Genome-wide effects of acute progressive feed restriction in liver and white adipose tissue

Acute progressive feed restriction (APFR) represents a specific form of caloric restriction in which feed availability is increasingly curtailed over a period of a few days to a few weeks. It is often used for control animals in toxicological and pharmacological studies on compounds causing body wei...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Toxicology and applied pharmacology 2008-07, Vol.230 (1), p.41-56
Hauptverfasser: Pohjanvirta, Raimo, Boutros, Paul C., Moffat, Ivy D., Lindén, Jere, Wendelin, Dominique, Okey, Allan B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 56
container_issue 1
container_start_page 41
container_title Toxicology and applied pharmacology
container_volume 230
creator Pohjanvirta, Raimo
Boutros, Paul C.
Moffat, Ivy D.
Lindén, Jere
Wendelin, Dominique
Okey, Allan B.
description Acute progressive feed restriction (APFR) represents a specific form of caloric restriction in which feed availability is increasingly curtailed over a period of a few days to a few weeks. It is often used for control animals in toxicological and pharmacological studies on compounds causing body weight loss to equalize weight changes between experimental and control groups and thereby, intuitively, to also set their metabolic states to the same phase. However, scientific justification for this procedure is lacking. In the present study, we analyzed by microarrays the impact on hepatic gene expression in rats of two APFR regimens that caused identical diminution of body weight (19%) but differed slightly in duration (4 vs. 10 days). In addition, white adipose tissue (WAT) was also subjected to the transcriptomic analysis on day-4. The data revealed that the two regimens led to distinct patterns of differentially expressed genes in liver, albeit some major pathways of energy metabolism were similarly affected (particularly fatty acid and amino acid catabolism). The reason for the divergence appeared to be entrainment by the longer APFR protocol of peripheral oscillator genes, which resulted in derailment of circadian rhythms and consequent interaction of altered diurnal fluctuations with metabolic adjustments in gene expression activities. WAT proved to be highly unresponsive to the 4-day APFR as only 17 mRNA levels were influenced by the treatment. This study demonstrates that body weight is a poor proxy of metabolic state and that the customary protocols of feed restriction can lead to rhythm entrainment.
doi_str_mv 10.1016/j.taap.2008.02.002
format Article
fullrecord <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_21140878</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0041008X08000707</els_id><sourcerecordid>19529814</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-d564d0fabac67e8ecdbc86a3071fe04fc7f9421bcd6636625d2800879d75ae9b3</originalsourceid><addsrcrecordid>eNp9kE2LFDEQhoMo7rj6BzxIQPTWbeWj093gZVl0FRa8KAgeQjqpuBl6kjHp3sV_b5oZ9OapKOqpot6HkJcMWgZMvdu3izHHlgMMLfAWgD8iOwajakAI8ZjsACRr6vT7BXlWyh4ARinZU3LBBjFKpYYd-XGDMR2weQgOKXqPdik0eWrsuiA95vQzYynhHqlHdLQ2Sw52CSnSEOlcB5ma6OjDXai8ceGYCtIllLLic_LEm7ngi3O9JN8-fvh6_am5_XLz-frqtrFSiqVxnZIOvJmMVT0OaN1kB2UE9MwjSG97P0rOJuuUEkrxzvGhhupH13cGx0lcktenu6ksQRdbP7F3NsVYw2jOmKzwUKm3J6qG-rXWHPoQisV5NhHTWjQbOz4OTFaQn0CbUykZvT7mcDD5t2agN_F6rzfxehOvgesqvi69Ol9fpwO6fytn0xV4cwZMsWb22UQbyl-Og-x60UPl3p84rMbuA-YtEEaLLuQtj0vhf3_8AdHuodg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19529814</pqid></control><display><type>article</type><title>Genome-wide effects of acute progressive feed restriction in liver and white adipose tissue</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Pohjanvirta, Raimo ; Boutros, Paul C. ; Moffat, Ivy D. ; Lindén, Jere ; Wendelin, Dominique ; Okey, Allan B.</creator><creatorcontrib>Pohjanvirta, Raimo ; Boutros, Paul C. ; Moffat, Ivy D. ; Lindén, Jere ; Wendelin, Dominique ; Okey, Allan B.