Logo image
Nitric oxide-mediated expression of Bax protein and DNA fragmentation during hypoxia in neuronal nuclei from newborn piglets
Journal article   Peer reviewed

Nitric oxide-mediated expression of Bax protein and DNA fragmentation during hypoxia in neuronal nuclei from newborn piglets

Alan B Zubrow, Maria Delivoria-Papadopoulos, Qazi M Ashraf, Juan R Ballesteros, Karen I Fritz and Om P Mishra
Brain research, v 954(1)
2002
PMID: 12393233

Abstract

Bax Bcl-2 DNA fragmentation Hypoxia Nitric oxide Nitric oxide synthase
The present study tests the hypothesis that nitric oxide mediates the hypoxia-induced increase in expression of Bax and in DNA fragmentation in the cerebral cortex of newborn piglets, and that administration of N-nitro- l-arginine (NNLA), a nitric oxide synthase inhibitor, will prevent a change in hypoxia-induced expression of apoptotic genes and DNA damage. Piglets were assigned to normoxic, hypoxic, or NNLA-pretreated hypoxic groups. Cerebral tissue hypoxia was documented biochemically by measuring ATP and phosphocreatine (PCr) levels. Cerebral cortical neuronal nuclei were isolated and nuclear proteins were separated electrophoretically and probed with specific antibodies against Bcl-2 or Bax proteins. Neuronal nuclear DNA from normoxic, hypoxic, and NNLA-pretreated hypoxic animals was isolated, separated by electrophoresis on 1% agarose gel and stained with ethidium bromide. Cerebral hypoxia resulted in an increase in nuclear membrane Bax protein levels from 121.33±47.7 optical density (OD)×mm 2 in normoxic to 273.67±67.3 OD×mm 2 in hypoxic group ( P<0.05 vs. normoxic), but levels in NNLA-pretreated hypoxic group were 155.78±48.3 OD×mm 2 ( P<0.05 vs. hypoxic, P=NS vs. normoxic). Similarly, cerebral hypoxia resulted in the density of DNA fragments increasing from 1530.3±309.8 OD/mm 2 in the normoxic group to 5383.3±775 OD/mm 2 in the hypoxic group ( P<0.05), while levels in NNLA-pretreated hypoxic group were 3574.0±952 OD/mm 2 ( P<0.05 compared to hypoxic and normoxic groups). The data show that NNLA-pretreatment prevents the hypoxia-induced increase in Bax expression and DNA fragmentation demonstrating that the hypoxia-induced Bax gene expression and the DNA fragmentation are NO-mediated.

Metrics

16 Record Views
58 citations in Scopus

Details

UN Sustainable Development Goals (SDGs)

This publication has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

InCites Highlights

Data related to this publication, from InCites Benchmarking & Analytics tool:

Collaboration types
Domestic collaboration
Web of Science research areas
Neurosciences
Logo image