Reducing brain Aβ burden ameliorates high-fat diet-induced fatty liver disease in APP/PS1 mice
High-fat diet (HFD)-induced fatty liver disease is a deteriorating risk factor for Alzheimer’s disease (AD). Mitigating fatty liver disease has been shown to attenuate AD-like pathology in animal models. However, it remains unclear whether enhancing Aβ clearance through immunotherapy would in turn a...
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Veröffentlicht in: | Biomedicine & pharmacotherapy 2024-04, Vol.173, p.116404-116404, Article 116404 |
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creator | Tsay, Huey-Jen Gan, Yu-Ling Su, Yu-Han Sun, Yu-Yo Yao, Heng-Hsiang Chen, Hui-Wen Hsu, Ying-Ting Hsu, John Tsu-An Wang, Horng-Dar Shie, Feng-Shiun |
description | High-fat diet (HFD)-induced fatty liver disease is a deteriorating risk factor for Alzheimer’s disease (AD). Mitigating fatty liver disease has been shown to attenuate AD-like pathology in animal models. However, it remains unclear whether enhancing Aβ clearance through immunotherapy would in turn attenuate HFD-induced fatty liver or whether its efficacy would be compromised by long-term exposure to HFD. Here, the therapeutic potentials of an anti-Aβ antibody, NP106, was investigated in APP/PS1 mice by HFD feeding for 44 weeks. The data demonstrate that NP106 treatment effectively reduced Aβ burden and pro-inflammatory cytokines in HFD-fed APP/PS1 mice and ameliorated HFD-aggravated cognitive impairments during the final 18 weeks of the study. The rejuvenating characteristics of microglia were evident in APP/PS1 mice with NP106 treatment, namely enhanced microglial Aβ phagocytosis and attenuated microglial lipid accumulation, which may explain the benefits of NP106. Surprisingly, NP106 also reduced HFD-induced hyperglycemia, fatty liver, liver fibrosis, and hepatic lipids, concomitant with modifications in the expressions of genes involved in hepatic lipogenesis and fatty acid oxidation. The data further reveal that brain Aβ burden and behavioral deficits were positively correlated with the severity of fatty liver disease and fasting serum glucose levels. In conclusion, our study shows for the first time that anti-Aβ immunotherapy using NP106, which alleviates AD-like disorders in APP/PS1 mice, ameliorates fatty liver disease. Minimizing AD-related pathology and symptoms may reduce the vicious interplay between central AD and peripheral fatty liver disease, thereby highlighting the importance of developing AD therapies from a systemic disease perspective.
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•NP106 treatment showed multiple therapeutic benefits in HFD-fed APP/PS1 mice.•Reducing AD-like pathology and symptoms attenuated HFD-induced fatty liver disease.•Brain disorders were positively correlated with indications of fatty liver disease. |
doi_str_mv | 10.1016/j.biopha.2024.116404 |
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[Display omitted]
•NP106 treatment showed multiple therapeutic benefits in HFD-fed APP/PS1 mice.•Reducing AD-like pathology and symptoms attenuated HFD-induced fatty liver disease.•Brain disorders were positively correlated with indications of fatty liver disease.</description><identifier>ISSN: 0753-3322</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2024.116404</identifier><identifier>PMID: 38471275</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Alzheimer Disease - metabolism ; Alzheimer’s disease ; Amyloid beta-Peptides - metabolism ; Amyloid beta-Protein Precursor - metabolism ; Animals ; Anti-Aβ antibody ; Brain - metabolism ; Diet, High-Fat - adverse effects ; Disease Models, Animal ; Fatty liver ; Fatty Liver - metabolism ; High-fat diet ; Liver Diseases - metabolism ; Mice ; Mice, Transgenic ; Microglial phagocytosis</subject><ispartof>Biomedicine & pharmacotherapy, 2024-04, Vol.173, p.116404-116404, Article 116404</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c357t-db7c45ec05c1192febf4f841a48ec701bb8b7e47cc9073f4056e8a64e9624c583</cites><orcidid>0000-0002-6608-1347 ; 0000-0001-9570-3611 ; 0000-0002-5774-6538</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0753332224002889$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38471275$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsay, Huey-Jen</creatorcontrib><creatorcontrib>Gan, Yu-Ling</creatorcontrib><creatorcontrib>Su, Yu-Han</creatorcontrib><creatorcontrib>Sun, Yu-Yo</creatorcontrib><creatorcontrib>Yao, Heng-Hsiang</creatorcontrib><creatorcontrib>Chen, Hui-Wen</creatorcontrib><creatorcontrib>Hsu, Ying-Ting</creatorcontrib><creatorcontrib>Hsu, John