Functional components in Luffa cylindrica and their effects on anti-inflammation of macrophage cells

► Phenolics, oleanolic acid, carotenoid and chlorophyll were found in Luffa. ► Luffa peel contained a higher amount of functional components than pulp. ► Luffa peel was superior to Luffa pulp in anti-inflammation of RAW 264.7 cells. ► Ethyl acetate extract of Luffa peel decreased the production of N...

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Veröffentlicht in:Food chemistry 2012-11, Vol.135 (2), p.386-395
Hauptverfasser: Kao, T.H., Huang, C.W., Chen, B.H.
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Chen, B.H.
description ► Phenolics, oleanolic acid, carotenoid and chlorophyll were found in Luffa. ► Luffa peel contained a higher amount of functional components than pulp. ► Luffa peel was superior to Luffa pulp in anti-inflammation of RAW 264.7 cells. ► Ethyl acetate extract of Luffa peel decreased the production of NO and IL-6. ► Ethyl acetate extract of Luffa peel inhibited the expression of iNOS and p-IκBα. The objectives of this study were to determine the distribution of functional components in peel and pulp of Luffa cylindrica and evaluate their anti-inflammatory activity on RAW 264.7 murine macrophage cells. Phenolics and flavonoids were present in abundant amounts in aqueous extract of peel, but in ethyl acetate extracts of peel, oleanolic acid, carotenoids and chlorophylls dominated. Both ethanol and ethyl acetate extracts in peel and pulp decreased production of nitric oxide in LPS-induced RAW 264.7 cells, whereas the ethanol extract mitigated secretion of prostaglandin E2. Furthermore, all the extracts significantly inhibited IL-6 production, but remained ineffective in retarding generation of IL-1β and TNF-α. Ethyl acetate extract of peel reduced expression of inducible nitric oxide synthase, but enhanced expression of cyclooxygenase 2. Both ethyl acetate extracts of peel and pulp mitigated expression of p-IκBα, while the latter attenuated expression of p-ERK, and all the extracts failed to inhibit JNK phosphorylation.
doi_str_mv 10.1016/j.foodchem.2012.04.128
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Psychology ; Inflammation - drug therapy ; Inflammation - genetics ; Inflammation - immunology ; Luffa - chemistry ; Luffa cylindrica ; Macrophage cell ; Macrophages - drug effects ; Macrophages - enzymology ; Macrophages - immunology ; Mice ; Nitric Oxide - immunology ; Nitric Oxide Synthase Type II - antagonists &amp; inhibitors ; Nitric Oxide Synthase Type II - genetics ; Nitric Oxide Synthase Type II - immunology ; Plant Extracts - analysis ; Plant Extracts - pharmacology</subject><ispartof>Food chemistry, 2012-11, Vol.135 (2), p.386-395</ispartof><rights>2012 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. 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The objectives of this study were to determine the distribution of functional components in peel and pulp of Luffa cylindrica and evaluate their anti-inflammatory activity on RAW 264.7 murine macrophage cells. Phenolics and flavonoids were present in abundant amounts in aqueous extract of peel, but in ethyl acetate extracts of peel, oleanolic acid, carotenoids and chlorophylls dominated. Both ethanol and ethyl acetate extracts in peel and pulp decreased production of nitric oxide in LPS-induced RAW 264.7 cells, whereas the ethanol extract mitigated secretion of prostaglandin E2. Furthermore, all the extracts significantly inhibited IL-6 production, but remained ineffective in retarding generation of IL-1β and TNF-α. Ethyl acetate extract of peel reduced expression of inducible nitric oxide synthase, but enhanced expression of cyclooxygenase 2. Both ethyl acetate extracts of peel and pulp mitigated expression of p-IκBα, while the latter attenuated expression of p-ERK, and all the extracts failed to inhibit JNK phosphorylation.</description><subject>Animals</subject><subject>Anti-inflammatory activity</subject><subject>Anti-Inflammatory Agents - analysis</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Antiinflammatory agents</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cyclooxygenase 2 - immunology</subject><subject>Cytokines - genetics</subject><subject>Cytokines - immunology</subject><subject>Dinoprostone - immunology</subject><subject>Food industries</subject><subject>Functional components</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - genetics</subject><subject>Inflammation - immunology</subject><subject>Luffa - chemistry</subject><subject>Luffa cylindrica</subject><subject>Macrophage cell</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - enzymology</subject><subject>Macrophages - immunology</subject><subject>Mice</subject><subject>Nitric Oxide - immunology</subject><subject>Nitric Oxide Synthase Type II - antagonists &amp; inhibitors</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - immunology</subject><subject>Plant Extracts - analysis</subject><subject>Plant Extracts - pharmacology</subject><issn>0308-8146</issn><issn>1873-7072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0U1v1DAQBmALgei28BcqX5C4JPgrtnMDVRQqrcQFzpbjjFmvEnuxE6T--zraLRzhZMl6ZjyeF6FbSlpKqPxwbH1KozvA3DJCWUtES5l-gXZUK94oothLtCOc6EZTIa_QdSlHQki1-jW6YkxLTYnYofF-jW4JKdoJuzSfUoS4FBwi3q_eW-wepxDHHJzFNo54OUDIGLwHV1WK9XIJTYh-svNstz44eTxbl9PpYH8CdjBN5Q165e1U4O3lvEE_7j9_v_va7L99ebj7tG-c4HRphKasZz31ne_6katBW-IlH5ntGe-4kppLB4O3fuA9GYaKtVKCeQacE9XxG_T-3PeU068VymLmULYJbIS0FlM3IUSvO_EflHCmuGZyo_JM66dKyeDNKYfZ5seKzBaGOZrnMMwWhiHC1DBq4e3ljXWYYfxT9rz9Ct5dgC3OTj7b6EL56yTtZUf76j6eHdTl_Q6QTXEBooMx5BqEGVP41yxPT22q1w</recordid><startdate>20121115</startdate><enddate>20121115</enddate><creator>Kao, T.H.