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Increased PIT1 and PIT2 Expression in Streptozotocin (STZ)-induced Diabetic Mice Contributes to Uptake of iAs(V)
This study aimed to investigate the susceptibility of mice with streptozotocin(STZ)-induced diabetes mellitus (TIDM) to the uptake of pentavalent inorganic arsenic (iAsV) and the possible molecular mechanism. TIDM was induced in mice by STZ. TIDM and normal mice were treated with 15.0 mg/kg Na2HAsO4...
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Published in: | Biomedical and environmental sciences 2017-11, Vol.30 (11), p.792-801 |
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creator | YU, Sha Li XU, Ling Fei WU, Jun Xia YAO, Chen Juan HU, Qiao Yun ZHANG, Chun Xue ZHAO, Xin Yuan WEI, Hai Yan WANG, Xiao Ke CHEN, Gang |
description | This study aimed to investigate the susceptibility of mice with streptozotocin(STZ)-induced diabetes mellitus (TIDM) to the uptake of pentavalent inorganic arsenic (iAsV) and the possible molecular mechanism.
TIDM was induced in mice by STZ. TIDM and normal mice were treated with 15.0 mg/kg Na2HAsO4·12H2O by intragastric administration. Then, the concentrations of arsenic in various tissues were measured by atomic fluorescence spectrometry. The gene expression levels of Pit1 and Pit2 were quantified by real-time RT-PCR, and their protein levels were detected by Western blotting in mouse heart, kidney, and liver tissues.
The concentrations of arsenic in STZ-induced TIDM mouse tissues were higher at 2 h after intragastric administration of Na2HAsO4·12H2O. Compared with the levels in normal mice, PIT1 and PIT2, which play a role in the uptake of iAsV, were upregulated in the livers and hearts of TIDM mice. PIT1 but not PIT2 was higher in TIDM mouse kidneys. The upregulation of Pit1 and Pit2 expression could be reversed by insulin treatment.
The increased uptake of iAsV in TIDM mouse tissues may be associated with increased PIT1 and/or PIT2 expression. |
doi_str_mv | 10.3967/bes2017.107 |
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TIDM was induced in mice by STZ. TIDM and normal mice were treated with 15.0 mg/kg Na2HAsO4·12H2O by intragastric administration. Then, the concentrations of arsenic in various tissues were measured by atomic fluorescence spectrometry. The gene expression levels of Pit1 and Pit2 were quantified by real-time RT-PCR, and their protein levels were detected by Western blotting in mouse heart, kidney, and liver tissues.
The concentrations of arsenic in STZ-induced TIDM mouse tissues were higher at 2 h after intragastric administration of Na2HAsO4·12H2O. Compared with the levels in normal mice, PIT1 and PIT2, which play a role in the uptake of iAsV, were upregulated in the livers and hearts of TIDM mice. PIT1 but not PIT2 was higher in TIDM mouse kidneys. The upregulation of Pit1 and Pit2 expression could be reversed by insulin treatment.