Tsu-An</creatorcontrib><creatorcontrib>Wang, Horng-Dar</creatorcontrib><creatorcontrib>Shie, Feng-Shiun</creatorcontrib><title>Reducing brain Aβ burden ameliorates high-fat diet-induced fatty liver disease in APP/PS1 mice</title><title>Biomedicine & pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>High-fat diet (HFD)-induced fatty liver disease is a deteriorating risk factor for Alzheimer’s disease (AD). Mitigating fatty liver disease has been shown to attenuate AD-like pathology in animal models. However, it remains unclear whether enhancing Aβ clearance through immunotherapy would in turn attenuate HFD-induced fatty liver or whether its efficacy would be compromised by long-term exposure to HFD. Here, the therapeutic potentials of an anti-Aβ antibody, NP106, was investigated in APP/PS1 mice by HFD feeding for 44 weeks. The data demonstrate that NP106 treatment effectively reduced Aβ burden and pro-inflammatory cytokines in HFD-fed APP/PS1 mice and ameliorated HFD-aggravated cognitive impairments during the final 18 weeks of the study. The rejuvenating characteristics of microglia were evident in APP/PS1 mice with NP106 treatment, namely enhanced microglial Aβ phagocytosis and attenuated microglial lipid accumulation, which may explain the benefits of NP106. Surprisingly, NP106 also reduced HFD-induced hyperglycemia, fatty liver, liver fibrosis, and hepatic lipids, concomitant with modifications in the expressions of genes involved in hepatic lipogenesis and fatty acid oxidation. The data further reveal that brain Aβ burden and behavioral deficits were positively correlated with the severity of fatty liver disease and fasting serum glucose levels. In conclusion, our study shows for the first time that anti-Aβ immunotherapy using NP106, which alleviates AD-like disorders in APP/PS1 mice, ameliorates fatty liver disease. Minimizing AD-related pathology and symptoms may reduce the vicious interplay between central AD and peripheral fatty liver disease, thereby highlighting the importance of developing AD therapies from a systemic disease perspective.
[Display omitted]
•NP106 treatment showed multiple therapeutic benefits in HFD-fed APP/PS1 mice.•Reducing AD-like pathology and symptoms attenuated HFD-induced fatty liver disease.•Brain disorders were positively correlated with indications of fatty liver disease.</description><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer’s disease</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Amyloid beta-Protein Precursor - metabolism</subject><subject>Animals</subject><subject>Anti-Aβ antibody</subject><subject>Brain - metabolism</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Fatty liver</subject><subject>Fatty Liver - metabolism</subject><subject>High-fat diet</subject><subject>Liver Diseases - metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Microglial phagocytosis</subject><issn>0753-3322</issn><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMlKBDEURYMo2g5_IJKlm2qTqky1EUScQLBxWIck9cpOU0ObVAn-lh_iN5mm1KWrB-_dex_3IHRMyZwSKs5Wc-v79dLMc5KzOaWCEbaFZrTkJBOEyG00I5IXWVHk-R7aj3FFCOGiULtor1BM0lzyGdKPUI3Od6_YBuM7fPH1ie0YKuiwaaHxfTADRLz0r8usNgOuPAyZ75IHKpwWwwdu_DuEdIhgIuBNxmJxtniiuPUODtFObZoIRz_zAL1cXz1f3mb3Dzd3lxf3mSu4HLLKSsc4OMIdpWVeg61ZrRg1TIGThFqrrAQmnSuJLGqWioAygkEpcua4Kg7Q6ZS7Dv3bCHHQrY8OmsZ00I9R5yUXQnElRZKySepCH2OAWq-Db0340JToDVq90hNavUGrJ7TJdvLzYbQtVH-mX5ZJcD4JIPV89xB0dB66BMoHcIOuev__h28Tfov0</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Tsay, Huey-Jen</creator><creator>Gan, Yu-Ling</creator><creator>Su, Yu-Han</creator><creator>Sun, Yu-Yo</creator><creator>Yao, Heng-Hsiang</creator><creator>Chen, Hui-Wen</creator><creator>Hsu, Ying-Ting</creator><creator>Hsu, John Tsu-An</creator><creator>Wang, Horng-Dar</creator><creator>Shie, Feng-Shiun</creator><general>Elsevier Masson SAS</general><scope>6I.</scope><scope>AAFTH</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><orcidid>https://orcid.org/0000-0002-6608-1347</orcidid><orcidid>https://orcid.org/0000-0001-9570-3611</orcidid><orcidid>https://orcid.org/0000-0002-5774-6538</orcidid></search><sort><creationdate>202404</creationdate><title>Reducing brain Aβ burden ameliorates high-fat diet-induced fatty liver disease in APP/PS1 mice</title><author>Tsay, Huey-Jen ; Gan, Yu-Ling ; Su, Yu-Han ; Sun, Yu-Yo ; Yao, Heng-Hsiang ; Chen, Hui-Wen ; Hsu, Ying-Ting ; Hsu, John Tsu-An ; Wang, Horng-Dar ; Shie, Feng-Shiun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-db7c45ec05c1192febf4f841a48ec701bb8b7e47cc9073f4056e8a64e9624c583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer’s