Caloric restrictions affect some factors involved in age-related hypercholesterolemia
Ageing has been defined as a progressive decrease in physiological capacity and a reduced ability to respond to environmental stresses. It has been observed that diet‐restricted animals show a minor morbidity in age‐related disease. Among these age‐related diseases, hypercholesterolemia is the most...
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description | Ageing has been defined as a progressive decrease in physiological capacity and a reduced ability to respond to environmental stresses. It has been observed that diet‐restricted animals show a minor morbidity in age‐related disease. Among these age‐related diseases, hypercholesterolemia is the most recurring one and it is often associated with cardiac failure. Several studies have been published indicating age‐dependent changes in circulating levels of cholesterol in both humans and in rodents; recently changes have also been reported in the proteins involved in cholesterol homeostasis, that is, 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase (HMG‐CoAR), Insig‐induced gene (Insig) protein, SREBP cleavage activating protein (SCAP), sterol regulatory element binding protein (SREBP), and low density lipoprotein receptor (LDLr). Most age‐related modifications of biochemical parameters are normalized or very improved in food‐restricted animals, so the aim of this work is to examine whether or not alterations of the factors involved in cholesterol homeostasis which occur during ageing could be counteracted by caloric restriction (CR). The data show that the diet restrictions used attenuate the age‐related effects on the factors involved in the synthesis and the degradation rate of HMG‐CoAR; in spite of this, CRs have a good effect on the age‐related hypercholesterolemia whose reduction seems to depend both on the correct membrane LDLr localization and on the proper restored HMG‐CoAR activity. J. Cell. Biochem. 101: 235–243, 2007. © 2007 Wiley‐Liss, Inc. |
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It has been observed that diet‐restricted animals show a minor morbidity in age‐related disease. Among these age‐related diseases, hypercholesterolemia is the most recurring one and it is often associated with cardiac failure. Several studies have been published indicating age‐dependent changes in circulating levels of cholesterol in both humans and in rodents; recently changes have also been reported in the proteins involved in cholesterol homeostasis, that is, 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase (HMG‐CoAR), Insig‐induced gene (Insig) protein, SREBP cleavage activating protein (SCAP), sterol regulatory element binding protein (SREBP), and low density lipoprotein receptor (LDLr). Most age‐related modifications of biochemical parameters are normalized or very improved in food‐restricted animals, so the aim of this work is to examine whether or not alterations of the factors involved in cholesterol homeostasis which occur during ageing could be counteracted by caloric restriction (CR). The data show that the diet restrictions used attenuate the age‐related effects on the factors involved in the synthesis and the degradation rate of HMG‐CoAR; in spite of this, CRs have a good effect on the age‐related hypercholesterolemia whose reduction seems to depend both on the correct membrane LDLr localization and on the proper restored HMG‐CoAR activity. J. Cell. Biochem. 101: 235–243, 2007. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.21158</identifier><identifier>PMID: 17203467</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>ageing ; Aging - physiology ; Animals ; Caloric Restriction ; cholesterol ; Cholesterol - blood ; Gene Expression Regulation ; HMG-CoA reductase ; Hydroxymethylglutaryl CoA Reductases - genetics ; Hydroxymethylglutaryl CoA Reductases - metabolism ; Hypercholesterolemia - genetics ; Hypercholesterolemia - metabolism ; Insig ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; LDLr ; Liver - metabolism ; Male ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Random Allocation ; rat liver ; Rats ; Rats, Sprague-Dawley ; Receptors, LDL - genetics ; Receptors, LDL - metabolism ; SREBPs</subject><ispartof>Journal of cellular biochemistry, 2007-05, Vol.101 (1), p.235-243</ispartof><rights>Copyright © 2007 Wiley‐Liss, Inc.