Abstract
In olfaction, to preserve the sensitivity of the response, the bioavailability of odor molecules is under the control of odorant-metabolizing enzymes (OMEs) expressed in the olfactory neuroepithelium. Although this enzymatic regulation has been shown to be involved in olfactory receptor activation and perceptual responses, it remains widely underestimated in vertebrates. In particular, the possible activity of OMEs in the nasal mucus, i.e. the aqueous layer that lined the nasal epithelium and forms the interface for airborne odorants to reach the olfactory sensory neurons, is poorly known. Here, we used the well-described model of the mammary pheromone (MP) and behavioral response in rabbit neonates to challenge the function of nasal mucus metabolism in an unprecedented way. First, we showed, in the olfactory epithelium, a rapid glutathione transferase activity toward the MP by ex vivo real-time mass spectrometry (PTR-MS) which supported an activity in the closest vicinity of both the odorants and olfactory receptors. Indeed and second, both the presence and activity of glutathione transferases were evidenced in the nasal mucus of neonates using proteomic and HPLC analysis respectively. Finally, we strikingly demonstrated that the deregulation of the MP metabolism by in vivo mucus washing modulates the newborn rabbit behavioral responsiveness to the MP. This is a step forward in the demonstration of the critical function of OMEs especially in the mucus, which is at the nasal front line of interaction with odorants and potentially subjected to physiopathological changes.
Highlights
In olfaction, to preserve the sensitivity of the response, the bioavailability of odor molecules is under the control of odorant-metabolizing enzymes (OMEs) expressed in the olfactory neuroepithelium
A fresh explant of olfactory mucosa (OM) was placed into a glassware trap, in which a known concentration of gaseous odorant was continuously delivered; in the same time the glassware headspace was continuously analyzed by PTR-MS instrument recording the mammary pheromone (MP) signal (m/z = 85.064791) (Figs 1 and S1)
The first assay was conducted with the MP at 10−9 g/ ml continuously delivered above the OM in the glassware trap, in comparison with controls without OM or with heated OM to denaturate the enzymes present in this olfactory tissue (Fig. 2A,B)
Summary
To preserve the sensitivity of the response, the bioavailability of odor molecules is under the control of odorant-metabolizing enzymes (OMEs) expressed in the olfactory neuroepithelium. We first demonstrated a high GST (phase II enzymes) activity toward the MP in the olfactory mucosa (OM) of newborn compared to weanling rabbits (at weaning the typical orocephalic movements are no longer displayed to the MP)[16] This suggested a direct function of GSTs in the active clearance of the MP from the perireceptor environment in this developmental period where a high sensitivity to the MP must be maintained to ensure survival[11,13].We further developed an ex vivo headspace gas-chromatography method to measure MP metabolism in quasi physiological exposure conditions, i.e., by suing intact OM fresh explants in contact with MP on gaseous form. Our goal and challenge were to study the GST velocity and enzymatic activity (to date not clearly evidenced) toward the MP in the OM and nasal mucus of the newborn rabbit In this purpose, we used here a previously developed and very sensitive mass spectrometry method based on PTR-Tof-MS (PTR-MS) instrument[5] to monitor, in real-time, the ex vivo olfactory metabolism of the MP. The newborn rabbits’ sucking-related behavior was tested in order to determine the influence of the nasal mucus, supposed to be containing enzymes, in the perception of the MP
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