Loading…
ClC-3 Expression and Its Association with Hyperglycemia Induced HT22 Hippocampal Neuronal Cell Apoptosis
Although apoptosis plays an important role in the development of Diabetic Encephalopathy (DE), the underlying molecular mechanisms remain unclear. With respect to this, the present work aims to study the variation in chloride/proton exchanger ClC-3 expression and its association with HT22 hippocampa...
Saved in:
Published in: | Journal of diabetes research 2016-01, Vol.2016 (2016), p.1-12 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323 |
---|---|
cites | cdi_FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323 |
container_end_page | 12 |
container_issue | 2016 |
container_start_page | 1 |
container_title | Journal of diabetes research |
container_volume | 2016 |
creator | Tu, Yanyang Fu, Jianfang Li, Qian Wang, Zhen Zhang, Pengxing Liu, Hui Ren, Dongni Wang, Xin Liu, Tao Fan, Feiyan Liu, Nan |
description | Although apoptosis plays an important role in the development of Diabetic Encephalopathy (DE), the underlying molecular mechanisms remain unclear. With respect to this, the present work aims to study the variation in chloride/proton exchanger ClC-3 expression and its association with HT22 hippocampal neuronal apoptosis under hyperglycemic condition in vitro. The cells were stimulated with added 0, 5, or 25 mM glucose or mannitol for up to 72 hours before assessing the rate of ClC-3 expression, cell viability, and apoptosis. In a consecutive experiment, cells received chloride channel blocker in addition to glucose. The rate of cellular death/apoptosis and viability was measured using Flow Cytometry and MTT assay, respectively. Changes in ClC-3 expression were assessed using immunofluorescence staining and western blot analysis. The results revealed a significant increase in cellular apoptosis and reduction in viability, associated with increased ClC-3 expression in high glucose group. Osmolarity had no role to play. Addition of chloride channel blocker completely abolished this effect. Thus we conclude that, with its increased expression, ClC-3 plays a major role in hyperglycemia induced hippocampal neuronal apoptosis. To strengthen our understanding of this aforesaid association, we conducted an extensive literature search which is presented in this paper. |
doi_str_mv | 10.1155/2016/2984380 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_1d0a949fd1c04e91a04e620f1d51c962</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_1d0a949fd1c04e91a04e620f1d51c962</doaj_id><sourcerecordid>1769628247</sourcerecordid><originalsourceid>FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323</originalsourceid><addsrcrecordid>eNqNkk2P0zAQhiMEYlfL3jgjS1yQIKzHdhznglRVC620gstythx_tK6SONgJS_89Li2F5YQP9mj86LXfmSmKl4DfA1TVDcHAb0gjGBX4SXFJKLCS1xV9eo5ZdVFcp7TDeTW0EZV4XlwQ3pCKEbgststuWVJ0-2OMNiUfBqQGg9ZTQouUgvZqOuQe_LRFq_1o46bba9t7hdaDmbU1aHVPCFr5cQxa9aPq0Gc7xzDkYGm7Di3GME4h-fSieOZUl-z16bwqvn68vV-uyrsvn9bLxV2pOa2m0rUUWkOcbjkXrXECt06B4Iy2ggkQzlndGm2EAua0w5QD1aQSNWsZqSihV8X6qGuC2skx-l7FvQzKy1-JEDdSxcnrzkowWDWscQY0ZrYBlXdOsANTgW74QevDUWuc294abYcpqu6R6OObwW_lJnyXrGbZDcsCb04CMXybbZpk75POdVGDDXOSUPP8jiCszujrf9BdmGOuY5KE4ZrT3GPI1LsjpWNIKVp3_gxgeZgIeZgIeZqIjL_628AZ_t3_DLw9Als_GPXg_1POZsY69YcGLHC2_BMDI8cw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2407638431</pqid></control><display><type>article</type><title>ClC-3 Expression and Its Association with Hyperglycemia Induced HT22 Hippocampal Neuronal Cell Apoptosis</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><source>Wiley Open Access</source><creator>Tu, Yanyang ; Fu, Jianfang ; Li, Qian ; Wang, Zhen ; Zhang, Pengxing ; Liu, Hui ; Ren, Dongni ; Wang, Xin ; Liu, Tao ; Fan, Feiyan ; Liu, Nan</creator><contributor>Mastrocola, Raffaella ; Raffaella Mastrocola</contributor><creatorcontrib>Tu, Yanyang ; Fu, Jianfang ; Li, Qian ; Wang, Zhen ; Zhang, Pengxing ; Liu, Hui ; Ren, Dongni ; Wang, Xin ; Liu, Tao ; Fan, Feiyan ; Liu, Nan ; Mastrocola, Raffaella ; Raffaella Mastrocola</creatorcontrib><description>Although apoptosis plays an important role in the development of Diabetic Encephalopathy (DE), the underlying molecular mechanisms remain unclear. With respect