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Investigation on oxidative stress of nitric oxide synthase interacting protein from Clonorchis sinensis
Numerous evidences indicate that excretory–secretory products (ESPs) from liver flukes trigger the generation of free radicals that are associated with the initial pathophysiological responses in host cells. In this study, we first constructed a Clonorchis sinensis (C. sinensis, Cs)-infected BALB/c...
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Published in: | Parasitology research (1987) 2016-01, Vol.115 (1), p.77-83 |
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description | Numerous evidences indicate that excretory–secretory products (ESPs) from liver flukes trigger the generation of free radicals that are associated with the initial pathophysiological responses in host cells. In this study, we first constructed a Clonorchis sinensis (C. sinensis, Cs)-infected BALB/c mouse model and examined relative results respectively at 3, 5, 7, and 9 weeks postinfection (p.i.). Quantitative reverse transcription (RT)-PCR indicated that the transcriptional level of both endothelial nitric oxide synthase (eNOS) and superoxide dismutase (SOD) gradually decreased with lastingness of infection, while the transcriptional level of inducible NOS (iNOS) significantly increased. The level of malondialdehyde (MDA) in sera of infected mouse significantly increased versus the healthy control group. These results showed that the liver of C. sinensis-infected mouse was in a state with elevated levels of oxidation stress. Previously, C. sinensis NOS interacting protein coding gene (named CsNOSIP) has been isolated and recombinant CsNOSIP (rCsNOSIP) has been expressed in Escherichia coli, which has been confirmed to be a component present in CsESPs and confirmed to play important roles in immune regulation of the host. In the present paper, we investigated the effects of rCsNOSIP on the lipopolysaccharide (LPS)-induced activated RAW264.7, a murine macrophage cell line. We found that endotoxin-free rCsNOSIP significantly promoted the levels of nitric oxide (NO) and reactive oxygen species (ROS) after pretreated with rCsNOSIP, while the level of SOD decreased. Furthermore, rCsNOSIP could also increase the level of lipid peroxidation MDA. Taken together, these results suggested that CsNOSIP was a key molecule which was involved in the production of nitric oxide (NO) and its reactive intermediates, and played an important role in oxidative stress during C. sinensis infection. |
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In this study, we first constructed a Clonorchis sinensis (C. sinensis, Cs)-infected BALB/c mouse model and examined relative results respectively at 3, 5, 7, and 9 weeks postinfection (p.i.). Quantitative reverse transcription (RT)-PCR indicated that the transcriptional level of both endothelial nitric oxide synthase (eNOS) and superoxide dismutase (SOD) gradually decreased with lastingness of infection, while the transcriptional level of inducible NOS (iNOS) significantly increased. The level of malondialdehyde (MDA) in sera of infected mouse significantly increased versus the healthy control group. These results showed that the liver of C. sinensis-infected mouse was in a state with elevated levels of oxidation stress. Previously, C. sinensis NOS interacting protein coding gene (named CsNOSIP) has been isolated and recombinant CsNOSIP (rCsNOSIP) has been expressed in Escherichia coli, which has been confirmed to be a component present in CsESPs and confirmed to play important roles in immune regulation of the host. In the present paper, we investigated the effects of rCsNOSIP on the lipopolysaccharide (LPS)-induced activated RAW264.7, a murine macrophage cell line. We found that endotoxin-free rCsNOSIP significantly promoted the levels of nitric oxide (NO) and reactive oxygen species (ROS) after pretreated with rCsNOSIP, while the level of SOD decreased. Furthermore, rCsNOSIP could also increase the level of lipid peroxidation MDA. Taken together, these results suggested that CsNOSIP was a key molecule which was involved in the production of nitric oxide (NO) and its reactive intermediates, and played an important role in oxidative stress during C. sinensis infection.