Possible role of the α7 nicotinic receptors in mediating nicotine’s effect on developing lung – implications in unexplained human perinatal death
© Lavezzi et al.; licensee BioMed Central Ltd. 2014
Received: 29 July 2013
Accepted: 24 January 2014
Published: 1 February 2014
It 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.
In 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.
We 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.
These 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.
KeywordsNicotinic receptors Human lung development Brainstem SIDS SIUDS Nicotine Maternal smoking in pregnancy
Maternal smoking during pregnancy has been associated with intrauterine growth retardation, low birth weight, neonatal morbidity and mortality, as well as an increased incidence of respiratory disorders and of an attention deficit in infants [1–6]. Nicotine, among thousands of compounds of tobacco smoke, is particularly involved in these pathological manifestations because, in cases of prenatal exposure, it readily crosses the placental barrier, so that levels of nicotine in the developing fetus closely mimic and also exceed the maternal levels .
Fetal damage caused by maternal smoking mainly result from the interaction of nicotine with nicotinic acetylcholine receptors (nAChRs) [8–10]. These receptors are ion channels in the cytoplasmic membrane consisting of a different combination of α and β subunits that can be opened not only by the neurotransmitter acetylcholine but also by nicotine – hence the name “nicotinic”. To date, a total of 10α and 4β different subunits have been described on the basis of the receptors sensitivity to nicotine .
It is well known that nAChRs regulate critical aspects of brain maturation during the intrauterine and early postnatal periods, mediating the neurochemical transmission of acetylcholine among the neurons [12–15]. Prenatal nicotine exposure significantly increases nAChR endogenous activation, above all in neuronal nuclei and/or in structures undergoing major phases of differentiation, that are consequently more sensitive to environmental stimuli.
The knowledge of the biology of nAChRs has expanded in recent years thanks to the identification of the nAChRs also in several peripheral organs, including the lungs [16, 17]. Although the origin of lung damage caused by maternal smoking in pregnancy is likely multifactorial, many respiratory diseases may be mediated by the interaction of nicotine with the nicotinic receptors that are widely expressed in the airway cells of the developing lung . In this scenario, the expression of nAChR provides a receptor-mediated mechanism that may help to understand, at the molecular level, how smoking affects lung development and leads to the well-documented decreased pulmonary function and increased respiratory symptoms observed in exposed infants after birth. Sekhon et al. [19, 20], in experimental studies using specific antibodies for different nAChR subunits (e.g., α3, α5, α7, β2), demonstrated a marked α7 immunostaining intensity, related to prenatal nicotine exposure, particularly in the airway epithelial cells and airway vessel walls of fetal and newborn lungs of monkeys. This means that nicotine absorption mainly upregulates the pulmonary expression of α7 nAChR, while other nicotinic receptor subtypes are more resistant. In addition, these authors indicated an association between α7 overexpression and an altered airway development, with a subsequent influence on respiratory health.
Previously, we have reported a high incidence of lung hypoplasia in subjects who died of Sudden Intrauterine Unexplained Death Syndrome (SIUDS) and Sudden Infant Death Syndrome (SIDS) [21, 22]. In the present study we aimed to investigate whether the lung hypodevelopment frequently observed in these victims may be due, as shown in experimental studies, to a specific hyperactivation of the α7 nAChR subunit in cases of nicotine absorption in pregnancy.
Among the many cases sent to our Research Center according to the guidelines stipulated by the Italian law n.31/2006 “Regulations for Diagnostic Post Mortem Investigation in Victims of SIDS and Unexpected Fetal Death”a and diagnosed as SIUDS and/or SIDS, we selected 60 cases, precisely 45 sudden late fetal deaths (32–39 gestational weeks) and 15 sudden neonatal deaths (within the first month of life), provided with completeness of data, namely a detailed collection of clinical/environmental information, including the maternal smoking habit.
Twenty-seven mothers of the SIUDS/SIDS group (45%) claimed to smoke before and during pregnancy, while the remaining 32 (55%) denied they smoked.
We included in the study a control group consisting of 24 age-matched subjects (16 fetuses and 8 newborns) in which the autopsy established a precise cause of death (specifically, respiratory infections, cardiomyopathies, sepsis in infant deaths; cardiomyopathies and chorioamnionitis in fetal deaths). Five of the 24 mothers of the control group (21%) reported a smoking habit, while 19 mothers (79%) were non-smokers.
