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Synergistic Effects of Ad-Libitum Low-Dose Fructose Drinking and Low-Dose Streptozotocin Treatment in Wistar Rats: A Mild Model of Type 2 Diabetes
To develop a convenient animal model of T2D by pretreatment with low-dose 10% w/v fructose (FRC) solution followed by the injection of low doses of streptozotocin (STZ) in Wistar rats. For this 8-week experimental study; rats were first fed a standard chow ad-libitum diet and either tap water (n=40)...
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Published in: | Acta medica Iranica 2017-05, Vol.55 (5), p.304-310 |
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description | To develop a convenient animal model of T2D by pretreatment with low-dose 10% w/v fructose (FRC) solution followed by the injection of low doses of streptozotocin (STZ) in Wistar rats. For this 8-week experimental study; rats were first fed a standard chow ad-libitum diet and either tap water (n=40) or 10% w/v FRC solution (n=40) for 4 weeks. Next, rats in each category were randomly allocated to 4 subgroups (n=10 each) of low-dose STZ (25,35, and 45 mg/kg). The final mean fasting blood sugar (FBG) of FRC+STZ45 (197±55.87 mg/dl) were significantly higher than that of the STZ45 (P=0.015) and FRC (P=0.019) groups. FRC+STZ45 showed the highest insulin resistance demonstrated by insulin tolerance test [area under the curve (AUC) of insulin tolerance test; P |
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For this 8-week experimental study; rats were first fed a standard chow ad-libitum diet and either tap water (n=40) or 10% w/v FRC solution (n=40) for 4 weeks. Next, rats in each category were randomly allocated to 4 subgroups (n=10 each) of low-dose STZ (25,35, and 45 mg/kg). The final mean fasting blood sugar (FBG) of FRC+STZ45 (197±55.87 mg/dl) were significantly higher than that of the STZ45 (P=0.015) and FRC (P=0.019) groups. FRC+STZ45 showed the highest insulin resistance demonstrated by insulin tolerance test [area under the curve (AUC) of insulin tolerance test; P<0.05]. AUC was not significantly different between the STZ45 and non-STZ groups and between FRC and non-FRC fed groups. Furthermore, FBG levels did not differ between FRC and non-FRC groups. Body weight measurement showed that the FRC+STZ45 group had the lowest body weight compared to all other groups. Our data provide the evidence that FRC and STZ45 synergistically could induce hyperglycemia and insulin resistance in Wistar rats. Here we presented a feasible model for initial forms of T2D by employing pretreatment with low-dose FRC solution and treatment with low-dose STZ.</description><identifier>ISSN: 0044-6025</identifier><identifier>EISSN: 1735-9694</identifier><identifier>PMID: 28724270</identifier><language>eng</language><publisher>Iran: Tehran University of Medical Sciences</publisher><subject>Animals ; Blood Glucose ; Diabetes ; Diabetes Mellitus, Experimental - physiopathology ; Diabetes Mellitus, Type 2 - physiopathology ; Diet ; Disease Models, Animal ; Experimental animal model ; Fructose ; Fructose - administration & dosage ; Hyperglycemia ; Hyperglycemia - physiopathology ; Insulin Resistance ; Male ; Rats ; Rats, Wistar ; Rodents ; Streptozocin - administration & dosage ; Streptozotocin ; Type 2 diabetes</subject><ispartof>Acta medica Iranica, 2017-05, Vol.55 (5), p.304-310</ispartof><rights>Copyright Tehran University of Medical Sciences 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1924965657/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1924965657?