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Expression of inducible nitric oxide synthase and cyclooxygenase‐2 after excitotoxic damage to the immature rat brain
Author(s) -
Acarin Laia,
Peluffo Hugo,
González Berta,
Castellano Bernardo
Publication year - 2002
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.10261
Subject(s) - nitric oxide synthase , lesion , microglia , biology , cyclooxygenase , nitric oxide , neuroinflammation , pathology , inflammation , enzyme , endocrinology , medicine , immunology , biochemistry
It is well established that after adult brain damage the enzymes cyclooxygenase‐2 (COX‐2) and inducible nitric oxide synthase (iNOS) play an important role in the inflammatory processes and oxidative stress, which are considered to be the leading factors contributing to delayed cell death. The contribution of these enzymes to postnatal brain damage, however, is poorly understood. In our study, excitotoxic lesions were induced by the injection of N ‐methyl‐ D ‐aspartate in the cortex of postnatal day 9 rats. After different survival times ranging from 4 hr to 7 days post‐lesion, brain sections were processed for the immunocytochemical demonstration of COX‐2 and iNOS and double labeling with neuronal, glial and neutrophil markers. First and maximal de novo induction of iNOS and COX‐2 expression was found at 10 hr post‐lesion. Expression of both enzymes started to diminish at 24 hr, reaching basal levels at day 3. iNOS‐expressing cells were mainly identified as infiltrated neutrophils as well as highly ramified protoplasmic astrocytes closely associated with blood vessels. Moreover, scattered iNOS‐positive neurons were found at the lesion borders. In contrast, COX‐2 was mainly observed in reactive microglial cells and neuronal cells. COX‐2‐positive neurons were found within the degenerating area at 10 hr and at the borders of the lesion later on. This study shows that maximal iNOS and COX‐2 expression precedes the period of massive neuronal death observed at 24 hr post‐lesion, and may therefore contribute to the evolution of the inflammatory response and the neurodegenerative process after an excitotoxic lesion to the postnatal brain. © 2002 Wiley‐Liss, Inc.