Case profiles of the study
Sudden perinatal deaths
2 h-27 d
2 h-25 d
Parents of all the victims of the study provided written informed consent to autopsy, with the Milan University “Lino Rossi” Research Center institutional review board approval.
A complete autopsy examination was carried out in every case including, in particular, an in-depth study of the brainstem and of the lungs. All organs were fixed in 10% phosphate-buffered formalin, processed and embedded in paraffin.
The brainstem was examined according to the protocol routinely applied in the “Lino Rossi” Research Center, available in our previous works [23, 24] and in the web site http://users.unimi.it/centrolinorossi/en/guidelines.html.
The routine histological evaluation of the brainstem was focused on the main nuclei checking the vital functions: the locus coeruleus, the Kölliker-Fuse and the rostral raphe nuclei (magnum and caudal linear nuclei) in the rostral pons/caudal mesencephalon; the retrotrapezoid, the parafacial, the superior olivary and the median raphe nuclei in the caudal pons; the hypoglossus, the dorsal motor vagus, the tractus solitarius, the ambiguus, the pre-Bötzinger, the inferior olivary, the arcuate, the obscurus and the pallidus raphe nuclei in the medulla oblongata.
In addition we performed a morphometric analysis of the main nuclei with an Image-Pro Plus Image Analyzer (Media Cybernetics, Silver Spring, Maryland, USA) in serial histological sections. The following parameters were evaluated for every nucleus: neuronal density, (number of neurons per unit area-mm 2 ) and volume. All the neurons with clearly defined edges and with a distinct nucleolus were counted using an optical microscope at 20× magnification. The volume was measured by three-dimensional reconstruction. A computer program developed by Voxblast (VayTek, Fairfield, Iowa) was used to digitize and display serial section reconstructions, to obtain volumetric measurements. The morphometric results were expressed as mean values and standard deviation. The statistical significance of direct comparisons between morphometric values obtained from sudden death cases and controls was determined using the analysis of variance. A diagnosis of hypoplasia related to a particular nucleus was formulated when its morphometric values were significantly lower than the reference values obtained from age-matched control cases.
Regarding the lung examination, the main focus of the study, samples were obtained from each lobe by cutting parallel to the frontal plane and passing through the hilus. The histological examination of the routinely stained sections by hematoxylin-eosin included the evaluation in terminal lung units (i.e., portions of parenchyma distal to the last respiratory bronchioles, identifiable by an incomplete epithelial lining) of the radial alveolar count (RAC). This is a reliable index of lung maturation in intrauterine and early postnatal development established by Emery and Mithal in 1960 , closely related to the gestational age in weeks for fetuses and to the postnatal age in months for newborns. The RAC is obtained by examining at least 10 random histological fields for each case in order to estimate the number of airspaces cut by a straight line drawn from the center of the most peripheral bronchiole to the nearest connective tissue septum or the pleura. Emery and Mithal also provided the RAC reference values at different ages. The normal mean value from 32 to 35 gestational weeks is 3.2 ± 0.9; from 36 to 39 gestational weeks 3.6 ± 0.9. The normal RAC from the first postnatal weeks to 4 months is 5.5 ± 1.4.
Immunohistochemical methods were applied to selected histological sections of lungs in order to evaluate the expression of α7 nAChRs by using specific rabbit polyclonal antibodies (aa 22–71, Abcam cod. ab10096). Sections, after dewax and rehydration, were immersed and boiled in a Citrate Buffer solution pH 6.0 (for α3) and in TRIS-EDTA Buffer (for α7 and β2) for the antigen retrieval with a microwave oven, having first blocked endogenous peroxidase by 3% hydrogen peroxide treatment. Then, sections were incubated with the primary antibodies overnight (diluitions: 1:75 for α3, 1:500 for α7 and 1:167 for β2) in a wet chamber. Samples were washed with PBS buffer and incubated with a secondary anti-rabbit antibody and then processed with a usual avidin-biotin-immunoperoxidase technique (VECTOR LABS, Burlingame, CA). Finally each section was counterstained with Mayer’s Hematoxylin and coverslipped.
