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Effects of early life stress on drinking and serotonin system activity in rhesus macaques: 5-hydroxyindoleacetic acid in cerebrospinal fluid predicts brain tissue levels
Abstract Early childhood stress is a risk factor for the development of substance-abuse disorders. A nonhuman primate model of early life stress, social impoverishment through nursery-rearing rather than mother-rearing, has been shown to produce increased impulsive and anxiety-like behaviors, cognit...
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Published in: | Alcohol (Fayetteville, N.Y.) N.Y.), 2012-06, Vol.46 (4), p.371-376 |
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creator | Huggins, Kimberly N Mathews, Tiffany A Locke, Jason L Szeliga, Kendall T Friedman, David P Bennett, Allyson J Jones, Sara R |
description | Abstract Early childhood stress is a risk factor for the development of substance-abuse disorders. A nonhuman primate model of early life stress, social impoverishment through nursery-rearing rather than mother-rearing, has been shown to produce increased impulsive and anxiety-like behaviors, cognitive and motor deficits, and increased alcohol consumption. These behavioral changes have been linked to changes in cerebrospinal fluid (CSF) levels of 5-hydroxyindoleacetic acid (5-HIAA), a serotonin (5-HT) metabolite. The effects of different rearing conditions on ethanol drinking and three measures of 5-HT function in the central nervous system were evaluated, including CSF 5-HIAA levels and tissue levels of 5-HT and 5-HIAA in brain samples. Brain samples were taken from the dorsal caudate, putamen, substantia nigra (SN) pars reticulata, SN pars compacta and hippocampus. There was a clear effect of rearing condition on the 5-HT system. Overall 5-HIAA and 5-HIAA/5-HT ratio measures of 5-HT turnover were significantly lower in nursery reared compared to mother-reared animals. In addition, there was a strong within-subject correlation between CSF and brain tissue 5-HIAA levels. Ethanol drinking was greater in nursery reared monkeys, consistent with previous results. These findings show that CSF 5-HIAA measurements can be used to predict brain 5-HT activity that may be involved in behavioral outcomes such as anxiety and alcohol consumption. Thus, CSF sampling may provide a minimally invasive test for neurochemical risk factors related to alcohol abuse. |
doi_str_mv | 10.1016/j.alcohol.2011.11.003 |
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A nonhuman primate model of early life stress, social impoverishment through nursery-rearing rather than mother-rearing, has been shown to produce increased impulsive and anxiety-like behaviors, cognitive and motor deficits, and increased alcohol consumption. These behavioral changes have been linked to changes in cerebrospinal fluid (CSF) levels of 5-hydroxyindoleacetic acid (5-HIAA), a serotonin (5-HT) metabolite. The effects of different rearing conditions on ethanol drinking and three measures of 5-HT function in the central nervous system were evaluated, including CSF 5-HIAA levels and tissue levels of 5-HT and 5-HIAA in brain samples. Brain samples were taken from the dorsal caudate, putamen, substantia nigra (SN) pars reticulata, SN pars compacta and hippocampus. There was a clear effect of rearing condition on the 5-HT system. Overall 5-HIAA and 5-HIAA/5-HT ratio measures of 5-HT turnover were significantly lower in nursery reared compared to mother-reared animals. In addition, there was a strong within-subject correlation between CSF and brain tissue 5-HIAA levels. Ethanol drinking was greater in nursery reared monkeys, consistent with previous results. These findings show that CSF 5-HIAA measurements can be used to predict brain 5-HT activity that may be involved in behavioral outcomes such as anxiety and alcohol consumption. Thus, CSF sampling may provide a minimally invasive test for neurochemical risk factors related to alcohol abuse.</description><identifier>ISSN: 0741-8329</identifier><identifier>EISSN: 1873-6823</identifier><identifier>DOI: 10.1016/j.alcohol.2011.11.003</identifier><identifier>PMID: 22445804</identifier><identifier>CODEN: ALCOEX</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alcohol Drinking - cerebrospinal fluid ; Alcohol Drinking - metabolism ; Alcohol use ; Alcoholism ; Analysis of Variance ; Animals ; Behavior ; Brain ; Brain - metabolism ; Caudate ; Chromatography ; Disease Models, Animal ; Ethanol ; Ethanol - pharmacology ; Fluids ; Hippocampus ; Hydroxyindoleacetic Acid - cerebrospinal fluid ; Hydroxyindoleacetic Acid - metabolism ; Macaca mulatta ; Male ; Maternal Deprivation ; Metabolite ; Metabolites ; Monkeys & apes ; Primates ; Psychiatry ; Putamen ; Serotonin ; Serotonin - metabolism ; Stress ; Studies ; Substantia nigra ; Tissue content</subject><ispartof>Alcohol (Fayetteville, N.Y.), 2012-06, Vol.46 (4), p.371-376</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><rights>2012 Elsevier Inc. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c583t-108280904ee707c859d2d8b74c1a8b5c648d8da031eb95b123a86242a31fe2683</citedby><cites>FETCH-LOGICAL-c583t-108280904ee707c859d2d8b74c1a8b5c648d8da031eb95b123a86242a31fe2683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1027214324/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1027214324?