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-015-4723-5</identifier><identifier>PMID: 26391171</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Cell Line ; Clonorchis sinensis ; Clonorchis sinensis - chemistry ; Clonorchis sinensis - genetics ; Clonorchis sinensis - metabolism ; Cyprinidae - parasitology ; Escherichia coli ; Health aspects ; Immunology ; Lipid Peroxidation ; Macrophages - metabolism ; Male ; Malondialdehyde - metabolism ; Medical Microbiology ; Mice ; Mice, Inbred BALB C ; Microbiology ; Nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase Type II - metabolism ; Nitric Oxide Synthase Type III - metabolism ; Observations ; Oriental liver fluke ; Original Paper ; Oxidative Stress ; Protein-protein interactions ; Random Allocation ; Reactive Oxygen Species - metabolism ; RNA, Messenger - metabolism ; Specific Pathogen-Free Organisms ; Superoxide Dismutase - antagonists & inhibitors ; Superoxide Dismutase - metabolism ; Trematoda ; Ubiquitin-Protein Ligases - metabolism ; Up-Regulation</subject><ispartof>Parasitology research (1987), 2016-01, Vol.115 (1), p.77-83</ispartof><rights>Springer-Verlag Berlin Heidelberg 2015</rights><rights>COPYRIGHT 2016 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-9af274442b7358cdfbef9a75a1b47f314723e1c1665c0a7ee9ab815b57ceda6c3</citedby><cites>FETCH-LOGICAL-c510t-9af274442b7358cdfbef9a75a1b47f314723e1c1665c0a7ee9ab815b57ceda6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26391171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bian, Meng</creatorcontrib><creatorcontrib>Xu, Qingxia</creatorcontrib><creatorcontrib>Xu, Yanquan</creatorcontrib><creatorcontrib>Li, Shan</creatorcontrib><creatorcontrib>Wang, Xiaoyun</creatorcontrib><creatorcontrib>Sheng, Jiahe</creatorcontrib><creatorcontrib>Wu, Zhongdao</creatorcontrib><creatorcontrib>Huang, Yan</creatorcontrib><creatorcontrib>Yu, Xinbing</creatorcontrib><title>Investigation on oxidative stress of nitric oxide synthase interacting protein from Clonorchis sinensis</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><addtitle>Parasitol Res</addtitle><description>Numerous evidences indicate that excretory–secretory products (ESPs) from liver flukes trigger the generation of free radicals that are associated with the initial pathophysiological responses in host cells. In this study, we first constructed a Clonorchis sinensis (C. sinensis, Cs)-infected BALB/c mouse model and examined relative results respectively at 3, 5, 7, and 9 weeks postinfection (p.i.). Quantitative reverse transcription (RT)-PCR indicated that the transcriptional level of both endothelial nitric oxide synthase (eNOS) and superoxide dismutase (SOD) gradually decreased with lastingness of infection, while the transcriptional level of inducible NOS (iNOS) significantly increased. The level of malondialdehyde (MDA) in sera of infected mouse significantly increased versus the healthy control group. These results showed that the liver of C. sinensis-infected mouse was in a state with elevated levels of oxidation stress. Previously, C. sinensis NOS interacting protein coding gene (named CsNOSIP) has been isolated and recombinant CsNOSIP (rCsNOSIP) has been expressed in Escherichia coli, which has been confirmed to be a component present in CsESPs and confirmed to play important roles in immune regulation of the host. In the present paper, we investigated the effects of rCsNOSIP on the lipopolysaccharide (LPS)-induced activated RAW264.7, a murine macrophage cell line. We found that endotoxin-free rCsNOSIP significantly promoted the levels of nitric oxide (NO) and reactive oxygen species (ROS) after pretreated with rCsNOSIP, while the level of SOD decreased. Furthermore, rCsNOSIP could also increase the level of lipid peroxidation MDA. Taken together, these results suggested that CsNOSIP was a key molecule which was involved in the production of nitric oxide (NO) and its reactive intermediates, and played an important role in oxidative stress during C. sinensis infection.