A set of sections from each group of the study was used as negative control. Precisely, the tissue samples were stained using the same procedure but omitting the primary antibody in order to verify that the immunolabeling was not due to nonspecific labeling by the secondary antibody. In fact, if specific staining occurs in negative control tissues, immunohistochemical results should be considered invalid.
nAChR immunohistochemistry quantification
The degree of positive immunoreactivity in the lungs was defined for every case by two independent and blinded observers as the number of cells with strong unequivocal immunostaining, divided by the total number of consecutive cells counted in the epithelium surrounding both alveoli and bronchioles or divided by the total number of the counted cells in the parenchima, expressed as percentage (nAChR index: nAChR-I). nAChR-I was classified as: “Class 0” for no staining (negativity); “Class 1” when the index was < 10% (weak positivity); “Class 2” with a percentage of immunopositive cells between 10 and 30% (moderate positivity); “Class 3” with an index > 30% of the counted cells (strong positivity).
Comparison among the observations carried out by the two pathologists was performed employing Kappa statistics (Kappa Index- KI) to evaluate inter-observer reproducibility. The Landis and Koch  system of KI interpretation was used, where 0 to 0.2 is slight agreement, 0.21 to 0.40 indicates fair agreement, 0.41 to 0.60 is moderate agreement, 0.61 to 0.80 is strong or substantial agreement, and 0.81 to 1.00 indicates very strong or almost perfect agreement (a value of 1.0 being perfect agreement). This analysis revealed a very satisfactory Kappa Index (KI = 0.85).
Markers for fibroblasts and collagen
Immunostaining procedures for Fibroblast-specific protein-1 (FSP-1; 11 kD) of the S100 superfamily were applied to identify fibroblasts in the lung vessel walls. Skin samples were used as positive controls; negative controls were prepared omitting the primary antibody and replacing only with PBS during incubations. Sections from paraffin-embedded tissue blocks were treated using commercially supplied 1:400 diluted rabbit monoclonal antibodies FSP-1 (Millipore #07-2274). Slides were boiled for the antigen retrieval in 0.01 M citrate buffer (pH 6.0), using a microwave oven, at 600 W for 3 times at 5 min each, and finally cooled. A standard ABC technique avidin-biotin complex (Vectastain elite ABC KIT, PK-6101) was used with HRP-DAB to visualize and develop the antigen-antibody reaction. Sections were counterstained with Mayer’s hematoxylin, than coverslipped.
Heidenhain’s trichrome staining (AZAN staining) was applied as histochemical staining procedure to identify the collagen around the airways and the vessels. In this method three acid dyes are used: azocarmine and a mixture of aniline blue and orange G. The azocarmine stain is combined with the mixture of aniline blue and orange G as counterstain, after mordanting with phosphotungstic acid. The collagen and cytoplasmic reticulum appear blue, muscle red to yellow, nuclear chromatine red.
Histological and immunohistochemical data were tabulated and analyzed for differences comparing pairs of groups by using the analysis of variance (ANOVA). Statistical calculations were carried out with a SPSS statistical software (version 11.0; SPSS Inc., Chicago, IL, USA). The selected threshold level for statistical significance was p < 0.05.
Lung examination in SIUDS/SIDS
Lung examination in controls
Mostly, in control subjects the RAC was within the normal reference values. Nevertheless, a “low grade of lung hypoplasia” in 2 newborns (8%) who died of pneumonia in the first two months of life, with a slightly lower lung maturation index than the mean value for the age (RAC value: 4; mean reference value: 5.5 ± 1.4).
A high α7 subunit immunoreactivity (“Class 3” of nAChR-I) was detected in the airway epithelium of 3 newborns, two of whom had died of respiratory infections and showed mild lung hypoplasia.
Correlation of lung observations with maternal smoking
A significant association between a strong expression of α7 nAChR, lung hypoplasia and prenatal cigarette smoke exposure (p < 0.01) occurred. In fact, 20 of the 27 cases with a smoker mother belonged to the SIUDS/SIDS group showing a high α7 immunopositivity and lower RAC values than the reference values. Moreover, the mothers of the 3 control infants with similar nAChR results and mild lung hypoplasia were active smokers in pregnancy.
