Literature DB >> 7510374

Inducible nitric oxide synthase in glial cells.

Y Nomura1, Y Kitamura.   

Abstract

Nitric oxide (NO), a free radical gas, has been suggested to mediate both synaptic plasticity and neuronal death. NO is generated by constitutive and inducible types of NO synthase (cNOS and iNOS, respectively). The neuronal cNOS was recently cloned, sequenced and characterized. In contrast, properties of iNOS in the brain are not fully understood. It is noted that glial cells can form NO and that microglial and reactive astroglial cells are accumulated around neurodegenerative sites in the brain, suggesting a relationship between neuronal injury and NO originated from glial cells. We found that several stimuli such as endotoxin (lipopolysaccharide) and cytokines induced iNOS in glial cells of rat brain. This article reviews recent findings on characteristics and the induction mechanism of iNOS in the glial cells, and discusses the possible pathophysiological functions of iNOS in the brain.

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Year:  1993        PMID: 7510374     DOI: 10.1016/0168-0102(93)90013-g

Source DB:  PubMed          Journal:  Neurosci Res        ISSN: 0168-0102            Impact factor:   3.304


  16 in total

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2.  Reovirus infection of the CNS enhances iNOS expression in areas of virus-induced injury.

Authors:  Robin J Goody; Cristen C Hoyt; Kenneth L Tyler
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Review 3.  Histochemistry of nitric oxide synthase in the nervous system.

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5.  Nitration as a mechanism of Na+, K+-ATPase modification during hypoxia in the cerebral cortex of the guinea pig fetus.

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8.  Nitric oxide (no), citrulline - no cycle enzymes, glutamine synthetase and oxidative stress in anoxia (hypobaric hypoxia) and reperfusion in rat brain.

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9.  Neurodegeneration and glia response in rat hippocampus following nitro-L-arginine methyl ester (L-NAME).

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Review 10.  Nitric oxide and the brain. Part 2: Effects following neonatal brain injury-friend or foe?

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Journal:  Pediatr Res       Date:  2020-06-20       Impact factor: 3.756

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