Acute effects of ayahuasca in a juvenile non-human primate model of depression

Detalhes bibliográficos
Autor(a) principal: da Silva,Flávia S.
Data de Publicação: 2019
Outros Autores: Silva,Erick A.S., Sousa Jr.,Geovan M. de, Maia-de-Oliveira,João P., Soares-Rachetti,Vanessa de Paula, de Araujo,Draulio B., Sousa,Maria B.C., Lobão-Soares,Bruno, Hallak,Jaime, Galvão-Coelho,Nicole L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Psychiatry (São Paulo. 1999. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462019000400280
Resumo: Objective: The incidence rate of major depression in adolescents reaches approximately 14%. This disorder is usually recurrent, without remission of symptoms even after pharmacological treatment, and persists throughout adult life. Since the effects of antidepressants take approximately 2 weeks to begin, new pharmacological therapies are under continuous exploration. Recent evidence suggests that psychedelics could produce rapid antidepressant effects. In this study, we evaluated the potential antidepressant effects of ayahuasca in a juvenile non-human primate model of depression. Methods: While living with their families, juvenile marmosets (8 males; 7 females) were observed on alternate days for four weeks during a baseline phase. This was followed by 8 weeks of an induced depressive state protocol, the social isolated context (IC), in which the animals were monitored in the first and last weeks. Subsequently, five males and four females were randomly selected for treatment, first with a single administration of saline vehicle (1.67 mL/300 g of body weight, via gavage), followed by a single dose of ayahuasca (1.67 mL/300 g of body weight, via gavage). Both phases lasted 1 week and the animals were monitored daily. A third week of sampling was called the tardive-pharmacological effects phase. In all phases the marmosets were assessed for behavior, fecal cortisol levels, and body weight. Results: After IC, the animals presented typical hypocortisolemia, but cortisol recovered to baseline levels 24 h after an acute dose of ayahuasca; this recovery was not observed in vehicle-treated animals. Additionally, in males, ayahuasca, but not the vehicle, reduced scratching, a stereotypic behavior, and increased feeding. Ayahuasca treatment also improved body weight to baseline levels in both sexes. The ayahuasca-induced behavioral response had long-term effects (14 days). Thus, in this translational juvenile animal model of depression, ayahuasca presented beneficial effects. Conclusions: These results can contribute to the validation of ayahuasca as an antidepressant drug and encourage new studies on psychedelic drugs as a tool for treating mood disorders, including for adolescents with early-onset depression.
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spelling Acute effects of ayahuasca in a juvenile non-human primate model of depressionTranslational animal modelnon-human primatecommon marmosetmarmosetcortisolearly-age depressionpsychedelic drugs Objective: The incidence rate of major depression in adolescents reaches approximately 14%. This disorder is usually recurrent, without remission of symptoms even after pharmacological treatment, and persists throughout adult life. Since the effects of antidepressants take approximately 2 weeks to begin, new pharmacological therapies are under continuous exploration. Recent evidence suggests that psychedelics could produce rapid antidepressant effects. In this study, we evaluated the potential antidepressant effects of ayahuasca in a juvenile non-human primate model of depression. Methods: While living with their families, juvenile marmosets (8 males; 7 females) were observed on alternate days for four weeks during a baseline phase. This was followed by 8 weeks of an induced depressive state protocol, the social isolated context (IC), in which the animals were monitored in the first and last weeks. Subsequently, five males and four females were randomly selected for treatment, first with a single administration of saline vehicle (1.67 mL/300 g of body weight, via gavage), followed by a single dose of ayahuasca (1.67 mL/300 g of body weight, via gavage). Both phases lasted 1 week and the animals were monitored daily. A third week of sampling was called the tardive-pharmacological effects phase. In all phases the marmosets were assessed for behavior, fecal cortisol levels, and body weight. Results: After IC, the animals presented typical hypocortisolemia, but cortisol recovered to baseline levels 24 h after an acute dose of ayahuasca; this recovery was not observed in vehicle-treated animals. Additionally, in males, ayahuasca, but not the vehicle, reduced scratching, a stereotypic behavior, and increased feeding. Ayahuasca treatment also improved body weight to baseline levels in both sexes. The ayahuasca-induced behavioral response had long-term effects (14 days). Thus, in this translational juvenile animal model of depression, ayahuasca presented beneficial effects. Conclusions: These results can contribute to the validation of ayahuasca as an antidepressant drug and encourage new studies on psychedelic drugs as a tool for treating mood disorders, including for adolescents with early-onset depression.Associação Brasileira de Psiquiatria2019-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462019000400280Brazilian Journal of Psychiatry v.41 n.4 2019reponame:Brazilian Journal of Psychiatry (São Paulo. 1999. Online)instname:Associação Brasileira de Psiquiatria (ABP)instacron:ABP10.1590/1516-4446-2018-0140info:eu-repo/semantics/openAccessda Silva,Flávia S.Silva,Erick A.S.Sousa Jr.,Geovan M. deMaia-de-Oliveira,João P.Soares-Rachetti,Vanessa de Paulade Araujo,Draulio B.Sousa,Maria B.C.Lobão-Soares,BrunoHallak,JaimeGalvão-Coelho,Nicole L.eng2019-10-11T00:00:00Zoai:scielo:S1516-44462019000400280Revistahttp://www.bjp.org.br/ahead_of_print.asphttps://old.scielo.br/oai/scielo-oai.php||rbp@abpbrasil.org.br1809-452X1516-4446opendoar:2019-10-11T00:00Brazilian Journal of Psychiatry (São Paulo. 1999. Online) - Associação Brasileira de Psiquiatria (ABP)false
dc.title.none.fl_str_mv Acute effects of ayahuasca in a juvenile non-human primate model of depression
title Acute effects of ayahuasca in a juvenile non-human primate model of depression
spellingShingle Acute effects of ayahuasca in a juvenile non-human primate model of depression
da Silva,Flávia S.
