Alcohol‐induced cognitive deficits are associated with decreased circulating levels of the neurotrophin BDNF in humans and rats
Chronic alcohol consumption is associated with neurocognitive and memory deficits, dramatically affecting plasticity and connectivity, with maximal expression as dementia. Neurotrophic factors may contribute to alcohol‐related cognitive decline. For further investigation, a cross‐sectional study was...
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Veröffentlicht in: | Addiction biology 2019-09, Vol.24 (5), p.1019-1033 |
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creator | Silva‐Peña, Daniel García‐Marchena, Nuria Alén, Francisco Araos, Pedro Rivera, Patricia Vargas, Antonio García‐Fernández, María Inmaculada Martín‐Velasco, Ana Isabel Villanúa, María Ángeles Castilla‐Ortega, Estela Santín, Luis Pavón, Francisco Javier Serrano, Antonia Rubio, Gabriel Rodríguez de Fonseca, Fernando Suárez, Juan |
description | Chronic alcohol consumption is associated with neurocognitive and memory deficits, dramatically affecting plasticity and connectivity, with maximal expression as dementia. Neurotrophic factors may contribute to alcohol‐related cognitive decline. For further investigation, a cross‐sectional study was performed to evaluate the association of cognitive impairment, by using frontal assessment battery, and memory loss, using memory failures everyday, with the circulating levels of the neurotrophin brain‐derived neurotrophic factor (BDNF) and neurotrophin 3 (NT‐3) in abstinent subjects with alcohol use disorders (AUDs, N = 58, average of 17.9 years of problematic use and 4.3 months of abstinence) compared with healthy control subjects (N = 22). This association was also explored in a pre‐clinical model of adolescent rats chronically exposed to alcohol up to adulthood (~77 days old) in a three‐bottle free‐choice (5–10–20 percent), repeated abstinence and relapse paradigm. AUD subjects had low educational level and cognitive impairment associated with teenage consumption and lower circulating levels of BDNF and NT‐3. Only BDNF concentration showed a positive correlation with frontal assessment battery in AUD patients. In the ethanol‐exposed rats, the plasma levels of BDNF and NT‐3 were also decreased, and a negative correlation between hippocampal Bdnf mRNA levels and recognition memory was found. The ethanol‐exposed rat hippocampus showed a decrease in the mRNA levels of neurotrophic (Bdnf and Ntf‐3) and neurogenic (Mki67, Sox2, Dcx, Ncam1 and Calb1) factors, associated to a deactivation of the neurogenic regulator mitogen‐activated protein kinase extracellular signal‐regulated kinase. Results suggest a relevant role of BDNF/extracellular signal‐regulated kinase 2 signaling in alcohol‐induced cognitive impairment and suggest that early alcohol exposure‐derived effects on cognition are associated with neurotrophin signaling deficits.
There was a negative correlation between plasma BDNF and cognition deficit in alcohol patients. Hippocampal Bdnf levels and recognition memory negatively correlated in alcohol‐exposed rats during adolescence, an effect that was associated with a neurogenic regulator ERK2 deactivation. Early alcohol‐induced cognitive decline is related to BDNF signaling deficits. |
doi_str_mv | 10.1111/adb.12668 |
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There was a negative correlation between plasma BDNF and cognition deficit in alcohol patients. Hippocampal Bdnf levels and recognition memory negatively correlated in alcohol‐exposed rats during adolescence, an effect that was associated with a neurogenic regulator ERK2 deactivation. Early alcohol‐induced cognitive decline is related to BDNF signaling deficits.