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,780,784,885,21376,21394,27924,27925,33611,33612,33769,33770,43733,43814,74221,74310</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22445804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huggins, Kimberly N</creatorcontrib><creatorcontrib>Mathews, Tiffany A</creatorcontrib><creatorcontrib>Locke, Jason L</creatorcontrib><creatorcontrib>Szeliga, Kendall T</creatorcontrib><creatorcontrib>Friedman, David P</creatorcontrib><creatorcontrib>Bennett, Allyson J</creatorcontrib><creatorcontrib>Jones, Sara R</creatorcontrib><title>Effects of early life stress on drinking and serotonin system activity in rhesus macaques: 5-hydroxyindoleacetic acid in cerebrospinal fluid predicts brain tissue levels</title><title>Alcohol (Fayetteville, N.Y.)</title><addtitle>Alcohol</addtitle><description>Abstract Early childhood stress is a risk factor for the development of substance-abuse disorders. A nonhuman primate model of early life stress, social impoverishment through nursery-rearing rather than mother-rearing, has been shown to produce increased impulsive and anxiety-like behaviors, cognitive and motor deficits, and increased alcohol consumption. These behavioral changes have been linked to changes in cerebrospinal fluid (CSF) levels of 5-hydroxyindoleacetic acid (5-HIAA), a serotonin (5-HT) metabolite. The effects of different rearing conditions on ethanol drinking and three measures of 5-HT function in the central nervous system were evaluated, including CSF 5-HIAA levels and tissue levels of 5-HT and 5-HIAA in brain samples. Brain samples were taken from the dorsal caudate, putamen, substantia nigra (SN) pars reticulata, SN pars compacta and hippocampus. There was a clear effect of rearing condition on the 5-HT system. Overall 5-HIAA and 5-HIAA/5-HT ratio measures of 5-HT turnover were significantly lower in nursery reared compared to mother-reared animals. In addition, there was a strong within-subject correlation between CSF and brain tissue 5-HIAA levels. Ethanol drinking was greater in nursery reared monkeys, consistent with previous results. These findings show that CSF 5-HIAA measurements can be used to predict brain 5-HT activity that may be involved in behavioral outcomes such as anxiety and alcohol consumption. Thus, CSF sampling may provide a minimally invasive test for neurochemical risk factors related to alcohol abuse.</description><subject>Alcohol Drinking - cerebrospinal fluid</subject><subject>Alcohol Drinking - metabolism</subject><subject>Alcohol use</subject><subject>Alcoholism</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Behavior</subject><subject>Brain</subject><subject>Brain - metabolism</subject><subject>Caudate</subject><subject>Chromatography</subject><subject>Disease Models, Animal</subject><subject>Ethanol</subject><subject>Ethanol - pharmacology</subject><subject>Fluids</subject><subject>Hippocampus</subject><subject>Hydroxyindoleacetic Acid - cerebrospinal fluid</subject><subject>Hydroxyindoleacetic Acid - metabolism</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>Maternal Deprivation</subject><subject>Metabolite</subject><subject>Metabolites</subject><subject>Monkeys & apes</subject><subject>Primates</subject><subject>Psychiatry</subject><subject>Putamen</subject><subject>Serotonin</subject><subject>Serotonin - metabolism</subject><subject>Stress</subject><subject>Studies</subject><subject>Substantia nigra</subject><subject>Tissue 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A nonhuman primate model of early life stress, social impoverishment through nursery-rearing rather than mother-rearing, has been shown to produce increased impulsive and anxiety-like behaviors, cognitive and motor deficits, and increased alcohol consumption. These behavioral changes have been linked to changes in cerebrospinal fluid (CSF) levels of 5-hydroxyindoleacetic acid (5-HIAA), a serotonin (5-HT) metabolite. The effects of different rearing conditions on ethanol drinking and three measures of 5-HT function in the central nervous system were evaluated, including CSF 5-HIAA levels and tissue levels of 5-HT and 5-HIAA in brain samples. Brain samples were taken from the dorsal caudate, putamen, substantia nigra (SN) pars reticulata, SN pars compacta and hippocampus. There was a clear effect of rearing condition on the 5-HT system. Overall 5-HIAA and 5-HIAA/5-HT ratio measures of 5-HT turnover were significantly lower in nursery reared compared to mother-reared animals. In addition, there was a strong within-subject correlation between CSF and brain tissue 5-HIAA levels. Ethanol drinking was greater in nursery reared monkeys, consistent with previous results. These findings show that CSF 5-HIAA measurements can be used to predict brain 5-HT activity that may be involved in behavioral outcomes such as anxiety and alcohol consumption. Thus, CSF sampling may provide a minimally invasive test for neurochemical risk factors related to alcohol abuse.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22445804</pmid><doi>10.1016/j.alcohol.2011.11.003</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Drinking - cerebrospinal fluid Alcohol Drinking - metabolism Alcohol use Alcoholism Analysis of Variance Animals Behavior Brain Brain - metabolism Caudate Chromatography Disease Models, Animal Ethanol Ethanol - pharmacology Fluids Hippocampus Hydroxyindoleacetic Acid - cerebrospinal fluid Hydroxyindoleacetic Acid - metabolism Macaca mulatta Male Maternal Deprivation Metabolite Metabolites Monkeys & apes Primates Psychiatry Putamen Serotonin Serotonin - metabolism Stress Studies Substantia nigra Tissue content |
title | Effects of early life stress on drinking and serotonin system activity in rhesus macaques: 5-hydroxyindoleacetic acid in cerebrospinal fluid predicts brain tissue levels |
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