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Reduced hypoxic ventilatory response in newborn mice knocked‐out for the progesterone receptor
Author(s) -
Potvin Catherine,
Rossignol Orlane,
Uppari NagaPraveena,
Dallongeville Arnaud,
Bairam Aida,
Joseph Vincent
Publication year - 2014
Publication title -
experimental physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 101
eISSN - 1469-445X
pISSN - 0958-0670
DOI - 10.1113/expphysiol.2014.080986
Subject(s) - endocrinology , medicine , hypoxic ventilatory response , hypoxia (environmental) , receptor , plethysmograph , respiratory system , progesterone receptor , endogeny , biology , chemistry , organic chemistry , cancer , estrogen receptor , oxygen , breast cancer
New FindingsWhat is the central question of this study? Progesterone has been proposed as an alternative to xanthine therapy for the treatment of idiopathic apnoeas in preterm neonates, but our knowledge of the respiratory function of progesterone in neonates is limited. We therefore asked whether endogenous progesterone is an efficient respiratory stimulant in newborn mice.What is the main finding and its importance? The present study shows that expression of the nuclear progesterone receptor is a key contributor to the hypoxic ventilatory response in newborn mice. This study will encourage further research on the role of other progesterone receptors in respiratory control in newborn mammals.Abstract Recent studies showed that progesterone stimulates the hypoxic ventilatory response and may reduce apnoea frequency in newborn rats, but so far we still do not know by what mechanisms and whether endogenous progesterone might contribute to respiratory control in neonates. We therefore determined the role of the nuclear progesterone receptor (PR; member of the steroid receptor superfamily) by using wild‐type (WT) and PR knock‐out (PRKO) mice at postnatal days (P) 1, 4 and 10. We measured the hypoxic ventilatory response (14 and 12% O 2 , 20 min each) and apnoea frequency in both male and female mice by using whole‐body plethysmography. In response to hypoxia, WT male mice had a marked hypoxic ventilatory response at P1 and P10, but not at P4. At P1 and P10, PRKO male mice had a lower hypoxic ventilatory response than WT males. Wild‐type female mice had a marked hypoxic ventilatory response at P10, but not at P1 and P4. At P1 and P10, PRKO female mice had a lower hypoxic ventilatory response than WT females. In basal conditions, apnoea frequency was similar in WT and PRKO mice at P1, P4 and P10. During hypoxia, apnoea frequency was higher in WT male mice compared with PRKO male mice and WT female mice at P1. We conclude that PR is a key contributor to the hypoxic ventilatory response in newborn mice, but PR deletion does not increase the frequency of apnoea during normoxia or hypoxia.