[Cell death in neonatal hypoxia-ischemia].

Abstract:

OBJECTIVES:To review the mechanisms of cell death (CD) in the developing brain after hypoxia-ischemia (HI). DEVELOPMENT:The possibility of limiting the CD which occurs in serious situations of cerebral HI is based on advances in the understanding of the underlying cellular and molecular mechanisms. Various experimental models offer the opportunity to study these mechanisms in reproducible situations. Relevant concepts are the focal HI as compared to global HI, with well-differentiated patterns of selective vulnerability which depend on vascular and neurochemical factors. In situations of infarct, the distinction between core and penumbra permits the identification of areas of brain tissue which potentially may recover, where the CD occurs, at least partially, more slowly and by apoptosis. Most of this CD occurs during the phase of reperfusion, when the reintroduction of oxygen activates the neurotoxic cascades. Amongst the molecules involved in the early marking of cell damage are the genes c-fos and c-jun, HSP, MAP-2, cytokines, GLUT3 and calpaines. Some of the recent attempts of block post-HI MC are treatments with trophic factors, glucocorticoids and hypothermia. CONCLUSIONS:Analysis of the time-course of MC in perinatal HI suggest the presence of a therapeutic window. The development of treatments for nerve rescue comes up against the complexity of the mechanisms involved in MC and their potential toxicity in immature brain.

journal_name

Rev Neurol

journal_title

Revista de neurologia

authors

Macaya A

subject

Has Abstract

pub_date

2000-10-16 00:00:00

pages

784-9

issue

8

eissn

0210-0010

issn

1576-6578

journal_volume

31

pub_type

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