Relationship between blood glucose levels and hepatic Fto mRNA expression in mice
► Intraperitoneal glucose injection reverses fasting-induced increase in hepatic Fto mRNA expression in mice. ► Hepatic Fto mRNA levels are inversely correlated with blood glucose levels independent of body weight in mice. ► Hepatic Fto mRNA levels are positively correlated with expression of glucon...
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creator | Poritsanos, Nicole J. Lew, Pei San Mizuno, Tooru M. |
description | ► Intraperitoneal glucose injection reverses fasting-induced increase in hepatic
Fto mRNA expression in mice. ► Hepatic
Fto mRNA levels are inversely correlated with blood glucose levels independent of body weight in mice. ► Hepatic
Fto mRNA levels are positively correlated with expression of gluconeogenic genes,
Pepck and
G6pase.
Common variants in the fat mass and obesity associated (
FTO) gene are associated with obesity and type 2 diabetes. Fto-deficient mice develop hepatic insulin resistance, leading to the hypothesis that hepatic Fto plays a role in the regulation of glucose metabolism and that hepatic Fto expression is regulated by metabolic states. We found that hepatic
Fto mRNA levels were increased by fasting in mice. Intraperitoneal glucose injection reduced hepatic
Fto mRNA levels without significant changes in body weight in fasted mice. The inverse correlation between
Fto mRNA and glucose remained significant after adjusting for body weight. There were positive correlations between hepatic
Fto mRNA expression and gluconeogenic gene expression. These data support the hypothesis that hepatic
Fto expression changes in response to metabolic states and glucose reduces hepatic
Fto mRNA expression independently of body weight. Hepatic Fto may participate in the feedback regulation of glucose metabolism via gluconeogenesis. |
doi_str_mv | 10.1016/j.bbrc.2010.08.133 |
format | Article |
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Fto mRNA expression in mice. ► Hepatic
Fto mRNA levels are inversely correlated with blood glucose levels independent of body weight in mice. ► Hepatic
Fto mRNA levels are positively correlated with expression of gluconeogenic genes,
Pepck and
G6pase.
Common variants in the fat mass and obesity associated (
FTO) gene are associated with obesity and type 2 diabetes. Fto-deficient mice develop hepatic insulin resistance, leading to the hypothesis that hepatic Fto plays a role in the regulation of glucose metabolism and that hepatic Fto expression is regulated by metabolic states. We found that hepatic
Fto mRNA levels were increased by fasting in mice. Intraperitoneal glucose injection reduced hepatic
Fto mRNA levels without significant changes in body weight in fasted mice. The inverse correlation between
Fto mRNA and glucose remained significant after adjusting for body weight. There were positive correlations between hepatic
Fto mRNA expression and gluconeogenic gene expression. These data support the hypothesis that hepatic
Fto expression changes in response to metabolic states and glucose reduces hepatic
Fto mRNA expression independently of body weight. Hepatic Fto may participate in the feedback regulation of glucose metabolism via gluconeogenesis.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2010.08.133</identifier><identifier>PMID: 20816934</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alpha-Ketoglutarate-Dependent Dioxygenase FTO ; Animals ; Blood ; Blood Glucose - genetics ; Body Weight - genetics ; Gene expression ; Gene Expression Regulation ; Gluconeogenesis ; Gluconeogenesis - genetics ; Glucose ; Liver - metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Nutrient ; Obesity ; Proteins - metabolism ; RNA, Messenger - metabolism</subject><ispartof>Biochemical and biophysical research communications, 2010-10, Vol.400 (4), p.713-717</ispartof><rights>2010 Elsevier Inc.</rights><rights>Copyright © 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-1d2ea5beba57e12174df823685501134a5f73b919fbfbdf0c4ad5e2235c940f33</citedby><cites>FETCH-LOGICAL-c387t-1d2ea5beba57e12174df823685501134a5f73b919fbfbdf0c4ad5e2235c940f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbrc.2010.08.133$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20816934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poritsanos, Nicole J.</creatorcontrib><creatorcontrib>Lew, Pei San</creatorcontrib><creatorcontrib>Mizuno, Tooru M.</creatorcontrib><title>Relationship between blood glucose levels and hepatic Fto mRNA expression in mice</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>► Intraperitoneal glucose injection reverses fasting-induced increase in hepatic
Fto mRNA expression in mice. ► Hepatic
Fto mRNA levels are inversely correlated with blood glucose levels independent of body weight in mice. ► Hepatic
Fto mRNA levels are positively correlated with expression of gluconeogenic genes,
Pepck and
G6pase.
