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Anti-inflammatory activity of herb products from Licania rigida Benth
•The extract is rich in phenolic compounds and flavonoids.•The extract presented an anti-inflammatory effect, affecting the metabolic route of arachidonic acid.•The extract showed a reduction in leukocyte migration, indicating an inhibition of cytokine production. The objective of the present study...
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Published in: | Complementary therapies in medicine 2019-08, Vol.45, p.254-261 |
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creator | Santos, Enaide Soares de Morais Oliveira, Cícera Datiane Alencar Menezes, Irwin Rose do Nascimento, Emmily Petícia Correia, Denise Bezerra de Alencar, Cícero Damon Carvalho de Fátima Sousa, Maria Fernandes Lima, Cícera Norma Monteiro, Álefe Brito de Souza, Camila Pedroso Estevam de Araújo Delmondes, Gyllyandeson Bezerra, Daniel Souza de Oliveira Garcia, Francisca Adilfa Boligon, Aline Augusti da Costa, José Galberto Martins Melo Coutinho, Henrique Douglas Bezerra Felipe, Cícero Francisco Kerntopf, Marta Regina |
description | •The extract is rich in phenolic compounds and flavonoids.•The extract presented an anti-inflammatory effect, affecting the metabolic route of arachidonic acid.•The extract showed a reduction in leukocyte migration, indicating an inhibition of cytokine production.
The objective of the present study was to evaluate the systemic anti-inflammatory activity of the hydroalcoholic extract of the leaves of Licania rigida Benth (EHFLR) on models of systemic inflammation in mice.
The quantitative chemical profiles of phenolic acids and flavonoids were performed by High-Performance Liquid Chromatography (HPLC). Systemic anti-inflammatory activity was determined from carrageenan and dextran-induced paw edema models and the animals were orally treated (p.o.) with EHFLR at doses of 25, 50, 100 mg/kg, indomethacin (10 mg/kg) for carrageenan-induced paw edema and promethazine (6 mg/kg) for dextran-induced paw edema. The possible mechanisms involved in the anti-inflammatory action of the extract were evaluated by the paw edema models induced by histamine and arachidonic acid, and by the model of carrageenan-induced peritonitis, where vascular permeability and leukocyte migration to the peritoneal cavity were evaluated.
The results of the HPLC identified the presence of phenolic acids and flavonoids, with chlorogenic acid (1.16%) and Caempferol (0.81%) as the main constituents. From the results, it was concluded that the extract has an LD50 ≥5000 mg/kg when administered orally in mice as this dose did not trigger deaths in any of the observed groups. EHFLR (25 mg/kg) showed a significant antiderematogenic effect on histamine and arachidonic acid-induced paw edema at the third hour of the tests, with a percentage of inhibition of 46.64% and 18.33%, respectively. The extract (25 mg/kg, p.o.) also significantly reduced vascular permeability and leukocyte migration in the peritoneal cavity.
It is concluded that EHFLR exerts a systemic anti-inflammatory action, which seems to depend, at least in part, on the inhibition of arachidonic acid metabolism and the action of vasoactive amines. In addition, the extract reduced the leukocyte migration in the peritoneal cavity, indicating that its action may be linked to the inhibition of pro-inflammatory cytokines. |
doi_str_mv | 10.1016/j.ctim.2019.06.001 |
format | article |
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The objective of the present study was to evaluate the systemic anti-inflammatory activity of the hydroalcoholic extract of the leaves of Licania rigida Benth (EHFLR) on models of systemic inflammation in mice.
The quantitative chemical profiles of phenolic acids and flavonoids were performed by High-Performance Liquid Chromatography (HPLC). Systemic anti-inflammatory activity was determined from carrageenan and dextran-induced paw edema models and the animals were orally treated (p.o.) with EHFLR at doses of 25, 50, 100 mg/kg, indomethacin (10 mg/kg) for carrageenan-induced paw edema and promethazine (6 mg/kg) for dextran-induced paw edema. The possible mechanisms involved in the anti-inflammatory action of the extract were evaluated by the paw edema models induced by histamine and arachidonic acid, and by the model of carrageenan-induced peritonitis, where vascular permeability and leukocyte migration to the peritoneal cavity were evaluated.
