Exposure to diazepam during pregnancy alters the breathing control in post-natal life

Detalhes bibliográficos
Autor(a) principal: da Silva Junior, Carlos Aparecido [UNESP]
Data de Publicação: 2019
Outros Autores: Biancardi, Vivian, Patrone, Luis Gustavo A. [UNESP], Gargaglioni, Luciane H. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/198494
Resumo: Introduction: Breathing is an important motor behavior that contributes to the maintenance of homeostasis. This behavior depends on the proper development of respiratory network located in brainstem that generates and controls the respiratory rhythm during the embryonic and post-natal ages. The development of this network can be affected by the use of psychiatric medications prescribed to mothers to treat general anxiety or panic disorders. One of the most common drugs prescribed is Diazepam (DZP), a benzodiazepine that binds to gamma-aminobutyric acid (GABAA) receptors enhancing the permeability of chloride channels. However, it is still unknown if the administration of DZP during pregnancy could have deleterious effects on breathing control during post-natal life. Objective: To understand the consequences of intrauterine exposure to DZP on the ventilatory responses of newborns rats, Material and Methods: We administered DZP (1mg/Kg) or its vehicle, via osmotic pump, to pregnant rats during whole pregnancy (21 day). We used newborns rats (male and female) at post-natal day 0 (P0) and P12. Ventilation (VE), tidal volume (VT), respiratory frequency (fR) and oxygen consumption (VO2) were measured by using head-out plethysmograph during 20 minutes of normocapnia, hypercapnia (7% CO2) and hypoxia (10% O2). Results: At P0, females treated with DZP had an attenuation of VT during hypoxia. At P12, males and females presented a decrease on VE during hypoxia and VE/VO2 was lower in DZP-treated animals. At this age, hypercapnic ventilatory response was also reduced in DZP groups due to an attenuation of VT. Conclusions: DZP during pregnancy promotes a decrease in ventilatory responses to CO2 and O2 in males and females, and this disturbance occurs at P12 that is considered the critical period for breathing control.
id UNSP_c70f7ba665aa243e14867757efb0599f
oai_identifier_str oai:repositorio.unesp.br:11449/198494
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Exposure to diazepam during pregnancy alters the breathing control in post-natal lifeAnimalBreathing controlDiazepamPregnancyIntroduction: Breathing is an important motor behavior that contributes to the maintenance of homeostasis. This behavior depends on the proper development of respiratory network located in brainstem that generates and controls the respiratory rhythm during the embryonic and post-natal ages. The development of this network can be affected by the use of psychiatric medications prescribed to mothers to treat general anxiety or panic disorders. One of the most common drugs prescribed is Diazepam (DZP), a benzodiazepine that binds to gamma-aminobutyric acid (GABAA) receptors enhancing the permeability of chloride channels. However, it is still unknown if the administration of DZP during pregnancy could have deleterious effects on breathing control during post-natal life. Objective: To understand the consequences of intrauterine exposure to DZP on the ventilatory responses of newborns rats, Material and Methods: We administered DZP (1mg/Kg) or its vehicle, via osmotic pump, to pregnant rats during whole pregnancy (21 day). We used newborns rats (male and female) at post-natal day 0 (P0) and P12. Ventilation (VE), tidal volume (VT), respiratory frequency (fR) and oxygen consumption (VO2) were measured by using head-out plethysmograph during 20 minutes of normocapnia, hypercapnia (7% CO2) and hypoxia (10% O2). Results: At P0, females treated with DZP had an attenuation of VT during hypoxia. At P12, males and females presented a decrease on VE during hypoxia and VE/VO2 was lower in DZP-treated animals. At this age, hypercapnic ventilatory response was also reduced in DZP groups due to an attenuation of VT. Conclusions: DZP during pregnancy promotes a decrease in ventilatory responses to CO2 and O2 in males and females, and this disturbance occurs at P12 that is considered the critical period for breathing control.