Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis

No === Cortical spreading depression (CSD) is a temporary disruption of local ionic homeostasis that propagates slowly across the cerebral cortex. Cortical spreading depression promotes lesion progression in experimental stroke, and may contribute to the initiation of migraine attacks. The purpose o...

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Main Authors: Urenjak, Jutta A., Obrenovitch, Tihomir P., Wang, M.
Language:en
Published: 2009
Subjects:
Online Access:http://hdl.handle.net/10454/3117
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spelling ndltd-BRADFORD-oai-bradscholars.brad.ac.uk-10454-31172019-08-31T03:02:20Z Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis Urenjak, Jutta A. Obrenovitch, Tihomir P. Wang, M. Spreading depression Nitric oxide Nitric oxide synthase L-NAME Migraine Sroke N-methyl-d-aspartate No Cortical spreading depression (CSD) is a temporary disruption of local ionic homeostasis that propagates slowly across the cerebral cortex. Cortical spreading depression promotes lesion progression in experimental stroke, and may contribute to the initiation of migraine attacks. The purpose of this study was to investigate the roles of the marked increase of nitric oxide (NO) formation that occurs with CSD. Microdialysis electrodes were implanted in the cortex of anesthetized rats to perform the following operations within the same region: (1) elicitation of CSD by perfusion of high K+ medium; (2) recording of CSD elicitation; (3) application of the NO synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME); and (4) recording of dialysate pH changes. The primary effect of L-NAME (0.3 to 3.0 mmol/L in the perfusion medium) was a marked widening of individual CSD wave, resulting essentially from a delayed initiation of the repolarization phase. This change was due to NO synthase inhibition because it was not observed with the inactive isomer D-NAME, and was reversed by L-arginine. This effect did not appear to be linked to the suppression of a sustained, NO-mediated vascular change associated with the superposition of NO synthase inhibition on high levels of extracellular K+. The delayed initiation of repolarization with local NO synthase inhibition may reflect the suppression of NO-mediated negative feedback mechanisms acting on neuronal or glial processes involved in CSD genesis. However, the possible abrogation of a very brief, NO-mediated vascular change associated with the early phase of CSD cannot be ruled out. 2009-07-27T09:22:56Z 2009-07-27T09:22:56Z 2009-07-27T09:22:56Z Article No full-text available in the repository Obrenovitch, T.P., Urenjak, J.A. and Wang, M. (2002). Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis. Journal of Cerebral Blood Flow & Metabolism. Vo. 22, No. 6, pp. 680-688. http://hdl.handle.net/10454/3117 en http://www.nature.com/jcbfm/journal/v22/n6/pdf/9591259a.pdf
collection NDLTD
language en
sources NDLTD
topic Spreading depression
Nitric oxide
Nitric oxide synthase
L-NAME
Migraine
Sroke
N-methyl-d-aspartate
spellingShingle Spreading depression
Nitric oxide
Nitric oxide synthase
L-NAME
Migraine
Sroke
N-methyl-d-aspartate
Urenjak, Jutta A.
Obrenovitch, Tihomir P.
Wang, M.
Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
description No === Cortical spreading depression (CSD) is a temporary disruption of local ionic homeostasis that propagates slowly across the cerebral cortex. Cortical spreading depression promotes lesion progression in experimental stroke, and may contribute to the initiation of migraine attacks. The purpose of this study was to investigate the roles of the marked increase of nitric oxide (NO) formation that occurs with CSD. Microdialysis electrodes were implanted in the cortex of anesthetized rats to perform the following operations within the same region: (1) elicitation of CSD by perfusion of high K+ medium; (2) recording of CSD elicitation; (3) application of the NO synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME); and (4) recording of dialysate pH changes. The primary effect of L-NAME (0.3 to 3.0 mmol/L in the perfusion medium) was a marked widening of individual CSD wave, resulting essentially from a delayed initiation of the repolarization phase. This change was due to NO synthase inhibition because it was not observed with the inactive isomer D-NAME, and was reversed by L-arginine. This effect did not appear to be linked to the suppression of a sustained, NO-mediated vascular change associated with the superposition of NO synthase inhibition on high levels of extracellular K+. The delayed initiation of repolarization with local NO synthase inhibition may reflect the suppression of NO-mediated negative feedback mechanisms acting on neuronal or glial processes involved in CSD genesis. However, the possible abrogation of a very brief, NO-mediated vascular change associated with the early phase of CSD cannot be ruled out.
author Urenjak, Jutta A.
Obrenovitch, Tihomir P.
Wang, M.
author_facet Urenjak, Jutta A.
Obrenovitch, Tihomir P.
Wang, M.
author_sort Urenjak, Jutta A.
title Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
title_short Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
title_full Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
title_fullStr Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
title_full_unstemmed Nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
title_sort nitric oxide formation during cortical spreading depression is critical for rapid subsequent recovery of ionic homeostasis
publishDate 2009
url http://hdl.handle.net/10454/3117
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AT wangm nitricoxideformationduringcorticalspreadingdepressioniscriticalforrapidsubsequentrecoveryofionichomeostasis
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