The results of the HPLC identified the presence of phenolic acids and flavonoids, with chlorogenic acid (1.16%) and Caempferol (0.81%) as the main constituents. From the results, it was concluded that the extract has an LD50 ≥5000 mg/kg when administered orally in mice as this dose did not trigger deaths in any of the observed groups. EHFLR (25 mg/kg) showed a significant antiderematogenic effect on histamine and arachidonic acid-induced paw edema at the third hour of the tests, with a percentage of inhibition of 46.64% and 18.33%, respectively. The extract (25 mg/kg, p.o.) also significantly reduced vascular permeability and leukocyte migration in the peritoneal cavity.
It is concluded that EHFLR exerts a systemic anti-inflammatory action, which seems to depend, at least in part, on the inhibition of arachidonic acid metabolism and the action of vasoactive amines. In addition, the extract reduced the leukocyte migration in the peritoneal cavity, indicating that its action may be linked to the inhibition of pro-inflammatory cytokines.</description><identifier>ISSN: 0965-2299</identifier><identifier>EISSN: 1873-6963</identifier><identifier>DOI: 10.1016/j.ctim.2019.06.001</identifier><identifier>PMID: 31331571</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Acids ; Amines ; Animal models ; Animals ; Anti-inflammatory agents ; Anti-Inflammatory Agents - pharmacology ; Arachidonic acid ; Carrageenan ; Carrageenan - pharmacology ; Cell adhesion & migration ; Chlorogenic acid ; Chromatography ; Chrysobalanaceae - chemistry ; Conflicts of interest ; Cytokines ; Dextran ; Edema ; Edema - chemically induced ; Edema - drug therapy ; Enzymes ; Flavonoids ; Flavonoids - pharmacology ; High performance liquid chromatography ; Histamine ; Hydroxybenzoates - pharmacology ; Indomethacin ; Inflammation ; Inflammation - chemically induced ; Inflammation - drug therapy ; Inhibition ; Leukocyte migration ; Licania rigida ; Liquid chromatography ; Male ; Metabolism ; Mice ; Nonsteroidal anti-inflammatory drugs ; Oral administration ; Organic chemistry ; Peritoneum ; Peritonitis ; Peritonitis - chemically induced ; Peritonitis - drug therapy ; Permeability ; Pharmaceutical industry ; Phenolic acids ; Phenols ; Phytotherapy - methods ; Plant Extracts - pharmacology ; Plant Leaves - chemistry ; Promethazine ; Vasoactive agents</subject><ispartof>Complementary therapies in medicine, 2019-08, Vol.45, p.254-261</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><rights>2019. Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-d2f891ebbd38e5edb8ba0b283cc037bceadfa8c748acfb20f388ebb4dc43dc743</citedby><cites>FETCH-LOGICAL-c384t-d2f891ebbd38e5edb8ba0b283cc037bceadfa8c748acfb20f388ebb4dc43dc743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31331571$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Santos, Enaide Soares</creatorcontrib><creatorcontrib>de Morais Oliveira, Cícera Datiane</creatorcontrib><creatorcontrib>Alencar Menezes, Irwin Rose</creatorcontrib><creatorcontrib>do Nascimento, Emmily Petícia</creatorcontrib><creatorcontrib>Correia, Denise Bezerra</creatorcontrib><creatorcontrib>de Alencar, Cícero Damon Carvalho</creatorcontrib><creatorcontrib>de Fátima Sousa, Maria</creatorcontrib><creatorcontrib>Fernandes Lima, Cícera Norma</creatorcontrib><creatorcontrib>Monteiro, Álefe Brito</creatorcontrib><creatorcontrib>de Souza, Camila Pedroso Estevam</creatorcontrib><creatorcontrib>de Araújo Delmondes, Gyllyandeson</creatorcontrib><creatorcontrib>Bezerra, Daniel Souza</creatorcontrib><creatorcontrib>de Oliveira Garcia, Francisca Adilfa</creatorcontrib><creatorcontrib>Boligon, Aline Augusti</creatorcontrib><creatorcontrib>da Costa, José Galberto Martins</creatorcontrib><creatorcontrib>Melo Coutinho, Henrique Douglas</creatorcontrib><creatorcontrib>Bezerra Felipe, Cícero Francisco</creatorcontrib><creatorcontrib>Kerntopf, Marta Regina</creatorcontrib><title>Anti-inflammatory activity of herb products from Licania rigida Benth</title><title>Complementary therapies in medicine</title><addtitle>Complement Ther Med</addtitle><description>•The extract is rich in phenolic compounds and flavonoids.•The extract presented an anti-inflammatory effect, affecting the metabolic route of arachidonic acid.•The extract showed a reduction in leukocyte migration, indicating an inhibition of cytokine production.