The increased uptake of iAsV in TIDM mouse tissues may be associated with increased PIT1 and/or PIT2 expression.</description><identifier>ISSN: 0895-3988</identifier><identifier>EISSN: 2214-0190</identifier><identifier>DOI: 10.3967/bes2017.107</identifier><identifier>PMID: 29216956</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Pentavalent inorganic arsenic ; Phosphate cotransporters ; Type I diabetes mellitus ; Uptake</subject><ispartof>Biomedical and environmental sciences, 2017-11, Vol.30 (11), p.792-801</ispartof><rights>2017 The Editorial Board of Biomedical and Environmental Sciences</rights><rights>Copyright © 2017 The Editorial Board of Biomedical and Environmental Sciences. Published by China CDC. All rights reserved.</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/bes/bes.jpg</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0895398817301290$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27901,27902,45756</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29216956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>YU, Sha Li</creatorcontrib><creatorcontrib>XU, Ling Fei</creatorcontrib><creatorcontrib>WU, Jun Xia</creatorcontrib><creatorcontrib>YAO, Chen Juan</creatorcontrib><creatorcontrib>HU, Qiao Yun</creatorcontrib><creatorcontrib>ZHANG, Chun Xue</creatorcontrib><creatorcontrib>ZHAO, Xin Yuan</creatorcontrib><creatorcontrib>WEI, Hai Yan</creatorcontrib><creatorcontrib>WANG, Xiao Ke</creatorcontrib><creatorcontrib>CHEN, Gang</creatorcontrib><title>Increased PIT1 and PIT2 Expression in Streptozotocin (STZ)-induced Diabetic Mice Contributes to Uptake of iAs(V)</title><title>Biomedical and environmental sciences</title><addtitle>Biomed Environ Sci</addtitle><description>This study aimed to investigate the susceptibility of mice with streptozotocin(STZ)-induced diabetes mellitus (TIDM) to the uptake of pentavalent inorganic arsenic (iAsV) and the possible molecular mechanism.
TIDM was induced in mice by STZ. TIDM and normal mice were treated with 15.0 mg/kg Na2HAsO4·12H2O by intragastric administration. Then, the concentrations of arsenic in various tissues were measured by atomic fluorescence spectrometry. The gene expression levels of Pit1 and Pit2 were quantified by real-time RT-PCR, and their protein levels were detected by Western blotting in mouse heart, kidney, and liver tissues.
The concentrations of arsenic in STZ-induced TIDM mouse tissues were higher at 2 h after intragastric administration of Na2HAsO4·12H2O. Compared with the levels in normal mice, PIT1 and PIT2, which play a role in the uptake of iAsV, were upregulated in the livers and hearts of TIDM mice. PIT1 but not PIT2 was higher in TIDM mouse kidneys. The upregulation of Pit1 and Pit2 expression could be reversed by insulin treatment.
The increased uptake of iAsV in TIDM mouse tissues may be associated with increased PIT1 and/or PIT2 expression.</description><subject>Pentavalent inorganic arsenic</subject><subject>Phosphate cotransporters</subject><subject>Type I diabetes mellitus</subject><subject>Uptake</subject><issn>0895-3988</issn><issn>2214-0190</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo1kUFvFDEMhSNERbeFE3eUA4ftYUqSmWSSY7WUslIrkLrlwCXKJB6UsptMkwxQfj2huz3Zlj7bz88IvaXkvFWi_zBAZoT255T0L9CCMdo1hCryEi2IVLxplZTH6CTne0I6qjr5Ch0zxahQXCzQtA42gcng8Nf1hmITnhKGL_9MCXL2MWAf8G1JMJX4N5Zoa7m83Xw_a3xws62NH70ZoHiLb7wFvIqhJD_MBTIuEd9NxfwEHEfsL_Ly29lrdDSabYY3h3iK7j5dblafm-svV-vVxXUDTIrSMMG5cVS0lDg7iM6OQ-v6jhEuDHFVu5KMA-Vc1eAME2IcnLO9JJKCa4f2FL3fz_1twmjCD30f5xTqRn3wi1JCWMWWe2xK8WGGXPTOZwvbrQkQ56yp6jmhXUtkRd8d0HnYgdNT8juTHvWzmRXgewDqXb88JJ2th1At8gls0S56TYn-_7RnEbXu239O_oVn</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>YU, Sha Li</creator><creator>XU, Ling Fei</creator><creator>WU, Jun Xia</creator><creator>YAO, Chen Juan</creator><creator>HU, Qiao Yun</creator><creator>ZHANG, Chun Xue</creator><creator>ZHAO, Xin Yuan</creator><creator>WEI, Hai