Loading…
A Dietary Ketone Ester Normalizes Abnormal Behavior in a Mouse Model of Alzheimer's Disease
Because of a decreased sensitivity toward insulin, a key regulator of pyruvate dehydrogenase (PDH), Alzheimer's patients have lower brain glucose utilization with reductions in Tricarboxylic Acid (TCA) cycle metabolites such as citrate, a precursor to n-acetyl-aspartate. In the 3xTgAd mouse mod...
Saved in:
Published in: | International journal of molecular sciences 2020-02, Vol.21 (3), p.1044 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883 |
---|---|
cites | cdi_FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883 |
container_end_page | |
container_issue | 3 |
container_start_page | 1044 |
container_title | International journal of molecular sciences |
container_volume | 21 |
creator | Pawlosky, Robert J Kashiwaya, Yoshihero King, M Todd Veech, Richard L |
description | Because of a decreased sensitivity toward insulin, a key regulator of pyruvate dehydrogenase (PDH), Alzheimer's patients have lower brain glucose utilization with reductions in Tricarboxylic Acid (TCA) cycle metabolites such as citrate, a precursor to n-acetyl-aspartate. In the 3xTgAd mouse model of Alzheimer's disease (AD), aging mice also demonstrate low brain glucose metabolism. Ketone metabolism can overcome PDH inhibition and restore TCA cycle metabolites, thereby enhancing amino acid biosynthesis. A ketone ester of d-β-hydroxybutyrate was incorporated into a diet (Ket) and fed to 3xTgAd mice. A control group was fed a calorically matched diet (Cho). At 15 months of age, the exploratory and avoidance-related behavior patterns of the mice were evaluated. At 16.5 months of age, the animals were euthanized, and their hippocampi were analyzed for citrate, α-ketoglutarate, and amino acids. In the hippocampi of the Ket-fed mice, there were higher concentrations of citrate and α-ketoglutarate as well as higher concentrations of glutamate, aspartate and n-acetyl-aspartate compared with controls. There were positive associations between (1) concentrations of aspartate and n-acetyl-aspartate (n = 14, R = 0.9327), and (2) α-ketoglutarate and glutamate (n = 14, R = 0.8521) in animals maintained on either diet. Hippocampal n-acetyl-aspartate predicted the outcome of several exploratory and avoidance-related behaviors. Ketosis restored citrate and α-ketoglutarate in the hippocampi of aging mice. Higher concentrations of n-acetyl-aspartate corresponded with greater exploratory activity and reduced avoidance-related behavior. |
doi_str_mv | 10.3390/ijms21031044 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7036949</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2352643561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883</originalsourceid><addsrcrecordid>eNpdkTtPwzAURi0EoqWwMSNLDDBQ8CuvBamU8hAFFpgYLCe5oa6SuNhJJfrrMbRUhcX2lY8-3aMPoUNKzjlPyIWeVo5RwikRYgt1qWCsT0gYbW-8O2jPuSkhjLMg2UUdzgjnTMRd9DbA1xoaZT_xAzSmBjxyDVj8ZGylSr0Ahwdp_TPgK5iouTYW6xor_GhaB_7MocSmwINyMQFdgT1xPtGBcrCPdgpVOjhY3T30ejN6Gd71x8-398PBuJ8Jypp-lBc8TlmesbCAJAAaqoJFQIss5SIORUKpKIiiXLGAREJ4MMtTmvHY-0dxzHvocpk7a9MK8gzqxqpSzqyuvJc0Ssu_P7WeyHczlxHhYSISH3C6CrDmowXXyEq7DMpS1eAtJeMBCwUPQurR43_o1LS29nqSBX7bhIhEeOpsSWXWOGehWC9DifxuTW625vGjTYE1_FsT_wJVMpJa</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2548690494</pqid></control><display><type>article</type><title>A Dietary Ketone Ester Normalizes Abnormal Behavior in a Mouse Model of Alzheimer's Disease</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><creator>Pawlosky, Robert J ; Kashiwaya, Yoshihero ; King, M Todd ; Veech, Richard L</creator><creatorcontrib>Pawlosky, Robert J ; Kashiwaya, Yoshihero ; King, M Todd ; Veech, Richard L</creatorcontrib><description>Because of a decreased sensitivity toward insulin, a key regulator of pyruvate dehydrogenase (PDH), Alzheimer's patients have lower brain glucose utilization with reductions in Tricarboxylic Acid (TCA) cycle metabolites such as citrate, a precursor to n-acetyl-aspartate. In the 3xTgAd mouse model of Alzheimer's disease (AD), aging mice also demonstrate low brain glucose metabolism. Ketone metabolism can overcome PDH inhibition and restore TCA cycle metabolites, thereby enhancing amino acid biosynthesis. A ketone ester of d-β-hydroxybutyrate was incorporated into a diet (Ket) and fed to 3xTgAd mice. A control group was fed a calorically matched diet (Cho). At 15 months of age, the exploratory and avoidance-related behavior patterns of the mice were evaluated. At 16.5 months of age, the animals were euthanized, and their hippocampi were analyzed for citrate, α-ketoglutarate, and amino acids. In the hippocampi of the Ket-fed mice, there were higher concentrations of citrate and α-ketoglutarate as well as higher concentrations of glutamate, aspartate and n-acetyl-aspartate compared with controls. There were positive associations between (1) concentrations of aspartate and n-acetyl-aspartate (n = 14, R = 0.9327), and (2) α-ketoglutarate and glutamate (n = 14, R = 0.8521) in animals maintained on either diet. Hippocampal n-acetyl-aspartate predicted the outcome of several exploratory and avoidance-related behaviors. Ketosis restored citrate and α-ketoglutarate in the hippocampi of aging mice. Higher concentrations of n-acetyl-aspartate corresponded with greater exploratory activity and reduced avoidance-related behavior.