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sao Paulo State University FCAV/UNESPUniversity Of AlbertaSao Paulo State University FCAV/UNESPUniversidade Estadual Paulista (Unesp)University Of Albertada Silva Junior, Carlos Aparecido [UNESP]Biancardi, VivianPatrone, Luis Gustavo A. [UNESP]Gargaglioni, Luciane H. [UNESP]2020-12-12T01:14:26Z2020-12-12T01:14:26Z2019-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleRevista Cubana de Investigaciones Biomedicas, v. 38, n. 5, 2019.1561-30110864-0300http://hdl.handle.net/11449/1984942-s2.0-85079133816Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista Cubana de Investigaciones Biomedicasinfo:eu-repo/semantics/openAccess2021-10-22T13:12:36Zoai:repositorio.unesp.br:11449/198494Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:30:29.221689Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Exposure to diazepam during pregnancy alters the breathing control in post-natal life
title Exposure to diazepam during pregnancy alters the breathing control in post-natal life
spellingShingle Exposure to diazepam during pregnancy alters the breathing control in post-natal life
da Silva Junior, Carlos Aparecido [UNESP]
Animal
Breathing control
Diazepam
Pregnancy
title_short Exposure to diazepam during pregnancy alters the breathing control in post-natal life
title_full Exposure to diazepam during pregnancy alters the breathing control in post-natal life
title_fullStr Exposure to diazepam during pregnancy alters the breathing control in post-natal life
title_full_unstemmed Exposure to diazepam during pregnancy alters the breathing control in post-natal life
title_sort Exposure to diazepam during pregnancy alters the breathing control in post-natal life
author da Silva Junior, Carlos Aparecido [UNESP]
author_facet da Silva Junior, Carlos Aparecido [UNESP]
Biancardi, Vivian
Patrone, Luis Gustavo A. [UNESP]
Gargaglioni, Luciane H. [UNESP]
author_role author
author2 Biancardi, Vivian
Patrone, Luis Gustavo A. [UNESP]
Gargaglioni, Luciane H. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
University Of Alberta
dc.contributor.author.fl_str_mv da Silva Junior, Carlos Aparecido [UNESP]
Biancardi, Vivian
Patrone, Luis Gustavo A. [UNESP]
Gargaglioni, Luciane H. [UNESP]
dc.subject.por.fl_str_mv Animal
Breathing control
Diazepam
Pregnancy
topic Animal
Breathing control
Diazepam
Pregnancy
description Introduction: Breathing is an important motor behavior that contributes to the maintenance of homeostasis. This behavior depends on the proper development of respiratory network located in brainstem that generates and controls the respiratory rhythm during the embryonic and post-natal ages. The development of this network can be affected by the use of psychiatric medications prescribed to mothers to treat general anxiety or panic disorders. One of the most common drugs prescribed is Diazepam (DZP), a benzodiazepine that binds to gamma-aminobutyric acid (GABAA) receptors enhancing the permeability of chloride channels. However, it is still unknown if the administration of DZP during pregnancy could have deleterious effects on breathing control during post-natal life. Objective: To understand the consequences of intrauterine exposure to DZP on the ventilatory responses of newborns rats, Material and Methods: We administered DZP (1mg/Kg) or its vehicle, via osmotic pump, to pregnant rats during whole pregnancy (21 day). We used newborns rats (male and female) at post-natal day 0 (P0) and P12. Ventilation (VE), tidal volume (VT), respiratory frequency (fR) and oxygen consumption (VO2) were measured by using head-out plethysmograph during 20 minutes of normocapnia, hypercapnia (7% CO2) and hypoxia (10% O2). Results: At P0, females treated with DZP had an attenuation of VT during hypoxia. At P12, males and females presented a decrease on VE during hypoxia and VE/VO2 was lower in DZP-treated animals. At this age, hypercapnic ventilatory response was also reduced in DZP groups due to an attenuation of VT. Conclusions: DZP during pregnancy promotes a decrease in ventilatory responses to CO2 and O2 in males and females, and this disturbance occurs at P12 that is considered the critical period for breathing control.
publishDate 2019
dc.date.none.fl_str_mv 2019-01-01
2020-12-12T01:14:26Z
2020-12-12T01:14:26Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Revista Cubana de Investigaciones Biomedicas, v. 38, n. 5, 2019.
1561-3011
0864-0300
http://hdl.handle.net/11449/198494
2-s2.0-85079133816
identifier_str_mv Revista Cubana de Investigaciones Biomedicas, v. 38, n. 5, 2019.
1561-3011
0864-0300
2-s2.0-85079133816
url http://hdl.handle.net/11449/198494
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista Cubana de Investigaciones Biomedicas
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808128524300582912