High-fat feeding alters both basal and stress-induced hypothalamic-pituitary-adrenal activity in the rat
1 Developmental Neuroendocrinology Laboratory, Douglas Hospital Research Center, and 2 Department of Neurology and Neurosurgery, McGill University, Montreal H4H-1R3; 3 Neuropeptide Physiology Laboratory, Montreal Children's Hospital Research Institute and Department of Pediatrics, McGill Uni...
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Veröffentlicht in: | American journal of physiology: endocrinology and metabolism 1997-12, Vol.273 (6), p.E1168-E1177 |
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container_title | American journal of physiology: endocrinology and metabolism |
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creator | Tannenbaum, B.M Brindley, D.N Tannenbaum, G.S Dallman, M.F McArthur, M.D Meaney, M.J |
description | 1 Developmental
Neuroendocrinology Laboratory, Douglas Hospital Research Center,
and 2 Department of Neurology and
Neurosurgery, McGill University, Montreal H4H-1R3;
3 Neuropeptide Physiology
Laboratory, Montreal Children's Hospital Research Institute and
Department of Pediatrics, McGill University, Montreal H3H-1P3;
4 Signal Transduction
Laboratories, Department of Biochemistry, University of Alberta,
Edmonton, Canada T6G-2S2; and
5 Department of Physiology,
University of California, San Francisco, California 94143
High-fat feeding induces insulin resistance
and increases the risk for the development of diabetes and coronary
artery disease. Glucocorticoids exacerbate this hyperinsulinemic state,
rendering an individual at further risk for chronic disease. The
present studies were undertaken to determine whether dietary
fat-induced increases in corticosterone (B) reflect alterations in the
regulatory components of the hypothalamic-pituitary-adrenal (HPA) axis.
Adult male rats were maintained on a high-fat (20%) or control (4%) diet for varying periods of time. Marked elevations in light-phase spontaneous basal B levels were evident as early as 7 days after fat
diet onset, and B concentrations remained significantly elevated up to
21 days after fat diet onset compared with controls. In contrast, there
were no significant effects on any parameters of spontaneous growth
hormone secretory profiles, thus providing support for the specificity
of the effects on the HPA axis. In a second study, all groups of rats
fed the high-fat diet for 1, 9, or 12 wk exhibited significantly
elevated levels of plasma adrenocorticotropic hormone, B, fatty acid,
and glucose before, during, and/or at 20, 60, and/or
120 min after the termination of a restraint stress. Furthermore, 12-wk
fat-fed animals showed a significant resistance to insulin compared
with normally fed controls. There were no differences in negative
feedback efficacy in high-fat-fed rats vs. controls. Taken together,
these results suggest that dietary fat intake acts as a background form
of chronic stress, elevating basal B levels and enhancing HPA responses
to stress.
glucocorticoids; adrenocorticotropic hormone; corticosterone; fatty
acid; glucose |
doi_str_mv | 10.1152/ajpendo.1997.273.6.e1168 |
format | Article |
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Neuroendocrinology Laboratory, Douglas Hospital Research Center,
and 2 Department of Neurology and
Neurosurgery, McGill University, Montreal H4H-1R3;
3 Neuropeptide Physiology
Laboratory, Montreal Children's Hospital Research Institute and
Department of Pediatrics, McGill University, Montreal H3H-1P3;
4 Signal Transduction
Laboratories, Department of Biochemistry, University of Alberta,
Edmonton, Canada T6G-2S2; and
5 Department of Physiology,
University of California, San Francisco, California 94143
High-fat feeding induces insulin resistance
and increases the risk for the development of diabetes and coronary
artery disease. Glucocorticoids exacerbate this hyperinsulinemic state,
rendering an individual at further risk for chronic disease. The
present studies were undertaken to determine whether dietary
fat-induced increases in corticosterone (B) reflect alterations in the
regulatory components of the hypothalamic-pituitary-adrenal (HPA) axis.
