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The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure
This study was carried out to determine the changes in the lungs of the rat pups exposed to tobacco smoke during pregnancy period and to investigate the protective effects of alpha lipoic acid, which is administered during pregnancy, on these changes. Spraque-Dawley female rats were divided into fou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031852/ https://www.ncbi.nlm.nih.gov/pubmed/29984187 http://dx.doi.org/10.1016/j.toxrep.2018.05.014 |
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author | Guzel, Elif Erdem Kaya, Nalan Ozan, Gonca Tektemur, Ahmet Dabak, Durrin Ozlem Ozan, Ibrahim Enver |
author_facet | Guzel, Elif Erdem Kaya, Nalan Ozan, Gonca Tektemur, Ahmet Dabak, Durrin Ozlem Ozan, Ibrahim Enver |
author_sort | Guzel, Elif Erdem |
collection | PubMed |
description | This study was carried out to determine the changes in the lungs of the rat pups exposed to tobacco smoke during pregnancy period and to investigate the protective effects of alpha lipoic acid, which is administered during pregnancy, on these changes. Spraque-Dawley female rats were divided into four groups: control, tobacco smoke (TS), tobacco smoke + alpha lipoic acid (TS + ALA) and alpha lipoic acid (ALA). The rats in control group were untreated. Rats were exposed to TS twice a day for one hour starting from eight weeks before mating and during pregnancy. 20 mg / kg of ALA was administered to rats. On 7(th) and 21(st) days 7 of the pups from each group were decapitated. Histological, morphometric, biochemical and quantitative real-time RT-PCR analyzes were performed. Histopathological and biochemical changes were observed in TS group. While a significant decrease was observed both in SP-A and VEGF immunoreactivities and mRNA levels, caspase-3 immunoreactivity and TUNEL positive cells were increased in TS group. It is suggested that prenatal TS exposure leads to morphological and histopathological changes on lung development by causing oxidative damage in lungs of neonatal rats and the maternal use of ALA can provide a limited protective effect on the neonatal lung development against this oxidative stress originating from TS. Although pregnant women are increasingly aware on health risks of smoking, environmental tobacco smoke exposure is still a widespread problem. For this reason, it is thought that this damage can be partially reduced by some antioxidant supplements in pregnancy. |
format | Online Article Text |
id | pubmed-6031852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60318522018-07-06 The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure Guzel, Elif Erdem Kaya, Nalan Ozan, Gonca Tektemur, Ahmet Dabak, Durrin Ozlem Ozan, Ibrahim Enver Toxicol Rep Article This study was carried out to determine the changes in the lungs of the rat pups exposed to tobacco smoke during pregnancy period and to investigate the protective effects of alpha lipoic acid, which is administered during pregnancy, on these changes. Spraque-Dawley female rats were divided into four groups: control, tobacco smoke (TS), tobacco smoke + alpha lipoic acid (TS + ALA) and alpha lipoic acid (ALA). The rats in control group were untreated. Rats were exposed to TS twice a day for one hour starting from eight weeks before mating and during pregnancy. 20 mg / kg of ALA was administered to rats. On 7(th) and 21(st) days 7 of the pups from each group were decapitated. Histological, morphometric, biochemical and quantitative real-time RT-PCR analyzes were performed. Histopathological and biochemical changes were observed in TS group. While a significant decrease was observed both in SP-A and VEGF immunoreactivities and mRNA levels, caspase-3 immunoreactivity and TUNEL positive cells were increased in TS group. It is suggested that prenatal TS exposure leads to morphological and histopathological changes on lung development by causing oxidative damage in lungs of neonatal rats and the maternal use of ALA can provide a limited protective effect on the neonatal lung development against this oxidative stress originating from TS. Although pregnant women are increasingly aware on health risks of smoking, environmental tobacco smoke exposure is still a widespread problem. For this reason, it is thought that this damage can be partially reduced by some antioxidant supplements in pregnancy. Elsevier 2018-06-05 /pmc/articles/PMC6031852/ /pubmed/29984187 http://dx.doi.org/10.1016/j.toxrep.2018.05.014 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Guzel, Elif Erdem Kaya, Nalan Ozan, Gonca Tektemur, Ahmet Dabak, Durrin Ozlem Ozan, Ibrahim Enver The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
title | The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
title_full | The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
title_fullStr | The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
title_full_unstemmed | The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
title_short | The investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
title_sort | investigation of effect of alpha lipoic acid against damage on neonatal rat lung to maternal tobacco smoke exposure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031852/ https://www.ncbi.nlm.nih.gov/pubmed/29984187 http://dx.doi.org/10.1016/j.toxrep.2018.05.014 |
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