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Vol. 303, Issue 2, 510-519, November 2002
Neurotoxicology Laboratory, Department of Medicinal Chemistry and
Molecular Pharmacology, Purdue University, West Lafayette, Indiana
A comparative study was conducted in rat primary cortical (CX) and
mesencephalic (MC) neurons to investigate intracellular cascades
activated during cyanide-induced injury and to determine the point at
which the cascades diverge to produce either apoptosis or necrosis.
Cyanide treatment (400 µM) for 24 h produced primarily apoptosis
in CX cells, whereas the same concentration of cyanide induced
predominantly necrosis in MC cells as indicated by increased propidium
iodide staining and cellular lactate dehydrogenase efflux. Cyanide
increased generation of cellular reactive oxygen species (ROS) in both
CX and MC cells, but the rate of formation and nature of the oxidative
species varied with cell type. Catalase decreased cyanide-induced ROS
generation in CX but not in MC cells. Nitric oxide generation was more
prominent after cyanide treatment of MC compared with CX cells.
N-Methyl-D-aspartate receptors were more involved in CX apoptosis than in MC necrosis. Mitochondrial membrane potential decreased moderately in CX cells on exposure to
cyanide, whereas MC cells responded with a more pronounced reduction in
potential. In CX cells cyanide produced a concentration-dependent release of cytochrome c from mitochondria and increased
caspase activity, whereas little change was seen in MC neurons. Thus, cyanide-induced necrosis of MC cells involved generation of excessive amounts of nitric oxide and superoxide accompanied by mitochondrial depolarization. In contrast cyanide causes a lower level of oxidative stress in CX cells, involving mainly hydrogen peroxide and superoxide, and a moderate change in mitochondrial membrane potential that lead to
cytochrome c release, caspase activation, and apoptosis.
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