Tissue Proteins
• Oligopeptides
• benzyloxycarbonyl-leucyl-glutamyl-histidyl-aspartic acid fluoromethyl ketone
• caspase-activated DNase inhibitor
• Phosphocreatine
• Adenosine Triphosphate
• Deoxyribonucleases
• caspase-activated deoxyribonuclease
• Caspase 3
• Caspase 9

Topics

• Adenosine Triphosphate (metabolism)
• Animals
• Animals, Newborn (physiology)
• Apoptosis Regulatory Proteins (biosynthesis, genetics)
• Caspase 3 (metabolism)
• Caspase 9 (physiology)
• Caspase Inhibitors
• Cell Nucleus (drug effects, enzymology, metabolism)
• Cerebral Cortex (metabolism)
• Cytosol (drug effects, enzymology, metabolism)
• DNA Fragmentation
• Deoxyribonucleases (biosynthesis, genetics)
• Electrophoresis, Agar Gel
• Enzyme Activation (physiology)
• Enzyme Inhibitors (pharmacology)
• Hypoxia (metabolism)
• Nerve Tissue Proteins (metabolism)
• Neurons (metabolism, ultrastructure)
• Oligopeptides (pharmacology)
• Phosphocreatine (metabolism)
• Swine