Brainstem examination in SIUDS/SIDS and controls
The in-depth histological examination, supported by the morphometric analysis, of the brainstem in SIUDS/SIDS cases frequently yielded a diagnosis of hypodevelopment of important nuclei and/or neuronal structures checking vital functions. Hypoplasia/agenesis of one or more nuclei of the raphe system (i.e., obscurus, pallidus, median, magnum, caudal linear raphe nuclei), a complex of nuclei that plays a trophic role in brain development, being responsible for serotonergic transmission , was the most frequent alteration (observed in 28 SIUDS and 8 SIDS).
In 11 SIUDS with hypoplasia of the obscurus and pallidus raphe nuclei in the medulla oblongata, we observed an association with hypoplasia of the pontine parafacial and Kölliker-Fuse nuclei, consisting of “pre-inspiratory” neurons with the hierarchical function of starting the first breathing movements [28, 29].
Hypoplasia of the medullary pre-Bötzinger nucleus, a critical structure for respiratory rhythmogenesis , and of the arcuate nucleus, involved in chemoreception , was simultaneously present in 12 SIUDS and 6 SIDS victims, five of whom showed agenesis of the raphe obscurus nucleus.
In most of these cases (15 SIUDS and 4 SIDS) the mother smoked during pregnancy.
A significant correlation was found between the neuropathological results and the above-reported lung alterations. In fact, in 20 SIUDS and 4 SIDS victims with a defective maturation of important brainstem centers, lung hypoplasia with a high α7 nicotinic receptor expression was discovered.
In controls hypoplasia of the arcuate nucleus was the only finding (observed in 3 cases), not related to maternal smoking. On the whole, SIUDS and SIDS cases displayed a significantly higher incidence of brainstem pathological findings as compared to age-matched controls (p < 0.01).
Sudden perinatal deaths
RAC (mean value)
α7 nAChR strong immunopositivity
Brainstem nuclei hypoplasia(1)
Further research aimed at evaluating nicotinic receptor expression in the brainstem is now in progress in our laboratory, and will be the subject of a forthcoming publication.
The lung, during its long process of maturation from the embryonic phase of development in utero up to adolescence, is highly susceptible to damage caused by exposure to environmental toxicants, and particularly to tobacco smoke in pregnancy [32–34].
In pregnant smokers nicotine, that in amniotic fluid reaches similar or higher levels than those present in maternal plasma , when crossing the placenta can directly affect fetal lung development. This is facilitated by the fact that the metabolic activity of the fetal liver is not yet well developed so leading to a higher half-life of nicotine with the ability to interfere in the development of especially the most vulnerable organs, including the lung . In addition the developing lung can be exposed during early childhood to nicotine ingestion through the breast milk from a smoking mother .
Previous experimental studies performed on Rhesus monkeys, an ideal model of pulmonary growth that is very similar to that of humans, demonstrated that nicotine administration during pregnancy causes lung hypodevelopment as a direct result of its interaction with the α7 subunit of the nicotinic receptors, that are widely distributed in the airways epithelium in prenatal life . Similar results were more recently obtained by Wongtrakool et al.  in mouse. These authors established that prenatal nicotine exposure leads to a decrease in pulmonary function and in alveolar surface, through interactions with α7 nAChRs.
The involvement of this specific subunit in lung pathophysiology is also proven by its strong manifestation in tobacco-induced cancers. Nicotine contributes directly to pulmonary tumorigenesis through stimulation of the α7 nAChR subunits in target cells, as shown by their overexpression particularly in non-small cell lung carcinomas of patients who smoked [38, 39].
Basing on these results, we propose a potential molecular mechanism responsible for the high incidence of lung hypoplasia in SIUDS and SIDS whose mothers smoked. We hypothesize that the overexpression of the α7 nicotinic receptors we found in these cases is the result of modifications of the corresponding gene expression. This is supported by the increased messenger RNA levels of several nAChR subunits (including α7 subunits) observed in the developing nervous system of rats as a consequence of nicotine absorption , leading to a remarkable increase in receptor protein synthesis. In human pulmonary cell cultures, Plummer et al.  likewise demonstrated a higher α7 mRNA and a consequent increase in α7 nicotinic receptor levels in the presence of nicotine-derived carcinogenic nitrosamine.