Translational animal model
non-human primate
common marmoset
marmoset
cortisol
early-age depression
psychedelic drugs
title_short Acute effects of ayahuasca in a juvenile non-human primate model of depression
title_full Acute effects of ayahuasca in a juvenile non-human primate model of depression
title_fullStr Acute effects of ayahuasca in a juvenile non-human primate model of depression
title_full_unstemmed Acute effects of ayahuasca in a juvenile non-human primate model of depression
title_sort Acute effects of ayahuasca in a juvenile non-human primate model of depression
author da Silva,Flávia S.
author_facet da Silva,Flávia S.
Silva,Erick A.S.
Sousa Jr.,Geovan M. de
Maia-de-Oliveira,João P.
Soares-Rachetti,Vanessa de Paula
de Araujo,Draulio B.
Sousa,Maria B.C.
Lobão-Soares,Bruno
Hallak,Jaime
Galvão-Coelho,Nicole L.
author_role author
author2 Silva,Erick A.S.
Sousa Jr.,Geovan M. de
Maia-de-Oliveira,João P.
Soares-Rachetti,Vanessa de Paula
de Araujo,Draulio B.
Sousa,Maria B.C.
Lobão-Soares,Bruno
Hallak,Jaime
Galvão-Coelho,Nicole L.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv da Silva,Flávia S.
Silva,Erick A.S.
Sousa Jr.,Geovan M. de
Maia-de-Oliveira,João P.
Soares-Rachetti,Vanessa de Paula
de Araujo,Draulio B.
Sousa,Maria B.C.
Lobão-Soares,Bruno
Hallak,Jaime
Galvão-Coelho,Nicole L.
dc.subject.por.fl_str_mv Translational animal model
non-human primate
common marmoset
marmoset
cortisol
early-age depression
psychedelic drugs
topic Translational animal model
non-human primate
common marmoset
marmoset
cortisol
early-age depression
psychedelic drugs
description Objective: The incidence rate of major depression in adolescents reaches approximately 14%. This disorder is usually recurrent, without remission of symptoms even after pharmacological treatment, and persists throughout adult life. Since the effects of antidepressants take approximately 2 weeks to begin, new pharmacological therapies are under continuous exploration. Recent evidence suggests that psychedelics could produce rapid antidepressant effects. In this study, we evaluated the potential antidepressant effects of ayahuasca in a juvenile non-human primate model of depression. Methods: While living with their families, juvenile marmosets (8 males; 7 females) were observed on alternate days for four weeks during a baseline phase. This was followed by 8 weeks of an induced depressive state protocol, the social isolated context (IC), in which the animals were monitored in the first and last weeks. Subsequently, five males and four females were randomly selected for treatment, first with a single administration of saline vehicle (1.67 mL/300 g of body weight, via gavage), followed by a single dose of ayahuasca (1.67 mL/300 g of body weight, via gavage). Both phases lasted 1 week and the animals were monitored daily. A third week of sampling was called the tardive-pharmacological effects phase. In all phases the marmosets were assessed for behavior, fecal cortisol levels, and body weight. Results: After IC, the animals presented typical hypocortisolemia, but cortisol recovered to baseline levels 24 h after an acute dose of ayahuasca; this recovery was not observed in vehicle-treated animals. Additionally, in males, ayahuasca, but not the vehicle, reduced scratching, a stereotypic behavior, and increased feeding. Ayahuasca treatment also improved body weight to baseline levels in both sexes. The ayahuasca-induced behavioral response had long-term effects (14 days). Thus, in this translational juvenile animal model of depression, ayahuasca presented beneficial effects. Conclusions: These results can contribute to the validation of ayahuasca as an antidepressant drug and encourage new studies on psychedelic drugs as a tool for treating mood disorders, including for adolescents with early-onset depression.
publishDate 2019
dc.date.none.fl_str_mv 2019-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462019000400280
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462019000400280
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1516-4446-2018-0140
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Brasileira de Psiquiatria
publisher.none.fl_str_mv Associação Brasileira de Psiquiatria
dc.source.none.fl_str_mv Brazilian Journal of Psychiatry v.41 n.4 2019
reponame:Brazilian Journal of Psychiatry (São Paulo. 1999. Online)
instname:Associação Brasileira de Psiquiatria (ABP)
instacron:ABP
instname_str Associação Brasileira de Psiquiatria (ABP)
instacron_str ABP
institution ABP
reponame_str Brazilian Journal of Psychiatry (São Paulo. 1999. Online)
collection Brazilian Journal of Psychiatry (São Paulo. 1999. Online)
repository.name.fl_str_mv Brazilian Journal of Psychiatry (São Paulo. 1999. Online) - Associação Brasileira de Psiquiatria (ABP)
repository.mail.fl_str_mv ||rbp@abpbrasil.org.br
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