</creatorcontrib><description>Acute progressive feed restriction (APFR) represents a specific form of caloric restriction in which feed availability is increasingly curtailed over a period of a few days to a few weeks. It is often used for control animals in toxicological and pharmacological studies on compounds causing body weight loss to equalize weight changes between experimental and control groups and thereby, intuitively, to also set their metabolic states to the same phase. However, scientific justification for this procedure is lacking. In the present study, we analyzed by microarrays the impact on hepatic gene expression in rats of two APFR regimens that caused identical diminution of body weight (19%) but differed slightly in duration (4 vs. 10 days). In addition, white adipose tissue (WAT) was also subjected to the transcriptomic analysis on day-4. The data revealed that the two regimens led to distinct patterns of differentially expressed genes in liver, albeit some major pathways of energy metabolism were similarly affected (particularly fatty acid and amino acid catabolism). The reason for the divergence appeared to be entrainment by the longer APFR protocol of peripheral oscillator genes, which resulted in derailment of circadian rhythms and consequent interaction of altered diurnal fluctuations with metabolic adjustments in gene expression activities. WAT proved to be highly unresponsive to the 4-day APFR as only 17 mRNA levels were influenced by the treatment. This study demonstrates that body weight is a poor proxy of metabolic state and that the customary protocols of feed restriction can lead to rhythm entrainment.</description><identifier>ISSN: 0041-008X</identifier><identifier>EISSN: 1096-0333</identifier><identifier>DOI: 10.1016/j.taap.2008.02.002</identifier><identifier>PMID: 18394668</identifier><identifier>CODEN: TXAPA9</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; ADIPOSE TISSUE ; Adipose Tissue, White - metabolism ; AMINO ACIDS ; Animals ; Biological and medical sciences ; CATABOLISM ; Energy metabolism ; Energy Metabolism - genetics ; Energy Metabolism - physiology ; Feed restriction ; FOOD ; Food Deprivation - physiology ; Food entrainment ; GENES ; Genome ; LIVER ; Liver - metabolism ; Male ; Medical sciences ; Microarrays ; Oligonucleotide Array Sequence Analysis ; Peripheral rhythms ; POLYMERASE CHAIN REACTION ; RATS ; Rats, Long-Evans ; Reverse Transcriptase Polymerase Chain Reaction ; RNA - genetics ; RNA - isolation &amp; purification ; RT-PCR ; STEROLS ; Toxicology ; TRANSCRIPTION ; TRANSCRIPTION FACTORS</subject><ispartof>Toxicology and applied pharmacology, 2008-07, Vol.230 (1), p.41-56</ispartof><rights>2008 Elsevier Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-d564d0fabac67e8ecdbc86a3071fe04fc7f9421bcd6636625d2800879d75ae9b3</citedby><cites>FETCH-LOGICAL-c443t-d564d0fabac67e8ecdbc86a3071fe04fc7f9421bcd6636625d2800879d75ae9b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041008X08000707$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20457370$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18394668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/21140878$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Pohjanvirta, Raimo</creatorcontrib><creatorcontrib>Boutros, Paul C.</creatorcontrib><creatorcontrib>Moffat, Ivy D.</creatorcontrib><creatorcontrib>Lindén, Jere</creatorcontrib><creatorcontrib>Wendelin, Dominique</creatorcontrib><creatorcontrib>Okey, Allan B.</creatorcontrib><title>Genome-wide effects of acute progressive feed restriction in liver and white adipose tissue</title><title>Toxicology and applied pharmacology</title><addtitle>Toxicol Appl Pharmacol</addtitle><description>Acute progressive feed restriction (APFR) represents a specific form of caloric restriction in which feed availability is increasingly curtailed over a period of a few days to a few weeks. It is often used for control animals in toxicological and pharmacological studies on compounds causing body weight loss to equalize weight changes between experimental and control groups and thereby, intuitively, to also set their metabolic states to the same phase. However, scientific justification for this procedure is lacking. In the present study, we analyzed by microarrays the impact on hepatic gene expression in rats of two APFR regimens that caused identical diminution of body weight (19%) but differed slightly in duration (4 vs. 10 days). In addition, white adipose tissue (WAT) was also subjected to the transcriptomic analysis on day-4. The data revealed that the two regimens led to