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HMG-CoA Reductase Inhibitors Do Not Improve Glucose Intolerance in Spontaneously Diabetic Goto–Kakizaki Rats
We examined whether 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) improve glucose intolerance in spontaneously diabetic Goto–Kakizaki (GK) rats or not. The fasting blood glucose, plasma insulin, and serum cholesterol levels were significantly higher in GK rats than t...
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Published in: | Biological & pharmaceutical bulletin 2005, Vol.28(11), pp.2092-2095 |
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creator | Satoh, Kumi Keimatsu, Natsue Kanda, Makoto Kasai, Toshinori Takaguri, Akira Sun, Fan Ichihara, Kazuo |
description | We examined whether 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) improve glucose intolerance in spontaneously diabetic Goto–Kakizaki (GK) rats or not. The fasting blood glucose, plasma insulin, and serum cholesterol levels were significantly higher in GK rats than those in age-matched Wistar rats. All rats were given orally once a day 0.5% carboxymethylcellulose, pravastatin 8 mg/kg, simvastatin 8 mg/kg, or atorvastatin 8 mg/kg. An oral glucose tolerance test (OGTT) was performed before and 3, 6 and 12 weeks after statin treatments. The hyperglycemic response to OGTT in GK rats significantly exceeded that in Wistar rats. The plasma insulin level in GK rats increased with age until 14-week-old (treated for 6 weeks), and then decreased. Glucose intake significantly increased the plasma insulin in almost all rats. The increment of plasma insulin due to OGTT in GK rats appeared to be less than that in Wistar rats, because the basal level was already high in GK rats. Pravastatin, simvastatin, and atorvastatin did not modify changes in blood glucose and plasma insulin induced by glucose intake. In conclusion, long-term treatments of GK rats with statins did not improve glucose intolerance observed during OGTT. |
doi_str_mv | 10.1248/bpb.28.2092 |
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The fasting blood glucose, plasma insulin, and serum cholesterol levels were significantly higher in GK rats than those in age-matched Wistar rats. All rats were given orally once a day 0.5% carboxymethylcellulose, pravastatin 8 mg/kg, simvastatin 8 mg/kg, or atorvastatin 8 mg/kg. An oral glucose tolerance test (OGTT) was performed before and 3, 6 and 12 weeks after statin treatments. The hyperglycemic response to OGTT in GK rats significantly exceeded that in Wistar rats. The plasma insulin level in GK rats increased with age until 14-week-old (treated for 6 weeks), and then decreased. Glucose intake significantly increased the plasma insulin in almost all rats. The increment of plasma insulin due to OGTT in GK rats appeared to be less than that in Wistar rats, because the basal level was already high in GK rats. Pravastatin, simvastatin, and atorvastatin did not modify changes in blood glucose and plasma insulin induced by glucose intake. In conclusion, long-term treatments of GK rats with statins did not improve glucose intolerance observed during OGTT.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.28.2092</identifier><identifier>PMID: 16272695</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Animals ; Atorvastatin ; Blood Glucose - metabolism ; Body Weight - drug effects ; Cholesterol - blood ; diabetes ; Diabetes Mellitus - genetics ; Glucose Intolerance - drug therapy ; Glucose Tolerance Test ; Goto–Kakizaki (GK) rat ; Heptanoic Acids - therapeutic use ; HMG-CoA reductase inhibitor ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology ; insulin ; Insulin - blood ; Insulin Resistance - physiology ; Male ; oral glucose tolerance test (OGTT) ; Pravastatin - therapeutic use ; Pyrroles - therapeutic use ; Rats ; Rats, Wistar ; Simvastatin - therapeutic use</subject><ispartof>Biological and Pharmaceutical Bulletin, 2005, Vol.28(11), pp.2092-2095</ispartof><rights>2005 