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Phosphatidylserine and the human brain
Abstract Objective The aim of this study was to assess the roles and importance of phosphatidylserine (PS), an endogenous phospholipid and dietary nutrient, in human brain biochemistry, physiology, and function. Methods A scientific literature search was conducted on MEDLINE for relevant articles re...
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Published in: | Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2015-06, Vol.31 (6), p.781-786 |
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description | Abstract Objective The aim of this study was to assess the roles and importance of phosphatidylserine (PS), an endogenous phospholipid and dietary nutrient, in human brain biochemistry, physiology, and function. Methods A scientific literature search was conducted on MEDLINE for relevant articles regarding PS and the human brain published before June 2014. Additional publications were identified from references provided in original papers; 127 articles were selected for inclusion in this review. Results A large body of scientific evidence describes the interactions among PS, cognitive activity, cognitive aging, and retention of cognitive functioning ability. Conclusion Phosphatidylserine is required for healthy nerve cell membranes and myelin. Aging of the human brain is associated with biochemical alterations and structural deterioration that impair neurotransmission. Exogenous PS (300–800 mg/d) is absorbed efficiently in humans, crosses the blood–brain barrier, and safely slows, halts, or reverses biochemical alterations and structural deterioration in nerve cells. It supports human cognitive functions, including the formation of short-term memory, the consolidation of long-term memory, the ability to create new memories, the ability to retrieve memories, the ability to learn and recall information, the ability to focus attention and concentrate, the ability to reason and solve problems, language skills, and the ability to communicate. It also supports locomotor functions, especially rapid reactions and reflexes. |
doi_str_mv | 10.1016/j.nut.2014.10.014 |
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Methods A scientific literature search was conducted on MEDLINE for relevant articles regarding PS and the human brain published before June 2014. Additional publications were identified from references provided in original papers; 127 articles were selected for inclusion in this review. Results A large body of scientific evidence describes the interactions among PS, cognitive activity, cognitive aging, and retention of cognitive functioning ability. Conclusion Phosphatidylserine is required for healthy nerve cell membranes and myelin. Aging of the human brain is associated with biochemical alterations and structural deterioration that impair neurotransmission. Exogenous PS (300–800 mg/d) is absorbed efficiently in humans, crosses the blood–brain barrier, and safely slows, halts, or reverses biochemical alterations and structural deterioration in nerve cells. It supports human cognitive functions, including the formation of short-term memory, the consolidation of long-term memory, the ability to create new memories, the ability to retrieve memories, the ability to learn and recall information, the ability to focus attention and concentrate, the ability to reason and solve problems, language skills, and the ability to communicate. It also supports locomotor functions, especially rapid reactions and reflexes.</description><identifier>ISSN: 0899-9007</identifier><identifier>EISSN: 1873-1244</identifier><identifier>DOI: 10.1016/j.nut.2014.10.014</identifier><identifier>PMID: 25933483</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aging ; Aging - drug effects ; Aging - metabolism ; Alzheimer's disease ; Blood-Brain Barrier ; Brain ; Brain - drug effects ; Brain - metabolism ; Cognition ; Cognition Disorders - metabolism ; Cognition Disorders - prevention & control ; Cognitive ability ; Cognitive aging ; Cognitive decline ; Cognitive function ; Dietary Supplements ; Endoplasmic reticulum ; Gastroenterology and Hepatology ; Humans ; Kinases ; Membranes ; Memory - drug effects ; Nervous system ; Neurotransmission ; Phosphatidylserine ; Phosphatidylserines - metabolism ; Phosphatidylserines - pharmacology ; Phosphatidylserines - therapeutic use ; Stress response</subject><ispartof>Nutrition (Burbank, Los Angeles County, Calif.), 2015-06, Vol.31 (6), p.781-786</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Jun 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-f7a03e7dad17c966395f956de25d6e690935cac2cb872a272fab1b9f2f8a16663</citedby><cites>FETCH-LOGICAL-c436t-f7a03e7dad17c966395f956de25d6e690935cac2cb872a272fab1b9f2f8a16663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25933483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Glade, Michael J., Ph.D</creatorcontrib><creatorcontrib>Smith, Kyl, D.C</creatorcontrib><title>Phosphatidylserine and the human brain</title><title>Nutrition (Burbank, Los Angeles County, Calif.)</title><addtitle>Nutrition</addtitle><description>Abstract Objective The aim of this study was to assess the roles and importance of phosphatidylserine (PS), an endogenous phospholipid and dietary nutrient, in human brain biochemistry, physiology, and function. Methods A scientific literature search was conducted on MEDLINE for relevant articles regarding PS and the human brain published before June 2014. Additional publications were identified from references provided in original papers; 127 articles were selected for inclusion in this review. Results A large body of scientific evidence describes the interactions among PS, cognitive activity, cognitive aging, and retention of cognitive functioning ability. Conclusion Phosphatidylserine is required for healthy nerve cell membranes and myelin. Aging of the human brain is associated with biochemical alterations and structural deterioration that impair neurotransmission. Exogenous PS (300–800 mg/d) is absorbed efficiently in humans, crosses the blood–brain barrier, and safely slows, halts, or reverses biochemical alterations and structural deterioration in nerve cells. It supports human cognitive functions, including the formation of short-term memory, the consolidation of long-term memory, the ability to create new memories, the ability to retrieve memories, the ability to learn and recall information, the ability to focus attention and concentrate, the ability to reason and solve problems, language skills, and the ability to communicate. It also supports locomotor functions, especially rapid reactions and reflexes.</description><subject>Aging</subject><subject>Aging - drug effects</subject><subject>Aging - metabolism</subject><subject>Alzheimer's disease</subject><subject>Blood-Brain Barrier</subject><subject>Brain</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Cognition</subject><subject>Cognition Disorders - metabolism</subject><subject>Cognition Disorders - prevention & control</subject><subject>Cognitive ability</subject><subject>Cognitive aging</subject><subject>Cognitive decline</subject><subject>Cognitive function</subject><subject>Dietary Supplements</subject><subject>Endoplasmic reticulum</subject><subject>Gastroenterology and Hepatology</subject><subject>Humans</subject><subject>Kinases</subject><subject>Membranes</subject><subject>Memory - drug effects</subject><subject>Nervous system</subject><subject>Neurotransmission</subject><subject>Phosphatidylserine</subject><subject>Phosphatidylserines - metabolism</subject><subject>Phosphatidylserines - pharmacology</subject><subject>Phosphatidylserines - therapeutic use</subject><subject>Stress response</subject><issn>0899-9007</issn><issn>1873-1244</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kUtLxDAUhYMoOj5-gBsZEMRNxzzapEEQRHzBgIK6Dmlyy2TspGPSCvPvTZlRwYWrQ5LvHHLPReiY4AnBhF_MJ77vJhSTPJ0nSbbQiJSCZYTm-TYa4VLKTGIs9tB-jHOMMZFc7qI9WkjG8pKN0NnzrI3Lme6cXTURgvMw1t6OuxmMZ_1C-3EVtPOHaKfW6f1oowfo7e729eYhmz7dP95cTzOTM95ltdCYgbDaEmEk50wWtSy4BVpYDlxiyQqjDTVVKaimgta6IpWsaV1qwhN_gM7XucvQfvQQO7Vw0UDTaA9tHxXhklJJsRjQ0z_ovO2DT79LVDkMKso8UWRNmdDGGKBWy-AWOqwUwWooUc1VKlENJQ5XSZLnZJPcVwuwP47v1hJwuQYgVfHpIKhoHHgD1gUwnbKt-zf-6o_bNM47o5t3WEH8nUJFqrB6GbY4LJHkGOcFZewL46WU4g</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Glade, Michael J., Ph.D</creator><creator>Smith, Kyl, D.C</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>3V.</scope><scope>7RQ</scope><scope>7RV</scope><scope>7TS</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150601</creationdate><title>Phosphatidylserine and the human brain</title><author>Glade, Michael J., Ph.D ; Smith, Kyl, D.