</description><identifier>ISSN: 1355-6215</identifier><identifier>EISSN: 1369-1600</identifier><identifier>DOI: 10.1111/adb.12668</identifier><identifier>PMID: 30277635</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Alcohol ; Brain-derived neurotrophic factor ; Cognition ; Cognitive ability ; Deactivation ; Dementia disorders ; Doublecortin protein ; ERK2 ; Ethanol ; Hippocampus ; Kinases ; Memory ; mRNA ; Neural networks ; Neurotrophic factors ; Neurotrophin 3 ; Plasma levels ; Protein kinase</subject><ispartof>Addiction biology, 2019-09, Vol.24 (5), p.1019-1033</ispartof><rights>2018 Society for the Study of Addiction</rights><rights>2018 Society for the Study of Addiction.</rights><rights>2019 Society for the Study of Addiction</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-ddc8b1addd44cc569f30205e5460476143a92518500245104224a0bb4db84fd83</citedby><cites>FETCH-LOGICAL-c3538-ddc8b1addd44cc569f30205e5460476143a92518500245104224a0bb4db84fd83</cites><orcidid>0000-0002-6436-1361 ; 0000-0002-4496-1167 ; 0000-0001-5254-9802 ; 0000-0002-5256-8904</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fadb.12668$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fadb.12668$$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/30277635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silva‐Peña, Daniel</creatorcontrib><creatorcontrib>García‐Marchena, Nuria</creatorcontrib><creatorcontrib>Alén, Francisco</creatorcontrib><creatorcontrib>Araos, Pedro</creatorcontrib><creatorcontrib>Rivera, Patricia</creatorcontrib><creatorcontrib>Vargas, Antonio</creatorcontrib><creatorcontrib>García‐Fernández, María Inmaculada</creatorcontrib><creatorcontrib>Martín‐Velasco, Ana Isabel</creatorcontrib><creatorcontrib>Villanúa, María Ángeles</creatorcontrib><creatorcontrib>Castilla‐Ortega, Estela</creatorcontrib><creatorcontrib>Santín, Luis</creatorcontrib><creatorcontrib>Pavón, Francisco Javier</creatorcontrib><creatorcontrib>Serrano, Antonia</creatorcontrib><creatorcontrib>Rubio, Gabriel</creatorcontrib><creatorcontrib>Rodríguez de Fonseca, Fernando</creatorcontrib><creatorcontrib>Suárez, Juan</creatorcontrib><title>Alcohol‐induced cognitive deficits are associated with decreased circulating levels of the neurotrophin BDNF in humans and rats</title><title>Addiction biology</title><addtitle>Addict Biol</addtitle><description>Chronic alcohol consumption is associated with neurocognitive and memory deficits, dramatically affecting plasticity and connectivity, with maximal expression as dementia. Neurotrophic factors may contribute to alcohol‐related cognitive decline. For further investigation, a cross‐sectional study was performed to evaluate the association of cognitive impairment, by using frontal assessment battery, and memory loss, using memory failures everyday, with the circulating levels of the neurotrophin brain‐derived neurotrophic factor (BDNF) and neurotrophin 3 (NT‐3) in abstinent subjects with alcohol use disorders (AUDs, N = 58, average of 17.9 years of problematic use and 4.3 months of abstinence) compared with healthy control subjects (N = 22). This association was also explored in a pre‐clinical model of adolescent rats chronically exposed to alcohol up to adulthood (~77 days old) in a three‐bottle free‐choice (5–10–20 percent), repeated abstinence and relapse paradigm. AUD subjects had low educational level and cognitive impairment associated with teenage consumption and lower circulating levels of BDNF and NT‐3. Only BDNF concentration showed a positive correlation with frontal assessment battery in AUD patients. In the ethanol‐exposed rats, the plasma levels of BDNF and NT‐3 were also decreased, and a negative correlation between hippocampal Bdnf mRNA levels and recognition memory was found. The ethanol‐exposed rat hippocampus showed a decrease in the mRNA levels of neurotrophic (Bdnf and Ntf‐3) and neurogenic (Mki67, Sox2, Dcx, Ncam1 and Calb1) factors, associated to a deactivation of the neurogenic regulator mitogen‐activated protein kinase extracellular signal‐regulated kinase. Results suggest a relevant role of BDNF/extracellular signal‐regulated kinase 2 signaling in alcohol‐induced cognitive impairment and suggest that early alcohol exposure‐derived effects on cognition are associated with neurotrophin signaling deficits.
