Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA
The influence of life span-prolonging dietary energy restriction on hepatic expression of glucose-regulated protein 78 and 94 (GRP78 and GRP94) RNA was investigated in female C3B10RF1 mice. Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivale...
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Veröffentlicht in: | The Journal of nutrition 1990-11, Vol.120 (11), p.1412-1417 |
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description | The influence of life span-prolonging dietary energy restriction on hepatic expression of glucose-regulated protein 78 and 94 (GRP78 and GRP94) RNA was investigated in female C3B10RF1 mice. Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. GRP mRNA levels are elevated by agents that increase the level of malfolded proteins in the endoplasmic reticulum. Thus, energy restriction may act to reduce malfolded proteins in the endoplasmic reticulum of hepatic cells. |
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Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. GRP mRNA levels are elevated by agents that increase the level of malfolded proteins in the endoplasmic reticulum. Thus, energy restriction may act to reduce malfolded proteins in the endoplasmic reticulum of hepatic cells.</description><identifier>ISSN: 0022-3166</identifier><identifier>EISSN: 1541-6100</identifier><identifier>DOI: 10.1093/jn/120.11.1412</identifier><identifier>PMID: 2231029</identifier><identifier>CODEN: JONUAI</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Aging - metabolism ; Animals ; ARN MENSAJERO ; ARN MESSAGER ; Biological and medical sciences ; Carrier Proteins - genetics ; Diet ; DIETA ; ENERGIA ; ENERGIE ; Energy Intake ; energy restriction ; Female ; FOIE ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation ; GLUCOSA ; GLUCOSE ; Glucose - administration & dosage ; Glucose - metabolism ; glucose-regulated protein ; GRP mRNA ; Heat-Shock Proteins ; HIGADO ; HSP70 Heat-Shock Proteins ; liver ; Liver - metabolism ; Liver. Bile. Biliary tracts ; Membrane Proteins - genetics ; Mice ; Molecular Chaperones ; mouse ; PROTEINAS ; PROTEINE ; RATON ; REGIME ALIMENTAIRE ; RNA, Messenger - analysis ; SOURIS ; Vertebrates: digestive system</subject><ispartof>The Journal of nutrition, 1990-11, Vol.120 (11), p.1412-1417</ispartof><rights>1990 American Society for Nutrition.</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3422-20950bba23c1b3d778b4c88c8935ad952cb4737493bc8ab81cb5d6f305b5847c3</citedby><cites>FETCH-LOGICAL-c3422-20950bba23c1b3d778b4c88c8935ad952cb4737493bc8ab81cb5d6f305b5847c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5043204$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2231029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spindler, Stephen R.</creatorcontrib><creatorcontrib>Crew, Mark D.</creatorcontrib><creatorcontrib>Mote, Patricia L.</creatorcontrib><creatorcontrib>Grizzle, Judith M.</creatorcontrib><creatorcontrib>Walford, Roy L.</creatorcontrib><title>Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA</title><title>The Journal of nutrition</title><addtitle>J Nutr</addtitle><description>The influence of life span-prolonging dietary energy restriction on hepatic expression of glucose-regulated protein 78 and 94 (GRP78 and GRP94) RNA was investigated in female C3B10RF1 mice. Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. GRP mRNA levels are elevated by agents that increase the level of malfolded proteins in the endoplasmic reticulum. Thus, energy restriction may act to reduce malfolded proteins in the endoplasmic reticulum of hepatic cells.</description><subject>Aging - metabolism</subject><subject>Animals</subject><subject>ARN MENSAJERO</subject><subject>ARN MESSAGER</subject><subject>Biological and medical sciences</subject><subject>Carrier Proteins - genetics</subject><subject>Diet</subject><subject>DIETA</subject><subject>ENERGIA</subject><subject>ENERGIE</subject><subject>Energy Intake</subject><subject>energy restriction</subject><subject>Female</subject><subject>FOIE</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation</subject><subject>GLUCOSA</subject><subject>GLUCOSE</subject><subject>Glucose - administration & dosage</subject><subject>Glucose - metabolism</subject><subject>glucose-regulated protein</subject><subject>GRP mRNA</subject><subject>Heat-Shock Proteins</subject><subject>HIGADO</subject><subject>HSP70 Heat-Shock Proteins</subject><subject>liver</subject><subject>Liver - metabolism</subject><subject>Liver. Bile. Biliary tracts</subject><subject>Membrane Proteins - genetics</subject><subject>Mice</subject><subject>Molecular Chaperones</subject><subject>mouse</subject><subject>PROTEINAS</subject><subject>PROTEINE</subject><subject>RATON</subject><subject>REGIME ALIMENTAIRE</subject><subject>RNA, Messenger - analysis</subject><subject>SOURIS</subject><subject>Vertebrates: digestive system</subject><issn>0022-3166</issn><issn>1541-6100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1vEzEQhi0EKmngygEJyQdUwWFTf23WPpYSWqQCVaBny56djRxt1sHeRfTf4yhRbxwsW36fGY8fQt5wtuDMyMvtcMlFOfMFV1w8IzNeK14tOWPPyYwxISrJl8uX5DznLWOMK6PPyJkQkjNhZiR-Dji69EhXA6bNI11jHlOAMcSBhoF-C4Dlrp0AM73FvRsD0NXffcKcD0js6E0_QcxYrXEz9W7Elt6nOGIpbjT98Cncf6RuaKlRdLf-fvWKvOhcn_H1aZ-Thy-rX9e31d2Pm6_XV3cVSFVmFszUzHsnJHAv26bRXoHWoI2sXWtqAV41slFGetDOaw6-bpedZLWvtWpAzsnFse8-xd9T-ZTdhQzY927AOGWrGTNa16yAiyMIKeacsLP7FHbFiOXMHgzb7WCLYcu5PRguBe9OnSe_w_YJPykt-ftT7jK4vktugJCfsJopKcqak7dHrHPRuk0qyMNPw8uLTJZQH0Msiv4ETDZDwAGwDQlhtG0M_xvvH5y2m_A</recordid><startdate>199011</startdate><enddate>199011</enddate><creator>Spindler, Stephen R.