Loading…
Cytotoxicity, nitric oxide and acetylcholinesterase inhibitory activity of three limonoids isolated from Trichilia welwitschii (Meliaceae)
Limonoids are highly oxygenated compounds with a prototypical structure. Their occurrence in the plant kingdom is mainly confined to plant families of Meliaceae and Rutaceae. Owing to their wide range of pharmacological and therapeutic properties, this study was aimed at investigating the potential...
Saved in:
Published in: | Biological research 2015-10, Vol.48 (1), p.57-57, Article 57 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603 |
---|---|
cites | cdi_FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603 |
container_end_page | 57 |
container_issue | 1 |
container_start_page | 57 |
container_title | Biological research |
container_volume | 48 |
creator | Dzoyem, Jean P Tsamo, Armelle T Melong, Raduis Mkounga, Pierre Nkengfack, Augustin E McGaw, Lyndy J Eloff, Jacobus N |
description | Limonoids are highly oxygenated compounds with a prototypical structure. Their occurrence in the plant kingdom is mainly confined to plant families of Meliaceae and Rutaceae. Owing to their wide range of pharmacological and therapeutic properties, this study was aimed at investigating the potential nitric oxide (NO) and acetylcholinesterase (AChE) inhibitory activity and the cytotoxicity of three limonoids: trichilia lactone D5 (1), rohituka 3 (2) and dregeanin DM4 (3), isolated from Trichilia welwitschii C.DC.
Results indicated that the three limonoids had low cytotoxicity towards Vero cells with LC50 values ranging from 89.17 to 75.82 μg/mL. Compounds (2) and (3) had lower cytotoxicity compared to puromycin and doxorubicin used as reference cytotoxic compounds. Compound (1) (LC50 of 23.55 μg/mL) had good antiproliferative activity against RAW 264.7 cancer cells. At the lowest concentration tested (0.5 µg/mL), compound (2) and (3) released the lowest amount of nitric oxide (2.97 and 2.93 µM, respectively). The three limonoids had anti-AChE activity with IC50 values ranged of 19.13 μg/mL for (1), 34.15 μg/mL for (2) and 45.66 μg/mL for (3), compared to galantamine (IC50 of 8.22 μg/mL) used as positive control.
The limonoid compounds studied in this work inhibited nitric oxide production in LPS-stimulated macrophages and had anti-AChE activity. Trichilia lactone D5 had potential antiproliferative activity against RAW 264.7 cancer cells. The limonoids had low cytotoxicity towards Vero cells lines. This study provided further examples of the importance of limonoids compounds as potential AChE inhibitors and anti-inflammatory agents targeting the inhibition of NO production. |
doi_str_mv | 10.1186/s40659-015-0049-0 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_5497d1a39ba741dd8da2456eb105eab4</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A541684919</galeid><scielo_id>S0716_97602015000100057</scielo_id><doaj_id>oai_doaj_org_article_5497d1a39ba741dd8da2456eb105eab4</doaj_id><sourcerecordid>A541684919</sourcerecordid><originalsourceid>FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603</originalsourceid><addsrcrecordid>eNpVUl1vFCEUnRiNrdUf4Ish8aVNnAosMDMvTZqNH5vUmNj6TBi4s3ubmaEC23b_gr9a1qm1E0KAyzkHzr23KN4yespYrT5GQZVsSspkSanIm2fFIa1YVSpeV8-f7A-KVzFeU8ol5eplccCVUAul6GHxe7lLPvl7tJh2H8iIKaAl-eyAmNERYyHtervxPY4QEwQTgeC4wRaTD7t8n_A2U4nvSNoEANLj4EePLhKMvjcJHOmCH8hVFt5gj4bcQX-HKeYTkuNvkEMWDJy8Ll50po_w5mE9Kn5-_nS1_FpefP-yWp5flFZVLJVKMG4sbYCBE0y0tJLZex685sxZXjfWNFLJVnWdNFJm_60UyrpaUGkUXRwVq0nXeXOtbwIOJuy0N6j_BnxYaxMS2h60FE3lmFk0rakEc652hgupoGVUgmlF1jqdtKJF6L2-9tsw5s_ry5x7pZtKUZ7LQyllecoqE84mws22HcBZGFMw_ewX85sRN3rtb7VQVCjOssDxg0Dwv7a5JHrAaKHvzQh-GzWrOBd8Qdn-rfcTdG2yFxw7nxXtHq7PpWCqFg1r_luYofJwMKD1I3SY4zPCyYyQMQnu09psY9Sryx9zLJuwNvgYA3SPThnV-x7WUw_rnCS972G9r8-7pyl6ZPxr2sUfyXTq1Q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1722423017</pqid></control><display><type>article</type><title>Cytotoxicity, nitric oxide and acetylcholinesterase inhibitory activity of three limonoids isolated from Trichilia welwitschii (Meliaceae)</title><source>SpringerLink Contemporary</source><source>Publicly Available Content (ProQuest)</source><source>SciELO</source><creator>Dzoyem, Jean P ; Tsamo, Armelle T ; Melong, Raduis ; Mkounga, Pierre ; Nkengfack, Augustin E ; McGaw, Lyndy J ; Eloff, Jacobus N</creator><creatorcontrib>Dzoyem, Jean P ; Tsamo, Armelle T ; Melong, Raduis ; Mkounga, Pierre ; Nkengfack, Augustin E ; McGaw, Lyndy J ; Eloff, Jacobus N</creatorcontrib><description>Limonoids are highly oxygenated compounds with a prototypical structure. Their occurrence in the plant kingdom is mainly confined to plant families of Meliaceae and Rutaceae. Owing to their wide range of pharmacological and therapeutic properties, this study was aimed at investigating the potential nitric oxide (NO) and acetylcholinesterase (AChE) inhibitory activity and the cytotoxicity of three limonoids: trichilia lactone D5 (1), rohituka 3 (2) and dregeanin DM4 (3), isolated from Trichilia welwitschii C.DC.