In our study, the α7 nAChR overexpression observed in lung epithelial cells in a high percentage of SIUDS/SIDS victims was exacerbated by the presence of developmental alterations of brainstem centers affecting not only breathing activity but, more in general, all the vital functions, thus amplifying the harmful effect of nicotine and leading to a fatal outcome. The results of the current research now in progress in our laboratory on the α7 nAChR expression in the brainstem, will validate this assertion. It is therefore clear that nicotine, after entering the fetal circulation and crossing the fetal blood–brain barrier, interacts with the α7 subunits and up-regulates its expression in both non-neuronal cells of the lung and in neuronal cells of the brainstem, thereby leading to impaired lung function and hypodevelopment of the respiratory neuronal centers.
The strong immunoexpression of the α7 nAChR subunit also observed in fibroblasts around lung vessels and airways must be underlined. The vascular walls, in particular, appear thicker, very likely due to interactions of nicotine with fibroblast receptors, thereby triggering a high collagen protein synthesis and hence causing accumulation of connective tissue. Nicotine can therefore directly stimulate α 7 nAChR-bearing fibroblasts to lay down an excessive amount of connective tissue.
These considerations are consistent with the report by Sekhon et al.  of a high expression of α7 subunits in fibroblasts of the lung vessels in monkey fetuses exposed to nicotine during pregnancy, with a significant accumulation of collagen in the tunica media.
Collagen deposition around the airways and pulmonary vessels certainly induces an increased airway resistance and decreased respiratory function, providing an explanation for the high incidence of persistent pulmonary hypertension observed in infants whose mothers smoked during pregnancy .
It is important to point out several limitations of this study. First, the exact mechanisms by which nicotine interacts with nAChR to alter lung development remain to be determined. This is due, in particular, to the impossibility to perform experimental studies in humans. However, based on our results we can hypothesize a link between α7 overexpression and delayed pulmonary development in SIUDS/SIDS victims. Secondly, pertaining to cigarette smoke exposure, is that available information on our cases did not provide evidence of an exposure ‘dose’. Furthermore, it should be considered that retrospective assessment of the maternal smoking, particularly if performed after a fatal event, is sometimes unreliable, due to the fact that mothers who smoke are reluctant to admit tobacco use, because of feelings of guilt . Finally, it is important to point out that our study was focused on the role of the increased α7 receptor expression in developing lung in relation to nicotine absorption. Hovewer we detain that other nAChR subtypes could likely play important roles in mediating the effects of nicotine on lung development. Therefore we plan to extend the study, using a wider range of nAChRs.
This article emphasizes the extreme vulnerability of the developing lung to maternal cigarette smoke absorption. In summary, we claim that nicotine in pregnant women is readily transported across the placenta, achieving sufficient levels to interact directly with the nicotinic receptors that are widely distributed in the lung cells in prenatal life. In particular, on the basis of our results and of previous experimental studies, we propose α7 nAChR as the main candidate mediating the pathobiologic effects of tobacco products on lung maturation and function. The specific interaction of nicotine molecules with α7 subunits, widespread in the cytoplasmic membrane of both lung epithelial cells and fibroblasts, leads to an overexpression of the corresponding receptors with a consequent severe inhibition of airway development in utero, as well as an airflow decrease in the first days of life and a high incidence of smoke-associated pediatric respiratory disorders. The relevance of this study is the significantly higher association highlighted among many factors (overexpression of α7 nAChRs, lung hypoplasia, developmental alterations of brainstem nuclei and maternal smoking) in SIUDS/SIDS, as compared to controls.
Despite the compelling evidence that prenatal nicotine absorption increases the incidence of pulmonary diseases in fetal and infant life, in addition to posing the well known risks of spontaneous abortion, preterm delivery, low birth weight and sudden perinatal death, a significant number of women continue to smoke during pregnancy.
The findings of this study further underline the importance of ensuring widespread information about the noxious potential of nicotine absorption in pregnancy, as well as the need to implement measures to prevent this major and avoidable cause of lung morbidity and mortality in fetuses and infants.
aThis law decrees that all infants suspected of SIDS, suddenly died in Italian regions within the first year of age, as well as all fetuses who died without any apparent cause (SIUDS), must undergo an in-depth anatomo-pathological examination, particularly of the autonomic nervous system.
The authors thank Ms. Mary Victoria Candace Pragnell, B.A. for English revision of this manuscript.
This study was supported by the Italian Health’s Ministry in accordance with the Law 31/2006 “Regulations for Diagnostic Post Mortem Investigation in Victims of Sudden Infant Death Syndrome (SIDS) and Unexpected Fetal Death”, and by the Convention with the Provincia autonoma of Trento, Italy (CONV 7436/555-12).