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21031044</identifier><identifier>PMID: 32033248</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aging ; Alzheimer's disease ; Amino acids ; Animal cognition ; Animals ; Anxiety ; Avoidance ; Avoidance behavior ; Biomarkers ; Biosynthesis ; Brain ; Citric acid ; Communication ; Diet ; Enzymes ; Exploratory behavior ; Glucose ; Glucose metabolism ; Hippocampus ; Insulin ; Insulin resistance ; Ketoglutaric acid ; Ketones ; Ketosis ; Memory ; Metabolism ; Metabolites ; Pyruvic acid ; Tricarboxylic acid cycle</subject><ispartof>International journal of molecular sciences, 2020-02, Vol.21 (3), p.1044</ispartof><rights>2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883</citedby><cites>FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2548690494/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2548690494?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32033248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pawlosky, Robert J</creatorcontrib><creatorcontrib>Kashiwaya, Yoshihero</creatorcontrib><creatorcontrib>King, M Todd</creatorcontrib><creatorcontrib>Veech, Richard L</creatorcontrib><title>A Dietary Ketone Ester Normalizes Abnormal Behavior in a Mouse Model of Alzheimer's Disease</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Because of a decreased sensitivity toward insulin, a key regulator of pyruvate dehydrogenase (PDH), Alzheimer's patients have lower brain glucose utilization with reductions in Tricarboxylic Acid (TCA) cycle metabolites such as citrate, a precursor to n-acetyl-aspartate. In the 3xTgAd mouse model of Alzheimer's disease (AD), aging mice also demonstrate low brain glucose metabolism. Ketone metabolism can overcome PDH inhibition and restore TCA cycle metabolites, thereby enhancing amino acid biosynthesis. A ketone ester of d-β-hydroxybutyrate was incorporated into a diet (Ket) and fed to 3xTgAd mice. A control group was fed a calorically matched diet (Cho). At 15 months of age, the exploratory and avoidance-related behavior patterns of the mice were evaluated. At 16.5 months of age, the animals were euthanized, and their hippocampi were analyzed for citrate, α-ketoglutarate, and amino acids. In the hippocampi of the Ket-fed mice, there were higher concentrations of citrate and α-ketoglutarate as well as higher concentrations of glutamate, aspartate and n-acetyl-aspartate compared with controls. There were positive associations between (1) concentrations of aspartate and n-acetyl-aspartate (n = 14, R = 0.9327), and (2) α-ketoglutarate and glutamate (n = 14, R = 0.8521) in animals maintained on either diet. Hippocampal n-acetyl-aspartate predicted the outcome of several exploratory and avoidance-related behaviors. Ketosis restored citrate and α-ketoglutarate in the hippocampi of aging mice. Higher concentrations of n-acetyl-aspartate corresponded with greater exploratory activity and reduced avoidance-related behavior.</description><subject>Aging</subject><subject>Alzheimer's disease</subject><subject>Amino acids</subject><subject>Animal cognition</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Avoidance</subject><subject>Avoidance behavior</subject><subject>Biomarkers</subject><subject>Biosynthesis</subject><subject>Brain</subject><subject>Citric acid</subject><subject>Communication</subject><subject>Diet</subject><subject>Enzymes</subject><subject>Exploratory behavior</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Hippocampus</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Ketoglutaric acid</subject><subject>Ketones</subject><subject>Ketosis</subject><subject>Memory</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Pyruvic acid</subject><subject>Tricarboxylic acid cycle</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkTtPwzAURi0EoqWwMSNLDDBQ8CuvBamU8hAFFpgYLCe5oa6SuNhJJfrrMbRUhcX2lY8-3aMPoUNKzjlPyIWeVo5RwikRYgt1qWCsT0gYbW-8O2jPuSkhjLMg2UUdzgjnTMRd9DbA1xoaZT_xAzSmBjxyDVj8ZGylSr0Ahwdp_TPgK5iouTYW6xor_GhaB_7MocSmwINyMQFdgT1xPtGBcrCPdgpVOjhY3T30ejN6Gd71x8-398PBuJ8Jypp-lBc8TlmesbCAJAAaqoJFQIss5SIORUKpKIiiXLGAREJ4MMtTmvHY-0dxzHvocpk7a9MK8gzqxqpSzqyuvJc0Ssu_P7WeyHczlxHhYSISH3C6CrDmowXXyEq7DMpS1eAtJeMBCwUPQurR43_o1LS29nqSBX7bhIhEeOpsSWXWOGehWC9DifxuTW625vGjTYE1_FsT_wJVMpJa</recordid><startdate>20200204</startdate><enddate>20200204</enddate><creator>Pawlosky, Robert J</creator><creator>Kashiwaya, Yoshihero</creator><creator>King, M