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-f7a03e7dad17c966395f956de25d6e690935cac2cb872a272fab1b9f2f8a16663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aging</topic><topic>Aging - drug effects</topic><topic>Aging - metabolism</topic><topic>Alzheimer's disease</topic><topic>Blood-Brain Barrier</topic><topic>Brain</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Cognition</topic><topic>Cognition Disorders - metabolism</topic><topic>Cognition Disorders - prevention & control</topic><topic>Cognitive ability</topic><topic>Cognitive aging</topic><topic>Cognitive decline</topic><topic>Cognitive function</topic><topic>Dietary Supplements</topic><topic>Endoplasmic reticulum</topic><topic>Gastroenterology and Hepatology</topic><topic>Humans</topic><topic>Kinases</topic><topic>Membranes</topic><topic>Memory - drug effects</topic><topic>Nervous system</topic><topic>Neurotransmission</topic><topic>Phosphatidylserine</topic><topic>Phosphatidylserines - metabolism</topic><topic>Phosphatidylserines - pharmacology</topic><topic>Phosphatidylserines - therapeutic use</topic><topic>Stress response</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Glade, Michael J., Ph.D</creatorcontrib><creatorcontrib>Smith, Kyl, D.C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Career & Technical Education Database</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Glade, Michael J., Ph.D</au><au>Smith, Kyl, D.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phosphatidylserine and the human brain</atitle><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle><addtitle>Nutrition</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>31</volume><issue>6</issue><spage>781</spage><epage>786</epage><pages>781-786</pages><issn>0899-9007</issn><eissn>1873-1244</eissn><abstract>Abstract Objective The aim of this study was to assess the roles and importance of phosphatidylserine (PS), an endogenous phospholipid and dietary nutrient, in human brain biochemistry, physiology, and function. Methods A scientific literature search was conducted on MEDLINE for relevant articles regarding PS and the human brain published before June 2014. Additional publications were identified from references provided in original papers; 127 articles were selected for inclusion in this review. Results A large body of scientific evidence describes the interactions among PS, cognitive activity, cognitive aging, and retention of cognitive functioning ability. Conclusion Phosphatidylserine is required for healthy nerve cell membranes and myelin. Aging of the human brain is associated with biochemical alterations and structural deterioration that impair neurotransmission. Exogenous PS (300–800 mg/d) is absorbed efficiently in humans, crosses the blood–brain barrier, and safely slows, halts, or reverses biochemical alterations and structural deterioration in nerve cells. It supports human cognitive functions, including the formation of short-term memory, the consolidation of long-term memory, the ability to create new memories, the ability to retrieve memories, the ability to learn and recall information, the ability to focus attention and concentrate, the ability to reason and solve problems, language skills, and the ability to communicate. It also supports locomotor functions, especially rapid reactions and reflexes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25933483</pmid><doi>10.1016/j.nut.2014.10.014</doi><tpages>6</tpages></addata></record> |
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subjects | Aging Aging - drug effects Aging - metabolism Alzheimer's disease Blood-Brain Barrier Brain Brain - drug effects Brain - metabolism Cognition Cognition Disorders - metabolism Cognition Disorders - prevention & control Cognitive ability Cognitive aging Cognitive decline Cognitive function Dietary Supplements Endoplasmic reticulum Gastroenterology and Hepatology Humans Kinases Membranes Memory - drug effects Nervous system Neurotransmission Phosphatidylserine Phosphatidylserines - metabolism Phosphatidylserines - pharmacology Phosphatidylserines - therapeutic use Stress response |
title | Phosphatidylserine and the human brain |
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