distinct patterns of differentially expressed genes in liver, albeit some major pathways of energy metabolism were similarly affected (particularly fatty acid and amino acid catabolism). The reason for the divergence appeared to be entrainment by the longer APFR protocol of peripheral oscillator genes, which resulted in derailment of circadian rhythms and consequent interaction of altered diurnal fluctuations with metabolic adjustments in gene expression activities. WAT proved to be highly unresponsive to the 4-day APFR as only 17 mRNA levels were influenced by the treatment. This study demonstrates that body weight is a poor proxy of metabolic state and that the customary protocols of feed restriction can lead to rhythm entrainment.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>ADIPOSE TISSUE</subject><subject>Adipose Tissue, White - metabolism</subject><subject>AMINO ACIDS</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CATABOLISM</subject><subject>Energy metabolism</subject><subject>Energy Metabolism - genetics</subject><subject>Energy Metabolism - physiology</subject><subject>Feed restriction</subject><subject>FOOD</subject><subject>Food Deprivation - physiology</subject><subject>Food entrainment</subject><subject>GENES</subject><subject>Genome</subject><subject>LIVER</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microarrays</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Peripheral rhythms</subject><subject>POLYMERASE CHAIN REACTION</subject><subject>RATS</subject><subject>Rats, Long-Evans</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA - genetics</subject><subject>RNA - isolation &amp; purification</subject><subject>RT-PCR</subject><subject>STEROLS</subject><subject>Toxicology</subject><subject>TRANSCRIPTION</subject><subject>TRANSCRIPTION FACTORS</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2LFDEQhoMo7rj6BzxIQPTWbeWj093gZVl0FRa8KAgeQjqpuBl6kjHp3sV_b5oZ9OapKOqpot6HkJcMWgZMvdu3izHHlgMMLfAWgD8iOwajakAI8ZjsACRr6vT7BXlWyh4ARinZU3LBBjFKpYYd-XGDMR2weQgOKXqPdik0eWrsuiA95vQzYynhHqlHdLQ2Sw52CSnSEOlcB5ma6OjDXai8ceGYCtIllLLic_LEm7ngi3O9JN8-fvh6_am5_XLz-frqtrFSiqVxnZIOvJmMVT0OaN1kB2UE9MwjSG97P0rOJuuUEkrxzvGhhupH13cGx0lcktenu6ksQRdbP7F3NsVYw2jOmKzwUKm3J6qG-rXWHPoQisV5NhHTWjQbOz4OTFaQn0CbUykZvT7mcDD5t2agN_F6rzfxehOvgesqvi69Ol9fpwO6fytn0xV4cwZMsWb22UQbyl-Og-x60UPl3p84rMbuA-YtEEaLLuQtj0vhf3_8AdHuodg</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Pohjanvirta, Raimo</creator><creator>Boutros, Paul C.</creator><creator>Moffat, Ivy D.</creator><creator>Lindén, Jere</creator><creator>Wendelin, Dominique</creator><creator>Okey, Allan B.</creator><general>Elsevier Inc</general><general>Elsevier</general><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>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>OTOTI</scope></search><sort><creationdate>20080701</creationdate><title>Genome-wide effects of acute progressive feed restriction in liver and white adipose tissue</title><author>Pohjanvirta, Raimo ; Boutros, Paul C. ; Moffat, Ivy D. ; Lindén, Jere ; Wendelin, Dominique ; Okey, Allan B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-d564d0fabac67e8ecdbc86a3071fe04fc7f9421bcd6636625d2800879d75ae9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>ADIPOSE TISSUE</topic><topic>Adipose Tissue, White - metabolism</topic><topic>AMINO ACIDS</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CATABOLISM</topic><topic>Energy metabolism</topic><topic>Energy Metabolism - genetics</topic><topic>Energy Metabolism - physiology</topic><topic>Feed restriction</topic><topic>FOOD</topic><topic>Food Deprivation - physiology</topic><topic>Food entrainment</topic><topic>GENES</topic><topic>Genome</topic><topic>LIVER</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microarrays</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Peripheral rhythms</topic><topic>POLYMERASE CHAIN REACTION</topic><topic>RATS</topic><topic>Rats, Long-Evans</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA - genetics</topic><topic>RNA - isolation &amp; purification</topic><topic>RT-PCR</topic><topic>STEROLS</topic><topic>Toxicology</topic><topic>TRANSCRIPTION</topic><topic>TRANSCRIPTION FACTORS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pohjanvirta, Raimo</creatorcontrib><creatorcontrib>Boutros, Paul C.