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Sexually dimorphic effects of prenatal diazepam exposure on respiratory control and the monoaminergic system of neonate and young rats

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Author(s):
da Silva Junior, Carlos Aparecido ; Patrone, Luis Gustavo A. ; Biancardi, Vivian ; Vilela-Costa, Heloisa H. ; Marques, Danuzia A. ; Cristina-Silva, Caroline ; da Costa Silva, Kaoma Stephani ; Bicego, Kenia C. ; Szawka, Raphael E. ; Gargaglioni, Luciane H.
Total Authors: 10
Document type: Journal article
Source: PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY; v. 474, n. 11, p. 16-pg., 2022-07-25.
Abstract

Pregnancy is highly affected by anxiety disorders, which may be treated with benzodiazepines, especially diazepam (DZP), that can cross the placental barrier and interact with the fetal GABAergic system. We tested whether prenatal exposure to DZP promotes sex-specific postnatal changes in the respiratory control of rats. We evaluated ventilation ((V)over dot(E)) and oxygen consumption ((V)over dot O-2) in resting conditions and under hypercapnia (7% CO2) and hypoxia (10% O-2) in newborn [postnatal day (P) 0-1 and (P12-13)] and young (P21-22) rats from mothers treated with DZP during pregnancy. We also analyzed brainstem monoamines at the same ages. DZP exposure had minimal effects on room air-breathing variables in females, but caused hypoventilation (drop in (V)Over dot(E)/(V)Over dot O-2) in P12-13 males, lasting until P21-22. The hypercapnic ventilatory response was attenuated in P0-1 and P12-13 DZP-treated females mainly by a decrease in tidal volume (V-T), whereas males had a reduction in respiratory frequency (f(R)) at P12-13. Minor changes were observed in hypoxia, but an attenuation in (V)over dot(E) was seen in P12-13 males. In the female brainstem, DZP increased dopamine concentration and decreased 5-hydroxyindole-3-acetic acid (5-HIAA) and the 3,4-dihydroxyphenylacetic acid (DOPAC)/dopamine ratio at P0-1, and reduced DOPAC concentration at P12-13. In males, DZP decreased brainstem noradrenaline at P0-1. Our results demonstrate that prenatal DZP exposure reduces CO2 chemoreflex only in postnatal females and does not affect hypoxia-induced hyperventilation in both sexes. In addition, prenatal DZP alters brainstem monoamine concentrations throughout development differently in male and female rats. (AU)

FAPESP's process: 17/05318-0 - Developmental consequences of intrauterine exposure to cannabinoids: impact on the cardiorespiratory system and sleep-wake cycle
Grantee:Luis Gustavo Alexandre Patrone
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 16/17681-9 - Pathophysiological changes during systemic inflammation
Grantee:Luiz Guilherme de Siqueira Branco
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 20/01702-2 - Physiopathology of CO2 sensitivity: role of locus coeruleus
Grantee:Luciane Helena Gargaglioni Batalhão
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 17/26367-9 - Developmental consequences of intra-uterine exposure to diazepam: impact on the ventilatory system of newborns rats
Grantee:Carlos Aparecido da Silva Junior
Support Opportunities: Scholarships in Brazil - Master