Multiple interacting cell death mechanisms in the mediation of excitotoxicity and ischemic brain damage: A challenge for neuroprotection.


Autoria(s): Puyal J.; Ginet V.; Clarke P.G.
Data(s)

2013

Resumo

There is currently no approved neuroprotective pharmacotherapy for acute conditions such as stroke and cerebral asphyxia. One of the reasons for this may be the multiplicity of cell death mechanisms, because inhibition of a particular mechanism leaves the brain vulnerable to alternative ones. It is therefore essential to understand the different cell death mechanisms and their interactions. We here review the multiple signaling pathways underlying each of the three main morphological types of cell death - apoptosis, autophagic cell death and necrosis - emphasizing their importance in the neuronal death that occurs during cerebral ischemia and hypoxia-ischemia, and we analyze the interactions between the different mechanisms. Finally, we discuss the implications of the multiplicity of cell death mechanisms for the design of neuroprotective strategies.

Identificador

https://serval.unil.ch/?id=serval:BIB_63839B33A37E

isbn:1873-5118 (Electronic)

pmid:23567504

doi:10.1016/j.pneurobio.2013.03.002

isiid:000320418400002

http://my.unil.ch/serval/document/BIB_63839B33A37E.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_63839B33A37E7

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

Progress in Neurobiology, vol. 105, pp. 24-48

Palavras-Chave #Neuronal death; Apoptosis; Necrosis; Autophagy; Stroke; Hypoxia-ischemia
Tipo

info:eu-repo/semantics/review

article