There was a negative correlation between plasma BDNF and cognition deficit in alcohol patients. Hippocampal Bdnf levels and recognition memory negatively correlated in alcohol‐exposed rats during adolescence, an effect that was associated with a neurogenic regulator ERK2 deactivation. Early alcohol‐induced cognitive decline is related to BDNF signaling deficits.</description><subject>Alcohol</subject><subject>Brain-derived neurotrophic factor</subject><subject>Cognition</subject><subject>Cognitive ability</subject><subject>Deactivation</subject><subject>Dementia disorders</subject><subject>Doublecortin protein</subject><subject>ERK2</subject><subject>Ethanol</subject><subject>Hippocampus</subject><subject>Kinases</subject><subject>Memory</subject><subject>mRNA</subject><subject>Neural networks</subject><subject>Neurotrophic factors</subject><subject>Neurotrophin 3</subject><subject>Plasma levels</subject><subject>Protein kinase</subject><issn>1355-6215</issn><issn>1369-1600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kcFuFSEUhomxsbW68AUMiZu6mBYYYGaWt61Vk6ZudE0YONOh4cIVmDbd6Rv4jD6JXG910aRn85-Ejy-QH6E3lBzTOifajseUSdk_Qwe0lUNDJSHPt7sQjWRU7KOXOd8QQlkn2hdovyWs62QrDtDPlTdxjv73j18u2MWAxSZeB1fcLWALkzOuZKwTYJ1zNE6XSty5MtdDk0Dn7QWXzOJ1ceEae7gFn3GccJkBB1hSLCluZhfw6fnVBa45L2sdqjNYnHTJr9DepH2G1w95iL5dfPh69qm5_PLx89nqsjGtaPvGWtOPVFtrOTdGyGGqnyACBJeEd5LyVg9M0F4QwrighDPGNRlHbseeT7ZvD9HRzrtJ8fsCuai1ywa81wHikhWjVHSCiWGo6LtH6E1cUqivU4x1jHLRky31fkeZFHNOMKlNcmud7hUlatuLqr2ov71U9u2DcRnXYP-T_4qowMkOuHMe7p82qdX56U75B6xHl7Q</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Silva‐Peña, Daniel</creator><creator>García‐Marchena, Nuria</creator><creator>Alén, Francisco</creator><creator>Araos, Pedro</creator><creator>Rivera, Patricia</creator><creator>Vargas, Antonio</creator><creator>García‐Fernández, María Inmaculada</creator><creator>Martín‐Velasco, Ana Isabel</creator><creator>Villanúa, María Ángeles</creator><creator>Castilla‐Ortega, Estela</creator><creator>Santín, Luis</creator><creator>Pavón, Francisco Javier</creator><creator>Serrano, Antonia</creator><creator>Rubio, Gabriel</creator><creator>Rodríguez de Fonseca, Fernando</creator><creator>Suárez, Juan</creator><general>John Wiley & Sons, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7T5</scope><scope>7TM</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6436-1361</orcidid><orcidid>https://orcid.org/0000-0002-4496-1167</orcidid><orcidid>https://orcid.org/0000-0001-5254-9802</orcidid><orcidid>https://orcid.org/0000-0002-5256-8904</orcidid></search><sort><creationdate>201909</creationdate><title>Alcohol‐induced cognitive deficits are associated with decreased circulating levels of the neurotrophin BDNF in humans and rats</title><author>Silva‐Peña, Daniel ; García‐Marchena, Nuria ; Alén, Francisco ; Araos, Pedro ; Rivera, Patricia ; Vargas, Antonio ; García‐Fernández, María Inmaculada ; Martín‐Velasco, Ana Isabel ; Villanúa, María Ángeles ; Castilla‐Ortega, Estela ; Santín, Luis ; Pavón, Francisco Javier ; Serrano, Antonia ; Rubio, Gabriel ; Rodríguez de Fonseca, Fernando ; Suárez, Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-ddc8b1addd44cc569f30205e5460476143a92518500245104224a0bb4db84fd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alcohol</topic><topic>Brain-derived neurotrophic factor</topic><topic>Cognition</topic><topic>Cognitive ability</topic><topic>Deactivation</topic><topic>Dementia disorders</topic><topic>Doublecortin protein</topic><topic>ERK2</topic><topic>Ethanol</topic><topic>Hippocampus</topic><topic>Kinases</topic><topic>Memory</topic><topic>mRNA</topic><topic>Neural networks</topic><topic>Neurotrophic factors</topic><topic>Neurotrophin 3</topic><topic>Plasma levels</topic><topic>Protein kinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silva‐Peña, Daniel</creatorcontrib><creatorcontrib>García‐Marchena, Nuria</creatorcontrib><creatorcontrib>Alén, Francisco</creatorcontrib><creatorcontrib>Araos, Pedro</creatorcontrib><creatorcontrib>Rivera, Patricia</creatorcontrib><creatorcontrib>Vargas, Antonio</creatorcontrib><creatorcontrib>García‐Fernández, María Inmaculada</creatorcontrib><creatorcontrib>Martín‐Velasco, Ana Isabel</creatorcontrib><creatorcontrib>Villanúa, María Ángeles</creatorcontrib><creatorcontrib>Castilla‐Ortega, Estela</creatorcontrib><creatorcontrib>Santín, Luis</creatorcontrib><creatorcontrib>Pavón, Francisco