Ability of Three Kind of Imidazole Dipeptides, Carnosine, Anserine, and Balenine, to Interact with Unsaturated Fatty Acid-Derived Aldehydes and Carbohydrate-Derived Aldehydes
Imidazole dipeptides (IDPs) such as carnosine (CAR), anserine (ANS), and balenine (BAL) are widely distributed in the skeletal muscle of vertebrates. Recently, several studies have revealed that CAR plays an important role in the detoxification of cytotoxic aldehydes arising from the peroxide of uns...
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description | Imidazole dipeptides (IDPs) such as carnosine (CAR), anserine (ANS), and balenine (BAL) are widely distributed in the skeletal muscle of vertebrates. Recently, several studies have revealed that CAR plays an important role in the detoxification of cytotoxic aldehydes arising from the peroxide of unsaturated fatty acids and carbohydrate metabolite. Although intensive studies on the detoxification of aldehydes by CAR have been performed, few studies have focused on the effects of detoxification by ANS and BAL. To determine the potential of minor IDPs such as ANS and BAL to react with cytotoxic aldehydes, the present study was established to investigate the consumption of IDP after co-incubation with cytotoxic aldehydes using high-performance liquid chromatography (HPLC). In the case of unsaturated fatty acid-derived aldehydes such as 4-hydroxy-2-
trans
-nonenal (from n-6 fatty acid) and 4-hydroxy-2-
trans
-hexenal (from n-3 fatty acid), ANS and CAR decreased considerably after co-incubation, but BAL did not. In the case of 3-deoxyglucosone and methylglyoxal as carbohydrate metabolites, no IDPs decreased after co-incubation; however, the absorbance at 336 nm of the CAR and BAL mixtures increased dramatically in a time-dependent manner. In the case of glyceraldehyde, which is also a carbohydrate metabolite, all IDPs, especially BAL, decreased after co-incubation and a new peak, surmised to represent an IDP-glyceraldehyde adduct, appeared on the HPLC chromatogram. These results can help explain the unique function and behavior of ANS and BAL in specific species. |
doi_str_mv | 10.1007/s10989-019-09975-4 |
format | Article |
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trans
-nonenal (from n-6 fatty acid) and 4-hydroxy-2-
trans
-hexenal (from n-3 fatty acid), ANS and CAR decreased considerably after co-incubation, but BAL did not. In the case of 3-deoxyglucosone and methylglyoxal as carbohydrate metabolites, no IDPs decreased after co-incubation; however, the absorbance at 336 nm of the CAR and BAL mixtures increased dramatically in a time-dependent manner. In the case of glyceraldehyde, which is also a carbohydrate metabolite, all IDPs, especially BAL, decreased after co-incubation and a new peak, surmised to represent an IDP-glyceraldehyde adduct, appeared on the HPLC chromatogram. These results can help explain the unique function and behavior of ANS and BAL in specific species.</description><identifier>ISSN: 1573-3149</identifier><identifier>EISSN: 1573-3904</identifier><identifier>DOI: 10.1007/s10989-019-09975-4</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Aldehydes ; Animal Anatomy ; Antifungal agents ; Biochemistry ; Biomedical and Life Sciences ; Carbohydrates ; Carnosine ; Cytotoxicity ; Detoxification ; Fatty acids ; Glyceraldehyde ; High-performance liquid chromatography ; Histology ; Imidazole ; Life Sciences ; Metabolites ; Molecular Medicine ; Morphology ; Peroxide ; Pharmaceutical Sciences/Technology ; Pharmacology/Toxicology ; Polymer Sciences ; Pyruvaldehyde ; Skeletal muscle</subject><ispartof>International journal of peptide research and therapeutics, 2020-09, Vol.26 (3), p.1651-1660</ispartof><rights>Springer Nature B.V. 2019</rights><rights>Springer Nature B.V. 2019.