Results indicated that the three limonoids had low cytotoxicity towards Vero cells with LC50 values ranging from 89.17 to 75.82 μg/mL. Compounds (2) and (3) had lower cytotoxicity compared to puromycin and doxorubicin used as reference cytotoxic compounds. Compound (1) (LC50 of 23.55 μg/mL) had good antiproliferative activity against RAW 264.7 cancer cells. At the lowest concentration tested (0.5 µg/mL), compound (2) and (3) released the lowest amount of nitric oxide (2.97 and 2.93 µM, respectively). The three limonoids had anti-AChE activity with IC50 values ranged of 19.13 μg/mL for (1), 34.15 μg/mL for (2) and 45.66 μg/mL for (3), compared to galantamine (IC50 of 8.22 μg/mL) used as positive control.
The limonoid compounds studied in this work inhibited nitric oxide production in LPS-stimulated macrophages and had anti-AChE activity. Trichilia lactone D5 had potential antiproliferative activity against RAW 264.7 cancer cells. The limonoids had low cytotoxicity towards Vero cells lines. This study provided further examples of the importance of limonoids compounds as potential AChE inhibitors and anti-inflammatory agents targeting the inhibition of NO production.</description><identifier>ISSN: 0717-6287</identifier><identifier>ISSN: 0716-9760</identifier><identifier>EISSN: 0717-6287</identifier><identifier>DOI: 10.1186/s40659-015-0049-0</identifier><identifier>PMID: 26463660</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acetylcholinesterase ; Animals ; Anti-Inflammatory Agents - pharmacology ; BIOLOGY ; Cell Proliferation - drug effects ; Cercopithecus aethiops ; Cholinesterase Inhibitors - pharmacology ; Cytotoxicity ; Inhibitory Concentration 50 ; Lactones - analysis ; Lactones - pharmacology ; Lethal Dose 50 ; Limonins - analysis ; Limonins - isolation & purification ; Limonins - pharmacology ; Limonoids ; Lipopolysaccharides ; Macrophages - drug effects ; Meliaceae ; Meliaceae - chemistry ; Mice ; Nitric oxide ; Nitric Oxide - analysis ; Nitric Oxide - antagonists & inhibitors ; Properties ; RAW 264.7 Cells ; Toxicity ; Trichilia welwitschii ; Vero Cells</subject><ispartof>Biological research, 2015-10, Vol.48 (1), p.57-57, Article 57</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Dzoyem et al. 2015</rights><rights>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603</citedby><cites>FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603</cites><orcidid>0000-0003-3568-6711</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,24151,27924,27925,37013</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26463660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dzoyem, Jean P</creatorcontrib><creatorcontrib>Tsamo, Armelle T</creatorcontrib><creatorcontrib>Melong, Raduis</creatorcontrib><creatorcontrib>Mkounga, Pierre</creatorcontrib><creatorcontrib>Nkengfack, Augustin E</creatorcontrib><creatorcontrib>McGaw, Lyndy J</creatorcontrib><creatorcontrib>Eloff, Jacobus N</creatorcontrib><title>Cytotoxicity, nitric oxide and acetylcholinesterase inhibitory activity of three limonoids isolated from Trichilia welwitschii (Meliaceae)</title><title>Biological research</title><addtitle>Biol Res</addtitle><description>Limonoids are highly oxygenated compounds with a prototypical structure. Their occurrence in the plant kingdom is mainly confined to plant families of Meliaceae and Rutaceae. Owing to their wide range of pharmacological and therapeutic properties, this study was aimed at investigating the potential nitric oxide (NO) and acetylcholinesterase (AChE) inhibitory activity and the cytotoxicity of three limonoids: trichilia lactone D5 (1), rohituka 3 (2) and dregeanin DM4 (3), isolated from Trichilia welwitschii C.DC.