Adult male rats were maintained on a high-fat (20%) or control (4%) diet for varying periods of time. Marked elevations in light-phase spontaneous basal B levels were evident as early as 7 days after fat
diet onset, and B concentrations remained significantly elevated up to
21 days after fat diet onset compared with controls. In contrast, there
were no significant effects on any parameters of spontaneous growth
hormone secretory profiles, thus providing support for the specificity
of the effects on the HPA axis. In a second study, all groups of rats
fed the high-fat diet for 1, 9, or 12 wk exhibited significantly
elevated levels of plasma adrenocorticotropic hormone, B, fatty acid,
and glucose before, during, and/or at 20, 60, and/or
120 min after the termination of a restraint stress. Furthermore, 12-wk
fat-fed animals showed a significant resistance to insulin compared
with normally fed controls. There were no differences in negative
feedback efficacy in high-fat-fed rats vs. controls. Taken together,
these results suggest that dietary fat intake acts as a background form
of chronic stress, elevating basal B levels and enhancing HPA responses
to stress.
glucocorticoids; adrenocorticotropic hormone; corticosterone; fatty
acid; glucose</description><identifier>ISSN: 0002-9513</identifier><identifier>ISSN: 0193-1849</identifier><identifier>EISSN: 2163-5773</identifier><identifier>EISSN: 1522-1555</identifier><identifier>DOI: 10.1152/ajpendo.1997.273.6.e1168</identifier><identifier>PMID: 9435533</identifier><language>eng</language><publisher>United States</publisher><subject>Adrenalectomy ; Adrenocorticotropic Hormone - blood ; Adrenocorticotropic Hormone - metabolism ; Animals ; Blood Glucose - metabolism ; Brain - metabolism ; Circadian Rhythm ; CORPS GRAS ; Corticosterone - blood ; Corticosterone - metabolism ; Dexamethasone - metabolism ; DIET ; DIETA ; Dietary Fats ; FATS ; Feedback ; Feeding Behavior ; GRASAS ; Growth Hormone - blood ; Growth Hormone - metabolism ; Hypothalamo-Hypophyseal System - physiology ; Male ; Pituitary-Adrenal System - physiology ; Rats ; Rats, Sprague-Dawley ; Receptors, Glucocorticoid - metabolism ; REGIME ALIMENTAIRE ; Restraint, Physical ; Space life sciences ; Species Specificity ; Stress, Psychological - physiopathology ; Time Factors ; Weight Gain</subject><ispartof>American journal of physiology: endocrinology and metabolism, 1997-12, Vol.273 (6), p.E1168-E1177</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-1b78222db79736733afbfe8c8c9cdf03af4c3d5e7160d2005888c2f626c083f03</citedby><cites>FETCH-LOGICAL-c543t-1b78222db79736733afbfe8c8c9cdf03af4c3d5e7160d2005888c2f626c083f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9435533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tannenbaum, B.M</creatorcontrib><creatorcontrib>Brindley, D.N</creatorcontrib><creatorcontrib>Tannenbaum, G.S</creatorcontrib><creatorcontrib>Dallman, M.F</creatorcontrib><creatorcontrib>McArthur, M.D</creatorcontrib><creatorcontrib>Meaney, M.J</creatorcontrib><title>High-fat feeding alters both basal and stress-induced hypothalamic-pituitary-adrenal activity in the rat</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol</addtitle><description>1 Developmental
Neuroendocrinology Laboratory, Douglas Hospital Research Center,
and 2 Department of Neurology and
Neurosurgery, McGill University, Montreal H4H-1R3;
3 Neuropeptide Physiology
Laboratory, Montreal Children's Hospital Research Institute and
Department of Pediatrics, McGill University, Montreal H3H-1P3;
4 Signal Transduction
Laboratories, Department of Biochemistry, University of Alberta,
Edmonton, Canada T6G-2S2; and
5 Department of Physiology,
University of California, San Francisco, California 94143
High-fat feeding induces insulin resistance
and increases the risk for the development of diabetes and coronary
artery disease. Glucocorticoids exacerbate this hyperinsulinemic state,
rendering an individual at further risk for chronic disease. The
present studies were undertaken to determine whether dietary
fat-induced increases in corticosterone (B) reflect alterations in the
regulatory components of the hypothalamic-pituitary-adrenal (HPA) axis.
Adult male rats were maintained on a high-fat (20%) or control (4%) diet for varying periods of time. Marked elevations in light-phase spontaneous basal B levels were evident as early as 7 days after fat
diet onset, and B concentrations remained significantly elevated up to
21 days after fat diet onset compared with controls. In contrast, there
were no significant effects on any parameters of spontaneous growth
hormone secretory profiles, thus providing support for the specificity
of the effects on the HPA axis. In a second study, all groups of rats
fed the high-fat diet for 1, 9, or 12 wk exhibited significantly
elevated levels of plasma adrenocorticotropic hormone, B, fatty acid,
and glucose before, during, and/or at 20, 60, and/or
120 min after the termination of a restraint stress. Furthermore, 12-wk
fat-fed animals showed a significant resistance to insulin compared
with normally fed controls. There were no differences in negative
feedback efficacy in high-fat-fed rats vs. controls. Taken together,
these results suggest that dietary fat intake acts as a background form
of chronic stress, elevating basal B levels and enhancing HPA responses
to stress.