The objective of the present study was to evaluate the systemic anti-inflammatory activity of the hydroalcoholic extract of the leaves of Licania rigida Benth (EHFLR) on models of systemic inflammation in mice.
The quantitative chemical profiles of phenolic acids and flavonoids were performed by High-Performance Liquid Chromatography (HPLC). Systemic anti-inflammatory activity was determined from carrageenan and dextran-induced paw edema models and the animals were orally treated (p.o.) with EHFLR at doses of 25, 50, 100 mg/kg, indomethacin (10 mg/kg) for carrageenan-induced paw edema and promethazine (6 mg/kg) for dextran-induced paw edema. The possible mechanisms involved in the anti-inflammatory action of the extract were evaluated by the paw edema models induced by histamine and arachidonic acid, and by the model of carrageenan-induced peritonitis, where vascular permeability and leukocyte migration to the peritoneal cavity were evaluated.
The results of the HPLC identified the presence of phenolic acids and flavonoids, with chlorogenic acid (1.16%) and Caempferol (0.81%) as the main constituents. From the results, it was concluded that the extract has an LD50 ≥5000 mg/kg when administered orally in mice as this dose did not trigger deaths in any of the observed groups. EHFLR (25 mg/kg) showed a significant antiderematogenic effect on histamine and arachidonic acid-induced paw edema at the third hour of the tests, with a percentage of inhibition of 46.64% and 18.33%, respectively. The extract (25 mg/kg, p.o.) also significantly reduced vascular permeability and leukocyte migration in the peritoneal cavity.
It is concluded that EHFLR exerts a systemic anti-inflammatory action, which seems to depend, at least in part, on the inhibition of arachidonic acid metabolism and the action of vasoactive amines. In addition, the extract reduced the leukocyte migration in the peritoneal cavity, indicating that its action may be linked to the inhibition of pro-inflammatory cytokines.</description><subject>Acids</subject><subject>Amines</subject><subject>Animal models</subject><subject>Animals</subject><subject>Anti-inflammatory agents</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Arachidonic acid</subject><subject>Carrageenan</subject><subject>Carrageenan - pharmacology</subject><subject>Cell adhesion & migration</subject><subject>Chlorogenic acid</subject><subject>Chromatography</subject><subject>Chrysobalanaceae - chemistry</subject><subject>Conflicts of interest</subject><subject>Cytokines</subject><subject>Dextran</subject><subject>Edema</subject><subject>Edema - chemically induced</subject><subject>Edema - drug therapy</subject><subject>Enzymes</subject><subject>Flavonoids</subject><subject>Flavonoids - pharmacology</subject><subject>High performance liquid chromatography</subject><subject>Histamine</subject><subject>Hydroxybenzoates - pharmacology</subject><subject>Indomethacin</subject><subject>Inflammation</subject><subject>Inflammation - chemically induced</subject><subject>Inflammation - drug therapy</subject><subject>Inhibition</subject><subject>Leukocyte migration</subject><subject>Licania rigida</subject><subject>Liquid chromatography</subject><subject>Male</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Oral administration</subject><subject>Organic chemistry</subject><subject>Peritoneum</subject><subject>Peritonitis</subject><subject>Peritonitis - chemically induced</subject><subject>Peritonitis - drug therapy</subject><subject>Permeability</subject><subject>Pharmaceutical industry</subject><subject>Phenolic