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Abstract
Annual Review of Pharmacology and Toxicology
Vol. 47: 117-141 (Volume publication date February 2007)
(doi:10.1146/annurev.pharmtox.47.120505.105311)
First published online as a Review in Advance on July 31, 2006
Cell Signaling and Neuronal Death

Makoto R. Hara1 and Solomon H. Snyder1,2,3
1The Solomon H. Snyder Department of Neuroscience,
2Department of Pharmacology and Molecular Science, and
3Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205; email: ,

Abstract The past few decades have revealed that cell death can be precisely programmed with two principal forms, apoptosis and necrosis. Besides pathophysiological alterations, physiologic processes, such as the pruning of neurons during normal development and the involution of the thymus, involve apoptosis. This review focuses on the role of inter- and intracellular signaling systems in cell death, especially in the nervous system. Among neurotransmitters, glutamate and nitric oxide have been most extensively characterized and contribute to cell death in excitotoxic damage, especially in stroke and possibly in neurodegenerative diseases. Within cells, calcium, the most prominent of all intracellular messengers, mediates diverse forms of cell death with actions modulated by many proteins, including IP3 receptors, calcineurin, calpain, and cytochrome c.

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Authors:
Makoto R. Hara
Solomon H. Snyder
Keywords:
glutamate
nitric oxide
calcium
S-nitrosylation
apoptosis

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