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Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring

It is increasingly recognized that intra-uterine growth restriction (IUGR) is associated with an increased risk of metabolic disorders in late life. Previous studies showed that mice exposed to LPS in late gestation induced fetal IUGR. The present study investigated the effects of maternal LPS expos...

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Autores principales: Liu, Xiao-Jing, Wang, Bi-Wei, Zhao, Mei, Zhang, Cheng, Chen, Yuan-Hua, Hu, Chun-Qiu, Zhao, Hui, Wang, Hua, Chen, Xi, Tao, Fang-Biao, Xu, De-Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257726/
https://www.ncbi.nlm.nih.gov/pubmed/25479255
http://dx.doi.org/10.1371/journal.pone.0114780
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author Liu, Xiao-Jing
Wang, Bi-Wei
Zhao, Mei
Zhang, Cheng
Chen, Yuan-Hua
Hu, Chun-Qiu
Zhao, Hui
Wang, Hua
Chen, Xi
Tao, Fang-Biao
Xu, De-Xiang
author_facet Liu, Xiao-Jing
Wang, Bi-Wei
Zhao, Mei
Zhang, Cheng
Chen, Yuan-Hua
Hu, Chun-Qiu
Zhao, Hui
Wang, Hua
Chen, Xi
Tao, Fang-Biao
Xu, De-Xiang
author_sort Liu, Xiao-Jing
collection PubMed
description It is increasingly recognized that intra-uterine growth restriction (IUGR) is associated with an increased risk of metabolic disorders in late life. Previous studies showed that mice exposed to LPS in late gestation induced fetal IUGR. The present study investigated the effects of maternal LPS exposure during pregnancy on metabolic phenotypes in female adult offspring. Pregnant mice were intraperitoneally injected with LPS (50 µg/kg) daily from gestational day (GD)15 to GD17. After lactation, female pups were fed with standard-chow diets (SD) or high-fat diets (HFD). Glucose tolerance test (GTT) and insulin tolerance test (ITT) were assessed 8 and 12 weeks after diet intervention. Hepatic triglyceride content was examined 12 weeks after diet intervention. As expected, maternal LPS exposure during pregnancy resulted in fetal IUGR. Although there was an increasing trend on fat mass in female offspring whose dams were exposed to LPS during pregnancy, maternal LPS exposure during pregnancy did not elevate the levels of fasting blood glucose and serum insulin and hepatic triglyceride content in female adult offspring. Moreover, maternal LPS exposure during pregnancy did not alter insulin sensitivity in adipose tissue and liver in female adult offspring. Further analysis showed that maternal LPS exposure during pregnancy did not exacerbate HFD-induced glucose tolerance and insulin resistance in female adult offspring. In addition, maternal LPS exposure during pregnancy did not aggravate HFD-induced elevation of hepatic triglyceride content in female adult offspring. In conclusion, LPS-induced IUGR does not alter metabolic phenotypes in adulthood.
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spelling pubmed-42577262014-12-15 Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring Liu, Xiao-Jing Wang, Bi-Wei Zhao, Mei Zhang, Cheng Chen, Yuan-Hua Hu, Chun-Qiu Zhao, Hui Wang, Hua Chen, Xi Tao, Fang-Biao Xu, De-Xiang PLoS One Research Article It is increasingly recognized that intra-uterine growth restriction (IUGR) is associated with an increased risk of metabolic disorders in late life. Previous studies showed that mice exposed to LPS in late gestation induced fetal IUGR. The present study investigated the effects of maternal LPS exposure during pregnancy on metabolic phenotypes in female adult offspring. Pregnant mice were intraperitoneally injected with LPS (50 µg/kg) daily from gestational day (GD)15 to GD17. After lactation, female pups were fed with standard-chow diets (SD) or high-fat diets (HFD). Glucose tolerance test (GTT) and insulin tolerance test (ITT) were assessed 8 and 12 weeks after diet intervention. Hepatic triglyceride content was examined 12 weeks after diet intervention. As expected, maternal LPS exposure during pregnancy resulted in fetal IUGR. Although there was an increasing trend on fat mass in female offspring whose dams were exposed to LPS during pregnancy, maternal LPS exposure during pregnancy did not elevate the levels of fasting blood glucose and serum insulin and hepatic triglyceride content in female adult offspring. Moreover, maternal LPS exposure during pregnancy did not alter insulin sensitivity in adipose tissue and liver in female adult offspring. Further analysis showed that maternal LPS exposure during pregnancy did not exacerbate HFD-induced glucose tolerance and insulin resistance in female adult offspring. In addition, maternal LPS exposure during pregnancy did not aggravate HFD-induced elevation of hepatic triglyceride content in female adult offspring. In conclusion, LPS-induced IUGR does not alter metabolic phenotypes in adulthood. Public Library of Science 2014-12-05 /pmc/articles/PMC4257726/ /pubmed/25479255 http://dx.doi.org/10.1371/journal.pone.0114780 Text en © 2014 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liu, Xiao-Jing
Wang, Bi-Wei
Zhao, Mei
Zhang, Cheng
Chen, Yuan-Hua
Hu, Chun-Qiu
Zhao, Hui
Wang, Hua
Chen, Xi
Tao, Fang-Biao
Xu, De-Xiang
Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring
title Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring
title_full Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring
title_fullStr Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring
title_full_unstemmed Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring
title_short Effects of Maternal LPS Exposure during Pregnancy on Metabolic Phenotypes in Female Offspring
title_sort effects of maternal lps exposure during pregnancy on metabolic phenotypes in female offspring
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257726/
https://www.ncbi.nlm.nih.gov/pubmed/25479255
http://dx.doi.org/10.1371/journal.pone.0114780
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