- Mathews TJ: Smoking during pregnancy, 1990–1996. Natl Vital Stat Rep. 1998, 47: 1-12.Google Scholar
- Wainright RL: Change in observed birth weight associated with change in maternal cigarette smoking. Am J Epidemiol. 1983, 117: 668-675.PubMedGoogle Scholar
- Aliyu MH, Salihu HM, Wilson RE, Kirby RS: Prenatal smoking and risk of intrapartum stillbirth. Arch Environ Occup Health. 2007, 62: 87-92. 10.3200/AEOH.62.2.87-92.View ArticlePubMedGoogle Scholar
- Kleinman JC, Pierre MBJ, Madans JH, Land GH, Schramm WF: The effects of maternal smoking on fetal and infant mortality. Am J Epidemiol. 1988, 127: 274-282.PubMedGoogle Scholar
- Taylor B, Wadsworth J: Maternal smoking during pregnancy and lower respiratory tract illness in early life. Arch Dis Child. 1987, 62: 786-791. 10.1136/adc.62.8.786.View ArticlePubMedPubMed CentralGoogle Scholar
- Julvez J, Ribas-Fito N, Torrent M, Forns M, Garcia-Esteban R, Sunyer J: Maternal smoking habits and cognitive development of children at age 4 years in a population-based birth cohort. Int J Epidemiol. 2007, 36: 825-832. 10.1093/ije/dym107.View ArticlePubMedGoogle Scholar
- Luck W, Nau H, Hansen R, Steldinger R: Extent of nicotine and cotinine transfer to the human fetus, placenta and amniotic fluid of smoking mothers. Dev Pharmacol Ther. 1985, 8: 384-395.PubMedGoogle Scholar
- Lindstrom J: Nicotinic acetylcholine receptors in health and disease. Mol Neurobiol. 1997, 15: 193-222. 10.1007/BF02740634.View ArticlePubMedGoogle Scholar
- Boyd RT: The molecular biology of neuronal nicotinic acetylcholine receptors. Crit Rev Toxicol. 1997, 27: 299-318. 10.3109/10408449709089897.View ArticlePubMedGoogle Scholar
- Albuquerque EX, Pereira EF, Alkondon M, Rogers SW: Mammalian nicotinic acetylcholine receptors: from structure to function. Physiol Rev. 2009, 89: 73-120. 10.1152/physrev.00015.2008.View ArticlePubMedPubMed CentralGoogle Scholar
- Fowler CD, Arends MA, Kenny PJ: Subtypes of nicotinic acetylcholine receptors in nicotine reward, dependence, and withdrawal: evidence from genetically modified mice. Behav Pharmacol. 2008, 19: 461-484. 10.1097/FBP.0b013e32830c360e.View ArticlePubMedPubMed CentralGoogle Scholar
- Itier V, Bertrand D: Neuronal nicotinic receptors: from protein structure to function. FEBS Lett. 2001, 504: 118-125. 10.1016/S0014-5793(01)02702-8.View ArticlePubMedGoogle Scholar
- Gotti C, Clementi F, Fornari A, Gaimarri A, Guiducci S, Manfredi I, Moretti M, Pedrazzi P, Pucci L, Zoli M: Structural and functional diversity of native brain neuronal nicotinic receptors. Biochem Pharmacol. 2009, 78: 703-711. 10.1016/j.bcp.2009.05.024.View ArticlePubMedGoogle Scholar
- Dwyer JB, McQuown SC, Leslie FM: The dynamic effects of nicotine on the developing brain. Pharmacol Ther. 2009, 122: 125-139. 10.1016/j.pharmthera.2009.02.003.View ArticlePubMedPubMed CentralGoogle Scholar
- Graham A, Court JA, Martin-Ruiz CM, Jaros E, Perry R, Volsen SG, Bose S, Evans N, Ince P, Kuryatov A, Lindstrom J, Gotti C, Perry EK: Immunohistochemical localisation of nicotinic acetylcholine receptor subunits in human cerebellum. Neuroscience. 2002, 113: 493-507. 10.1016/S0306-4522(02)00223-3.View ArticlePubMedGoogle Scholar
- Wessler I, Kirkpatrick CJ: Acetylcholine beyond neurons: the Non-neuronal cholinergic system in humans. Brit J Pharmacol. 2008, 154: 1558-1571.View ArticleGoogle Scholar
