Literature DB >> 10079211

Perinatal exposure to aged and diluted sidestream cigarette smoke produces airway hyperresponsiveness in older rats.

J P Joad1, J M Bric, J L Peake, K E Pinkerton.   

Abstract

Exposing rats to aged and diluted sidestream cigarette smoke (ADSS) throughout in utero and postnatal life results in airway hyperresponsiveness and an increase in pulmonary neuroendocrine cells (PNECs) and neuroepithelial bodies (NEBs) in 7- to 10-week-old rats. Since human epidemiologic studies suggest that perinatal exposure to environmental tobacco smoke (ETS) may be detrimental to the lung function of older children, this study was designed to determine if perinatal exposure alone results in airway hyperresponsiveness and increased PNECs/NEBs later in life in rats. Pregnant Sprague-Dawley rats were exposed to filtered air (FA, n = 7) or ADSS (1 mg/m3 total suspended particulates, n = 7) for 4 to 6 h/day starting on Day 3 of gestation. Their pups continued to receive the same exposure regimen postnatally until 21 days of age. Thereafter all pups were exposed to FA until about 8 weeks of age. The airway responsiveness of one female pup from each litter was then assessed using an isolated perfused lung system whereby increasing doses of methacholine (-9.25 to -7.50 log mol) were administered into the pulmonary artery and lung resistance (Rl), dynamic compliance (Cdyn), and pulmonary pressure (Ppa) were measured. The number of PNECs/NEBs and mast cells per millimeter basal lamina were determined using immunocytochemical and histological staining and morphometric analysis. Statistics were performed using an unpaired Student's t test and repeated measures analysis of variance. Perinatal ADSS exposure enhanced methacholine-induced changes in Rl (p = 0.02), Cdyn (p = 0.004), and Ppa (p = 0.007). At the highest dose of methacholine, Rl in the ADSS-exposed lungs was threefold that in FA-exposed lungs. Although total PNEC number increased approximately twofold in the ADSS-exposed animals, this change was not found to be statistically significant. Mast cell number also was not different between groups. These data suggest that exposure to ADSS during the perinatal period followed by 5 weeks exposure to FA induces airway hyperresponsiveness in the absence of a significant change in PNECs, NEBs, or mast cells. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10079211     DOI: 10.1006/taap.1998.8612

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  9 in total

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3.  PPARγ agonist rosiglitazone prevents perinatal nicotine exposure-induced asthma in rat offspring.

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5.  Neonatal hyperoxia enhances the inflammatory response in adult mice infected with influenza A virus.

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6.  Effect of perinatal secondhand tobacco smoke exposure on in vivo and intrinsic airway structure/function in non-human primates.

Authors:  Jesse P Joad; Kayleen S Kott; John M Bric; Janice L Peake; Kent E Pinkerton
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Review 7.  The mammalian respiratory system and critical windows of exposure for children's health.

Authors:  K E Pinkerton; J P Joad
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8.  Effects of nicotine during pregnancy: human and experimental evidence.

Authors:  R Wickström
Journal:  Curr Neuropharmacol       Date:  2007-09       Impact factor: 7.363

9.  In utero exposure to environmental tobacco smoke potentiates adult responses to allergen in BALB/c mice.

Authors:  Arthur L Penn; Rodney L Rouse; David W Horohov; Michael T Kearney; Daniel B Paulsen; Larry Lomax
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  9 in total

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