glucocorticoids; adrenocorticotropic hormone; corticosterone; fatty
acid; glucose</description><subject>Adrenalectomy</subject><subject>Adrenocorticotropic Hormone - blood</subject><subject>Adrenocorticotropic Hormone - metabolism</subject><subject>Animals</subject><subject>Blood Glucose - metabolism</subject><subject>Brain - metabolism</subject><subject>Circadian Rhythm</subject><subject>CORPS GRAS</subject><subject>Corticosterone - blood</subject><subject>Corticosterone - metabolism</subject><subject>Dexamethasone - metabolism</subject><subject>DIET</subject><subject>DIETA</subject><subject>Dietary Fats</subject><subject>FATS</subject><subject>Feedback</subject><subject>Feeding Behavior</subject><subject>GRASAS</subject><subject>Growth Hormone - blood</subject><subject>Growth Hormone - metabolism</subject><subject>Hypothalamo-Hypophyseal System - physiology</subject><subject>Male</subject><subject>Pituitary-Adrenal System - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Glucocorticoid - metabolism</subject><subject>REGIME ALIMENTAIRE</subject><subject>Restraint, Physical</subject><subject>Space life sciences</subject><subject>Species Specificity</subject><subject>Stress, Psychological - physiopathology</subject><subject>Time Factors</subject><subject>Weight Gain</subject><issn>0002-9513</issn><issn>0193-1849</issn><issn>2163-5773</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtu1DAUhi1EVYbCIyB5xS7BlzhO2KGqN6kSi7Zry7GPJ64ySbAdIG-PoxkKLFhZR__F53wIYUpKSgX7pJ9nGO1U0raVJZO8rEugtG5eoR2jNS-ElPw12hFCWNEKyt-gtzE-55EKXp2j87biQnC-Q_2t3_eF0wk7AOvHPdZDghBxN6UedzrqAevR4pgCxFj40S4GLO7XOet60AdvitmnxScd1kLbAOOWMMl_92nFfsSpBxx0eofOnB4ivD-9F-jp-urx8ra4_3pzd_nlvjCi4qmgnWwYY7aTreS15Fy7zkFjGtMa60geK8OtAElrYhkhomkaw1zNakMang0X6OOxdw7TtwViUgcfDQyDHmFaopKtYJRUIhubo9GEKcYATs3BH_IVihK1QVYnyGqDrDJkVaurDXKOfjj9sXQHsC_BE9Wsl0e9z3B_-ABq7tfop2Hary-t_xZ-_n_gehmGR_iZfif_CqrZuj_bOD0pvQ8-qqeHbWciWSVa_gvEf6qK</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>Tannenbaum, B.M</creator><creator>Brindley, D.N</creator><creator>Tannenbaum, G.S</creator><creator>Dallman, M.F</creator><creator>McArthur, M.D</creator><creator>Meaney, M.J</creator><scope>FBQ</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>19971201</creationdate><title>High-fat feeding alters both basal and stress-induced hypothalamic-pituitary-adrenal activity in the rat</title><author>Tannenbaum, B.M ; Brindley, D.N ; Tannenbaum, G.S ; Dallman, M.F ; McArthur, M.D ; Meaney, M.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c543t-1b78222db79736733afbfe8c8c9cdf03af4c3d5e7160d2005888c2f626c083f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adrenalectomy</topic><topic>Adrenocorticotropic Hormone - blood</topic><topic>Adrenocorticotropic Hormone - metabolism</topic><topic>Animals</topic><topic>Blood Glucose - metabolism</topic><topic>Brain - metabolism</topic><topic>Circadian Rhythm</topic><topic>CORPS GRAS</topic><topic>Corticosterone - blood</topic><topic>Corticosterone - metabolism</topic><topic>Dexamethasone - metabolism</topic><topic>DIET</topic><topic>DIETA</topic><topic>Dietary Fats</topic><topic>FATS</topic><topic>Feedback</topic><topic>Feeding Behavior</topic><topic>GRASAS</topic><topic>Growth Hormone - blood</topic><topic>Growth Hormone - metabolism</topic><topic>Hypothalamo-Hypophyseal System - physiology</topic><topic>Male</topic><topic>Pituitary-Adrenal System - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Glucocorticoid - metabolism</topic><topic>REGIME ALIMENTAIRE</topic><topic>Restraint, Physical</topic><topic>Space life sciences</topic><topic>Species Specificity</topic><topic>Stress, Psychological - physiopathology</topic><topic>Time Factors</topic><topic>Weight Gain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tannenbaum, B.M</creatorcontrib><creatorcontrib>Brindley, D.N</creatorcontrib><creatorcontrib>Tannenbaum, G.S</creatorcontrib><creatorcontrib>Dallman, M.F</creatorcontrib><creatorcontrib>McArthur, M.D</creatorcontrib><creatorcontrib>Meaney, M.J</creatorcontrib><collection>AGRIS</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>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tannenbaum, B.M</au><au>Brindley, D.N</au><au>Tannenbaum, G.S</au><au>Dallman, M.F</au><au>McArthur, M.D</au><au>Meaney, M.