to this, the present work aims to study the variation in chloride/proton exchanger ClC-3 expression and its association with HT22 hippocampal neuronal apoptosis under hyperglycemic condition in vitro. The cells were stimulated with added 0, 5, or 25 mM glucose or mannitol for up to 72 hours before assessing the rate of ClC-3 expression, cell viability, and apoptosis. In a consecutive experiment, cells received chloride channel blocker in addition to glucose. The rate of cellular death/apoptosis and viability was measured using Flow Cytometry and MTT assay, respectively. Changes in ClC-3 expression were assessed using immunofluorescence staining and western blot analysis. The results revealed a significant increase in cellular apoptosis and reduction in viability, associated with increased ClC-3 expression in high glucose group. Osmolarity had no role to play. Addition of chloride channel blocker completely abolished this effect. Thus we conclude that, with its increased expression, ClC-3 plays a major role in hyperglycemia induced hippocampal neuronal apoptosis. To strengthen our understanding of this aforesaid association, we conducted an extensive literature search which is presented in this paper.</description><identifier>ISSN: 2314-6745</identifier><identifier>EISSN: 2314-6753</identifier><identifier>DOI: 10.1155/2016/2984380</identifier><identifier>PMID: 26925421</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Antibodies ; Apoptosis ; Blotting, Western ; Cell culture ; Cell cycle ; Cell Line ; Cell Survival ; Chloride ; Chloride Channels - analysis ; Chloride Channels - physiology ; Diabetes ; Flow Cytometry ; Glucose ; Hippocampus - pathology ; Hyperglycemia ; Hyperglycemia - pathology ; Mice ; Nitrobenzoates - pharmacology ; Oxidative Stress ; Proteins ; Studies</subject><ispartof>Journal of diabetes research, 2016-01, Vol.2016 (2016), p.1-12</ispartof><rights>Copyright © 2016 Feiyan Fan et al.</rights><rights>Copyright © 2016 Feiyan Fan et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2016 Feiyan Fan et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323</citedby><cites>FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323</cites><orcidid>0000-0002-4372-5920 ; 0000-0002-1846-540X ; 0000-0002-2173-5976 ; 0000-0002-9233-2170 ; 0000-0001-7462-6274 ; 0000-0003-3255-8108 ; 0000-0002-4822-9555</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2407638431/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2407638431?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26925421$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Mastrocola, Raffaella</contributor><contributor>Raffaella Mastrocola</contributor><creatorcontrib>Tu, Yanyang</creatorcontrib><creatorcontrib>Fu, Jianfang</creatorcontrib><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Wang, Zhen</creatorcontrib><creatorcontrib>Zhang, Pengxing</creatorcontrib><creatorcontrib>Liu, Hui</creatorcontrib><creatorcontrib>Ren, Dongni</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Liu, Tao</creatorcontrib><creatorcontrib>Fan, Feiyan</creatorcontrib><creatorcontrib>Liu, Nan</creatorcontrib><title>ClC-3 Expression and Its Association with Hyperglycemia Induced HT22 Hippocampal Neuronal Cell Apoptosis</title><title>Journal of diabetes research</title><addtitle>J Diabetes Res</addtitle><description>Although apoptosis plays an important role in the development of Diabetic Encephalopathy (DE), the underlying molecular mechanisms remain unclear. With respect to this, the present work aims to study the variation in chloride/proton exchanger ClC-3 expression and its association with HT22 hippocampal neuronal apoptosis under hyperglycemic condition in vitro. The cells were stimulated with added 0, 5, or 25 mM glucose or mannitol for up to 72 hours before assessing the rate of ClC-3 expression, cell viability, and apoptosis. In a consecutive experiment, cells received chloride channel blocker in addition to glucose. The rate of cellular death/apoptosis and viability was measured using Flow Cytometry and MTT assay, respectively. Changes in ClC-3 expression were assessed using immunofluorescence staining and western blot analysis. The results revealed a significant increase in cellular apoptosis and reduction in viability, associated with increased ClC-3 expression in high glucose group. Osmolarity had no role to play. Addition of chloride channel blocker completely abolished this effect. Thus we conclude that, with its increased expression, ClC-3 plays a major role in hyperglycemia induced hippocampal neuronal apoptosis. To strengthen our understanding of this aforesaid association, we conducted an extensive literature search which is presented in this paper.