Todd</creator><creator>Veech, Richard L</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200204</creationdate><title>A Dietary Ketone Ester Normalizes Abnormal Behavior in a Mouse Model of Alzheimer's Disease</title><author>Pawlosky, Robert J ; Kashiwaya, Yoshihero ; King, M Todd ; Veech, Richard L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aging</topic><topic>Alzheimer's disease</topic><topic>Amino acids</topic><topic>Animal cognition</topic><topic>Animals</topic><topic>Anxiety</topic><topic>Avoidance</topic><topic>Avoidance behavior</topic><topic>Biomarkers</topic><topic>Biosynthesis</topic><topic>Brain</topic><topic>Citric acid</topic><topic>Communication</topic><topic>Diet</topic><topic>Enzymes</topic><topic>Exploratory behavior</topic><topic>Glucose</topic><topic>Glucose metabolism</topic><topic>Hippocampus</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Ketoglutaric acid</topic><topic>Ketones</topic><topic>Ketosis</topic><topic>Memory</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Pyruvic acid</topic><topic>Tricarboxylic acid cycle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pawlosky, Robert J</creatorcontrib><creatorcontrib>Kashiwaya, Yoshihero</creatorcontrib><creatorcontrib>King, M Todd</creatorcontrib><creatorcontrib>Veech, Richard L</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pawlosky, Robert J</au><au>Kashiwaya, Yoshihero</au><au>King, M Todd</au><au>Veech, Richard L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Dietary Ketone Ester Normalizes Abnormal Behavior in a Mouse Model of Alzheimer's Disease</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2020-02-04</date><risdate>2020</risdate><volume>21</volume><issue>3</issue><spage>1044</spage><pages>1044-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Because of a decreased sensitivity toward insulin, a key regulator of pyruvate dehydrogenase (PDH), Alzheimer's patients have lower brain glucose utilization with reductions in Tricarboxylic Acid (TCA) cycle metabolites such as citrate, a precursor to n-acetyl-aspartate. In the 3xTgAd mouse model of Alzheimer's disease (AD), aging mice also demonstrate low brain glucose metabolism. Ketone metabolism can overcome PDH inhibition and restore TCA cycle metabolites, thereby enhancing amino acid biosynthesis. A ketone ester of d-β-hydroxybutyrate was incorporated into a diet (Ket) and fed to 3xTgAd mice. A control group was fed a calorically matched diet (Cho). At 15 months of age, the exploratory and avoidance-related behavior patterns of the mice were evaluated. At 16.5 months of age, the animals were euthanized, and their hippocampi were analyzed for citrate, α-ketoglutarate, and amino acids. In the hippocampi of the Ket-fed mice, there were higher concentrations of citrate and α-ketoglutarate as well as higher concentrations of glutamate, aspartate and n-acetyl-aspartate compared with controls. There were positive associations between (1) concentrations of aspartate and n-acetyl-aspartate (n = 14, R = 0.9327), and (2) α-ketoglutarate and glutamate (n = 14, R = 0.8521) in animals maintained on either diet. Hippocampal n-acetyl-aspartate predicted the outcome of several exploratory and avoidance-related behaviors. Ketosis restored citrate and α-ketoglutarate in the hippocampi of aging mice. Higher concentrations of n-acetyl-aspartate corresponded with greater exploratory activity and reduced avoidance-related behavior.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>32033248</pmid><doi>10.3390/ijms21031044</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2020-02, Vol.21 (3), p.1044 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7036949 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Aging Alzheimer's disease Amino acids Animal cognition Animals Anxiety Avoidance Avoidance behavior Biomarkers Biosynthesis Brain Citric acid Communication Diet Enzymes Exploratory behavior Glucose Glucose metabolism Hippocampus Insulin Insulin resistance Ketoglutaric acid Ketones Ketosis Memory Metabolism Metabolites Pyruvic acid Tricarboxylic acid cycle |
title | A Dietary Ketone Ester Normalizes Abnormal Behavior in a Mouse Model of Alzheimer's Disease |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T17%3A54%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Dietary%20Ketone%20Ester%20Normalizes%20Abnormal%20Behavior%20in%20a%20Mouse%20Model%20of%20Alzheimer's%20Disease&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Pawlosky,%20Robert%20J&rft.date=2020-02-04&rft.volume=21&rft.issue=3&rft.spage=1044&rft.pages=1044-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms21031044&rft_dat=%3Cproquest_pubme%3E2352643561%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c412t-7df38b2dc26fe95e16af27e1fcb348649114f0a13a250744dc2cdb1c383397883%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2548690494&rft_id=info:pmid/32033248&rfr_iscdi=true |