Apigenin glycosides from green pepper enhance longevity and stress resistance in Caenorhabditis elegans
Peppers are a rich source of bioactive compounds with several health benefits. However, most of the knowledge about these benefits has been obtained through in vitro studies, and less is known about their in vivo health-promoting and stress resistance effects. Therefore, we hypothesized that the int...
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Veröffentlicht in: | Nutrition research (New York, N.Y.) N.Y.), 2022-06, Vol.102, p.23-34 |
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creator | Elkhedir, Abdeen E. Iqbal, Aamir Zogona, Daniel Mohammed, Hammad Hamed Murtaza, Ayesha Xu, Xiaoyun |
description | Peppers are a rich source of bioactive compounds with several health benefits. However, most of the knowledge about these benefits has been obtained through in vitro studies, and less is known about their in vivo health-promoting and stress resistance effects. Therefore, we hypothesized that the intake of apigenin glycosides (XAp-G) from Xiaomila green pepper (Capsicum frutescens) could protect against stress factors and promote longevity of Caenorhabditis elegans. Synchronized worms were treated with XAp-G and the lifespan and stress resistance were examined. XAp-G treatment strongly enhanced the average lifespan of worms by 23.9% compared with control by reducing the reactive oxygen species (ROS) level. Ultrahigh performance liquid chromatography-electrospray ionization-quadrupole time-of-flight mass spectometry analysis showed that Xiaomila pepper (polyamide fraction) contained significant amount of flavone glycosides with m/z 563.14 (apigenin glycosides). Green fluorescent protein fluorescence and real-time polymerase chain reaction analyses showed that XAp-G-treatment could regulate the expression of anti-aging related genes, including daf-2, daf-16, sod-3, hsp-16.2, skn-1, gst-4, gcs-1, jnk-1, and sir-2.1 in C elegans, thereby promoting the translocation of DAF-16 and SKN-1 into the nucleus. However, it could not extend the lifespan of daf-16, skn-1, and sir-2.1 knocked-down mutants. XAp-G treatment significantly reduced ROS under normal and stress conditions (juglone, hydrogen peroxide), and thereby promotes longevity of C elegans via the insulin/insulin-like growth factor-1 signaling pathway.
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doi_str_mv | 10.1016/j.nutres.2022.02.003 |
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[Display omitted]</description><identifier>ISSN: 0271-5317</identifier><identifier>EISSN: 1879-0739</identifier><identifier>DOI: 10.1016/j.nutres.2022.02.003</identifier><identifier>PMID: 35366456</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apigenin - pharmacology ; Apigenin glycosides ; Caenorhabditis elegans ; Caenorhabditis elegans - genetics ; Caenorhabditis elegans - metabolism ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Capsicum ; Forkhead Transcription Factors - genetics ; Forkhead Transcription Factors - metabolism ; Glycosides - pharmacology ; Insulin/IGF-1 pathway ; Lifespan ; Longevity ; Oxidative Stress ; Reactive Oxygen Species - metabolism ; UPLC-ESI-Q-TOF-MS/PDA</subject><ispartof>Nutrition research (New York, N.Y.), 2022-06, Vol.102, p.23-34</ispartof><rights>2022</rights><rights>Copyright © 2022. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-346e813f0bfe6e8b934b6fa4a85223647f2808d91f20c0ae8125bf14fbb4549b3</citedby><cites>FETCH-LOGICAL-c362t-346e813f0bfe6e8b934b6fa4a85223647f2808d91f20c0ae8125bf14fbb4549b3</cites><orcidid>0000-0002-6787-2941</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.nutres.2022.02.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35366456$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Elkhedir, Abdeen E.</creatorcontrib><creatorcontrib>Iqbal, Aamir</creatorcontrib><creatorcontrib>Zogona, Daniel</creatorcontrib><creatorcontrib>Mohammed, Hammad Hamed</creatorcontrib><creatorcontrib>Murtaza, Ayesha</creatorcontrib><creatorcontrib>Xu, Xiaoyun</creatorcontrib><title>Apigenin glycosides from green pepper enhance longevity and stress resistance in Caenorhabditis elegans</title><title>Nutrition research (New York, N.Y.)