Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult

Electron paramagnetic resonance (EPR) was used as a method for recording the content of the nitric oxide (NO) in hippocampal tissues of intact rats and rats after modelling of ischaemic and haemorrhagic stroke. Based on direct measurements of NO by EPR spectroscopy, it was shown that, within 5 hours...

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Main Authors: Khalil L. Gainutdinov, Svetlana G. Pashkevich, Vyatcheslav V. Andrianov, Guzel G. Yafarova, Margarita O. Dosina, Tatiana Kh. Bogodvid, Julia P. Stukach, Dinara I. Silant'eva, Aleksandra S. Zamaro, Timur V. Sushko, Vladimir Kulchitsky
Format: Article
Language:English
Published: Pensoft Publishers 2017-10-01
Series:BioDiscovery
Subjects:
Online Access:https://biodiscovery.pensoft.net/article/14810/download/pdf/
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author Khalil L. Gainutdinov
Svetlana G. Pashkevich
Vyatcheslav V. Andrianov
Guzel G. Yafarova
Margarita O. Dosina
Tatiana Kh. Bogodvid
Julia P. Stukach
Dinara I. Silant'eva
Aleksandra S. Zamaro
Timur V. Sushko
Vladimir Kulchitsky
author_facet Khalil L. Gainutdinov
Svetlana G. Pashkevich
Vyatcheslav V. Andrianov
Guzel G. Yafarova
Margarita O. Dosina
Tatiana Kh. Bogodvid
Julia P. Stukach
Dinara I. Silant'eva
Aleksandra S. Zamaro
Timur V. Sushko
Vladimir Kulchitsky
author_sort Khalil L. Gainutdinov
collection DOAJ
description Electron paramagnetic resonance (EPR) was used as a method for recording the content of the nitric oxide (NO) in hippocampal tissues of intact rats and rats after modelling of ischaemic and haemorrhagic stroke. Based on direct measurements of NO by EPR spectroscopy, it was shown that, within 5 hours after the onset of symptoms of ischaemic and haemorrhagic stroke, the formation of NO in the hippocampus was reduced by a factor of 2-3 and this reduction was maintained for a period of between 24 and 72 hours. The results show that a systemic character of a decrease in the intensity of NO production during the modelling of ischaemic events in the brain reflects the effects of central dysregulation of the functions at the level of the whole organism such that it is appropriate to consider implementing the correction of the vital systems of the body in a stroke. It has indicated that non-selective NO-synthase blocker L-NAME reduced the low level of NO production by a factor of 3 by its administration within 72 hours after post-ischaemic and haemorrhagic stroke. It was discovered however that L-NAME returns the level of NO production to baseline (control) by its administration within 5 hours after ischaemia.
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spelling doaj.art-8968f35e7f214bb5a972952c9584bc2c2022-12-21T23:16:11ZengPensoft PublishersBioDiscovery2050-29662017-10-012011310.3897/biodiscovery.20.e1481014810Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic InsultKhalil L. Gainutdinov0Svetlana G. Pashkevich1Vyatcheslav V. Andrianov2Guzel G. Yafarova3Margarita O. Dosina4Tatiana Kh. Bogodvid5Julia P. Stukach6Dinara I. Silant'eva7Aleksandra S. Zamaro 8Timur V. Sushko9Vladimir Kulchitsky10Russian Academy of SciencesNational Academy of Sciences of BelarusRussian Academy of SciencesRussian Academy of SciencesNational Academy of Sciences of BelarusKazan Federal UniversityNational Academy of Sciences of BelarusKazan Federal UniversityNational Academy of Sciences of BelarusNational Academy of Sciences of BelarusNational Academy of Sciences of BelarusElectron paramagnetic resonance (EPR) was used as a method for recording the content of the nitric oxide (NO) in hippocampal tissues of intact rats and rats after modelling of ischaemic and haemorrhagic stroke. Based on direct measurements of NO by EPR spectroscopy, it was shown that, within 5 hours after the onset of symptoms of ischaemic and haemorrhagic stroke, the formation of NO in the hippocampus was reduced by a factor of 2-3 and this reduction was maintained for a period of between 24 and 72 hours. The results show that a systemic character of a decrease in the intensity of NO production during the modelling of ischaemic events in the brain reflects the effects of central dysregulation of the functions at the level of the whole organism such that it is appropriate to consider implementing the correction of the vital systems of the body in a stroke. It has indicated that non-selective NO-synthase blocker L-NAME reduced the low level of NO production by a factor of 3 by its administration within 72 hours after post-ischaemic and haemorrhagic stroke. It was discovered however that L-NAME returns the level of NO production to baseline (control) by its administration within 5 hours after ischaemia.https://biodiscovery.pensoft.net/article/14810/download/pdf/Nitric oxideElectron paramagnetic resonance
spellingShingle Khalil L. Gainutdinov
Svetlana G. Pashkevich
Vyatcheslav V. Andrianov
Guzel G. Yafarova
Margarita O. Dosina
Tatiana Kh. Bogodvid
Julia P. Stukach
Dinara I. Silant'eva
Aleksandra S. Zamaro
Timur V. Sushko
Vladimir Kulchitsky
Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult
BioDiscovery
Nitric oxide
Electron paramagnetic resonance
title Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult
title_full Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult
title_fullStr Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult
title_full_unstemmed Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult
title_short Participation of NO-synthase in Control of Nitric Oxide Level in Rat Hippocampus after Modelling of Ischaemic and Haemorrhagic Insult
title_sort participation of no synthase in control of nitric oxide level in rat hippocampus after modelling of ischaemic and haemorrhagic insult
topic Nitric oxide
Electron paramagnetic resonance
url https://biodiscovery.pensoft.net/article/14810/download/pdf/
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