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,36989,36990,44566,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28724270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sadeghi, Asie</creatorcontrib><creatorcontrib>Beigy, Maani</creatorcontrib><creatorcontrib>Alizadeh, Samira</creatorcontrib><creatorcontrib>Mazloom, Hossein</creatorcontrib><creatorcontrib>Vakili, Sanaz</creatorcontrib><creatorcontrib>Ahmadi, Saideh</creatorcontrib><creatorcontrib>Meshkani, Reza</creatorcontrib><title>Synergistic Effects of Ad-Libitum Low-Dose Fructose Drinking and Low-Dose Streptozotocin Treatment in Wistar Rats: A Mild Model of Type 2 Diabetes</title><title>Acta medica Iranica</title><addtitle>Acta Med Iran</addtitle><description>To develop a convenient animal model of T2D by pretreatment with low-dose 10% w/v fructose (FRC) solution followed by the injection of low doses of streptozotocin (STZ) in Wistar rats. For this 8-week experimental study; rats were first fed a standard chow ad-libitum diet and either tap water (n=40) or 10% w/v FRC solution (n=40) for 4 weeks. Next, rats in each category were randomly allocated to 4 subgroups (n=10 each) of low-dose STZ (25,35, and 45 mg/kg). The final mean fasting blood sugar (FBG) of FRC+STZ45 (197±55.87 mg/dl) were significantly higher than that of the STZ45 (P=0.015) and FRC (P=0.019) groups. FRC+STZ45 showed the highest insulin resistance demonstrated by insulin tolerance test [area under the curve (AUC) of insulin tolerance test; P<0.05]. AUC was not significantly different between the STZ45 and non-STZ groups and between FRC and non-FRC fed groups. Furthermore, FBG levels did not differ between FRC and non-FRC groups. Body weight measurement showed that the FRC+STZ45 group had the lowest body weight compared to all other groups. Our data provide the evidence that FRC and STZ45 synergistically could induce hyperglycemia and insulin resistance in Wistar rats. Here we presented a feasible model for initial forms of T2D by employing pretreatment with low-dose FRC solution and treatment with low-dose STZ.</description><subject>Animals</subject><subject>Blood Glucose</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Experimental - physiopathology</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diet</subject><subject>Disease Models, Animal</subject><subject>Experimental animal model</subject><subject>Fructose</subject><subject>Fructose - administration & dosage</subject><subject>Hyperglycemia</subject><subject>Hyperglycemia - physiopathology</subject><subject>Insulin Resistance</subject><subject>Male</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rodents</subject><subject>Streptozocin - administration & dosage</subject><subject>Streptozotocin</subject><subject>Type 2 diabetes</subject><issn>0044-6025</issn><issn>1735-9694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkctO3DAUhiNUBFPgFZAlNt1EcnxJnO5GDFCkQUgwiGV0bJ-MPE3iqe2omj4GT9xMuVRidW6f_nM7yGZFxWVel7X4ks0oFSIvKZPH2dcYN5RyxYrqKDtmqmKCVXSWvTzuBgxrF5Mz5Kpt0aRIfEvmNl867dLYk6X_nS98RHIdRpP2ziK44acb1gQG-7_8mAJuk__jkzduIKuAkHocEpmC56kBBPIAKX4nc3LnOkvuvMVu32u12yJhZOFAY8J4mh220EU8e7Mn2dP11eryR768v7m9nC9zyxhNOVfGCmWQai3AoOQUwWpgttWF0gCamZqVhZAVU5oKbRVtpTLCGiE4NZKfZLevutbDptkG10PYNR5c8y_hw7qBMJ2lw6a2lWUSLbaaCV4qVVsJpVGshsIIKSatb69a2-B_jRhT07tosOtgQD_GpqhZUXAqJZ3Qi0_oxo9hmDbdU6IuZSmriTp_o0bdo_0Y7_1z_C8ZzpWk</recordid><startdate>201705</startdate><enddate>201705</enddate><creator>Sadeghi, Asie</creator><creator>Beigy, Maani</creator><creator>Alizadeh, Samira</creator><creator>Mazloom, Hossein</creator><creator>Vakili, Sanaz</creator><creator>Ahmadi, Saideh</creator><creator>Meshkani, Reza</creator><general>Tehran University of Medical Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>CWDGH</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>201705</creationdate><title>Synergistic Effects of Ad-Libitum Low-Dose Fructose Drinking and Low-Dose Streptozotocin Treatment in Wistar Rats: A Mild Model of Type 2 Diabetes</title><author>Sadeghi, Asie ; Beigy, Maani ; Alizadeh, Samira ; Mazloom, Hossein ; Vakili, Sanaz ; Ahmadi, Saideh ; Meshkani, Reza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d220t-38cd48ce0bb4ace530eadba2dfb18baab2c926145728b04bd80f58c4dc4430c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Blood