</title><addtitle>Nutr Res</addtitle><description>Peppers are a rich source of bioactive compounds with several health benefits. However, most of the knowledge about these benefits has been obtained through in vitro studies, and less is known about their in vivo health-promoting and stress resistance effects. Therefore, we hypothesized that the intake of apigenin glycosides (XAp-G) from Xiaomila green pepper (Capsicum frutescens) could protect against stress factors and promote longevity of Caenorhabditis elegans. Synchronized worms were treated with XAp-G and the lifespan and stress resistance were examined. XAp-G treatment strongly enhanced the average lifespan of worms by 23.9% compared with control by reducing the reactive oxygen species (ROS) level. Ultrahigh performance liquid chromatography-electrospray ionization-quadrupole time-of-flight mass spectometry analysis showed that Xiaomila pepper (polyamide fraction) contained significant amount of flavone glycosides with m/z 563.14 (apigenin glycosides). Green fluorescent protein fluorescence and real-time polymerase chain reaction analyses showed that XAp-G-treatment could regulate the expression of anti-aging related genes, including daf-2, daf-16, sod-3, hsp-16.2, skn-1, gst-4, gcs-1, jnk-1, and sir-2.1 in C elegans, thereby promoting the translocation of DAF-16 and SKN-1 into the nucleus. However, it could not extend the lifespan of daf-16, skn-1, and sir-2.1 knocked-down mutants. XAp-G treatment significantly reduced ROS under normal and stress conditions (juglone, hydrogen peroxide), and thereby promotes longevity of C elegans via the insulin/insulin-like growth factor-1 signaling pathway.
[Display omitted]</description><subject>Animals</subject><subject>Apigenin - pharmacology</subject><subject>Apigenin glycosides</subject><subject>Caenorhabditis elegans</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans - metabolism</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Capsicum</subject><subject>Forkhead Transcription Factors - genetics</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Glycosides - pharmacology</subject><subject>Insulin/IGF-1 pathway</subject><subject>Lifespan</subject><subject>Longevity</subject><subject>Oxidative Stress</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>UPLC-ESI-Q-TOF-MS/PDA</subject><issn>0271-5317</issn><issn>1879-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rGzEQhkVJaBy3_6AUHXtZV1-r3b0Ugmk-INBLcxbS7mgts9ZuNGuD_33l2skxMEgDemZe9BDyjbMVZ1z_3K7ifk6AK8GEWLFcTH4iC15XTcEq2VyRBRMVL0rJqxtyi7hljFdcys_kRpZSa1XqBenvptBDDJH2w7EdMXSA1KdxR_sEEOkE0wSJQtzY2AIdxtjDIcxHamNH8ZSPNB8B5__vec_aQhzTxrouzAEpDNDbiF_ItbcDwtfLvSQv97__rh-L5z8PT-u756KVWsyFVBpqLj1zHnLnGqmc9lbZuhRCalV5UbO6a7gXrGU2s6J0nivvnCpV4-SS_DjvndL4ugeczS5gC8NgI4x7NEIrXYmyEVVG1Rlt04iYwJsphZ1NR8OZOSk2W3NWbE6KDcvFZB77fknYux1070NvTjPw6wxA_uchQDLYBsh2upCgnU03ho8T_gH_KZDB</recordid><startdate>202206</startdate><enddate>202206</enddate><creator>Elkhedir, Abdeen E.</creator><creator>Iqbal, Aamir</creator><creator>Zogona, Daniel</creator><creator>Mohammed, Hammad Hamed</creator><creator>Murtaza, Ayesha</creator><creator>Xu, Xiaoyun</creator><general>Elsevier Inc</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>7X8</scope><orcidid>https://orcid.org/0000-0002-6787-2941</orcidid></search><sort><creationdate>202206</creationdate><title>Apigenin glycosides from green pepper enhance longevity and stress resistance in Caenorhabditis elegans</title><author>Elkhedir, Abdeen E. ; Iqbal, Aamir ; Zogona, Daniel ; Mohammed, Hammad Hamed ; Murtaza, Ayesha ; Xu, Xiaoyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-346e813f0bfe6e8b934b6fa4a85223647f2808d91f20c0ae8125bf14fbb4549b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Apigenin - pharmacology</topic><topic>Apigenin glycosides</topic><topic>Caenorhabditis elegans</topic><topic>Caenorhabditis