acids</subject><subject>Phenols</subject><subject>Phytotherapy - methods</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Leaves - chemistry</subject><subject>Promethazine</subject><subject>Vasoactive agents</subject><issn>0965-2299</issn><issn>1873-6963</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE1rGzEQQEVIiR23f6CHsJBLL7sdSfuhhV6SkKYFQy_JWehj1Mh4dx1Ja_C_r1wnOfTQ04B4esw8Qj5TqCjQ9uumMskPFQPaV9BWAPSMLKnoeNn2LT8nS-jbpmSs7xfkMsYNAPS84xdkwSnntOnoktzfjMmXfnRbNQwqTeFQqGzd-3QoJlc8Y9DFLkx2NikWLkxDsfZGjV4Vwf_2VhW3OKbnj-SDU9uIn17nijx9v3-8-1Gufz38vLtZl4aLOpWWOdFT1NpygQ1aLbQCzQQ3BninDSrrlDBdLZRxmoHjQmS6tqbmNj_zFfly8uaVXmaMSQ4-Gtxu1YjTHCXLZ7WcN0Azev0PupnmMObtJGMt1NDTHGlF2IkyYYoxoJO74AcVDpKCPEaWG3mMLI-RJbQS_qqvXtWzHtC-f3mrmoFvJwBzi73HIKPxOBq0PqBJ0k7-f_4_DEuOSA</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>Santos, Enaide Soares</creator><creator>de Morais Oliveira, Cícera Datiane</creator><creator>Alencar Menezes, Irwin Rose</creator><creator>do Nascimento, Emmily Petícia</creator><creator>Correia, Denise Bezerra</creator><creator>de Alencar, Cícero Damon Carvalho</creator><creator>de Fátima Sousa, Maria</creator><creator>Fernandes Lima, Cícera Norma</creator><creator>Monteiro, Álefe Brito</creator><creator>de Souza, Camila Pedroso Estevam</creator><creator>de Araújo Delmondes, Gyllyandeson</creator><creator>Bezerra, Daniel Souza</creator><creator>de Oliveira Garcia, Francisca Adilfa</creator><creator>Boligon, Aline Augusti</creator><creator>da Costa, José Galberto Martins</creator><creator>Melo Coutinho, Henrique Douglas</creator><creator>Bezerra Felipe, Cícero Francisco</creator><creator>Kerntopf, Marta Regina</creator><general>Elsevier Ltd</general><general>Elsevier Limited</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>3V.</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201908</creationdate><title>Anti-inflammatory activity of herb products from Licania rigida Benth</title><author>Santos, Enaide Soares ; de Morais Oliveira, Cícera Datiane ; Alencar Menezes, Irwin Rose ; do Nascimento, Emmily Petícia ; Correia, Denise Bezerra ; de Alencar, Cícero Damon Carvalho ; de Fátima Sousa, Maria ; Fernandes Lima, Cícera Norma ; Monteiro, Álefe Brito ; de Souza, Camila Pedroso Estevam ; de Araújo Delmondes, Gyllyandeson ; Bezerra, Daniel Souza ; de Oliveira Garcia, Francisca Adilfa ; Boligon, Aline Augusti ; da Costa, José Galberto Martins ; Melo Coutinho, Henrique Douglas ; Bezerra Felipe, Cícero Francisco ; Kerntopf, Marta Regina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-d2f891ebbd38e5edb8ba0b283cc037bceadfa8c748acfb20f388ebb4dc43dc743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acids</topic><topic>Amines</topic><topic>Animal models</topic><topic>Animals</topic><topic>Anti-inflammatory agents</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Arachidonic acid</topic><topic>Carrageenan</topic><topic>Carrageenan - pharmacology</topic><topic>Cell adhesion & migration</topic><topic>Chlorogenic acid</topic><topic>Chromatography</topic><topic>Chrysobalanaceae - chemistry</topic><topic>Conflicts of interest</topic><topic>Cytokines</topic><topic>Dextran</topic><topic>Edema</topic><topic>Edema - chemically induced</topic><topic>Edema - drug therapy</topic><topic>Enzymes</topic><topic>Flavonoids</topic><topic>Flavonoids - pharmacology</topic><topic>High performance liquid chromatography</topic><topic>Histamine</topic><topic>Hydroxybenzoates - pharmacology</topic><topic>Indomethacin</topic><topic>Inflammation</topic><topic>Inflammation - chemically induced</topic><topic>Inflammation - drug therapy</topic><topic>Inhibition</topic><topic>Leukocyte