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-792e054a0057b0d9dbe8246faebee6823b6954c3c30a9047c15db13b244afe9e3</citedby><cites>FETCH-LOGICAL-c363t-792e054a0057b0d9dbe8246faebee6823b6954c3c30a9047c15db13b244afe9e3</cites><orcidid>0000-0003-4044-3474</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10989-019-09975-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10989-019-09975-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids></links><search><creatorcontrib>Mori, Akihiro</creatorcontrib><creatorcontrib>Hatate, Hideo</creatorcontrib><creatorcontrib>Tanaka, Ryusuke</creatorcontrib><title>Ability of Three Kind of Imidazole Dipeptides, Carnosine, Anserine, and Balenine, to Interact with Unsaturated Fatty Acid-Derived Aldehydes and Carbohydrate-Derived Aldehydes</title><title>International journal of peptide research and therapeutics</title><addtitle>Int J Pept Res Ther</addtitle><description>Imidazole dipeptides (IDPs) such as carnosine (CAR), anserine (ANS), and balenine (BAL) are widely distributed in the skeletal muscle of vertebrates. Recently, several studies have revealed that CAR plays an important role in the detoxification of cytotoxic aldehydes arising from the peroxide of unsaturated fatty acids and carbohydrate metabolite. Although intensive studies on the detoxification of aldehydes by CAR have been performed, few studies have focused on the effects of detoxification by ANS and BAL. To determine the potential of minor IDPs such as ANS and BAL to react with cytotoxic aldehydes, the present study was established to investigate the consumption of IDP after co-incubation with cytotoxic aldehydes using high-performance liquid chromatography (HPLC). In the case of unsaturated fatty acid-derived aldehydes such as 4-hydroxy-2-
trans
-nonenal (from n-6 fatty acid) and 4-hydroxy-2-
trans
-hexenal (from n-3 fatty acid), ANS and CAR decreased considerably after co-incubation, but BAL did not. In the case of 3-deoxyglucosone and methylglyoxal as carbohydrate metabolites, no IDPs decreased after co-incubation; however, the absorbance at 336 nm of the CAR and BAL mixtures increased dramatically in a time-dependent manner. In the case of glyceraldehyde, which is also a carbohydrate metabolite, all IDPs, especially BAL, decreased after co-incubation and a new peak, surmised to represent an IDP-glyceraldehyde adduct, appeared on the HPLC chromatogram. These results can help explain the unique function and behavior of ANS and BAL in specific species.</description><subject>Aldehydes</subject><subject>Animal Anatomy</subject><subject>Antifungal agents</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Carbohydrates</subject><subject>Carnosine</subject><subject>Cytotoxicity</subject><subject>Detoxification</subject><subject>Fatty acids</subject><subject>Glyceraldehyde</subject><subject>High-performance liquid chromatography</subject><subject>Histology</subject><subject>Imidazole</subject><subject>Life Sciences</subject><subject>Metabolites</subject><subject>Molecular Medicine</subject><subject>Morphology</subject><subject>Peroxide</subject><subject>Pharmaceutical Sciences/Technology</subject><subject>Pharmacology/Toxicology</subject><subject>Polymer Sciences</subject><subject>Pyruvaldehyde</subject><subject>Skeletal muscle</subject><issn>1573-3149</issn><issn>1573-3904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UctOAjEUnRhNRPQHXDVxy2hfM0OXI4oSSdzAuulM70jJ0MG2aPCj_EYLaFyYuGh6T3MeuT1JcknwNcG4uPEEi6FIMYlHiCJL-VHSI1nBUiYwP_6ZCRenyZn3S4wzWhDcSz7LyrQmbFHXoNnCAaAnY_UOTVZGq4-uBXRn1rAORoMfoJFytvPGwgCV1oPbTyoqblULdo9ChyY2gFN1QO8mLNDcehU2TgXQaKxCDCtro9O7qH6LT2WrYbGN7nufGFB1Ee7ofynnyUmjWg8X33c_mY_vZ6PHdPr8MBmV07RmOQtpISjgjKu4ZlFhLXQFQ8rzRkEFkA8pq3KR8ZrVDKv4P0VNMl0RVlHOVQMCWD-5OviuXfe6AR_ksts4GyMl5XRIi4zlPLLogVW7znsHjVw7s1JuKwmWu17koRcZe5H7XuROxA4iH8n2Bdyv9T-qL_uTkqg</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Mori, Akihiro</creator><creator>Hatate, Hideo</creator><creator>Tanaka, Ryusuke</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><orcidid>https://orcid.org/0000-0003-4044-3474</orcidid></search><sort><creationdate>20200901</creationdate><title>Ability of Three Kind of Imidazole Dipeptides, Carnosine, Anserine, and Balenine, to Interact with Unsaturated Fatty Acid-Derived Aldehydes and Carbohydrate-Derived Aldehydes</title><author>Mori, Akihiro ; Hatate, Hideo ; Tanaka, Ryusuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-792e054a0057b0d9dbe8246faebee6823b6954c3c30a9047c15db13b244afe9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aldehydes</topic><topic>Animal