Premium
Blunted response to low oxygen of rat respiratory network after perinatal ethanol exposure: involvement of inhibitory control
Author(s) -
Dubois C.,
Houchi H.,
Naassila M.,
Daoust M.,
Pierrefiche O.
Publication year - 2008
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2007.147165
Subject(s) - strychnine , anesthesia , respiratory center , ventilation (architecture) , hypoxia (environmental) , ethanol , respiratory system , endocrinology , control of respiration , chemistry , medicine , pharmacology , oxygen , biochemistry , mechanical engineering , organic chemistry , engineering
Acute ethanol depresses respiration, but little is known about chronic ethanol exposure during gestation and breathing, while the deleterious effects of ethanol on CNS development have been clearly described. In a recent study we demonstrated that pre‐ and postnatal ethanol exposure induced low minute ventilation in juvenile rats. The present study analysed in juvenile rats the respiratory response to hypoxia in vivo by plethysmography and the phrenic (Phr) nerve response to ischaemia in situ . Glycinergic neurotransmission was assessed in situ with strychnine application and [ 3 H]strychnine binding experiments performed in the medulla. After chronic ethanol exposure, hyperventilation during hypoxia was blunted in vivo . In situ Phr nerve response to ischaemia was also impaired, while gasping activity occurred earlier and recovery was delayed. Strychnine applications in situ (0.05–0.5 μ m ) demonstrated a higher sensitivity of expiratory duration in ethanol‐exposed animals compared to control animals. Moreover, [ 3 H]strychnine binding density was increased after ethanol and was associated with higher affinity. Furthermore, 0.2 μ m strychnine in ethanol‐exposed animals restored the low basal Phr nerve frequency, but also the Phr nerve response to ischaemia and the time to recovery, while gasping activity appeared even earlier with a higher frequency. Polycythaemia was present after ethanol exposure whereas lung and heart weights were not altered. We conclude that chronic ethanol exposure during rat brain development (i) induced polycythaemia to compensate for low minute ventilation at rest; (ii) impaired the respiratory network adaptive response to low oxygen because of an increase in central glycinergic tonic inhibitions, and (iii) did not affect gasping mechanisms. We suggest that ethanol exposure during early life can be a risk factor for the newborn respiratory adaptive mechanisms to a low oxygen environment.