Results indicated that the three limonoids had low cytotoxicity towards Vero cells with LC50 values ranging from 89.17 to 75.82 μg/mL. Compounds (2) and (3) had lower cytotoxicity compared to puromycin and doxorubicin used as reference cytotoxic compounds. Compound (1) (LC50 of 23.55 μg/mL) had good antiproliferative activity against RAW 264.7 cancer cells. At the lowest concentration tested (0.5 µg/mL), compound (2) and (3) released the lowest amount of nitric oxide (2.97 and 2.93 µM, respectively). The three limonoids had anti-AChE activity with IC50 values ranged of 19.13 μg/mL for (1), 34.15 μg/mL for (2) and 45.66 μg/mL for (3), compared to galantamine (IC50 of 8.22 μg/mL) used as positive control.
The limonoid compounds studied in this work inhibited nitric oxide production in LPS-stimulated macrophages and had anti-AChE activity. Trichilia lactone D5 had potential antiproliferative activity against RAW 264.7 cancer cells. The limonoids had low cytotoxicity towards Vero cells lines. This study provided further examples of the importance of limonoids compounds as potential AChE inhibitors and anti-inflammatory agents targeting the inhibition of NO production.</description><subject>Acetylcholinesterase</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>BIOLOGY</subject><subject>Cell Proliferation - drug effects</subject><subject>Cercopithecus aethiops</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Cytotoxicity</subject><subject>Inhibitory Concentration 50</subject><subject>Lactones - analysis</subject><subject>Lactones - pharmacology</subject><subject>Lethal Dose 50</subject><subject>Limonins - analysis</subject><subject>Limonins - isolation & purification</subject><subject>Limonins - pharmacology</subject><subject>Limonoids</subject><subject>Lipopolysaccharides</subject><subject>Macrophages - drug effects</subject><subject>Meliaceae</subject><subject>Meliaceae - chemistry</subject><subject>Mice</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - analysis</subject><subject>Nitric Oxide - antagonists & inhibitors</subject><subject>Properties</subject><subject>RAW 264.7 Cells</subject><subject>Toxicity</subject><subject>Trichilia welwitschii</subject><subject>Vero Cells</subject><issn>0717-6287</issn><issn>0716-9760</issn><issn>0717-6287</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVUl1vFCEUnRiNrdUf4Ish8aVNnAosMDMvTZqNH5vUmNj6TBi4s3ubmaEC23b_gr9a1qm1E0KAyzkHzr23KN4yespYrT5GQZVsSspkSanIm2fFIa1YVSpeV8-f7A-KVzFeU8ol5eplccCVUAul6GHxe7lLPvl7tJh2H8iIKaAl-eyAmNERYyHtervxPY4QEwQTgeC4wRaTD7t8n_A2U4nvSNoEANLj4EePLhKMvjcJHOmCH8hVFt5gj4bcQX-HKeYTkuNvkEMWDJy8Ll50po_w5mE9Kn5-_nS1_FpefP-yWp5flFZVLJVKMG4sbYCBE0y0tJLZex685sxZXjfWNFLJVnWdNFJm_60UyrpaUGkUXRwVq0nXeXOtbwIOJuy0N6j_BnxYaxMS2h60FE3lmFk0rakEc652hgupoGVUgmlF1jqdtKJF6L2-9tsw5s_ry5x7pZtKUZ7LQyllecoqE84mws22HcBZGFMw_ewX85sRN3rtb7VQVCjOssDxg0Dwv7a5JHrAaKHvzQh-GzWrOBd8Qdn-rfcTdG2yFxw7nxXtHq7PpWCqFg1r_luYofJwMKD1I3SY4zPCyYyQMQnu09psY9Sryx9zLJuwNvgYA3SPThnV-x7WUw_rnCS972G9r8-7pyl6ZPxr2sUfyXTq1Q</recordid><startdate>20151013</startdate><enddate>20151013</enddate><creator>Dzoyem, Jean P</creator><creator>Tsamo, Armelle T</creator><creator>Melong, Raduis</creator><creator>Mkounga, Pierre</creator><creator>Nkengfack, Augustin E</creator><creator>McGaw, Lyndy J</creator><creator>Eloff, Jacobus N</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>Sociedad de Biología de Chile</general><general>BMC</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>ISR</scope><scope>INF</scope><scope>7X8</scope><scope>5PM</scope><scope>GPN</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3568-6711</orcidid></search><sort><creationdate>20151013</creationdate><title>Cytotoxicity, nitric oxide and acetylcholinesterase inhibitory activity of three