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Meal time shift disturbs circadian rhythmicity along with metabolic and behavioral alterations in mice
In modern society, growing numbers of people are engaged in various forms of shift works or trans-meridian travels. Such circadian misalignment is known to disturb endogenous diurnal rhythms, which may lead to harmful physiological consequences including metabolic syndrome, obesity, cancer, cardiova...
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Published in: | PloS one 2012-08, Vol.7 (8), p.e44053 |
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description | In modern society, growing numbers of people are engaged in various forms of shift works or trans-meridian travels. Such circadian misalignment is known to disturb endogenous diurnal rhythms, which may lead to harmful physiological consequences including metabolic syndrome, obesity, cancer, cardiovascular disorders, and gastric disorders as well as other physical and mental disorders. However, the precise mechanism(s) underlying these changes are yet unclear. The present work, therefore examined the effects of 6 h advance or delay of usual meal time on diurnal rhythmicities in home cage activity (HCA), body temperature (BT), blood metabolic markers, glucose homeostasis, and expression of genes that are involved in cholesterol homeostasis by feeding young adult male mice in a time-restrictive manner. Delay of meal time caused locomotive hyperactivity in a significant portion (42%) of subjects, while 6 h advance caused a torpor-like symptom during the late scotophase. Accordingly, daily rhythms of blood glucose and triglyceride were differentially affected by time-restrictive feeding regimen with concurrent metabolic alterations. Along with these physiological changes, time-restrictive feeding also influenced the circadian expression patterns of low density lipoprotein receptor (LDLR) as well as most LDLR regulatory factors. Strikingly, chronic advance of meal time induced insulin resistance, while chronic delay significantly elevated blood glucose levels. Taken together, our findings indicate that persistent shifts in usual meal time impact the diurnal rhythms of carbohydrate and lipid metabolisms in addition to HCA and BT, thereby posing critical implications for the health and diseases of shift workers. |
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Such circadian misalignment is known to disturb endogenous diurnal rhythms, which may lead to harmful physiological consequences including metabolic syndrome, obesity, cancer, cardiovascular disorders, and gastric disorders as well as other physical and mental disorders. However, the precise mechanism(s) underlying these changes are yet unclear. The present work, therefore examined the effects of 6 h advance or delay of usual meal time on diurnal rhythmicities in home cage activity (HCA), body temperature (BT), blood metabolic markers, glucose homeostasis, and expression of genes that are involved in cholesterol homeostasis by feeding young adult male mice in a time-restrictive manner. Delay of meal time caused locomotive hyperactivity in a significant portion (42%) of subjects, while 6 h advance caused a torpor-like symptom during the late scotophase. Accordingly, daily rhythms of blood glucose and triglyceride were differentially affected by time-restrictive feeding regimen with concurrent metabolic alterations. Along with these physiological changes, time-restrictive feeding also influenced the circadian expression patterns of low density lipoprotein receptor (LDLR) as well as most LDLR regulatory factors. Strikingly, chronic advance of meal time induced insulin resistance, while chronic delay significantly elevated blood glucose levels. Taken together, our findings indicate that persistent shifts in usual meal time impact the diurnal rhythms of carbohydrate and lipid metabolisms in addition to HCA and BT, thereby posing critical implications for the health and diseases of shift workers.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0044053</identifier><identifier>PMID: 22952870</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis of Variance ; Animals ; Behavior, Animal - drug effects ; Behavior, Animal - physiology ; Biology ; Blood ; Blood glucose ; Blood Glucose - metabolism ; Body temperature ; Body Temperature - drug effects ; Body Temperature - physiology ; Body Weight - drug effects ; Cancer ; Carbohydrates ; Cholesterol ; Cholesterol - metabolism ; Circadian rhythm ; Circadian Rhythm - drug effects ; Circadian Rhythm - genetics ; Circadian Rhythm - physiology ; Circadian rhythms ; Delay ; Diurnal ; Drinking Behavior - drug effects ; Fasting - blood ; Feeding ; Feeding Behavior - drug effects ; Feeding Behavior - physiology ; Food ; Gene expression ; Gene Expression Regulation - drug effects ; Glucose ; Glucose Tolerance Test ; Homeostasis ; Homeostasis - drug effects ; Homeostasis - genetics ; Human behavior ; Hyperactivity ; Hyperglycemia ; Insulin ; Insulin - pharmacology ; Insulin resistance ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Legal medicine ; Liver - drug effects ; Liver - metabolism ; Low density lipoprotein receptors ; Male ; Meals - drug effects ; Meals - physiology ; Medicine ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mental disorders ; Metabolic syndrome ; Metabolism - drug effects ; Metabolism - genetics ; Mice ; Mice, Inbred C57BL ; Misalignment ; Neurodegeneration ; Neurosciences ; Nighttime ; Obesity ; Occupational health ; Physiology ; Receptor density ; Receptors, LDL - genetics ; Receptors, LDL - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Rodents ; Shift work ; Sterol Regulatory Element Binding Protein 1 - genetics ; Sterol Regulatory Element Binding Protein 1 - metabolism ; Torpor ; Trends ; Workers ; Young adults</subject><ispartof>PloS one, 2012-08, Vol.7 (8), p.e44053</ispartof><rights>Yoon et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 Yoon et al 2012 Yoon et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-f4e29f917eace6d4929f4667b0c768e49f941d7355249a3f7d9688445a44e5843</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1326543620/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1326543620?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22952870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Bartell, Paul A.</contributor><creatorcontrib>Yoon, Ji-Ae</creatorcontrib><creatorcontrib>Han, Dong-Hee</creatorcontrib><creatorcontrib>Noh, Jong-Yun</creatorcontrib><creatorcontrib>Kim, Mi-Hee</creatorcontrib><creatorcontrib>Son, Gi Hoon</creatorcontrib><creatorcontrib>Kim, Kyungjin</creatorcontrib><creatorcontrib>Kim, Chang-Ju</creatorcontrib><creatorcontrib>Pak, Youngmi Kim</creatorcontrib><creatorcontrib>Cho, Sehyung</creatorcontrib><title>Meal time shift disturbs circadian rhythmicity along with metabolic and behavioral alterations in mice</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>In modern society, growing numbers of people are engaged in various forms of shift works or trans-meridian travels. Such circadian misalignment is known to disturb endogenous diurnal rhythms, which may lead to harmful physiological consequences including metabolic syndrome, obesity, cancer, cardiovascular disorders, and gastric disorders as well as other physical and mental disorders. However, the precise mechanism(s) underlying these changes are yet unclear. The present work, therefore examined the effects of 6 h advance or delay of usual meal time on diurnal rhythmicities in home cage activity (HCA), body temperature (BT), blood metabolic markers, glucose homeostasis, and expression of genes that are involved in cholesterol homeostasis by feeding young adult male mice in a time-restrictive manner. Delay of meal time caused locomotive hyperactivity in a significant portion (42%) of subjects, while 6 h advance caused a torpor-like symptom during the late scotophase. Accordingly, daily rhythms of blood glucose and triglyceride were differentially affected by time-restrictive feeding regimen with concurrent metabolic alterations. Along with these physiological changes, time-restrictive feeding also influenced the circadian expression patterns of low density lipoprotein receptor (LDLR) as well as most LDLR regulatory factors. Strikingly, chronic advance of meal time induced insulin resistance, while chronic delay significantly elevated blood glucose levels. Taken together, our findings indicate that persistent shifts in usual meal time impact the diurnal rhythms of carbohydrate and lipid metabolisms in addition to HCA and BT, thereby posing critical implications for the health and diseases of shift workers.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Behavior, Animal - physiology</subject><subject>Biology</subject><subject>Blood</subject><subject>Blood glucose</subject><subject>Blood Glucose - metabolism</subject><subject>Body temperature</subject><subject>Body Temperature - drug effects</subject><subject>Body Temperature - physiology</subject><subject>Body Weight - drug effects</subject><subject>Cancer</subject><subject>Carbohydrates</subject><subject>Cholesterol</subject><subject>Cholesterol - metabolism</subject><subject>Circadian rhythm</subject><subject>Circadian Rhythm - drug effects</subject><subject>Circadian Rhythm - genetics</subject><subject>Circadian Rhythm - physiology</subject><subject>Circadian rhythms</subject><subject>Delay</subject><subject>Diurnal</subject><subject>Drinking Behavior - drug effects</subject><subject>Fasting - blood</subject><subject>Feeding</subject><subject>Feeding Behavior - drug effects</subject><subject>Feeding Behavior - physiology</subject><subject>Food</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Glucose</subject><subject>Glucose Tolerance