Glucose</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Experimental - physiopathology</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diet</topic><topic>Disease Models, Animal</topic><topic>Experimental animal model</topic><topic>Fructose</topic><topic>Fructose - administration & dosage</topic><topic>Hyperglycemia</topic><topic>Hyperglycemia - physiopathology</topic><topic>Insulin Resistance</topic><topic>Male</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Rodents</topic><topic>Streptozocin - administration & dosage</topic><topic>Streptozotocin</topic><topic>Type 2 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sadeghi, Asie</creatorcontrib><creatorcontrib>Beigy, Maani</creatorcontrib><creatorcontrib>Alizadeh, Samira</creatorcontrib><creatorcontrib>Mazloom, Hossein</creatorcontrib><creatorcontrib>Vakili, Sanaz</creatorcontrib><creatorcontrib>Ahmadi, Saideh</creatorcontrib><creatorcontrib>Meshkani, Reza</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</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>DOAJ Directory of Open Access Journals</collection><jtitle>Acta medica Iranica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sadeghi, Asie</au><au>Beigy, Maani</au><au>Alizadeh, Samira</au><au>Mazloom, Hossein</au><au>Vakili, Sanaz</au><au>Ahmadi, Saideh</au><au>Meshkani, Reza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic Effects of Ad-Libitum Low-Dose Fructose Drinking and Low-Dose Streptozotocin Treatment in Wistar Rats: A Mild Model of Type 2 Diabetes</atitle><jtitle>Acta medica Iranica</jtitle><addtitle>Acta Med Iran</addtitle><date>2017-05</date><risdate>2017</risdate><volume>55</volume><issue>5</issue><spage>304</spage><epage>310</epage><pages>304-310</pages><issn>0044-6025</issn><eissn>1735-9694</eissn><abstract>To develop a convenient animal model of T2D by pretreatment with low-dose 10% w/v fructose (FRC) solution followed by the injection of low doses of streptozotocin (STZ) in Wistar rats. For this 8-week experimental study; rats were first fed a standard chow ad-libitum diet and either tap water (n=40) or 10% w/v FRC solution (n=40) for 4 weeks. Next, rats in each category were randomly allocated to 4 subgroups (n=10 each) of low-dose STZ (25,35, and 45 mg/kg). The final mean fasting blood sugar (FBG) of FRC+STZ45 (197±55.87 mg/dl) were significantly higher than that of the STZ45 (P=0.015) and FRC (P=0.019) groups. FRC+STZ45 showed the highest insulin resistance demonstrated by insulin tolerance test [area under the curve (AUC) of insulin tolerance test; P<0.05]. AUC was not significantly different between the STZ45 and non-STZ groups and between FRC and non-FRC fed groups. Furthermore, FBG levels did not differ between FRC and non-FRC groups. Body weight measurement showed that the FRC+STZ45 group had the lowest body weight compared to all other groups. Our data provide the evidence that FRC and STZ45 synergistically could induce hyperglycemia and insulin resistance in Wistar rats. Here we presented a feasible model for initial forms of T2D by employing pretreatment with low-dose FRC solution and treatment with low-dose STZ.</abstract><cop>Iran</cop><pub>Tehran University of Medical Sciences</pub><pmid>28724270</pmid><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood Glucose Diabetes Diabetes Mellitus, Experimental - physiopathology Diabetes Mellitus, Type 2 - physiopathology Diet Disease Models, Animal Experimental animal model Fructose Fructose - administration & dosage Hyperglycemia Hyperglycemia - physiopathology Insulin Resistance Male Rats Rats, Wistar Rodents Streptozocin - administration & dosage Streptozotocin Type 2 diabetes |
title | Synergistic Effects of Ad-Libitum Low-Dose Fructose Drinking and Low-Dose Streptozotocin Treatment in Wistar Rats: A Mild Model of Type 2 Diabetes |
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