Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice

Abstract Background Epidemiological studies in China have revealed that Schistosoma japonicum infection is inversely correlated with metabolic syndrome, even after repeated chemotherapy with praziquantel (PZQ). We investigated the effect of chronic S. japonicum infection, PZQ chemotherapy, and solub...

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Main Authors: Xiaofeng Luo, Yuxiao Zhu, Ran Liu, Jingwei Song, Fan Zhang, Wenyue Zhang, Zhipeng Xu, Min Hou, Bingya Yang, Lin Chen, Minjun Ji
Format: Article
Language:English
Published: BMC 2017-10-01
Series:Parasites & Vectors
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13071-017-2400-5
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author Xiaofeng Luo
Yuxiao Zhu
Ran Liu
Jingwei Song
Fan Zhang
Wenyue Zhang
Zhipeng Xu
Min Hou
Bingya Yang
Lin Chen
Minjun Ji
author_facet Xiaofeng Luo
Yuxiao Zhu
Ran Liu
Jingwei Song
Fan Zhang
Wenyue Zhang
Zhipeng Xu
Min Hou
Bingya Yang
Lin Chen
Minjun Ji
author_sort Xiaofeng Luo
collection DOAJ
description Abstract Background Epidemiological studies in China have revealed that Schistosoma japonicum infection is inversely correlated with metabolic syndrome, even after repeated chemotherapy with praziquantel (PZQ). We investigated the effect of chronic S. japonicum infection, PZQ chemotherapy, and soluble egg antigen (SEA) treatment on whole-body metabolic homeostasis and hepatic insulin sensitivity in mouse models. Results Infection with S. japonicum was found to increase whole-body and hepatic insulin sensitivity in mice. PZQ chemotherapy significantly improved the physiological status of infected mice, maintaining Th2 immune-deviation and enhancing hepatic insulin sensitivity. Multiple linear regression analysis revealed positive correlations between anti-inflammatory cytokine expression and insulin signalling-related genes in the liver, as demonstrated by an in vitro stimulated hepatic cell line with IL-13 and IL-22. SEA treatment also improved the glucose tolerance and insulin sensitivity in Lepr db/db mice. Conclusions This study indicated that chronic S. japonicum infection with PZQ chemotherapy and SEA treatment can regulate metabolic homeostasis and protect against metabolic syndrome by promoting Th2 and regulatory responses in the liver.
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spelling doaj.art-57962a49754f412b9ba07466423618322022-12-21T18:49:38ZengBMCParasites & Vectors1756-33052017-10-0110111210.1186/s13071-017-2400-5Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in miceXiaofeng Luo0Yuxiao Zhu1Ran Liu2Jingwei Song3Fan Zhang4Wenyue Zhang5Zhipeng Xu6Min Hou7Bingya Yang8Lin Chen9Minjun Ji10Department of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityDepartment of Pathogen Biology, Nanjing Medical UniversityAbstract Background Epidemiological studies in China have revealed that Schistosoma japonicum infection is inversely correlated with metabolic syndrome, even after repeated chemotherapy with praziquantel (PZQ). We investigated the effect of chronic S. japonicum infection, PZQ chemotherapy, and soluble egg antigen (SEA) treatment on whole-body metabolic homeostasis and hepatic insulin sensitivity in mouse models. Results Infection with S. japonicum was found to increase whole-body and hepatic insulin sensitivity in mice. PZQ chemotherapy significantly improved the physiological status of infected mice, maintaining Th2 immune-deviation and enhancing hepatic insulin sensitivity. Multiple linear regression analysis revealed positive correlations between anti-inflammatory cytokine expression and insulin signalling-related genes in the liver, as demonstrated by an in vitro stimulated hepatic cell line with IL-13 and IL-22. SEA treatment also improved the glucose tolerance and insulin sensitivity in Lepr db/db mice. Conclusions This study indicated that chronic S. japonicum infection with PZQ chemotherapy and SEA treatment can regulate metabolic homeostasis and protect against metabolic syndrome by promoting Th2 and regulatory responses in the liver.http://link.springer.com/article/10.1186/s13071-017-2400-5Schistosoma japonicumGlucose metabolismInsulin resistanceAnti-inflammatory cytokines
spellingShingle Xiaofeng Luo
Yuxiao Zhu
Ran Liu
Jingwei Song
Fan Zhang
Wenyue Zhang
Zhipeng Xu
Min Hou
Bingya Yang
Lin Chen
Minjun Ji
Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
Parasites & Vectors
Schistosoma japonicum
Glucose metabolism
Insulin resistance
Anti-inflammatory cytokines
title Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
title_full Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
title_fullStr Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
title_full_unstemmed Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
title_short Praziquantel treatment after Schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
title_sort praziquantel treatment after schistosoma japonicum infection maintains hepatic insulin sensitivity and improves glucose metabolism in mice
topic Schistosoma japonicum
Glucose metabolism
Insulin resistance
Anti-inflammatory cytokines
url http://link.springer.com/article/10.1186/s13071-017-2400-5
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