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-fat feeding alters both basal and stress-induced hypothalamic-pituitary-adrenal activity in the rat</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol</addtitle><date>1997-12-01</date><risdate>1997</risdate><volume>273</volume><issue>6</issue><spage>E1168</spage><epage>E1177</epage><pages>E1168-E1177</pages><issn>0002-9513</issn><issn>0193-1849</issn><eissn>2163-5773</eissn><eissn>1522-1555</eissn><abstract>1 Developmental
Neuroendocrinology Laboratory, Douglas Hospital Research Center,
and 2 Department of Neurology and
Neurosurgery, McGill University, Montreal H4H-1R3;
3 Neuropeptide Physiology
Laboratory, Montreal Children's Hospital Research Institute and
Department of Pediatrics, McGill University, Montreal H3H-1P3;
4 Signal Transduction
Laboratories, Department of Biochemistry, University of Alberta,
Edmonton, Canada T6G-2S2; and
5 Department of Physiology,
University of California, San Francisco, California 94143
High-fat feeding induces insulin resistance
and increases the risk for the development of diabetes and coronary
artery disease. Glucocorticoids exacerbate this hyperinsulinemic state,
rendering an individual at further risk for chronic disease. The
present studies were undertaken to determine whether dietary
fat-induced increases in corticosterone (B) reflect alterations in the
regulatory components of the hypothalamic-pituitary-adrenal (HPA) axis.
Adult male rats were maintained on a high-fat (20%) or control (4%) diet for varying periods of time. Marked elevations in light-phase spontaneous basal B levels were evident as early as 7 days after fat
diet onset, and B concentrations remained significantly elevated up to
21 days after fat diet onset compared with controls. In contrast, there
were no significant effects on any parameters of spontaneous growth
hormone secretory profiles, thus providing support for the specificity
of the effects on the HPA axis. In a second study, all groups of rats
fed the high-fat diet for 1, 9, or 12 wk exhibited significantly
elevated levels of plasma adrenocorticotropic hormone, B, fatty acid,
and glucose before, during, and/or at 20, 60, and/or
120 min after the termination of a restraint stress. Furthermore, 12-wk
fat-fed animals showed a significant resistance to insulin compared
with normally fed controls. There were no differences in negative
feedback efficacy in high-fat-fed rats vs. controls. Taken together,
these results suggest that dietary fat intake acts as a background form
of chronic stress, elevating basal B levels and enhancing HPA responses
to stress.
glucocorticoids; adrenocorticotropic hormone; corticosterone; fatty
acid; glucose</abstract><cop>United States</cop><pmid>9435533</pmid><doi>10.1152/ajpendo.1997.273.6.e1168</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-9513 |
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issn | 0002-9513 0193-1849 2163-5773 1522-1555 |
language | eng |
recordid | cdi_highwire_physiology_ajpendo_273_6_E1168 |
source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adrenalectomy Adrenocorticotropic Hormone - blood Adrenocorticotropic Hormone - metabolism Animals Blood Glucose - metabolism Brain - metabolism Circadian Rhythm CORPS GRAS Corticosterone - blood Corticosterone - metabolism Dexamethasone - metabolism DIET DIETA Dietary Fats FATS Feedback Feeding Behavior GRASAS Growth Hormone - blood Growth Hormone - metabolism Hypothalamo-Hypophyseal System - physiology Male Pituitary-Adrenal System - physiology Rats Rats, Sprague-Dawley Receptors, Glucocorticoid - metabolism REGIME ALIMENTAIRE Restraint, Physical Space life sciences Species Specificity Stress, Psychological - physiopathology Time Factors Weight Gain |
title | High-fat feeding alters both basal and stress-induced hypothalamic-pituitary-adrenal activity in the rat |
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