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A role of sea buckthorn on Alzheimer’s disease
Summary Evidence suggests that diets rich in antioxidants reduce the risk factors of Alzheimer’s disease (AD). Hippophae rhamnoides, commonly known as sea buckthorn (SB), is rich in antioxidants which could have direct effects on amyloid‐beta (Aβ) levels and consequently influence AD pathogenesis. I...
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Published in: | International journal of food science & technology 2020-09, Vol.55 (9), p.3073-3081 |
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creator | Dong, Ke Fernando, Warnakulasuriya M. A. D. Binosha Durham, Rosalie Stockmann, Regine W. Jayatunga, Dona Pamoda Jayasena, Vijay |
description | Summary
Evidence suggests that diets rich in antioxidants reduce the risk factors of Alzheimer’s disease (AD). Hippophae rhamnoides, commonly known as sea buckthorn (SB), is rich in antioxidants which could have direct effects on amyloid‐beta (Aβ) levels and consequently influence AD pathogenesis. In this study, sea buckthorn powder (SBP) was administered at varying concentrations (0.6, 0.9, 1.2, 1.5 and 1.8 µg mL−1) to cell cultures (BE(2)‐M17) with 20 mm Aβ for 72 h. MTS test indicated that SB significantly increased cell viability in Aβ‐induced cells up to 95%. Results of Western blot showed maximum 38% inhibition of Aβ compared to the control (Aβ only). ELISA demonstrated significantly lower amyloid‐β level (6672 pg mL−1) than the control (10189 pg mL−1). Images of AFM further confirmed the presence of low quantity of amyloid beta in SBP‐treated cells. These findings suggest that SB warrants further investigation as potential therapeutic agent in the treatment of AD.
This research has outlined the role of sea buckthorn on Alzheimer’s disease. Significant reduction of amyloid beta concentration was observed in MTS, BCA, Western blot, ELISA and AFM since sea buckthorn powder was treated with cells. |
doi_str_mv | 10.1111/ijfs.14571 |
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Evidence suggests that diets rich in antioxidants reduce the risk factors of Alzheimer’s disease (AD). Hippophae rhamnoides, commonly known as sea buckthorn (SB), is rich in antioxidants which could have direct effects on amyloid‐beta (Aβ) levels and consequently influence AD pathogenesis. In this study, sea buckthorn powder (SBP) was administered at varying concentrations (0.6, 0.9, 1.2, 1.5 and 1.8 µg mL−1) to cell cultures (BE(2)‐M17) with 20 mm Aβ for 72 h. MTS test indicated that SB significantly increased cell viability in Aβ‐induced cells up to 95%. Results of Western blot showed maximum 38% inhibition of Aβ compared to the control (Aβ only). ELISA demonstrated significantly lower amyloid‐β level (6672 pg mL−1) than the control (10189 pg mL−1). Images of AFM further confirmed the presence of low quantity of amyloid beta in SBP‐treated cells. These findings suggest that SB warrants further investigation as potential therapeutic agent in the treatment of AD.
This research has outlined the role of sea buckthorn on Alzheimer’s disease. Significant reduction of amyloid beta concentration was observed in MTS, BCA, Western blot, ELISA and AFM since sea buckthorn powder was treated with cells.</description><identifier>ISSN: 0950-5423</identifier><identifier>EISSN: 1365-2621</identifier><identifier>DOI: 10.1111/ijfs.14571</identifier><language>eng</language><publisher>Oxford: Wiley Subscription Services, Inc</publisher><subject>AFM ; Alzheimer's disease ; amyloid beta ; Antioxidants ; Cell viability ; Chemical compounds ; ELISA ; Neurodegenerative diseases ; Pathogenesis ; Pharmacology ; Risk analysis ; Risk factors ; Sea buckthorn ; Western blotting</subject><ispartof>International journal of food science & technology, 2020-09, Vol.55 (9), p.3073-3081</ispartof><rights>2020 Institute of Food Science and Technology</rights><rights>International Journal of Food Science and Technology © 2020 Institute of Food Science and Technology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3011-f50919bbd15d507ebd79e3252a911da4366a425bdc70db3c5b31113dcfd78fec3</citedby><cites>FETCH-LOGICAL-c3011-f50919bbd15d507ebd79e3252a911da4366a425bdc70db3c5b31113dcfd78fec3</cites><orcidid>0000-0002-5181-6734 ; 0000-0002-8364-7808 ; 0000-0001-8681-0626</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27898,27899</link.rule.ids></links><search><creatorcontrib>Dong, Ke</creatorcontrib><creatorcontrib>Fernando, Warnakulasuriya M. A. D. Binosha</creatorcontrib><creatorcontrib>Durham, Rosalie</creatorcontrib><creatorcontrib>Stockmann, Regine</creatorcontrib><creatorcontrib>W. Jayatunga, Dona Pamoda</creatorcontrib><creatorcontrib>Jayasena, Vijay</creatorcontrib><title>A role of sea buckthorn on Alzheimer’s disease</title><title>International journal of food science & technology</title><description>Summary
Evidence suggests that diets rich in antioxidants reduce the risk factors of Alzheimer’s disease (AD). Hippophae rhamnoides, commonly known as sea buckthorn (SB), is rich in antioxidants which could have direct effects on amyloid‐beta (Aβ) levels and consequently influence AD pathogenesis. In this study, sea buckthorn powder (SBP) was administered at varying concentrations (0.6, 0.9, 1.2, 1.5 and 1.8 µg mL−1) to cell cultures (BE(2)‐M17) with 20 mm Aβ for 72 h. MTS test indicated that SB significantly increased cell viability in Aβ‐induced cells up to 95%. Results of Western blot showed maximum 38% inhibition of Aβ compared to the control (Aβ only). ELISA demonstrated significantly lower amyloid‐β level (6672 pg mL−1) than the control (10189 pg mL−1). Images of AFM further confirmed the presence of low quantity of amyloid beta in SBP‐treated cells. These findings suggest that SB warrants further investigation as potential therapeutic agent in the treatment of AD.
