Abstract

BackgroundIt is well known that maternal smoking during pregnancy is very harmful to the fetus. Prenatal nicotine absorption, in particular, is associated with alterations in lung development and functions at birth and with respiratory disorders in infancy. Many of the pulmonary disorders are mediated by the interaction of nicotine with the nicotinic receptors (nAChRs), above all with the α7 nAChR subunits that are widely expressed in the developing lung. To determine whether the lung hypoplasia frequently observed in victims of sudden fetal and neonatal death with a smoker mother may result from nicotine interacting with lung nicotinic receptors, we investigated by immunohistochemistry the possible presence of the α7 nAChR subunit overexpression in these pathologies.MethodsIn lung histological sections from 45 subjects who died of sudden intrauterine unexplained death syndrome (SIUDS) and 15 subjects who died of sudden infant death syndrome (SIDS), we applied the radial alveolar count (RAC) to evaluate the degree of lung maturation, and the immunohistochemical technique for nAChRs, in particular for the α7 nAChR subunit identification. In the same cases, an in-depth study of the autonomic nervous system was performed to highlight possible developmental alterations of the main vital centers located in the brainstem.ResultsWe diagnosed a “lung hypoplasia”, on the basis of RAC values lower than the normal reference values, in 63% of SIUDS/SIDS cases and 8% of controls. In addition, we observed a significantly higher incidence of strong α7 nAChR immunostaining in lung epithelial cells and lung vessel walls in sudden fetal and infant death cases with a smoker mother than in age-matched controls. Hypoplasia of the raphe, the parafacial, the Kölliker-Fuse, the arcuate and the pre-Bötzinger nuclei was at the same time present in the brainstem of these victims.ConclusionsThese findings demonstrate that when crossing the placenta, nicotine can interact with nicotinic receptors of both neuronal and non-neuronal cells, leading to lung and nervous system defective development, respectively. This work stresses the importance of implementing preventable measures to decrease the noxious potential of nicotine in pregnancy.

Highlights

  • It is well known that maternal smoking during pregnancy is very harmful to the fetus

  • Lung examination in sudden intrauterine unexplained death syndrome (SIUDS)/Sudden Infant Death Syndrome (SIDS) Histology In 38 cases (63%) of sudden death (33 SIUDS and 5 SIDS), a paucity of pulmonary alveoli was highlighted in histological sections demonstrating lower radial counts than the normal reference values (Figure 1)

  • 20 of the 27 cases with a smoker mother belonged to the SIUDS/ SIDS group showing a high α7 immunopositivity and lower radial alveolar count (RAC) values than the reference values

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Summary

Introduction

It is well known that maternal smoking during pregnancy is very harmful to the fetus. Many of the pulmonary disorders are mediated by the interaction of nicotine with the nicotinic receptors (nAChRs), above all with the α7 nAChR subunits that are widely expressed in the developing lung. Fetal damage caused by maternal smoking mainly result from the interaction of nicotine with nicotinic acetylcholine receptors (nAChRs) [8,9,10]. These receptors are ion channels in the cytoplasmic membrane consisting of a different combination of α and β subunits that can be opened by the neurotransmitter acetylcholine and by nicotine – the name “nicotinic”. Prenatal nicotine exposure significantly increases nAChR endogenous activation, above all in neuronal nuclei and/or in structures undergoing major phases of differentiation, that are more sensitive to environmental stimuli

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