migration</topic><topic>Licania rigida</topic><topic>Liquid chromatography</topic><topic>Male</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Oral administration</topic><topic>Organic chemistry</topic><topic>Peritoneum</topic><topic>Peritonitis</topic><topic>Peritonitis - chemically induced</topic><topic>Peritonitis - drug therapy</topic><topic>Permeability</topic><topic>Pharmaceutical industry</topic><topic>Phenolic acids</topic><topic>Phenols</topic><topic>Phytotherapy - methods</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves - chemistry</topic><topic>Promethazine</topic><topic>Vasoactive agents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santos, Enaide Soares</creatorcontrib><creatorcontrib>de Morais Oliveira, Cícera Datiane</creatorcontrib><creatorcontrib>Alencar Menezes, Irwin Rose</creatorcontrib><creatorcontrib>do Nascimento, Emmily Petícia</creatorcontrib><creatorcontrib>Correia, Denise Bezerra</creatorcontrib><creatorcontrib>de Alencar, Cícero Damon Carvalho</creatorcontrib><creatorcontrib>de Fátima Sousa, Maria</creatorcontrib><creatorcontrib>Fernandes Lima, Cícera Norma</creatorcontrib><creatorcontrib>Monteiro, Álefe Brito</creatorcontrib><creatorcontrib>de Souza, Camila Pedroso Estevam</creatorcontrib><creatorcontrib>de Araújo Delmondes, Gyllyandeson</creatorcontrib><creatorcontrib>Bezerra, Daniel Souza</creatorcontrib><creatorcontrib>de Oliveira Garcia, Francisca Adilfa</creatorcontrib><creatorcontrib>Boligon, Aline Augusti</creatorcontrib><creatorcontrib>da Costa, José Galberto Martins</creatorcontrib><creatorcontrib>Melo Coutinho, Henrique Douglas</creatorcontrib><creatorcontrib>Bezerra Felipe, Cícero Francisco</creatorcontrib><creatorcontrib>Kerntopf, Marta Regina</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Physical Education Index</collection><collection>Health & Medical Complete (ProQuest Database)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Health Management Database (Proquest)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest research library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</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 One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Complementary therapies in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santos, Enaide Soares</au><au>de Morais Oliveira, Cícera Datiane</au><au>Alencar Menezes, Irwin Rose</au><au>do Nascimento, Emmily Petícia</au><au>Correia, Denise Bezerra</au><au>de Alencar, Cícero Damon Carvalho</au><au>de Fátima Sousa, Maria</au><au>Fernandes Lima, Cícera Norma</au><au>Monteiro, Álefe Brito</au><au>de Souza, Camila Pedroso Estevam</au><au>de Araújo Delmondes, Gyllyandeson</au><au>Bezerra, Daniel Souza</au><au>de Oliveira Garcia, Francisca Adilfa</au><au>Boligon, Aline Augusti</au><au>da Costa, José Galberto Martins</au><au>Melo Coutinho, Henrique Douglas</au><au>Bezerra Felipe, Cícero Francisco</au><au>Kerntopf, Marta Regina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-inflammatory activity of herb products from Licania rigida Benth</atitle><jtitle>Complementary therapies in medicine</jtitle><addtitle>Complement Ther Med</addtitle><date>2019-08</date><risdate>2019</risdate><volume>45</volume><spage>254</spage><epage>261</epage><pages>254-261</pages><issn>0965-2299</issn><eissn>1873-6963</eissn><abstract>•The extract is rich in phenolic compounds and flavonoids.•The extract presented an anti-inflammatory effect, affecting the metabolic route of arachidonic acid.•The extract showed a reduction in leukocyte migration, indicating an inhibition of cytokine production.