- Spindel ER: Neuronal nicotinic acetylcholine receptors: not just in brain. Am J Physiol Lung Cell Mol Physiol. 2003, 285: 1201-1202.View ArticleGoogle Scholar
- Fu XW, Lindstrom J, Spindel ER: Nicotine activates and up-regulates nicotinic acetylcholine receptors in bronchial epithelial cells. Am J Physiol Lung Cell Mol Biol. 2009, 41: 93-99.Google Scholar
- Sekhon HS, Jia Y, Raab R, Kuryatov A, Pankow JF, Whitsett JA, Lindstrom J, Spindel ER: Prenatal nicotine increases pulmonary alpha7 nicotinic receptor expression and alters fetal lung development in monkeys. J Clin Invest. 1999, 103: 637-647. 10.1172/JCI5232.View ArticlePubMedPubMed CentralGoogle Scholar
- Sekhon HS, Keller JA, Benowitz NL, Spindel ER: Prenatal nicotine exposure alters pulmonary function in newborn rhesus monkeys. Am J Respir Crit Care Med. 2001, 164: 989-994. 10.1164/ajrccm.164.6.2011097.View ArticlePubMedGoogle Scholar
- Matturri L, Lavezzi AM, Cappellini A, Ottaviani G, Minoli I, Rubino B, Rossi L: Association between pulmonary hypoplasia and hypoplasia of arcuate nucleus in stillbirth. J Perinatol. 2003, 23: 328-332.View ArticlePubMedGoogle Scholar
- Ottaviani G, Mingrone R, Lavezzi AM, Matturri L: Infant and perinatal pulmonary hypoplasia frequently associated with brainstem hypodevelopment. Virchows Arch. 2009, 454: 451-456. 10.1007/s00428-009-0754-6.View ArticlePubMedGoogle Scholar
- Matturri L, Ottaviani G, Lavezzi AM: Techniques and criteria in pathologic and forensic-medical diagnostics of sudden unexpected infant and perinatal death. Am J Clin Pathol. 2005, 124: 259-268. 10.1309/J6AREY41HKBEYVHX.View ArticlePubMedGoogle Scholar
- Matturri L, Ottaviani G, Lavezzi AM: Guidelines for neuropathologic diagnostics of perinatal unexpected loss and sudden infant death syndrome (SIDS): a technical protocol. Virchows Arch. 2008, 452: 19-25. 10.1007/s00428-007-0527-z.View ArticlePubMedGoogle Scholar
- Emery JL, Mithal A: The number of alveoli in the terminal respiratory unit of man during late intrauterine life and childhood. Arch Dis Child. 1960, 35: 544-547. 10.1136/adc.35.184.544.View ArticlePubMedPubMed CentralGoogle Scholar
- Landis RJ, Koch GG: The measurement of observer agreement for categorical data. Biometrics. 1977, 33: 159-174. 10.2307/2529310.View ArticlePubMedGoogle Scholar
- Hornung JP: The human raphe nuclei and the serotonergic system. J Chem Neuroanat. 2003, 26: 331-343. 10.1016/j.jchemneu.2003.10.002.View ArticlePubMedGoogle Scholar
- Lavezzi AM, Matturri L: Hypoplasia of the parafacial/facial complex: a very frequent finding in sudden unexplained fetal death. Open Neurosci J. 2008, 2008 (2): 1-5.View ArticleGoogle Scholar
- Lavezzi AM, Ottaviani G, Rossi L, Matturri L: Hypoplasia of the Parabrachial/Kölliker-Fuse complex in perinatal death. Biol Neonate. 2004, 86: 92-97. 10.1159/000078310.View ArticlePubMedGoogle Scholar
- Lavezzi AM, Matturri L: Functional neuroanatomy of the human pre-Bötzinger complex with particular reference to sudden unexplained perinatal and infant death. Neuropathology. 2008, 28: 10-16. 10.1111/j.1440-1789.2007.00824.x.View ArticlePubMedGoogle Scholar
- Matturri L, Minoli I, Lavezzi AM, Cappellini A, Ramos S, Rossi L: Hypoplasia of medullary arcuate nucleus in unexpected late fetal death (stillborn infants): a pathologic study. Pediatrics. 2002, 109: E43-10.1542/peds.109.3.e43.View ArticlePubMedGoogle Scholar
