Abstract

We mapped and characterized changes in the activity of brainstem cell groups under hypoxia in one-day-old newborn mice, an animal model in which the central nervous system at birth is particularly immature. The classical biphasic respiratory response characterized by transient hyperventilation, followed by severe ventilation decline, was associated with increased c-FOS immunoreactivity in brainstem cell groups: the nucleus of the solitary tract, ventral reticular nucleus of the medulla, retrotrapezoid/parafacial region, parapyramidal group, raphe magnus nucleus, lateral, and medial parabrachial nucleus, and dorsal subcoeruleus nucleus. In contrast, the hypoglossal nucleus displayed decreased c-FOS immunoreactivity. There were fewer or no activated catecholaminergic cells activated in the medulla oblongata, whereas ~45% of the c-FOS-positive cells in the dorsal subcoeruleus were co-labeled. Approximately 30% of the c-FOS-positive cells in the parapyramidal group were serotoninergic, whereas only a small portion were labeled for serotonin in the raphe magnus nucleus. None of the c-FOS-positive cells in the retrotrapezoid/parafacial region were co-labeled for PHOX2B. Thus, the hypoxia-activated brainstem neuronal network of one-day-old mice is characterized by (i) the activation of catecholaminergic cells of the dorsal subcoeruleus nucleus, a structure implicated in the strong depressive pontine influence previously reported in the fetus but not in newborns, (ii) the weak activation of catecholaminergic cells of the ventral reticular nucleus of the medulla, an area involved in hypoxic hyperventilation, and (iii) the absence of PHOX2B-positive cells activated in the retrotrapezoid/parafacial region. Based on these results, one-day-old mice could highlight characteristics for modeling the breathing network of premature infants.

Highlights

  • Human infants, premature infants, display frequent episodes of apnea, and bradypnea, and very common episodes of hypoxia during the postnatal period (Bryan et al, 1986; Carroll and Agarwal, 2010; Teppema and Dahan, 2010; Mathew, 2011)

  • Our results revealed that the hypoxia-activated brainstem neuronal network of oneday-old mice is characterized by weak or absent activation of cells in areas involved in hypoxic hyperventilation i.e., catecholaminergic neurons of the ventral reticular nucleus of the medulla (VLM) and PHOX2B cells of the retrotrapezoid/parafacial region (Erickson and Millhorn, 1991, 1994; Takakura et al, 2006) as suggested by the scarcity or absence of tyrosine hydroxylase (TH)-positive or PHOX2B-positive cells among the c-FOS-positive-cells

  • This study significantly contributes to the knowledge of key brainstem cell populations, for which the activity is modulated during hypoxia using an animal model characterized by its immaturity relative to other mammals, the one-day-old mouse (Gauda, 2006; Gaultier et al, 2006; Teppema and Dahan, 2010; Darnall et al, 2016; Mallard and Vexler, 2015)

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Summary

Introduction

Premature infants, display frequent episodes of apnea, and bradypnea, and very common episodes of hypoxia during the postnatal period (Bryan et al, 1986; Carroll and Agarwal, 2010; Teppema and Dahan, 2010; Mathew, 2011). Central mechanisms contribute to a decline in ventilation in parallel with peripheral chemoreceptor activation; if the Abbreviations: 5HT, serotonin; A5, A5 region; cNTS, commissural part of the nucleus of the solitary tract; cVLM, caudal part of the ventrolateral reticular nucleus of the medulla; dSubC, dorsal part of the subcoeruleus nucleus; f R, respiratory frequency; HVD, hypoxic ventilatory depression; HVR, hypoxic ventilatory response; KF, Kölliker-Fuse nucleus; LC, locus coeruleus nucleus, lPB, lateral parabrachial nucleus; mNTS, medial part of the nucleus of the solitary tract; mPB, medial parabrachial nucleus; n7, facial nucleus; PP, parapyramidal group; RMg, raphe magnus nucleus; ROb, raphe obscurus nucleus; RPa, raphe pallidus nucleus; RTN/pFRG, retrotrapezoid nucleus/parafacial respiratory group region; rVLM, rostral part of the ventrolateral reticular nucleus of the medulla; SIDS, Sudden Infant Death Syndrome; TH, tyrosine hydroxylase; V E, ventilation minute; vlNTS, ventrolateral part of the nucleus of the solitary tract; vSubC, ventral part of the Subcoeruleus nucleus; VT, tidal volume

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