The objective of the present study was to evaluate the systemic anti-inflammatory activity of the hydroalcoholic extract of the leaves of Licania rigida Benth (EHFLR) on models of systemic inflammation in mice.
The quantitative chemical profiles of phenolic acids and flavonoids were performed by High-Performance Liquid Chromatography (HPLC). Systemic anti-inflammatory activity was determined from carrageenan and dextran-induced paw edema models and the animals were orally treated (p.o.) with EHFLR at doses of 25, 50, 100 mg/kg, indomethacin (10 mg/kg) for carrageenan-induced paw edema and promethazine (6 mg/kg) for dextran-induced paw edema. The possible mechanisms involved in the anti-inflammatory action of the extract were evaluated by the paw edema models induced by histamine and arachidonic acid, and by the model of carrageenan-induced peritonitis, where vascular permeability and leukocyte migration to the peritoneal cavity were evaluated.
The results of the HPLC identified the presence of phenolic acids and flavonoids, with chlorogenic acid (1.16%) and Caempferol (0.81%) as the main constituents. From the results, it was concluded that the extract has an LD50 ≥5000 mg/kg when administered orally in mice as this dose did not trigger deaths in any of the observed groups. EHFLR (25 mg/kg) showed a significant antiderematogenic effect on histamine and arachidonic acid-induced paw edema at the third hour of the tests, with a percentage of inhibition of 46.64% and 18.33%, respectively. The extract (25 mg/kg, p.o.) also significantly reduced vascular permeability and leukocyte migration in the peritoneal cavity.
It is concluded that EHFLR exerts a systemic anti-inflammatory action, which seems to depend, at least in part, on the inhibition of arachidonic acid metabolism and the action of vasoactive amines. In addition, the extract reduced the leukocyte migration in the peritoneal cavity, indicating that its action may be linked to the inhibition of pro-inflammatory cytokines.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>31331571</pmid><doi>10.1016/j.ctim.2019.06.001</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0965-2299 |
ispartof | Complementary therapies in medicine, 2019-08, Vol.45, p.254-261 |
issn | 0965-2299 1873-6963 |
language | eng |
recordid | cdi_proquest_miscellaneous_2331633501 |
source | ScienceDirect Journals |
subjects | Acids Amines Animal models Animals Anti-inflammatory agents Anti-Inflammatory Agents - pharmacology Arachidonic acid Carrageenan Carrageenan - pharmacology Cell adhesion & migration Chlorogenic acid Chromatography Chrysobalanaceae - chemistry Conflicts of interest Cytokines Dextran Edema Edema - chemically induced Edema - drug therapy Enzymes Flavonoids Flavonoids - pharmacology High performance liquid chromatography Histamine Hydroxybenzoates - pharmacology Indomethacin Inflammation Inflammation - chemically induced Inflammation - drug therapy Inhibition Leukocyte migration Licania rigida Liquid chromatography Male Metabolism Mice Nonsteroidal anti-inflammatory drugs Oral administration Organic chemistry Peritoneum Peritonitis Peritonitis - chemically induced Peritonitis - drug therapy Permeability Pharmaceutical industry Phenolic acids Phenols Phytotherapy - methods Plant Extracts - pharmacology Plant Leaves - chemistry Promethazine Vasoactive agents |
title | Anti-inflammatory activity of herb products from Licania rigida Benth |
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