Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders

The management of neurological disorders have huge and increasing human and economic costs. Despite this, there is a scarcity of effective therapeutics, and there is an extreme urgency for new and real treatments. In this short review we analyze some promising advancements in the search of new bioac...

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Main Authors: Cristina Maccallini, Rosa Amoroso
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Neural Regeneration Research
Subjects:
Online Access:http://www.nrronline.org/article.asp?issn=1673-5374;year=2016;volume=11;issue=11;spage=1731;epage=1734;aulast=Maccallini
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spelling doaj-661b1ae17a364a88b82bcb043cc85de82020-11-25T03:51:44ZengWolters Kluwer Medknow PublicationsNeural Regeneration Research1673-53742016-01-0111111731173410.4103/1673-5374.194707Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disordersCristina MaccalliniRosa AmorosoThe management of neurological disorders have huge and increasing human and economic costs. Despite this, there is a scarcity of effective therapeutics, and there is an extreme urgency for new and real treatments. In this short review we analyze some promising advancements in the search of new bioactive molecules targeting neuronal nitric oxide synthase (nNOS), an enzyme deputed to the biosynthesis of nitric oxide (NO). In different conditions of neuronal damages, this molecule is overproduced, contributing to the pathogenesis and progression of neuronal diseases. Two main approaches to modulate nNOS are discussed: a first one consisting in the direct inhibition of the enzyme by means of small organic molecules, which can be also active against other different targets involved in such diseases. A second section is dedicated to molecules able to prevent the formation of the ternary complex N-methyl-D-aspartate (NMDA)-type glutamate receptors, postsynaptic density-95 (PSD95) protein-nNOS, which is necessary to activate the latter for the biosynthesis of NO.http://www.nrronline.org/article.asp?issn=1673-5374;year=2016;volume=11;issue=11;spage=1731;epage=1734;aulast=Maccalliniamidines; carbonic anhydrase; inhibitors; neurological diseases; neuronal nitric oxide synthase; NMDAR; PSD95
collection DOAJ
language English
format Article
sources DOAJ
author Cristina Maccallini
Rosa Amoroso
spellingShingle Cristina Maccallini
Rosa Amoroso
Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
Neural Regeneration Research
amidines; carbonic anhydrase; inhibitors; neurological diseases; neuronal nitric oxide synthase; NMDAR; PSD95
author_facet Cristina Maccallini
Rosa Amoroso
author_sort Cristina Maccallini
title Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
title_short Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
title_full Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
title_fullStr Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
title_full_unstemmed Targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
title_sort targeting neuronal nitric oxide synthase as a valuable strategy for the therapy of neurological disorders
publisher Wolters Kluwer Medknow Publications
series Neural Regeneration Research
issn 1673-5374
publishDate 2016-01-01
description The management of neurological disorders have huge and increasing human and economic costs. Despite this, there is a scarcity of effective therapeutics, and there is an extreme urgency for new and real treatments. In this short review we analyze some promising advancements in the search of new bioactive molecules targeting neuronal nitric oxide synthase (nNOS), an enzyme deputed to the biosynthesis of nitric oxide (NO). In different conditions of neuronal damages, this molecule is overproduced, contributing to the pathogenesis and progression of neuronal diseases. Two main approaches to modulate nNOS are discussed: a first one consisting in the direct inhibition of the enzyme by means of small organic molecules, which can be also active against other different targets involved in such diseases. A second section is dedicated to molecules able to prevent the formation of the ternary complex N-methyl-D-aspartate (NMDA)-type glutamate receptors, postsynaptic density-95 (PSD95) protein-nNOS, which is necessary to activate the latter for the biosynthesis of NO.
topic amidines; carbonic anhydrase; inhibitors; neurological diseases; neuronal nitric oxide synthase; NMDAR; PSD95
url http://www.nrronline.org/article.asp?issn=1673-5374;year=2016;volume=11;issue=11;spage=1731;epage=1734;aulast=Maccallini
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