elegans - genetics</topic><topic>Caenorhabditis elegans - metabolism</topic><topic>Caenorhabditis elegans Proteins - genetics</topic><topic>Caenorhabditis elegans Proteins - metabolism</topic><topic>Capsicum</topic><topic>Forkhead Transcription Factors - genetics</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>Glycosides - pharmacology</topic><topic>Insulin/IGF-1 pathway</topic><topic>Lifespan</topic><topic>Longevity</topic><topic>Oxidative Stress</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>UPLC-ESI-Q-TOF-MS/PDA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elkhedir, Abdeen E.</creatorcontrib><creatorcontrib>Iqbal, Aamir</creatorcontrib><creatorcontrib>Zogona, Daniel</creatorcontrib><creatorcontrib>Mohammed, Hammad Hamed</creatorcontrib><creatorcontrib>Murtaza, Ayesha</creatorcontrib><creatorcontrib>Xu, Xiaoyun</creatorcontrib><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>Nutrition research (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elkhedir, Abdeen E.</au><au>Iqbal, Aamir</au><au>Zogona, Daniel</au><au>Mohammed, Hammad Hamed</au><au>Murtaza, Ayesha</au><au>Xu, Xiaoyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apigenin glycosides from green pepper enhance longevity and stress resistance in Caenorhabditis elegans</atitle><jtitle>Nutrition research (New York, N.Y.)</jtitle><addtitle>Nutr Res</addtitle><date>2022-06</date><risdate>2022</risdate><volume>102</volume><spage>23</spage><epage>34</epage><pages>23-34</pages><issn>0271-5317</issn><eissn>1879-0739</eissn><abstract>Peppers are a rich source of bioactive compounds with several health benefits. However, most of the knowledge about these benefits has been obtained through in vitro studies, and less is known about their in vivo health-promoting and stress resistance effects. Therefore, we hypothesized that the intake of apigenin glycosides (XAp-G) from Xiaomila green pepper (Capsicum frutescens) could protect against stress factors and promote longevity of Caenorhabditis elegans. Synchronized worms were treated with XAp-G and the lifespan and stress resistance were examined. XAp-G treatment strongly enhanced the average lifespan of worms by 23.9% compared with control by reducing the reactive oxygen species (ROS) level. Ultrahigh performance liquid chromatography-electrospray ionization-quadrupole time-of-flight mass spectometry analysis showed that Xiaomila pepper (polyamide fraction) contained significant amount of flavone glycosides with m/z 563.14 (apigenin glycosides). Green fluorescent protein fluorescence and real-time polymerase chain reaction analyses showed that XAp-G-treatment could regulate the expression of anti-aging related genes, including daf-2, daf-16, sod-3, hsp-16.2, skn-1, gst-4, gcs-1, jnk-1, and sir-2.1 in C elegans, thereby promoting the translocation of DAF-16 and SKN-1 into the nucleus. However, it could not extend the lifespan of daf-16, skn-1, and sir-2.1 knocked-down mutants. XAp-G treatment significantly reduced ROS under normal and stress conditions (juglone, hydrogen peroxide), and thereby promotes longevity of C elegans via the insulin/insulin-like growth factor-1 signaling pathway.
[Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>35366456</pmid><doi>10.1016/j.nutres.2022.02.003</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-6787-2941</orcidid></addata></record> |
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subjects | Animals Apigenin - pharmacology Apigenin glycosides Caenorhabditis elegans Caenorhabditis elegans - genetics Caenorhabditis elegans - metabolism Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Capsicum Forkhead Transcription Factors - genetics Forkhead Transcription Factors - metabolism Glycosides - pharmacology Insulin/IGF-1 pathway Lifespan Longevity Oxidative Stress Reactive Oxygen Species - metabolism UPLC-ESI-Q-TOF-MS/PDA |
title | Apigenin glycosides from green pepper enhance longevity and stress resistance in Caenorhabditis elegans |
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