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Line</subject><subject>Clonorchis sinensis</subject><subject>Clonorchis sinensis - chemistry</subject><subject>Clonorchis sinensis - genetics</subject><subject>Clonorchis sinensis - metabolism</subject><subject>Cyprinidae - parasitology</subject><subject>Escherichia coli</subject><subject>Health aspects</subject><subject>Immunology</subject><subject>Lipid Peroxidation</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>Medical Microbiology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Observations</subject><subject>Oriental liver fluke</subject><subject>Original Paper</subject><subject>Oxidative Stress</subject><subject>Protein-protein interactions</subject><subject>Random Allocation</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Specific Pathogen-Free Organisms</subject><subject>Superoxide Dismutase - antagonists & inhibitors</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Trematoda</subject><subject>Ubiquitin-Protein Ligases - metabolism</subject><subject>Up-Regulation</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFUk1v1DAQtRCILgs_gAvkyCXFE38lx2rFR6VKHKBny3HGqavELra3av89XlI4gmzJ45n3RvP8TMhboOdAqfqYKeVMthREy1XHWvGM7ICzroVBiOdkR4caUwB2Rl7lfEspKMn5S3LWSTYAKNiR-TLcYy5-NsXH0Jz2g5_q5R6bXBLm3ETXBF-St79LNf0Yyo3J2PhQMBlbfJibuxQL-tC4FNfmsMQQk73xuck-YMg-vyYvnFkyvnk69-T686cfh6_t1bcvl4eLq9YKoKUdjOsU57wbFRO9ndyIbjBKGBi5cgxOMhEsSCksNQpxMGMPYhTK4mSkZXvyYetbB_p5rMr06rPFZTEB4zFr6GXPqOIC_g9VgtOei0rYk_MNOpsFtQ8uliq8rglXb2NA52v-gisKvGOsqwTYCDbFnBM6fZf8atKjBqpP3unNO1290ydRWlTOu6d5juOK01_GH7MqoNsAuZbCjEnfxmMK9Tn_2fX9RnImajMnn_X1946CrL-BD4MU7BcdAK7p</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Bian, Meng</creator><creator>Xu, Qingxia</creator><creator>Xu, Yanquan</creator><creator>Li, Shan</creator><creator>Wang, Xiaoyun</creator><creator>Sheng, Jiahe</creator><creator>Wu, Zhongdao</creator><creator>Huang, Yan</creator><creator>Yu, Xinbing</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>M7N</scope></search><sort><creationdate>20160101</creationdate><title>Investigation on oxidative stress of nitric oxide synthase interacting protein from Clonorchis sinensis</title><author>Bian, Meng ; Xu, Qingxia ; Xu, Yanquan ; Li, Shan ; Wang, Xiaoyun ; Sheng, Jiahe ; Wu, Zhongdao ; Huang, Yan ; Yu, Xinbing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-9af274442b7358cdfbef9a75a1b47f314723e1c1665c0a7ee9ab815b57ceda6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Line</topic><topic>Clonorchis sinensis</topic><topic>Clonorchis sinensis - chemistry</topic><topic>Clonorchis sinensis - genetics</topic><topic>Clonorchis sinensis - metabolism</topic><topic>Cyprinidae - parasitology</topic><topic>Escherichia coli</topic><topic>Health aspects</topic><topic>Immunology</topic><topic>Lipid Peroxidation</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Malondialdehyde - metabolism</topic><topic>Medical Microbiology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Observations</topic><topic>Oriental liver fluke</topic><topic>Original Paper</topic><topic>Oxidative Stress</topic><topic>Protein-protein interactions</topic><topic>Random Allocation</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Specific Pathogen-Free Organisms</topic><topic>Superoxide Dismutase - antagonists & inhibitors</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Trematoda</topic><topic>Ubiquitin-Protein Ligases - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bian, Meng</creatorcontrib><creatorcontrib>Xu, Qingxia</creatorcontrib><creatorcontrib>Xu, Yanquan</creatorcontrib><creatorcontrib>Li, Shan</creatorcontrib><creatorcontrib>Wang, Xiaoyun</creatorcontrib><creatorcontrib>Sheng, Jiahe</creatorcontrib><creatorcontrib>Wu, Zhongdao</creatorcontrib><creatorcontrib>Huang, Yan</creatorcontrib><creatorcontrib>Yu, Xinbing</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bian, Meng</au><au>Xu, Qingxia</au><au>Xu, Yanquan</au><au>Li, Shan</au><au>Wang, Xiaoyun</au><au>Sheng, Jiahe</au><au>Wu, Zhongdao</au><au>Huang, Yan</au><au>Yu, Xinbing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation on oxidative stress of nitric oxide synthase interacting protein from Clonorchis sinensis</atitle><jtitle>Parasitology research (1987)</jtitle><stitle>Parasitol Res</stitle><addtitle>Parasitol Res</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>115</volume><issue>1</issue><spage>77</spage><epage>83</epage><pages>77-83</pages><issn>0932-0113</issn><eissn>1432-1955</eissn><abstract>Numerous evidences indicate that excretory–secretory products (ESPs) from liver flukes trigger the generation of free radicals that are associated with the initial pathophysiological responses in host cells. In this study, we first constructed a Clonorchis sinensis (C. sinensis, Cs)-infected BALB/c mouse model and examined relative results respectively at 3, 5, 7, and 9 weeks postinfection (p.i.). Quantitative reverse transcription (RT)-PCR indicated that the transcriptional level of both endothelial nitric oxide synthase (eNOS) and superoxide dismutase (SOD) gradually decreased with lastingness of infection, while the transcriptional level of inducible NOS (iNOS) significantly increased. The level of malondialdehyde (MDA) in sera of infected mouse significantly increased versus the healthy control group. These results showed that the liver of C. sinensis-infected mouse was in a state with elevated levels of oxidation stress. Previously, C. sinensis NOS interacting protein coding gene (named CsNOSIP) has been isolated and recombinant CsNOSIP (rCsNOSIP) has been expressed in Escherichia coli, which has been confirmed to be a component present in CsESPs and confirmed to play important roles in immune regulation of the host. In the present paper, we investigated the effects of rCsNOSIP on the lipopolysaccharide (LPS)-induced activated RAW264.7, a murine macrophage cell line. We found that endotoxin-free rCsNOSIP significantly promoted the levels of nitric oxide (NO) and reactive oxygen species (ROS) after pretreated with rCsNOSIP, while the level of SOD decreased. Furthermore, rCsNOSIP could also increase the level of lipid peroxidation MDA. Taken together, these results suggested that CsNOSIP was a key molecule which was involved in the production of nitric oxide (NO) and its reactive intermediates, and played an important role in oxidative stress during C. sinensis infection.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26391171</pmid><doi>10.1007/s00436-015-4723-5</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Cell Line Clonorchis sinensis Clonorchis sinensis - chemistry Clonorchis sinensis - genetics Clonorchis sinensis - metabolism Cyprinidae - parasitology Escherichia coli Health aspects Immunology Lipid Peroxidation Macrophages - metabolism Male Malondialdehyde - metabolism Medical Microbiology Mice Mice, Inbred BALB C Microbiology Nitric oxide Nitric Oxide - metabolism Nitric Oxide Synthase Type II - metabolism Nitric Oxide Synthase Type III - metabolism Observations Oriental liver fluke Original Paper Oxidative Stress Protein-protein interactions Random Allocation Reactive Oxygen Species - metabolism RNA, Messenger - metabolism Specific Pathogen-Free Organisms Superoxide Dismutase - antagonists & inhibitors Superoxide Dismutase - metabolism Trematoda Ubiquitin-Protein Ligases - metabolism Up-Regulation |
title | Investigation on oxidative stress of nitric oxide synthase interacting protein from Clonorchis sinensis |
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