Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters

This paper presents an up-to-date review of the evidence indicating that atypical neurotransmitters such as nitric oxide (NO) and endocannabinoids (eCBs) play an important role in the regulation of aversive responses in the periaqueductal gray (PAG). Among the results supporting this role, several studies have shown that inhibitors of neuronal NO synthase or cannabinoid receptor type 1 (CB1) receptor agonists cause clear anxiolytic responses when injected into this region. The nitrergic and eCB systems can regulate the activity of classical neurotransmitters such as glutamate and γ-aminobutyric acid (GABA) that control PAG activity. We propose that they exert a ‘fine-tuning’ regulatory control of defensive responses in this area. This control, however, is probably complex, which may explain the usually bell-shaped dose-response curves observed with drugs that act on NO- or CB1-mediated neurotransmission. Even if the mechanisms responsible for this complex interaction are still poorly understood, they are beginning to be recognized. For example, activation of transient receptor potential vanilloid type-1 channel (TRPV1) receptors by anandamide seems to counteract the anxiolytic effects induced by CB1 receptor activation caused by this compound. Further studies, however, are needed to identify other mechanisms responsible for this fine-tuning effect.

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Main Authors: Fogaça,M.V., Lisboa,S.F., Aguiar,D.C., Moreira,F.A., Gomes,F.V., Casarotto,P.C., Guimarães,F.S.
Format: Digital revista
Language:English
Published: Associação Brasileira de Divulgação Científica 2012
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000400010
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spelling oai:scielo:S0100-879X20120004000102012-04-05Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmittersFogaça,M.V.Lisboa,S.F.Aguiar,D.C.Moreira,F.A.Gomes,F.V.Casarotto,P.C.Guimarães,F.S. Endocannabinoid Anandamide Nitric oxide Endovanilloid TRPV1 This paper presents an up-to-date review of the evidence indicating that atypical neurotransmitters such as nitric oxide (NO) and endocannabinoids (eCBs) play an important role in the regulation of aversive responses in the periaqueductal gray (PAG). Among the results supporting this role, several studies have shown that inhibitors of neuronal NO synthase or cannabinoid receptor type 1 (CB1) receptor agonists cause clear anxiolytic responses when injected into this region. The nitrergic and eCB systems can regulate the activity of classical neurotransmitters such as glutamate and γ-aminobutyric acid (GABA) that control PAG activity. We propose that they exert a ‘fine-tuning’ regulatory control of defensive responses in this area. This control, however, is probably complex, which may explain the usually bell-shaped dose-response curves observed with drugs that act on NO- or CB1-mediated neurotransmission. Even if the mechanisms responsible for this complex interaction are still poorly understood, they are beginning to be recognized. For example, activation of transient receptor potential vanilloid type-1 channel (TRPV1) receptors by anandamide seems to counteract the anxiolytic effects induced by CB1 receptor activation caused by this compound. Further studies, however, are needed to identify other mechanisms responsible for this fine-tuning effect.info:eu-repo/semantics/openAccessAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research v.45 n.4 20122012-04-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000400010en10.1590/S0100-879X2012007500029
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language English
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author Fogaça,M.V.
Lisboa,S.F.
Aguiar,D.C.
Moreira,F.A.
Gomes,F.V.
Casarotto,P.C.
Guimarães,F.S.
spellingShingle Fogaça,M.V.
Lisboa,S.F.
Aguiar,D.C.
Moreira,F.A.
Gomes,F.V.
Casarotto,P.C.
Guimarães,F.S.
Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
author_facet Fogaça,M.V.
Lisboa,S.F.
Aguiar,D.C.
Moreira,F.A.
Gomes,F.V.
Casarotto,P.C.
Guimarães,F.S.
author_sort Fogaça,M.V.
title Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
title_short Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
title_full Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
title_fullStr Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
title_full_unstemmed Fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
title_sort fine-tuning of defensive behaviors in the dorsal periaqueductal gray by atypical neurotransmitters
description This paper presents an up-to-date review of the evidence indicating that atypical neurotransmitters such as nitric oxide (NO) and endocannabinoids (eCBs) play an important role in the regulation of aversive responses in the periaqueductal gray (PAG). Among the results supporting this role, several studies have shown that inhibitors of neuronal NO synthase or cannabinoid receptor type 1 (CB1) receptor agonists cause clear anxiolytic responses when injected into this region. The nitrergic and eCB systems can regulate the activity of classical neurotransmitters such as glutamate and γ-aminobutyric acid (GABA) that control PAG activity. We propose that they exert a ‘fine-tuning’ regulatory control of defensive responses in this area. This control, however, is probably complex, which may explain the usually bell-shaped dose-response curves observed with drugs that act on NO- or CB1-mediated neurotransmission. Even if the mechanisms responsible for this complex interaction are still poorly understood, they are beginning to be recognized. For example, activation of transient receptor potential vanilloid type-1 channel (TRPV1) receptors by anandamide seems to counteract the anxiolytic effects induced by CB1 receptor activation caused by this compound. Further studies, however, are needed to identify other mechanisms responsible for this fine-tuning effect.
publisher Associação Brasileira de Divulgação Científica
publishDate 2012
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000400010
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