Common variants in the fat mass and obesity associated (
FTO) gene are associated with obesity and type 2 diabetes. Fto-deficient mice develop hepatic insulin resistance, leading to the hypothesis that hepatic Fto plays a role in the regulation of glucose metabolism and that hepatic Fto expression is regulated by metabolic states. We found that hepatic
Fto mRNA levels were increased by fasting in mice. Intraperitoneal glucose injection reduced hepatic
Fto mRNA levels without significant changes in body weight in fasted mice. The inverse correlation between
Fto mRNA and glucose remained significant after adjusting for body weight. There were positive correlations between hepatic
Fto mRNA expression and gluconeogenic gene expression. These data support the hypothesis that hepatic
Fto expression changes in response to metabolic states and glucose reduces hepatic
Fto mRNA expression independently of body weight. Hepatic Fto may participate in the feedback regulation of glucose metabolism via gluconeogenesis.</description><subject>Alpha-Ketoglutarate-Dependent Dioxygenase FTO</subject><subject>Animals</subject><subject>Blood</subject><subject>Blood Glucose - genetics</subject><subject>Body Weight - genetics</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Gluconeogenesis</subject><subject>Gluconeogenesis - genetics</subject><subject>Glucose</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Nutrient</subject><subject>Obesity</subject><subject>Proteins - metabolism</subject><subject>RNA, Messenger - metabolism</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1r3DAQQEVoaLZp_0AORbeevBlJlm1BLiE0bSEkJLTQm9DHuNFiW67kTZN_Xy2b5ticBoY3j-ERcsJgzYA1p5u1tcmtOZQFdGsmxAFZMVBQcQb1G7ICgKbiiv08Iu9y3gAwVjfqLTni0LFGiXpFbu9wMEuIU74PM7W4_EGcqB1i9PTXsHUxIx3wAYdMzeTpPc6FdvRyiXS8uz6n-DgnzLkIaJjoGBy-J4e9GTJ-eJ7H5Mfl5-8XX6urmy_fLs6vKie6dqmY52ikRWtki4yztvZ9x0XTSVneFLWRfSusYqq3vfU9uNp4iZwL6VQNvRDH5NPeO6f4e4t50WPIDofBTBi3WXdNraTkAl4lW9k0UrXACsn3pEsx54S9nlMYTXrSDPSuud7oXXO9a66h06V5Ofr4rN_aEf3Lyb_IBTjbA6UiPgRMOruAk0MfErpF-xj-5_8Lp6OSIg</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Poritsanos, Nicole J.</creator><creator>Lew, Pei San</creator><creator>Mizuno, Tooru M.</creator><general>Elsevier Inc</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>7X8</scope><scope>7TM</scope></search><sort><creationdate>20101001</creationdate><title>Relationship between blood glucose levels and hepatic Fto mRNA expression in mice</title><author>Poritsanos, Nicole J. ; Lew, Pei San ; Mizuno, Tooru M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-1d2ea5beba57e12174df823685501134a5f73b919fbfbdf0c4ad5e2235c940f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Alpha-Ketoglutarate-Dependent Dioxygenase FTO</topic><topic>Animals</topic><topic>Blood</topic><topic>Blood Glucose - genetics</topic><topic>Body Weight - genetics</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Gluconeogenesis</topic><topic>Gluconeogenesis - genetics</topic><topic>Glucose</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nutrient</topic><topic>Obesity</topic><topic>Proteins - metabolism</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poritsanos, Nicole J.</creatorcontrib><creatorcontrib>Lew, Pei San</creatorcontrib><creatorcontrib>Mizuno, Tooru M.</creatorcontrib><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>Nucleic Acids Abstracts</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poritsanos, Nicole J.</au><au>Lew, Pei San</au><au>Mizuno, Tooru M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship between blood glucose levels and hepatic Fto mRNA expression in mice</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>400</volume><issue>4</issue><spage>713</spage><epage>717</epage><pages>713-717</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>► Intraperitoneal glucose injection reverses fasting-induced increase in hepatic
Fto mRNA expression in mice. ► Hepatic
Fto mRNA levels are inversely correlated with blood glucose levels independent of body weight in mice. ► Hepatic
Fto mRNA levels are positively correlated with expression of gluconeogenic genes,
Pepck and
G6pase.
Common variants in the fat mass and obesity associated (
FTO) gene are associated with obesity and type 2 diabetes. Fto-deficient mice develop hepatic insulin resistance, leading to the hypothesis that hepatic Fto plays a role in the regulation of glucose metabolism and that hepatic Fto expression is regulated by metabolic states. We found that hepatic
Fto mRNA levels were increased by fasting in mice. Intraperitoneal glucose injection reduced hepatic
Fto mRNA levels without significant changes in body weight in fasted mice. The inverse correlation between
Fto mRNA and glucose remained significant after adjusting for body weight. There were positive correlations between hepatic
Fto mRNA expression and gluconeogenic gene expression. These data support the hypothesis that hepatic
Fto expression changes in response to metabolic states and glucose reduces hepatic
Fto mRNA expression independently of body weight. Hepatic Fto may participate in the feedback regulation of glucose metabolism via gluconeogenesis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>20816934</pmid><doi>10.1016/j.bbrc.2010.08.133</doi><tpages>5</tpages></addata></record> |
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subjects | Alpha-Ketoglutarate-Dependent Dioxygenase FTO Animals Blood Blood Glucose - genetics Body Weight - genetics Gene expression Gene Expression Regulation Gluconeogenesis Gluconeogenesis - genetics Glucose Liver - metabolism Male Mice Mice, Inbred C57BL Nutrient Obesity Proteins - metabolism RNA, Messenger - metabolism |
title | Relationship between blood glucose levels and hepatic Fto mRNA expression in mice |
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