- Kajekar R: Environmental factors and developmental outcomes in the lung. Pharmacol Therap. 2007, 114: 129-145. 10.1016/j.pharmthera.2007.01.011.View ArticleGoogle Scholar
- Burri PH: Fetal and postnatal development of the lung. Annu Rev Physiol. 1984, 46: 617-628. 10.1146/annurev.ph.46.030184.003153.View ArticlePubMedGoogle Scholar
- Maritz GS, Windvogel S: Chronic maternal nicotine exposure during gestation and lactation and the development of the lung parenchyma in the offspring. Response to nicotine withdrawal. Pathophysiology. 2003, 10: 69-75. 10.1016/j.pathophys.2003.10.001.View ArticlePubMedGoogle Scholar
- Frank L, Sosenko IR: Prenatal development of lung antioxidant enzymes in four species. J Pediatr. 1987, 110: 106-110. 10.1016/S0022-3476(87)80300-1.View ArticlePubMedGoogle Scholar
- Stepans MB, Wilkerson N: Physiologic effects of maternal smoking on breast-feeding infants. J Am Acad Nurse Pract. 1993, 5: 105-113. 10.1111/j.1745-7599.1993.tb00850.x.View ArticlePubMedGoogle Scholar
- Wongtrakool C, Wang N, Hyde DM, Roman J, Spindel ER: Prenatal nicotine exposure alters lung function and airway geometry through α7 nicotinic receptors. Am J Respir Cell Mol Biol. 2012, 46: 695-702. 10.1165/rcmb.2011-0028OC.View ArticlePubMedPubMed CentralGoogle Scholar
- Schuller HM, Jull BA, Sheppard BJ, Plummer HK: Interaction of tobacco-specific toxicants with the neuronal α7 nicotinic acetylcholine receptor and its associated mitogenic signal transduction pathway: potential role in lung carcinogenesis and pediatric lung disorders. Eur J Pharmacol. 2000, 393: 265-277. 10.1016/S0014-2999(00)00094-7.View ArticlePubMedGoogle Scholar
- Paleari L, Catassi A, Ciarlo M, Cavalieri Z, Bruzzo C, Servent D, Cesario A, Chessa L, Cilli M, Piccardi F, Granone P, Russo P: Role of alpha7-nicotinic acetylcholine receptor in human non-small cell lung cancer proliferation. Cell Prolif. 2008, 41: 936-959. 10.1111/j.1365-2184.2008.00566.x.View ArticlePubMedGoogle Scholar
- Shacka JJ, Robinson SE: Exposure to prenatal nicotine transiently increases neuronal nicotinic receptor subunit α7, α4 and β2 messenger RNASs in the postnatal rat brain. Neuroscience. 1998, 84: 1151-1161. 10.1016/S0306-4522(97)00564-2.View ArticlePubMedGoogle Scholar
- Plummer HK, Dhar M, Schuller HM: Expression of the alpha7 nicotinic acetylcholine receptor in human lung cells. Respir Res. 2005, 6: 29-37. 10.1186/1465-9921-6-29.View ArticlePubMedPubMed CentralGoogle Scholar
- Sekhon HS, Proskocil BJ, Clark JA, Spindel ER: Prenatal nicotine exposure increases connective tissue expression in foetal monkey pulmonary vessels. Eur Respir J. 2004, 23: 906-915. 10.1183/09031936.04.00069604.View ArticlePubMedGoogle Scholar
- Bearer C, Emerson RK, O’Riordan MA, Roitman E, Shackleton C: Maternal tobacco smoke exposure and persistent pulmonary hypertension of the newborn. Environ Health Perspect. 1997, 105: 202-206. 10.1289/ehp.97105202.View ArticlePubMedPubMed CentralGoogle Scholar
- Heath AC, Knopik VS, Madden PA, Neuman RJ, Lynskey MJ, Slutske WS, Jacob T, Martin NG: Accuracy of mothers’ retrospective reports of smoking during pregnancy: comparison with twin sister informant rating. Twin Res. 2003, 6: 297-301. 10.1375/136905203322296656.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2466/14/11/prepub
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