Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
Neuronal subclass-selective loss of pyruvate dehydrogenase immunoreactivity following canine cardiac arrest and resuscitation.
Y E Bogaert; K F Sheu; P R Hof; A M Brown; J P Blass; R E Rosenthal; G Fiskum (Profiled Authors: Gary M Fiskum; Robert E Rosenthal)
Department of Biochemistry, George Washington University School of Medicine, Washington, DC, 20031, USA.
Experimental neurology 2000;161(1):115-26.
Chronic impairment of aerobic energy metabolism accompanies global cerebral ischemia and reperfusion and likely contributes to delayed neuronal cell death. Reperfusion-dependent inhibition of pyruvate dehydrogenase complex (PDHC) enzyme activity has been described and proposed to be at least partially responsible for this metabolic abnormality. This study tested the hypothesis that global cerebral ischemia and reperfusion results in the loss of pyruvate dehydrogenase immunoreactivity and that such loss is associated with selective neuronal vulnerability to transient ischemia. Following 10 min canine cardiac arrest, resuscitation, and 2 or 24 h of restoration of spontaneous circulation, brains were either perfusion fixed for immunohistochemical analyses or biopsy samples were removed for Western immunoblot analyses of PDHC immunoreactivity. A significant decrease in immunoreactivity was observed in frontal cortex homogenates from both 2 and 24 h reperfused animals compared to samples from nonischemic control animals. These results were supported by confocal microscopic immunohistochemical determinations of pyruvate dehydrogenase immunoreactivity in the neuronal cell bodies located within different layers of the frontal cortex. Loss of immunoreactivity was greatest for pyramidal neurons located in layer V compared to neurons in layers IIIc/IV, which correlates with a greater vulnerability of layer V neurons to delayed death caused by transient global cerebral ischemia.
1 Originating Grant
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1.
Fiskum, Gary
Molecular Mechanisms of Ischemia Reperfusion Brain Injury
1 May 1995 - 31 December 2008
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Publications
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1.
1994Y E Bogaert; R E Rosenthal; G Fiskum
Postischemic inhibition of cerebral cortex pyruvate dehydrogenase.
Free radical biology & medicine 1994;16(6):811-20. -
2.
2007Erica M Richards; Gary Fiskum; Robert E Rosenthal; Irene Hopkins; Mary C McKenna
Hyperoxic reperfusion after global ischemia decreases hippocampal energy metabolism.
Stroke; a journal of cerebral circulation 2007;38(5):1578-84. -
3.
2006Viktoria Vereczki; Erica Martin; Robert E Rosenthal; Patrick R Hof; Gloria E Hoffman; Gary Fiskum
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2006;26(6):821-35.
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