Literature DB >> 9262869

Modulation of glutamine synthesis in cultured astrocytes by nitric oxide.

M D Miñana1, E Kosenko, G Marcaida, C Hermenegildo, C Montoliu, S Grisolía, V Felipo.   

Abstract

1. Previous results suggest that glutamine synthesis in brain could be modulated by nitric oxide. The aim of this work was to assess this possibility. 2. As glutamine synthetase in brain is located mainly in astrocytes, we used primary cultures of astrocytes to assess the effects of increasing or decreasing nitric oxide levels on glutamine synthesis in intact astrocytes. 3. Nitric oxide levels were decreased by adding nitroarginine, an inhibitor of nitric oxide synthase. To increase nitric oxide we used S-nitroso-N-acetylpenicillamine, a nitric oxide generating agent. 4. It is shown that S-nitroso-N-acetylpenicillamine decreases glutamine synthesis in intact astrocytes by approximately 40-50%. Nitroarginine increases glutamine synthesis slightly in intact astrocytes. 5. These results indicate that brain glutamine synthesis may be modulated in vivo by nitric oxide.

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Year:  1997        PMID: 9262869     DOI: 10.1023/a:1026339428059

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  31 in total

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Journal:  J Neurochem       Date:  1981-07       Impact factor: 5.372

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6.  Nitroarginine, an inhibitor of nitric oxide synthetase, attenuates ammonia toxicity and ammonia-induced alterations in brain metabolism.

Authors:  E Kosenko; Y Kaminsky; E Grau; M D Miñana; S Grisolía; V Felipo
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Authors:  P. Marin; M. Lafon-Cazal; J. Bockaert
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Authors:  J F Brown; P J Hanson; B J Whittle
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Authors:  G J McBean; K B Doorty; K F Tipton; H Kollegger
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10.  Nitric oxide and nitric oxide-generating agents induce a reversible inactivation of protein kinase C activity and phorbol ester binding.

Authors:  R Gopalakrishna; Z H Chen; U Gundimeda
Journal:  J Biol Chem       Date:  1993-12-25       Impact factor: 5.157

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Review 10.  Critical Evaluation of the Changes in Glutamine Synthetase Activity in Models of Cerebral Stroke.

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