Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review

Detalhes bibliográficos
Autor(a) principal: Santos, Patrícia
Data de Publicação: 2019
Outros Autores: Herrmann, Ana Paula, Elisabetsky, Elaine, Piato, Angelo Luis Stapassoli
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/197547
Resumo: Objective: Anxiety disorders are highly prevalent and the efficacy of the available anxiolytic drugs is less than desired. Adverse effects also compromise patient quality of life and adherence to treatment. Accumulating evidence shows that the pathophysiology of anxiety and related disorders is multifactorial, involving oxidative stress, neuroinflammation, and glutamatergic dysfunction. The aim of this review was to evaluate data from animal studies and clinical trials showing the anxiolytic effects of agents whose mechanisms of action target these multiple domains. Methods: The PubMed database was searched for multitarget agents that had been evaluated in animal models of anxiety, as well as randomized double-blind placebo-controlled clinical trials of anxiety and/or anxiety related disorders. Results: The main multitarget agents that have shown consistent anxiolytic effects in various animal models of anxiety, as well in clinical trials, are agomelatine, N-acetylcysteine (NAC), and omega-3 fatty acids. Data from clinical trials are preliminary at best, but reveal good safety profiles and tolerance to adverse effects. Conclusion: Agomelatine, NAC and omega-3 fatty acids show beneficial effects in clinical conditions where mainstream treatments are ineffective. These three multitarget agents are considered promising candidates for innovative, effective, and better-tolerated anxiolytics.
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spelling Santos, PatríciaHerrmann, Ana PaulaElisabetsky, ElainePiato, Angelo Luis Stapassoli2019-07-31T02:30:14Z20191516-4446http://hdl.handle.net/10183/197547001093319Objective: Anxiety disorders are highly prevalent and the efficacy of the available anxiolytic drugs is less than desired. Adverse effects also compromise patient quality of life and adherence to treatment. Accumulating evidence shows that the pathophysiology of anxiety and related disorders is multifactorial, involving oxidative stress, neuroinflammation, and glutamatergic dysfunction. The aim of this review was to evaluate data from animal studies and clinical trials showing the anxiolytic effects of agents whose mechanisms of action target these multiple domains. Methods: The PubMed database was searched for multitarget agents that had been evaluated in animal models of anxiety, as well as randomized double-blind placebo-controlled clinical trials of anxiety and/or anxiety related disorders. Results: The main multitarget agents that have shown consistent anxiolytic effects in various animal models of anxiety, as well in clinical trials, are agomelatine, N-acetylcysteine (NAC), and omega-3 fatty acids. Data from clinical trials are preliminary at best, but reveal good safety profiles and tolerance to adverse effects. Conclusion: Agomelatine, NAC and omega-3 fatty acids show beneficial effects in clinical conditions where mainstream treatments are ineffective. These three multitarget agents are considered promising candidates for innovative, effective, and better-tolerated anxiolytics.application/pdfengRevista brasileira de psiquiatria = Brazilian journal of psychiatry. São Paulo. Vol. 41, n. 2 (mar./abr. 2019), p. 168-178AnsiolíticosÁcidos graxos ômega-3AcetilcisteínaAnxietyAgomelatineN-acetylcysteineOmega-3 fatty acidsAnxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a reviewinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001093319.pdf.txt001093319.pdf.txtExtracted Texttext/plain66834http://www.lume.ufrgs.br/bitstream/10183/197547/2/001093319.pdf.txt4a62de99d76e92ad0cd5fad00c66465cMD52ORIGINAL001093319.pdfTexto completo (inglês)application/pdf185581http://www.lume.ufrgs.br/bitstream/10183/197547/1/001093319.pdf8ed7f8e5d32f27ebb8ab344c99b98677MD5110183/1975472023-09-02 03:34:54.510342oai:www.lume.ufrgs.br:10183/197547Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-09-02T06:34:54Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
title Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
spellingShingle Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
Santos, Patrícia
Ansiolíticos
Ácidos graxos ômega-3
Acetilcisteína
Anxiety
Agomelatine
N-acetylcysteine
Omega-3 fatty acids
title_short Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
title_full Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
title_fullStr Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
title_full_unstemmed Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
title_sort Anxiolytic properties of compounds that counteract oxidative stress, neuroinflammation, and glutamatergic dysfunction : a review
author Santos, Patrícia
author_facet Santos, Patrícia
Herrmann, Ana Paula
Elisabetsky, Elaine
Piato, Angelo Luis Stapassoli
author_role author
author2 Herrmann, Ana Paula
Elisabetsky, Elaine
Piato, Angelo Luis Stapassoli
author2_role author
author
author
dc.contributor.author.fl_str_mv Santos, Patrícia
Herrmann, Ana Paula
Elisabetsky, Elaine
Piato, Angelo Luis Stapassoli
dc.subject.por.fl_str_mv Ansiolíticos
Ácidos graxos ômega-3
Acetilcisteína
topic Ansiolíticos
Ácidos graxos ômega-3
Acetilcisteína
Anxiety
Agomelatine
N-acetylcysteine
Omega-3 fatty acids
dc.subject.eng.fl_str_mv Anxiety
Agomelatine
N-acetylcysteine
Omega-3 fatty acids
description Objective: Anxiety disorders are highly prevalent and the efficacy of the available anxiolytic drugs is less than desired. Adverse effects also compromise patient quality of life and adherence to treatment. Accumulating evidence shows that the pathophysiology of anxiety and related disorders is multifactorial, involving oxidative stress, neuroinflammation, and glutamatergic dysfunction. The aim of this review was to evaluate data from animal studies and clinical trials showing the anxiolytic effects of agents whose mechanisms of action target these multiple domains. Methods: The PubMed database was searched for multitarget agents that had been evaluated in animal models of anxiety, as well as randomized double-blind placebo-controlled clinical trials of anxiety and/or anxiety related disorders. Results: The main multitarget agents that have shown consistent anxiolytic effects in various animal models of anxiety, as well in clinical trials, are agomelatine, N-acetylcysteine (NAC), and omega-3 fatty acids. Data from clinical trials are preliminary at best, but reveal good safety profiles and tolerance to adverse effects. Conclusion: Agomelatine, NAC and omega-3 fatty acids show beneficial effects in clinical conditions where mainstream treatments are ineffective. These three multitarget agents are considered promising candidates for innovative, effective, and better-tolerated anxiolytics.
publishDate 2019
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dc.relation.ispartof.pt_BR.fl_str_mv Revista brasileira de psiquiatria = Brazilian journal of psychiatry. São Paulo. Vol. 41, n. 2 (mar./abr. 2019), p. 168-178
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