</creator><creator>Huang, C.W.</creator><creator>Chen, B.H.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</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><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20121115</creationdate><title>Functional components in Luffa cylindrica and their effects on anti-inflammation of macrophage cells</title><author>Kao, T.H. ; Huang, C.W. ; Chen, B.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-48129291f5f59d37b8a0f63d2a9235376836cebfafb390bb29287742f2e330753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Anti-inflammatory activity</topic><topic>Anti-Inflammatory Agents - analysis</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Antiinflammatory agents</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cyclooxygenase 2 - immunology</topic><topic>Cytokines - genetics</topic><topic>Cytokines - immunology</topic><topic>Dinoprostone - immunology</topic><topic>Food industries</topic><topic>Functional components</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - genetics</topic><topic>Inflammation - immunology</topic><topic>Luffa - chemistry</topic><topic>Luffa cylindrica</topic><topic>Macrophage cell</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - enzymology</topic><topic>Macrophages - immunology</topic><topic>Mice</topic><topic>Nitric Oxide - immunology</topic><topic>Nitric Oxide Synthase Type II - antagonists &amp; inhibitors</topic><topic>Nitric Oxide Synthase Type II - genetics</topic><topic>Nitric Oxide Synthase Type II - immunology</topic><topic>Plant Extracts - analysis</topic><topic>Plant Extracts - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kao, T.H.</creatorcontrib><creatorcontrib>Huang, C.W.</creatorcontrib><creatorcontrib>Chen, B.H.</creatorcontrib><collection>Pascal-Francis</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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kao, T.H.</au><au>Huang, C.W.</au><au>Chen, B.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional components in Luffa cylindrica and their effects on anti-inflammation of macrophage cells</atitle><jtitle>Food chemistry</jtitle><addtitle>Food Chem</addtitle><date>2012-11-15</date><risdate>2012</risdate><volume>135</volume><issue>2</issue><spage>386</spage><epage>395</epage><pages>386-395</pages><issn>0308-8146</issn><eissn>1873-7072</eissn><coden>FOCHDJ</coden><abstract>► Phenolics, oleanolic acid, carotenoid and chlorophyll were found in Luffa. ► Luffa peel contained a higher amount of functional components than pulp. ► Luffa peel was superior to Luffa pulp in anti-inflammation of RAW 264.7 cells. ► Ethyl acetate extract of Luffa peel decreased the production of NO and IL-6. ► Ethyl acetate extract of Luffa peel inhibited the expression of iNOS and p-IκBα. The objectives of this study were to determine the distribution of functional components in peel and pulp of Luffa cylindrica and evaluate their anti-inflammatory activity on RAW 264.7 murine macrophage cells. Phenolics and flavonoids were present in abundant amounts in aqueous extract of peel, but in ethyl acetate extracts of peel, oleanolic acid, carotenoids and chlorophylls dominated. Both ethanol and ethyl acetate extracts in peel and pulp decreased production of nitric oxide in LPS-induced RAW 264.7 cells, whereas the ethanol extract mitigated secretion of prostaglandin E2. Furthermore, all the extracts significantly inhibited IL-6 production, but remained ineffective in retarding generation of IL-1β and TNF-α. Ethyl acetate extract of peel reduced expression of inducible nitric oxide synthase, but enhanced expression of cyclooxygenase 2. Both ethyl acetate extracts of peel and pulp mitigated expression of p-IκBα, while the latter attenuated expression of p-ERK, and all the extracts failed to inhibit JNK phosphorylation.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>22868104</pmid><doi>10.1016/j.foodchem.2012.04.128</doi><tpages>10</tpages></addata></record>
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subjects Animals
Anti-inflammatory activity
Anti-Inflammatory Agents - analysis
Anti-Inflammatory Agents - pharmacology
Antiinflammatory agents
Biological and medical sciences
Cell Line
Cyclooxygenase 2 - genetics
Cyclooxygenase 2 - immunology
Cytokines - genetics
Cytokines - immunology
Dinoprostone - immunology
Food industries
Functional components
Fundamental and applied biological sciences. Psychology
Inflammation - drug therapy
Inflammation - genetics
Inflammation - immunology
Luffa - chemistry
Luffa cylindrica
Macrophage cell
Macrophages - drug effects
Macrophages - enzymology
Macrophages - immunology
Mice
Nitric Oxide - immunology
Nitric Oxide Synthase Type II - antagonists & inhibitors
Nitric Oxide Synthase Type II - genetics
Nitric Oxide Synthase Type II - immunology
Plant Extracts - analysis
Plant Extracts - pharmacology
title Functional components in Luffa cylindrica and their effects on anti-inflammation of macrophage cells
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