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-4dc69b3f5dad391583f445127bd84e6465004d7e4b58385e0ea3cc92d2d3d233</citedby><cites>FETCH-LOGICAL-c501t-4dc69b3f5dad391583f445127bd84e6465004d7e4b58385e0ea3cc92d2d3d233</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/16272695$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Satoh, Kumi</creatorcontrib><creatorcontrib>Keimatsu, Natsue</creatorcontrib><creatorcontrib>Kanda, Makoto</creatorcontrib><creatorcontrib>Kasai, Toshinori</creatorcontrib><creatorcontrib>Takaguri, Akira</creatorcontrib><creatorcontrib>Sun, Fan</creatorcontrib><creatorcontrib>Ichihara, Kazuo</creatorcontrib><title>HMG-CoA Reductase Inhibitors Do Not Improve Glucose Intolerance in Spontaneously Diabetic Goto–Kakizaki Rats</title><title>Biological & pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>We examined whether 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) improve glucose intolerance in spontaneously diabetic Goto–Kakizaki (GK) rats or not. The fasting blood glucose, plasma insulin, and serum cholesterol levels were significantly higher in GK rats than those in age-matched Wistar rats. All rats were given orally once a day 0.5% carboxymethylcellulose, pravastatin 8 mg/kg, simvastatin 8 mg/kg, or atorvastatin 8 mg/kg. An oral glucose tolerance test (OGTT) was performed before and 3, 6 and 12 weeks after statin treatments. The hyperglycemic response to OGTT in GK rats significantly exceeded that in Wistar rats. The plasma insulin level in GK rats increased with age until 14-week-old (treated for 6 weeks), and then decreased. Glucose intake significantly increased the plasma insulin in almost all rats. The increment of plasma insulin due to OGTT in GK rats appeared to be less than that in Wistar rats, because the basal level was already high in GK rats. Pravastatin, simvastatin, and atorvastatin did not modify changes in blood glucose and plasma insulin induced by glucose intake. In conclusion, long-term treatments of GK rats with statins did not improve glucose intolerance observed during OGTT.</description><subject>Animals</subject><subject>Atorvastatin</subject><subject>Blood Glucose - metabolism</subject><subject>Body Weight - drug effects</subject><subject>Cholesterol - blood</subject><subject>diabetes</subject><subject>Diabetes Mellitus - genetics</subject><subject>Glucose Intolerance - drug therapy</subject><subject>Glucose Tolerance Test</subject><subject>Goto–Kakizaki (GK) rat</subject><subject>Heptanoic Acids - therapeutic use</subject><subject>HMG-CoA reductase inhibitor</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology</subject><subject>insulin</subject><subject>Insulin - blood</subject><subject>Insulin Resistance - physiology</subject><subject>Male</subject><subject>oral glucose tolerance test (OGTT)</subject><subject>Pravastatin - therapeutic use</subject><subject>Pyrroles - therapeutic use</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Simvastatin - therapeutic use</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpdkctOIzEQRS0EgsCwYo8sIbFBnfGzH0sITIgGGAnYW267Ah067WC7kWDFP8wfzpeMIQEkFlW1qKOrW3UR2qNkSJkof9aLesjKISMVW0MDykWRSUblOhqQipZZTmW5hbZDmBFCCsL4JtqiOStYXskB6s4vx9nIHeNrsL2JOgCedPdN3UTnAz51-MpFPJkvvHsCPG57496J6FrwujOAmw7fLFwXdQeuD-0zPm10DbExeOyi-_f697d-aF5S4Wsdww-0MdVtgN3V3EG3v85uR-fZxZ_xZHR8kRlJaMyENXlV86m02vIqHcCnQkjKitqWAnKRS0KELUDUaVVKIKC5MRWzzHLLON9Bh0vZ5PuxhxDVvAkG2nbpUuVlka4XeQIPvoEz1_suWVNUiIoLKjhL1NGSMt6F4GGqFr6Za_-sKFFvGaiUgWKlessg0fsrzb6eg_1iV09PwMkSmIWo7-AT0D69rYUPMUo_elL9XJp77RV0_D8aZ5nO</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Satoh, Kumi</creator><creator>Keimatsu, Natsue</creator><creator>Kanda, Makoto</creator><creator>Kasai, Toshinori</creator><creator>Takaguri, Akira</creator><creator>Sun, Fan</creator><creator>Ichihara, Kazuo</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20051101</creationdate><title>HMG-CoA Reductase Inhibitors Do Not Improve Glucose Intolerance in Spontaneously Diabetic Goto–Kakizaki Rats</title><author>Satoh, Kumi ; Keimatsu, Natsue ; Kanda, Makoto ; Kasai, Toshinori ; Takaguri, Akira ; Sun, Fan ; Ichihara, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-4dc69b3f5dad391583f445127bd84e6465004d7e4b58385e0ea3cc92d2d3d233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Atorvastatin</topic><topic>Blood Glucose - metabolism</topic><topic>Body Weight - drug effects</topic><topic>Cholesterol - blood</topic><topic>diabetes</topic><topic>Diabetes Mellitus - genetics</topic><topic>Glucose Intolerance - drug therapy</topic><topic>Glucose Tolerance Test</topic><topic>Goto–Kakizaki (GK) rat</topic><topic>Heptanoic Acids - therapeutic use</topic><topic>HMG-CoA reductase inhibitor</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology</topic><topic>insulin</topic><topic>Insulin - blood</topic><topic>Insulin Resistance - physiology</topic><topic>Male</topic><topic>oral glucose tolerance test (OGTT)</topic><topic>Pravastatin - therapeutic use</topic><topic>Pyrroles - therapeutic use</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Simvastatin - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Satoh, Kumi</creatorcontrib><creatorcontrib>Keimatsu, Natsue</creatorcontrib><creatorcontrib>Kanda, Makoto</creatorcontrib><creatorcontrib>Kasai, Toshinori</creatorcontrib><creatorcontrib>Takaguri, Akira</creatorcontrib><creatorcontrib>Sun, Fan</creatorcontrib><creatorcontrib>Ichihara, Kazuo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Satoh, Kumi</au><au>Keimatsu, Natsue</au><au>Kanda, Makoto</au><au>Kasai, Toshinori</au><au>Takaguri, Akira</au><au>Sun, Fan</au><au>Ichihara, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HMG-CoA Reductase Inhibitors Do Not Improve Glucose Intolerance in Spontaneously Diabetic Goto–Kakizaki Rats</atitle><jtitle>Biological & pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>28</volume><issue>11</issue><spage>2092</spage><epage>2095</epage><pages>2092-2095</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>We examined whether 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) improve glucose intolerance in spontaneously diabetic Goto–Kakizaki (GK) rats or not. The fasting blood glucose, plasma insulin, and serum cholesterol levels were significantly higher in GK rats than those in age-matched Wistar rats. All rats were given orally once a day 0.5% carboxymethylcellulose, pravastatin 8 mg/kg, simvastatin 8 mg/kg, or atorvastatin 8 mg/kg. An oral glucose tolerance test (OGTT) was performed before and 3, 6 and 12 weeks after statin treatments. The hyperglycemic response to OGTT in GK rats significantly exceeded that in Wistar rats. The plasma insulin level in GK rats increased with age until 14-week-old (treated for 6 weeks), and then decreased. Glucose intake significantly increased the plasma insulin in almost all rats. The increment of plasma insulin due to OGTT in GK rats appeared to be less than that in Wistar rats, because the basal level was already high in GK rats. Pravastatin, simvastatin, and atorvastatin did not modify changes in blood glucose and plasma insulin induced by glucose intake. In conclusion, long-term treatments of GK rats with statins did not improve glucose intolerance observed during OGTT.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>16272695</pmid><doi>10.1248/bpb.28.2092</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Atorvastatin Blood Glucose - metabolism Body Weight - drug effects Cholesterol - blood diabetes Diabetes Mellitus - genetics Glucose Intolerance - drug therapy Glucose Tolerance Test Goto–Kakizaki (GK) rat Heptanoic Acids - therapeutic use HMG-CoA reductase inhibitor Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology insulin Insulin - blood Insulin Resistance - physiology Male oral glucose tolerance test (OGTT) Pravastatin - therapeutic use Pyrroles - therapeutic use Rats Rats, Wistar Simvastatin - therapeutic use |
title | HMG-CoA Reductase Inhibitors Do Not Improve Glucose Intolerance in Spontaneously Diabetic Goto–Kakizaki Rats |
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