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Apoptosis</subject><subject>Blotting, Western</subject><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Cell Line</subject><subject>Cell Survival</subject><subject>Chloride</subject><subject>Chloride Channels - analysis</subject><subject>Chloride Channels - physiology</subject><subject>Diabetes</subject><subject>Flow Cytometry</subject><subject>Glucose</subject><subject>Hippocampus - pathology</subject><subject>Hyperglycemia</subject><subject>Hyperglycemia - pathology</subject><subject>Mice</subject><subject>Nitrobenzoates - pharmacology</subject><subject>Oxidative Stress</subject><subject>Proteins</subject><subject>Studies</subject><issn>2314-6745</issn><issn>2314-6753</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk2P0zAQhiMEYlfL3jgjS1yQIKzHdhznglRVC620gstythx_tK6SONgJS_89Li2F5YQP9mj86LXfmSmKl4DfA1TVDcHAb0gjGBX4SXFJKLCS1xV9eo5ZdVFcp7TDeTW0EZV4XlwQ3pCKEbgststuWVJ0-2OMNiUfBqQGg9ZTQouUgvZqOuQe_LRFq_1o46bba9t7hdaDmbU1aHVPCFr5cQxa9aPq0Gc7xzDkYGm7Di3GME4h-fSieOZUl-z16bwqvn68vV-uyrsvn9bLxV2pOa2m0rUUWkOcbjkXrXECt06B4Iy2ggkQzlndGm2EAua0w5QD1aQSNWsZqSihV8X6qGuC2skx-l7FvQzKy1-JEDdSxcnrzkowWDWscQY0ZrYBlXdOsANTgW74QevDUWuc294abYcpqu6R6OObwW_lJnyXrGbZDcsCb04CMXybbZpk75POdVGDDXOSUPP8jiCszujrf9BdmGOuY5KE4ZrT3GPI1LsjpWNIKVp3_gxgeZgIeZgIeZqIjL_628AZ_t3_DLw9Als_GPXg_1POZsY69YcGLHC2_BMDI8cw</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Tu, Yanyang</creator><creator>Fu, Jianfang</creator><creator>Li, Qian</creator><creator>Wang, Zhen</creator><creator>Zhang, Pengxing</creator><creator>Liu, Hui</creator><creator>Ren, Dongni</creator><creator>Wang, Xin</creator><creator>Liu, Tao</creator><creator>Fan, Feiyan</creator><creator>Liu, Nan</creator><general>Hindawi Publishing Corporation</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4372-5920</orcidid><orcidid>https://orcid.org/0000-0002-1846-540X</orcidid><orcidid>https://orcid.org/0000-0002-2173-5976</orcidid><orcidid>https://orcid.org/0000-0002-9233-2170</orcidid><orcidid>https://orcid.org/0000-0001-7462-6274</orcidid><orcidid>https://orcid.org/0000-0003-3255-8108</orcidid><orcidid>https://orcid.org/0000-0002-4822-9555</orcidid></search><sort><creationdate>20160101</creationdate><title>ClC-3 Expression and Its Association with Hyperglycemia Induced HT22 Hippocampal Neuronal Cell Apoptosis</title><author>Tu, Yanyang ; Fu, Jianfang ; Li, Qian ; Wang, Zhen ; Zhang, Pengxing ; Liu, Hui ; Ren, Dongni ; Wang, Xin ; Liu, Tao ; Fan, Feiyan ; Liu, Nan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Apoptosis</topic><topic>Blotting, Western</topic><topic>Cell culture</topic><topic>Cell cycle</topic><topic>Cell Line</topic><topic>Cell Survival</topic><topic>Chloride</topic><topic>Chloride Channels - analysis</topic><topic>Chloride Channels - physiology</topic><topic>Diabetes</topic><topic>Flow Cytometry</topic><topic>Glucose</topic><topic>Hippocampus - pathology</topic><topic>Hyperglycemia</topic><topic>Hyperglycemia - pathology</topic><topic>Mice</topic><topic>Nitrobenzoates - pharmacology</topic><topic>Oxidative Stress</topic><topic>Proteins</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tu, Yanyang</creatorcontrib><creatorcontrib>Fu, Jianfang</creatorcontrib><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Wang, Zhen</creatorcontrib><creatorcontrib>Zhang, Pengxing</creatorcontrib><creatorcontrib>Liu, Hui</creatorcontrib><creatorcontrib>Ren, Dongni</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Liu, Tao</creatorcontrib><creatorcontrib>Fan, Feiyan</creatorcontrib><creatorcontrib>Liu, Nan</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database (Proquest)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Journal