Javier</creatorcontrib><creatorcontrib>Serrano, Antonia</creatorcontrib><creatorcontrib>Rubio, Gabriel</creatorcontrib><creatorcontrib>Rodríguez de Fonseca, Fernando</creatorcontrib><creatorcontrib>Suárez, Juan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Addiction biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silva‐Peña, Daniel</au><au>García‐Marchena, Nuria</au><au>Alén, Francisco</au><au>Araos, Pedro</au><au>Rivera, Patricia</au><au>Vargas, Antonio</au><au>García‐Fernández, María Inmaculada</au><au>Martín‐Velasco, Ana Isabel</au><au>Villanúa, María Ángeles</au><au>Castilla‐Ortega, Estela</au><au>Santín, Luis</au><au>Pavón, Francisco Javier</au><au>Serrano, Antonia</au><au>Rubio, Gabriel</au><au>Rodríguez de Fonseca, Fernando</au><au>Suárez, Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alcohol‐induced cognitive deficits are associated with decreased circulating levels of the neurotrophin BDNF in humans and rats</atitle><jtitle>Addiction biology</jtitle><addtitle>Addict Biol</addtitle><date>2019-09</date><risdate>2019</risdate><volume>24</volume><issue>5</issue><spage>1019</spage><epage>1033</epage><pages>1019-1033</pages><issn>1355-6215</issn><eissn>1369-1600</eissn><abstract>Chronic alcohol consumption is associated with neurocognitive and memory deficits, dramatically affecting plasticity and connectivity, with maximal expression as dementia. Neurotrophic factors may contribute to alcohol‐related cognitive decline. For further investigation, a cross‐sectional study was performed to evaluate the association of cognitive impairment, by using frontal assessment battery, and memory loss, using memory failures everyday, with the circulating levels of the neurotrophin brain‐derived neurotrophic factor (BDNF) and neurotrophin 3 (NT‐3) in abstinent subjects with alcohol use disorders (AUDs, N = 58, average of 17.9 years of problematic use and 4.3 months of abstinence) compared with healthy control subjects (N = 22). This association was also explored in a pre‐clinical model of adolescent rats chronically exposed to alcohol up to adulthood (~77 days old) in a three‐bottle free‐choice (5–10–20 percent), repeated abstinence and relapse paradigm. AUD subjects had low educational level and cognitive impairment associated with teenage consumption and lower circulating levels of BDNF and NT‐3. Only BDNF concentration showed a positive correlation with frontal assessment battery in AUD patients. In the ethanol‐exposed rats, the plasma levels of BDNF and NT‐3 were also decreased, and a negative correlation between hippocampal Bdnf mRNA levels and recognition memory was found. The ethanol‐exposed rat hippocampus showed a decrease in the mRNA levels of neurotrophic (Bdnf and Ntf‐3) and neurogenic (Mki67, Sox2, Dcx, Ncam1 and Calb1) factors, associated to a deactivation of the neurogenic regulator mitogen‐activated protein kinase extracellular signal‐regulated kinase. Results suggest a relevant role of BDNF/extracellular signal‐regulated kinase 2 signaling in alcohol‐induced cognitive impairment and suggest that early alcohol exposure‐derived effects on cognition are associated with neurotrophin signaling deficits.
There was a negative correlation between plasma BDNF and cognition deficit in alcohol patients. Hippocampal Bdnf levels and recognition memory negatively correlated in alcohol‐exposed rats during adolescence, an effect that was associated with a neurogenic regulator ERK2 deactivation. Early alcohol‐induced cognitive decline is related to BDNF signaling deficits.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>30277635</pmid><doi>10.1111/adb.12668</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-6436-1361</orcidid><orcidid>https://orcid.org/0000-0002-4496-1167</orcidid><orcidid>https://orcid.org/0000-0001-5254-9802</orcidid><orcidid>https://orcid.org/0000-0002-5256-8904</orcidid></addata></record> |
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subjects | Alcohol Brain-derived neurotrophic factor Cognition Cognitive ability Deactivation Dementia disorders Doublecortin protein ERK2 Ethanol Hippocampus Kinases Memory mRNA Neural networks Neurotrophic factors Neurotrophin 3 Plasma levels Protein kinase |
title | Alcohol‐induced cognitive deficits are associated with decreased circulating levels of the neurotrophin BDNF in humans and rats |
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