</creator><creator>Crew, Mark D.</creator><creator>Mote, Patricia L.</creator><creator>Grizzle, Judith M.</creator><creator>Walford, Roy L.</creator><general>Elsevier Inc</general><general>American Society for Nutritional Sciences</general><scope>FBQ</scope><scope>IQODW</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>7X8</scope></search><sort><creationdate>199011</creationdate><title>Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA</title><author>Spindler, Stephen R. ; Crew, Mark D. ; Mote, Patricia L. ; Grizzle, Judith M. ; Walford, Roy L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3422-20950bba23c1b3d778b4c88c8935ad952cb4737493bc8ab81cb5d6f305b5847c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Aging - metabolism</topic><topic>Animals</topic><topic>ARN MENSAJERO</topic><topic>ARN MESSAGER</topic><topic>Biological and medical sciences</topic><topic>Carrier Proteins - genetics</topic><topic>Diet</topic><topic>DIETA</topic><topic>ENERGIA</topic><topic>ENERGIE</topic><topic>Energy Intake</topic><topic>energy restriction</topic><topic>Female</topic><topic>FOIE</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation</topic><topic>GLUCOSA</topic><topic>GLUCOSE</topic><topic>Glucose - administration & dosage</topic><topic>Glucose - metabolism</topic><topic>glucose-regulated protein</topic><topic>GRP mRNA</topic><topic>Heat-Shock Proteins</topic><topic>HIGADO</topic><topic>HSP70 Heat-Shock Proteins</topic><topic>liver</topic><topic>Liver - metabolism</topic><topic>Liver. Bile. Biliary tracts</topic><topic>Membrane Proteins - genetics</topic><topic>Mice</topic><topic>Molecular Chaperones</topic><topic>mouse</topic><topic>PROTEINAS</topic><topic>PROTEINE</topic><topic>RATON</topic><topic>REGIME ALIMENTAIRE</topic><topic>RNA, Messenger - analysis</topic><topic>SOURIS</topic><topic>Vertebrates: digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spindler, Stephen R.</creatorcontrib><creatorcontrib>Crew, Mark D.</creatorcontrib><creatorcontrib>Mote, Patricia L.</creatorcontrib><creatorcontrib>Grizzle, Judith M.</creatorcontrib><creatorcontrib>Walford, Roy L.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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><jtitle>The Journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spindler, Stephen R.</au><au>Crew, Mark D.</au><au>Mote, Patricia L.</au><au>Grizzle, Judith M.</au><au>Walford, Roy L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA</atitle><jtitle>The Journal of nutrition</jtitle><addtitle>J Nutr</addtitle><date>1990-11</date><risdate>1990</risdate><volume>120</volume><issue>11</issue><spage>1412</spage><epage>1417</epage><pages>1412-1417</pages><issn>0022-3166</issn><eissn>1541-6100</eissn><coden>JONUAI</coden><abstract>The influence of life span-prolonging dietary energy restriction on hepatic expression of glucose-regulated protein 78 and 94 (GRP78 and GRP94) RNA was investigated in female C3B10RF1 mice. Mice were either fed ad libitum or fed diets reduced 20 or 40% in energy but containing approximately equivalent amounts of protein, fats, vitamins and minerals. Aging produced no changes in GRP mRNA. However, GRP78 and GRP94 mRNA levels were reduced ∼ 50 and 40%, respectively, by 40% energy restriction. This level of energy restriction produced a 43% reduction in the mean plasma glucose levels of young and old mice. The changes in GRP mRNA expression appear to be specific, because the levels of these RNAs were normalized to the level of polyadenylated RNA, and no changes were detected in the levels of a number of other mRNAs. Although extreme glucose deprivation increases GRP mRNA levels in cultured cell lines, physiologically relevant reductions in blood glucose had the opposite effect in the liver, in vivo. The regulatory pathway responsible for these effects is not known. GRP mRNA levels are elevated by agents that increase the level of malfolded proteins in the endoplasmic reticulum. Thus, energy restriction may act to reduce malfolded proteins in the endoplasmic reticulum of hepatic cells.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>2231029</pmid><doi>10.1093/jn/120.11.1412</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging - metabolism Animals ARN MENSAJERO ARN MESSAGER Biological and medical sciences Carrier Proteins - genetics Diet DIETA ENERGIA ENERGIE Energy Intake energy restriction Female FOIE Fundamental and applied biological sciences. Psychology Gene Expression Regulation GLUCOSA GLUCOSE Glucose - administration & dosage Glucose - metabolism glucose-regulated protein GRP mRNA Heat-Shock Proteins HIGADO HSP70 Heat-Shock Proteins liver Liver - metabolism Liver. Bile. Biliary tracts Membrane Proteins - genetics Mice Molecular Chaperones mouse PROTEINAS PROTEINE RATON REGIME ALIMENTAIRE RNA, Messenger - analysis SOURIS Vertebrates: digestive system |
title | Dietary Energy Restriction in Mice Reduces Hepatic Expression of Glucose-Regulated Protein 78 (BiP) and 94 mRNA |
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