of diabetes research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tu, Yanyang</au><au>Fu, Jianfang</au><au>Li, Qian</au><au>Wang, Zhen</au><au>Zhang, Pengxing</au><au>Liu, Hui</au><au>Ren, Dongni</au><au>Wang, Xin</au><au>Liu, Tao</au><au>Fan, Feiyan</au><au>Liu, Nan</au><au>Mastrocola, Raffaella</au><au>Raffaella Mastrocola</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ClC-3 Expression and Its Association with Hyperglycemia Induced HT22 Hippocampal Neuronal Cell Apoptosis</atitle><jtitle>Journal of diabetes research</jtitle><addtitle>J Diabetes Res</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>2016</volume><issue>2016</issue><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>2314-6745</issn><eissn>2314-6753</eissn><abstract>Although apoptosis plays an important role in the development of Diabetic Encephalopathy (DE), the underlying molecular mechanisms remain unclear. With respect to this, the present work aims to study the variation in chloride/proton exchanger ClC-3 expression and its association with HT22 hippocampal neuronal apoptosis under hyperglycemic condition in vitro. The cells were stimulated with added 0, 5, or 25 mM glucose or mannitol for up to 72 hours before assessing the rate of ClC-3 expression, cell viability, and apoptosis. In a consecutive experiment, cells received chloride channel blocker in addition to glucose. The rate of cellular death/apoptosis and viability was measured using Flow Cytometry and MTT assay, respectively. Changes in ClC-3 expression were assessed using immunofluorescence staining and western blot analysis. The results revealed a significant increase in cellular apoptosis and reduction in viability, associated with increased ClC-3 expression in high glucose group. Osmolarity had no role to play. Addition of chloride channel blocker completely abolished this effect. Thus we conclude that, with its increased expression, ClC-3 plays a major role in hyperglycemia induced hippocampal neuronal apoptosis. To strengthen our understanding of this aforesaid association, we conducted an extensive literature search which is presented in this paper.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>26925421</pmid><doi>10.1155/2016/2984380</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-4372-5920</orcidid><orcidid>https://orcid.org/0000-0002-1846-540X</orcidid><orcidid>https://orcid.org/0000-0002-2173-5976</orcidid><orcidid>https://orcid.org/0000-0002-9233-2170</orcidid><orcidid>https://orcid.org/0000-0001-7462-6274</orcidid><orcidid>https://orcid.org/0000-0003-3255-8108</orcidid><orcidid>https://orcid.org/0000-0002-4822-9555</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2314-6745 |
ispartof | Journal of diabetes research, 2016-01, Vol.2016 (2016), p.1-12 |
issn | 2314-6745 2314-6753 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_1d0a949fd1c04e91a04e620f1d51c962 |
source | Open Access: PubMed Central; Publicly Available Content Database; Wiley Open Access |
subjects | Animals Antibodies Apoptosis Blotting, Western Cell culture Cell cycle Cell Line Cell Survival Chloride Chloride Channels - analysis Chloride Channels - physiology Diabetes Flow Cytometry Glucose Hippocampus - pathology Hyperglycemia Hyperglycemia - pathology Mice Nitrobenzoates - pharmacology Oxidative Stress Proteins Studies |
title | ClC-3 Expression and Its Association with Hyperglycemia Induced HT22 Hippocampal Neuronal Cell Apoptosis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T23%3A32%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ClC-3%20Expression%20and%20Its%20Association%20with%20Hyperglycemia%20Induced%20HT22%20Hippocampal%20Neuronal%20Cell%20Apoptosis&rft.jtitle=Journal%20of%20diabetes%20research&rft.au=Tu,%20Yanyang&rft.date=2016-01-01&rft.volume=2016&rft.issue=2016&rft.spage=1&rft.epage=12&rft.pages=1-12&rft.issn=2314-6745&rft.eissn=2314-6753&rft_id=info:doi/10.1155/2016/2984380&rft_dat=%3Cproquest_doaj_%3E1769628247%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c635t-fb31bd2fcb668bdf80bfa18643b84818ffecbdcd8a14fcf03613c25874b425323%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2407638431&rft_id=info:pmid/26925421&rfr_iscdi=true |