Anatomy</topic><topic>Antifungal agents</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Carbohydrates</topic><topic>Carnosine</topic><topic>Cytotoxicity</topic><topic>Detoxification</topic><topic>Fatty acids</topic><topic>Glyceraldehyde</topic><topic>High-performance liquid chromatography</topic><topic>Histology</topic><topic>Imidazole</topic><topic>Life Sciences</topic><topic>Metabolites</topic><topic>Molecular Medicine</topic><topic>Morphology</topic><topic>Peroxide</topic><topic>Pharmaceutical Sciences/Technology</topic><topic>Pharmacology/Toxicology</topic><topic>Polymer Sciences</topic><topic>Pyruvaldehyde</topic><topic>Skeletal muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mori, Akihiro</creatorcontrib><creatorcontrib>Hatate, Hideo</creatorcontrib><creatorcontrib>Tanaka, Ryusuke</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science 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><jtitle>International journal of peptide research and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mori, Akihiro</au><au>Hatate, Hideo</au><au>Tanaka, Ryusuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ability of Three Kind of Imidazole Dipeptides, Carnosine, Anserine, and Balenine, to Interact with Unsaturated Fatty Acid-Derived Aldehydes and Carbohydrate-Derived Aldehydes</atitle><jtitle>International journal of peptide research and therapeutics</jtitle><stitle>Int J Pept Res Ther</stitle><date>2020-09-01</date><risdate>2020</risdate><volume>26</volume><issue>3</issue><spage>1651</spage><epage>1660</epage><pages>1651-1660</pages><issn>1573-3149</issn><eissn>1573-3904</eissn><abstract>Imidazole dipeptides (IDPs) such as carnosine (CAR), anserine (ANS), and balenine (BAL) are widely distributed in the skeletal muscle of vertebrates. Recently, several studies have revealed that CAR plays an important role in the detoxification of cytotoxic aldehydes arising from the peroxide of unsaturated fatty acids and carbohydrate metabolite. Although intensive studies on the detoxification of aldehydes by CAR have been performed, few studies have focused on the effects of detoxification by ANS and BAL. To determine the potential of minor IDPs such as ANS and BAL to react with cytotoxic aldehydes, the present study was established to investigate the consumption of IDP after co-incubation with cytotoxic aldehydes using high-performance liquid chromatography (HPLC). In the case of unsaturated fatty acid-derived aldehydes such as 4-hydroxy-2-
trans
-nonenal (from n-6 fatty acid) and 4-hydroxy-2-
trans
-hexenal (from n-3 fatty acid), ANS and CAR decreased considerably after co-incubation, but BAL did not. In the case of 3-deoxyglucosone and methylglyoxal as carbohydrate metabolites, no IDPs decreased after co-incubation; however, the absorbance at 336 nm of the CAR and BAL mixtures increased dramatically in a time-dependent manner. In the case of glyceraldehyde, which is also a carbohydrate metabolite, all IDPs, especially BAL, decreased after co-incubation and a new peak, surmised to represent an IDP-glyceraldehyde adduct, appeared on the HPLC chromatogram. These results can help explain the unique function and behavior of ANS and BAL in specific species.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10989-019-09975-4</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4044-3474</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aldehydes Animal Anatomy Antifungal agents Biochemistry Biomedical and Life Sciences Carbohydrates Carnosine Cytotoxicity Detoxification Fatty acids Glyceraldehyde High-performance liquid chromatography Histology Imidazole Life Sciences Metabolites Molecular Medicine Morphology Peroxide Pharmaceutical Sciences/Technology Pharmacology/Toxicology Polymer Sciences Pyruvaldehyde Skeletal muscle |
title | Ability of Three Kind of Imidazole Dipeptides, Carnosine, Anserine, and Balenine, to Interact with Unsaturated Fatty Acid-Derived Aldehydes and Carbohydrate-Derived Aldehydes |
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