This research has outlined the role of sea buckthorn on Alzheimer’s disease. Significant reduction of amyloid beta concentration was observed in MTS, BCA, Western blot, ELISA and AFM since sea buckthorn powder was treated with cells.</description><subject>AFM</subject><subject>Alzheimer's disease</subject><subject>amyloid beta</subject><subject>Antioxidants</subject><subject>Cell viability</subject><subject>Chemical compounds</subject><subject>ELISA</subject><subject>Neurodegenerative diseases</subject><subject>Pathogenesis</subject><subject>Pharmacology</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Sea buckthorn</subject><subject>Western blotting</subject><issn>0950-5423</issn><issn>1365-2621</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1OwzAQRi0EEqGw4QSW2CGleOw4IcuooqWoEgtgbcV_akIaF7sRKiuuwfU4CS5hzWxm875vRg-hSyBTiHPTtDZMIeMFHKEEWM5TmlM4RgkpOUl5RtkpOguhJYRQVmQJIhX2rjPYWRxMjeWgXndr53vselx1H2vTbIz__vwKWDcRCOYcndi6C-bib0_Qy_zueXafrh4Xy1m1ShUjAKnlpIRSSg1cc1IYqYvSMMppXQLoOmN5XmeUS60KoiVTXLL4P9PK6uLWGsUm6Grs3Xr3NpiwE60bfB9PChrTQGkJNFLXI6W8C8EbK7a-2dR-L4CIgxFxMCJ-jUQYRvi96cz-H1IsH-ZPY-YH_4Binw</recordid><startdate>202009</startdate><enddate>202009</enddate><creator>Dong, Ke</creator><creator>Fernando, Warnakulasuriya M. 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Binosha ; Durham, Rosalie ; Stockmann, Regine ; W. Jayatunga, Dona Pamoda ; Jayasena, Vijay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3011-f50919bbd15d507ebd79e3252a911da4366a425bdc70db3c5b31113dcfd78fec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>AFM</topic><topic>Alzheimer's disease</topic><topic>amyloid beta</topic><topic>Antioxidants</topic><topic>Cell viability</topic><topic>Chemical compounds</topic><topic>ELISA</topic><topic>Neurodegenerative diseases</topic><topic>Pathogenesis</topic><topic>Pharmacology</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Sea buckthorn</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dong, Ke</creatorcontrib><creatorcontrib>Fernando, Warnakulasuriya M. A. D. 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Jayatunga, Dona Pamoda</creatorcontrib><creatorcontrib>Jayasena, Vijay</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>International journal of food science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dong, Ke</au><au>Fernando, Warnakulasuriya M. A. D. Binosha</au><au>Durham, Rosalie</au><au>Stockmann, Regine</au><au>W. Jayatunga, Dona Pamoda</au><au>Jayasena, Vijay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A role of sea buckthorn on Alzheimer’s disease</atitle><jtitle>International journal of food science & technology</jtitle><date>2020-09</date><risdate>2020</risdate><volume>55</volume><issue>9</issue><spage>3073</spage><epage>3081</epage><pages>3073-3081</pages><issn>0950-5423</issn><eissn>1365-2621</eissn><abstract>Summary
Evidence suggests that diets rich in antioxidants reduce the risk factors of Alzheimer’s disease (AD). Hippophae rhamnoides, commonly known as sea buckthorn (SB), is rich in antioxidants which could have direct effects on amyloid‐beta (Aβ) levels and consequently influence AD pathogenesis. In this study, sea buckthorn powder (SBP) was administered at varying concentrations (0.6, 0.9, 1.2, 1.5 and 1.8 µg mL−1) to cell cultures (BE(2)‐M17) with 20 mm Aβ for 72 h. MTS test indicated that SB significantly increased cell viability in Aβ‐induced cells up to 95%. Results of Western blot showed maximum 38% inhibition of Aβ compared to the control (Aβ only). ELISA demonstrated significantly lower amyloid‐β level (6672 pg mL−1) than the control (10189 pg mL−1). Images of AFM further confirmed the presence of low quantity of amyloid beta in SBP‐treated cells. These findings suggest that SB warrants further investigation as potential therapeutic agent in the treatment of AD.
This research has outlined the role of sea buckthorn on Alzheimer’s disease. Significant reduction of amyloid beta concentration was observed in MTS, BCA, Western blot, ELISA and AFM since sea buckthorn powder was treated with cells.</abstract><cop>Oxford</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/ijfs.14571</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5181-6734</orcidid><orcidid>https://orcid.org/0000-0002-8364-7808</orcidid><orcidid>https://orcid.org/0000-0001-8681-0626</orcidid></addata></record> |
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subjects | AFM Alzheimer's disease amyloid beta Antioxidants Cell viability Chemical compounds ELISA Neurodegenerative diseases Pathogenesis Pharmacology Risk analysis Risk factors Sea buckthorn Western blotting |
title | A role of sea buckthorn on Alzheimer’s disease |
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