Test</subject><subject>Homeostasis</subject><subject>Homeostasis - drug effects</subject><subject>Homeostasis - genetics</subject><subject>Human behavior</subject><subject>Hyperactivity</subject><subject>Hyperglycemia</subject><subject>Insulin</subject><subject>Insulin - pharmacology</subject><subject>Insulin resistance</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Legal medicine</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Low density lipoprotein receptors</subject><subject>Male</subject><subject>Meals - drug effects</subject><subject>Meals - physiology</subject><subject>Medicine</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mental disorders</subject><subject>Metabolic syndrome</subject><subject>Metabolism - drug effects</subject><subject>Metabolism - genetics</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Misalignment</subject><subject>Neurodegeneration</subject><subject>Neurosciences</subject><subject>Nighttime</subject><subject>Obesity</subject><subject>Occupational health</subject><subject>Physiology</subject><subject>Receptor density</subject><subject>Receptors, LDL - genetics</subject><subject>Receptors, LDL - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Shift work</subject><subject>Sterol Regulatory Element Binding Protein 1 - 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Such circadian misalignment is known to disturb endogenous diurnal rhythms, which may lead to harmful physiological consequences including metabolic syndrome, obesity, cancer, cardiovascular disorders, and gastric disorders as well as other physical and mental disorders. However, the precise mechanism(s) underlying these changes are yet unclear. The present work, therefore examined the effects of 6 h advance or delay of usual meal time on diurnal rhythmicities in home cage activity (HCA), body temperature (BT), blood metabolic markers, glucose homeostasis, and expression of genes that are involved in cholesterol homeostasis by feeding young adult male mice in a time-restrictive manner. Delay of meal time caused locomotive hyperactivity in a significant portion (42%) of subjects, while 6 h advance caused a torpor-like symptom during the late scotophase. Accordingly, daily rhythms of blood glucose and triglyceride were differentially affected by time-restrictive feeding regimen with concurrent metabolic alterations. Along with these physiological changes, time-restrictive feeding also influenced the circadian expression patterns of low density lipoprotein receptor (LDLR) as well as most LDLR regulatory factors. Strikingly, chronic advance of meal time induced insulin resistance, while chronic delay significantly elevated blood glucose levels. Taken together, our findings indicate that persistent shifts in usual meal time impact the diurnal rhythms of carbohydrate and lipid metabolisms in addition to HCA and BT, thereby posing critical implications for the health and diseases of shift workers.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22952870</pmid><doi>10.1371/journal.pone.0044053</doi><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_1326543620 |
source | PubMed Central(OA); ProQuest - Publicly Available Content Database |
subjects | Analysis of Variance Animals Behavior, Animal - drug effects Behavior, Animal - physiology Biology Blood Blood glucose Blood Glucose - metabolism Body temperature Body Temperature - drug effects Body Temperature - physiology Body Weight - drug effects Cancer Carbohydrates Cholesterol Cholesterol - metabolism Circadian rhythm Circadian Rhythm - drug effects Circadian Rhythm - genetics Circadian Rhythm - physiology Circadian rhythms Delay Diurnal Drinking Behavior - drug effects Fasting - blood Feeding Feeding Behavior - drug effects Feeding Behavior - physiology Food Gene expression Gene Expression Regulation - drug effects Glucose Glucose Tolerance Test Homeostasis Homeostasis - drug effects Homeostasis - genetics Human behavior Hyperactivity Hyperglycemia Insulin Insulin - pharmacology Insulin resistance Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism Legal medicine Liver - drug effects Liver - metabolism Low density lipoprotein receptors Male Meals - drug effects Meals - physiology Medicine Membrane Proteins - genetics Membrane Proteins - metabolism Mental disorders Metabolic syndrome Metabolism - drug effects Metabolism - genetics Mice Mice, Inbred C57BL Misalignment Neurodegeneration Neurosciences Nighttime Obesity Occupational health Physiology Receptor density Receptors, LDL - genetics Receptors, LDL - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Rodents Shift work Sterol Regulatory Element Binding Protein 1 - genetics Sterol Regulatory Element Binding Protein 1 - metabolism Torpor Trends Workers Young adults |
title | Meal time shift disturbs circadian rhythmicity along with metabolic and behavioral alterations in mice |
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