</creatorcontrib><creatorcontrib>Moffat, Ivy D.</creatorcontrib><creatorcontrib>Lindén, Jere</creatorcontrib><creatorcontrib>Wendelin, Dominique</creatorcontrib><creatorcontrib>Okey, Allan B.</creatorcontrib><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>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>OSTI.GOV</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pohjanvirta, Raimo</au><au>Boutros, Paul C.</au><au>Moffat, Ivy D.</au><au>Lindén, Jere</au><au>Wendelin, Dominique</au><au>Okey, Allan B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-wide effects of acute progressive feed restriction in liver and white adipose tissue</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>230</volume><issue>1</issue><spage>41</spage><epage>56</epage><pages>41-56</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Acute progressive feed restriction (APFR) represents a specific form of caloric restriction in which feed availability is increasingly curtailed over a period of a few days to a few weeks. It is often used for control animals in toxicological and pharmacological studies on compounds causing body weight loss to equalize weight changes between experimental and control groups and thereby, intuitively, to also set their metabolic states to the same phase. However, scientific justification for this procedure is lacking. In the present study, we analyzed by microarrays the impact on hepatic gene expression in rats of two APFR regimens that caused identical diminution of body weight (19%) but differed slightly in duration (4 vs. 10 days). In addition, white adipose tissue (WAT) was also subjected to the transcriptomic analysis on day-4. The data revealed that the two regimens led to distinct patterns of differentially expressed genes in liver, albeit some major pathways of energy metabolism were similarly affected (particularly fatty acid and amino acid catabolism). The reason for the divergence appeared to be entrainment by the longer APFR protocol of peripheral oscillator genes, which resulted in derailment of circadian rhythms and consequent interaction of altered diurnal fluctuations with metabolic adjustments in gene expression activities. WAT proved to be highly unresponsive to the 4-day APFR as only 17 mRNA levels were influenced by the treatment. This study demonstrates that body weight is a poor proxy of metabolic state and that the customary protocols of feed restriction can lead to rhythm entrainment.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>18394668</pmid><doi>10.1016/j.taap.2008.02.002</doi><tpages>16</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0041-008X
ispartof Toxicology and applied pharmacology, 2008-07, Vol.230 (1), p.41-56
issn 0041-008X
1096-0333
language eng
recordid cdi_osti_scitechconnect_21140878
source MEDLINE; Elsevier ScienceDirect Journals
subjects 60 APPLIED LIFE SCIENCES
ADIPOSE TISSUE
Adipose Tissue, White - metabolism
AMINO ACIDS
Animals
Biological and medical sciences
CATABOLISM
Energy metabolism
Energy Metabolism - genetics
Energy Metabolism - physiology
Feed restriction
FOOD
Food Deprivation - physiology
Food entrainment
GENES
Genome
LIVER
Liver - metabolism
Male
Medical sciences
Microarrays
Oligonucleotide Array Sequence Analysis
Peripheral rhythms
POLYMERASE CHAIN REACTION
RATS
Rats, Long-Evans
Reverse Transcriptase Polymerase Chain Reaction
RNA - genetics
RNA - isolation & purification
RT-PCR
STEROLS
Toxicology
TRANSCRIPTION
TRANSCRIPTION FACTORS
title Genome-wide effects of acute progressive feed restriction in liver and white adipose tissue
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T05%3A02%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genome-wide%20effects%20of%20acute%20progressive%20feed%20restriction%20in%20liver%20and%20white%20adipose%20tissue&rft.jtitle=Toxicology%20and%20applied%20pharmacology&rft.au=Pohjanvirta,%20Raimo&rft.date=2008-07-01&rft.volume=230&rft.issue=1&rft.spage=41&rft.epage=56&rft.pages=41-56&rft.issn=0041-008X&rft.eissn=1096-0333&rft.coden=TXAPA9&rft_id=info:doi/10.1016/j.taap.2008.02.002&rft_dat=%3Cproquest_osti_%3E19529814%3C/proquest_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19529814&rft_id=info:pmid/18394668&rft_els_id=S0041008X08000707&rfr_iscdi=true