Yan</creator><creator>WANG, Xiao Ke</creator><creator>CHEN, Gang</creator><general>Elsevier B.V</general><general>Department of Environmental Health, School of Public Health, Nantong University, Nantong 226019, Jiangsu, China%Department of Molecular Oral Physiology, Institute of Biomedical Sciences, Tokushima University Graduate School, 770-8504, Japan</general><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20171101</creationdate><title>Increased PIT1 and PIT2 Expression in Streptozotocin (STZ)-induced Diabetic Mice Contributes to Uptake of iAs(V)</title><author>YU, Sha Li ; XU, Ling Fei ; WU, Jun Xia ; YAO, Chen Juan ; HU, Qiao Yun ; ZHANG, Chun Xue ; ZHAO, Xin Yuan ; WEI, Hai Yan ; WANG, Xiao Ke ; CHEN, Gang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e286t-2655ad16310dcb64cfb3d742056a0d6959825e155925eda266fbddc78081ed3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Pentavalent inorganic arsenic</topic><topic>Phosphate cotransporters</topic><topic>Type I diabetes mellitus</topic><topic>Uptake</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YU, Sha Li</creatorcontrib><creatorcontrib>XU, Ling Fei</creatorcontrib><creatorcontrib>WU, Jun Xia</creatorcontrib><creatorcontrib>YAO, Chen Juan</creatorcontrib><creatorcontrib>HU, Qiao Yun</creatorcontrib><creatorcontrib>ZHANG, Chun Xue</creatorcontrib><creatorcontrib>ZHAO, Xin Yuan</creatorcontrib><creatorcontrib>WEI, Hai Yan</creatorcontrib><creatorcontrib>WANG, Xiao Ke</creatorcontrib><creatorcontrib>CHEN, Gang</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Biomedical and environmental sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YU, Sha Li</au><au>XU, Ling Fei</au><au>WU, Jun Xia</au><au>YAO, Chen Juan</au><au>HU, Qiao Yun</au><au>ZHANG, Chun Xue</au><au>ZHAO, Xin Yuan</au><au>WEI, Hai Yan</au><au>WANG, Xiao Ke</au><au>CHEN, Gang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased PIT1 and PIT2 Expression in Streptozotocin (STZ)-induced Diabetic Mice Contributes to Uptake of iAs(V)</atitle><jtitle>Biomedical and environmental sciences</jtitle><addtitle>Biomed Environ Sci</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>30</volume><issue>11</issue><spage>792</spage><epage>801</epage><pages>792-801</pages><issn>0895-3988</issn><eissn>2214-0190</eissn><abstract>This study aimed to investigate the susceptibility of mice with streptozotocin(STZ)-induced diabetes mellitus (TIDM) to the uptake of pentavalent inorganic arsenic (iAsV) and the possible molecular mechanism.
TIDM was induced in mice by STZ. TIDM and normal mice were treated with 15.0 mg/kg Na2HAsO4·12H2O by intragastric administration. Then, the concentrations of arsenic in various tissues were measured by atomic fluorescence spectrometry. The gene expression levels of Pit1 and Pit2 were quantified by real-time RT-PCR, and their protein levels were detected by Western blotting in mouse heart, kidney, and liver tissues.
The concentrations of arsenic in STZ-induced TIDM mouse tissues were higher at 2 h after intragastric administration of Na2HAsO4·12H2O. Compared with the levels in normal mice, PIT1 and PIT2, which play a role in the uptake of iAsV, were upregulated in the livers and hearts of TIDM mice. PIT1 but not PIT2 was higher in TIDM mouse kidneys. The upregulation of Pit1 and Pit2 expression could be reversed by insulin treatment.
The increased uptake of iAsV in TIDM mouse tissues may be associated with increased PIT1 and/or PIT2 expression.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29216956</pmid><doi>10.3967/bes2017.107</doi><tpages>10</tpages></addata></record> |
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subjects | Pentavalent inorganic arsenic Phosphate cotransporters Type I diabetes mellitus Uptake |
title | Increased PIT1 and PIT2 Expression in Streptozotocin (STZ)-induced Diabetic Mice Contributes to Uptake of iAs(V) |
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