</rights><rights>(c) 2007 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4278-eefc7a4534400ed3c5e3abec5943b09519885108f316aa5eb51db97c510749493</citedby><cites>FETCH-LOGICAL-c4278-eefc7a4534400ed3c5e3abec5943b09519885108f316aa5eb51db97c510749493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcb.21158$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcb.21158$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17203467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martini, Chiara</creatorcontrib><creatorcontrib>Pallottini, Valentina</creatorcontrib><creatorcontrib>Cavallini, Gabriella</creatorcontrib><creatorcontrib>Donati, Alessio</creatorcontrib><creatorcontrib>Bergamini, Ettore</creatorcontrib><creatorcontrib>Trentalance, Anna</creatorcontrib><title>Caloric restrictions affect some factors involved in age-related hypercholesterolemia</title><title>Journal of cellular biochemistry</title><addtitle>J. Cell. Biochem</addtitle><description>Ageing has been defined as a progressive decrease in physiological capacity and a reduced ability to respond to environmental stresses. It has been observed that diet‐restricted animals show a minor morbidity in age‐related disease. Among these age‐related diseases, hypercholesterolemia is the most recurring one and it is often associated with cardiac failure. Several studies have been published indicating age‐dependent changes in circulating levels of cholesterol in both humans and in rodents; recently changes have also been reported in the proteins involved in cholesterol homeostasis, that is, 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase (HMG‐CoAR), Insig‐induced gene (Insig) protein, SREBP cleavage activating protein (SCAP), sterol regulatory element binding protein (SREBP), and low density lipoprotein receptor (LDLr). Most age‐related modifications of biochemical parameters are normalized or very improved in food‐restricted animals, so the aim of this work is to examine whether or not alterations of the factors involved in cholesterol homeostasis which occur during ageing could be counteracted by caloric restriction (CR). The data show that the diet restrictions used attenuate the age‐related effects on the factors involved in the synthesis and the degradation rate of HMG‐CoAR; in spite of this, CRs have a good effect on the age‐related hypercholesterolemia whose reduction seems to depend both on the correct membrane LDLr localization and on the proper restored HMG‐CoAR activity. J. Cell. Biochem. 101: 235–243, 2007. © 2007 Wiley‐Liss, Inc.</description><subject>ageing</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Caloric Restriction</subject><subject>cholesterol</subject><subject>Cholesterol - blood</subject><subject>Gene Expression Regulation</subject><subject>HMG-CoA reductase</subject><subject>Hydroxymethylglutaryl CoA Reductases - genetics</subject><subject>Hydroxymethylglutaryl CoA Reductases - metabolism</subject><subject>Hypercholesterolemia - genetics</subject><subject>Hypercholesterolemia - metabolism</subject><subject>Insig</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>LDLr</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Random Allocation</subject><subject>rat liver</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, LDL - genetics</subject><subject>Receptors, LDL - metabolism</subject><subject>SREBPs</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOwzAQRS0EgvJY8AMoKyQWgXFsx_ESKiiPCiQeYmk57gQCSV3stNC_x9ACK1Z3xjpzZF1CdikcUoDs6MWWhxmlolghPQpKpjznfJX0QDJIM0azDbIZwgsAKMWydbJBZQaM57JHHvqmcb62icfQxexqNw6JqSq0XRJci0llbOd8SOrxzDUzHMUhMU-YemxMF9fn-QS9fXZNFKCP0dZmm6xVpgm4s8wt8nB2et8_T4c3g4v-8TC1PJNFilhZabhgnAPgiFmBzJRoheKsBCWoKgpBoagYzY0RWAo6KpW08U1yxRXbIvsL78S7t2n8gG7rYLFpzBjdNGgJTCrKiggeLEDrXQgeKz3xdWv8XFPQXx3q2KH-7jCye0vptGxx9EcuS4vA0QJ4rxuc_2_Sl_2TH2W6uKhjRx-_F8a_6uiTQj9eD3R-NYTB7eWdztknx7yKsw</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Martini, Chiara</creator><creator>Pallottini, Valentina</creator><creator>Cavallini, Gabriella</creator><creator>Donati, Alessio</creator><creator>Bergamini, Ettore</creator><creator>Trentalance, Anna</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>20070501</creationdate><title>Caloric restrictions affect some factors involved in age-related hypercholesterolemia</title><author>Martini, Chiara ; Pallottini, Valentina ; Cavallini, Gabriella ; Donati, Alessio ; Bergamini, Ettore ; Trentalance, Anna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4278-eefc7a4534400ed3c5e3abec5943b09519885108f316aa5eb51db97c510749493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>ageing</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Caloric Restriction</topic><topic>cholesterol</topic><topic>Cholesterol - blood</topic><topic>Gene Expression Regulation</topic><topic>HMG-CoA reductase</topic><topic>Hydroxymethylglutaryl CoA Reductases - genetics</topic><topic>Hydroxymethylglutaryl CoA Reductases - metabolism</topic><topic>Hypercholesterolemia - genetics</topic><topic>Hypercholesterolemia - metabolism</topic><topic>Insig</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>LDLr</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Random Allocation</topic><topic>rat liver</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, LDL - genetics</topic><topic>Receptors, LDL - metabolism</topic><topic>SREBPs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martini, Chiara</creatorcontrib><creatorcontrib>Pallottini, Valentina</creatorcontrib><creatorcontrib>Cavallini, Gabriella</creatorcontrib><creatorcontrib>Donati, Alessio</creatorcontrib><creatorcontrib>Bergamini, Ettore</creatorcontrib><creatorcontrib>Trentalance, Anna</creatorcontrib><collection>Istex</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>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martini, Chiara</au><au>Pallottini, Valentina</au><au>Cavallini, Gabriella</au><au>Donati, Alessio</au><au>Bergamini, Ettore</au><au>Trentalance, Anna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caloric restrictions affect some factors involved in age-related hypercholesterolemia</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J. Cell. Biochem</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>101</volume><issue>1</issue><spage>235</spage><epage>243</epage><pages>235-243</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><abstract>Ageing has been defined as a progressive decrease in physiological capacity and a reduced ability to respond to environmental stresses. It has been observed that diet‐restricted animals show a minor morbidity in age‐related disease. Among these age‐related diseases, hypercholesterolemia is the most recurring one and it is often associated with cardiac failure. Several studies have been published indicating age‐dependent changes in circulating levels of cholesterol in both humans and in rodents; recently changes have also been reported in the proteins involved in cholesterol homeostasis, that is, 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase (HMG‐CoAR), Insig‐induced gene (Insig) protein, SREBP cleavage activating protein (SCAP), sterol regulatory element binding protein (SREBP), and low density lipoprotein receptor (LDLr). Most age‐related modifications of biochemical parameters are normalized or very improved in food‐restricted animals, so the aim of this work is to examine whether or not alterations of the factors involved in cholesterol homeostasis which occur during ageing could be counteracted by caloric restriction (CR). The data show that the diet restrictions used attenuate the age‐related effects on the factors involved in the synthesis and the degradation rate of HMG‐CoAR; in spite of this, CRs have a good effect on the age‐related hypercholesterolemia whose reduction seems to depend both on the correct membrane LDLr localization and on the proper restored HMG‐CoAR activity. J. Cell. Biochem. 101: 235–243, 2007. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17203467</pmid><doi>10.1002/jcb.21158</doi><tpages>9</tpages></addata></record> |
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subjects | ageing Aging - physiology Animals Caloric Restriction cholesterol Cholesterol - blood Gene Expression Regulation HMG-CoA reductase Hydroxymethylglutaryl CoA Reductases - genetics Hydroxymethylglutaryl CoA Reductases - metabolism Hypercholesterolemia - genetics Hypercholesterolemia - metabolism Insig Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism LDLr Liver - metabolism Male Membrane Proteins - genetics Membrane Proteins - metabolism Random Allocation rat liver Rats Rats, Sprague-Dawley Receptors, LDL - genetics Receptors, LDL - metabolism SREBPs |
title | Caloric restrictions affect some factors involved in age-related hypercholesterolemia |
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