disease</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Amyloid beta-Protein Precursor - metabolism</topic><topic>Animals</topic><topic>Anti-Aβ antibody</topic><topic>Brain - metabolism</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Fatty liver</topic><topic>Fatty Liver - metabolism</topic><topic>High-fat diet</topic><topic>Liver Diseases - metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Microglial phagocytosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsay, Huey-Jen</creatorcontrib><creatorcontrib>Gan, Yu-Ling</creatorcontrib><creatorcontrib>Su, Yu-Han</creatorcontrib><creatorcontrib>Sun, Yu-Yo</creatorcontrib><creatorcontrib>Yao, Heng-Hsiang</creatorcontrib><creatorcontrib>Chen, Hui-Wen</creatorcontrib><creatorcontrib>Hsu, Ying-Ting</creatorcontrib><creatorcontrib>Hsu, John Tsu-An</creatorcontrib><creatorcontrib>Wang, Horng-Dar</creatorcontrib><creatorcontrib>Shie, Feng-Shiun</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Biomedicine & pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsay, Huey-Jen</au><au>Gan, Yu-Ling</au><au>Su, Yu-Han</au><au>Sun, Yu-Yo</au><au>Yao, Heng-Hsiang</au><au>Chen, Hui-Wen</au><au>Hsu, Ying-Ting</au><au>Hsu, John Tsu-An</au><au>Wang, Horng-Dar</au><au>Shie, Feng-Shiun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reducing brain Aβ burden ameliorates high-fat diet-induced fatty liver disease in APP/PS1 mice</atitle><jtitle>Biomedicine & pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2024-04</date><risdate>2024</risdate><volume>173</volume><spage>116404</spage><epage>116404</epage><pages>116404-116404</pages><artnum>116404</artnum><issn>0753-3322</issn><eissn>1950-6007</eissn><abstract>High-fat diet (HFD)-induced fatty liver disease is a deteriorating risk factor for Alzheimer’s disease (AD). Mitigating fatty liver disease has been shown to attenuate AD-like pathology in animal models. However, it remains unclear whether enhancing Aβ clearance through immunotherapy would in turn attenuate HFD-induced fatty liver or whether its efficacy would be compromised by long-term exposure to HFD. Here, the therapeutic potentials of an anti-Aβ antibody, NP106, was investigated in APP/PS1 mice by HFD feeding for 44 weeks. The data demonstrate that NP106 treatment effectively reduced Aβ burden and pro-inflammatory cytokines in HFD-fed APP/PS1 mice and ameliorated HFD-aggravated cognitive impairments during the final 18 weeks of the study. The rejuvenating characteristics of microglia were evident in APP/PS1 mice with NP106 treatment, namely enhanced microglial Aβ phagocytosis and attenuated microglial lipid accumulation, which may explain the benefits of NP106. Surprisingly, NP106 also reduced HFD-induced hyperglycemia, fatty liver, liver fibrosis, and hepatic lipids, concomitant with modifications in the expressions of genes involved in hepatic lipogenesis and fatty acid oxidation. The data further reveal that brain Aβ burden and behavioral deficits were positively correlated with the severity of fatty liver disease and fasting serum glucose levels. In conclusion, our study shows for the first time that anti-Aβ immunotherapy using NP106, which alleviates AD-like disorders in APP/PS1 mice, ameliorates fatty liver disease. Minimizing AD-related pathology and symptoms may reduce the vicious interplay between central AD and peripheral fatty liver disease, thereby highlighting the importance of developing AD therapies from a systemic disease perspective.
[Display omitted]
•NP106 treatment showed multiple therapeutic benefits in HFD-fed APP/PS1 mice.•Reducing AD-like pathology and symptoms attenuated HFD-induced fatty liver disease.•Brain disorders were positively correlated with indications of fatty liver disease.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>38471275</pmid><doi>10.1016/j.biopha.2024.116404</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-6608-1347</orcidid><orcidid>https://orcid.org/0000-0001-9570-3611</orcidid><orcidid>https://orcid.org/0000-0002-5774-6538</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - metabolism Alzheimer’s disease Amyloid beta-Peptides - metabolism Amyloid beta-Protein Precursor - metabolism Animals Anti-Aβ antibody Brain - metabolism Diet, High-Fat - adverse effects Disease Models, Animal Fatty liver Fatty Liver - metabolism High-fat diet Liver Diseases - metabolism Mice Mice, Transgenic Microglial phagocytosis |
title | Reducing brain Aβ burden ameliorates high-fat diet-induced fatty liver disease in APP/PS1 mice |
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