limonoids isolated from Trichilia welwitschii (Meliaceae)</title><author>Dzoyem, Jean P ; Tsamo, Armelle T ; Melong, Raduis ; Mkounga, Pierre ; Nkengfack, Augustin E ; McGaw, Lyndy J ; Eloff, Jacobus N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acetylcholinesterase</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>BIOLOGY</topic><topic>Cell Proliferation - drug effects</topic><topic>Cercopithecus aethiops</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Cytotoxicity</topic><topic>Inhibitory Concentration 50</topic><topic>Lactones - analysis</topic><topic>Lactones - pharmacology</topic><topic>Lethal Dose 50</topic><topic>Limonins - analysis</topic><topic>Limonins - isolation & purification</topic><topic>Limonins - pharmacology</topic><topic>Limonoids</topic><topic>Lipopolysaccharides</topic><topic>Macrophages - drug effects</topic><topic>Meliaceae</topic><topic>Meliaceae - chemistry</topic><topic>Mice</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - analysis</topic><topic>Nitric Oxide - antagonists & inhibitors</topic><topic>Properties</topic><topic>RAW 264.7 Cells</topic><topic>Toxicity</topic><topic>Trichilia welwitschii</topic><topic>Vero Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dzoyem, Jean P</creatorcontrib><creatorcontrib>Tsamo, Armelle T</creatorcontrib><creatorcontrib>Melong, Raduis</creatorcontrib><creatorcontrib>Mkounga, Pierre</creatorcontrib><creatorcontrib>Nkengfack, Augustin E</creatorcontrib><creatorcontrib>McGaw, Lyndy J</creatorcontrib><creatorcontrib>Eloff, Jacobus N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>Informe Revistas en Espanol</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SciELO</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dzoyem, Jean P</au><au>Tsamo, Armelle T</au><au>Melong, Raduis</au><au>Mkounga, Pierre</au><au>Nkengfack, Augustin E</au><au>McGaw, Lyndy J</au><au>Eloff, Jacobus N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytotoxicity, nitric oxide and acetylcholinesterase inhibitory activity of three limonoids isolated from Trichilia welwitschii (Meliaceae)</atitle><jtitle>Biological research</jtitle><addtitle>Biol Res</addtitle><date>2015-10-13</date><risdate>2015</risdate><volume>48</volume><issue>1</issue><spage>57</spage><epage>57</epage><pages>57-57</pages><artnum>57</artnum><issn>0717-6287</issn><issn>0716-9760</issn><eissn>0717-6287</eissn><abstract>Limonoids are highly oxygenated compounds with a prototypical structure. Their occurrence in the plant kingdom is mainly confined to plant families of Meliaceae and Rutaceae. Owing to their wide range of pharmacological and therapeutic properties, this study was aimed at investigating the potential nitric oxide (NO) and acetylcholinesterase (AChE) inhibitory activity and the cytotoxicity of three limonoids: trichilia lactone D5 (1), rohituka 3 (2) and dregeanin DM4 (3), isolated from Trichilia welwitschii C.DC.
Results indicated that the three limonoids had low cytotoxicity towards Vero cells with LC50 values ranging from 89.17 to 75.82 μg/mL. Compounds (2) and (3) had lower cytotoxicity compared to puromycin and doxorubicin used as reference cytotoxic compounds. Compound (1) (LC50 of 23.55 μg/mL) had good antiproliferative activity against RAW 264.7 cancer cells. At the lowest concentration tested (0.5 µg/mL), compound (2) and (3) released the lowest amount of nitric oxide (2.97 and 2.93 µM, respectively). The three limonoids had anti-AChE activity with IC50 values ranged of 19.13 μg/mL for (1), 34.15 μg/mL for (2) and 45.66 μg/mL for (3), compared to galantamine (IC50 of 8.22 μg/mL) used as positive control.
The limonoid compounds studied in this work inhibited nitric oxide production in LPS-stimulated macrophages and had anti-AChE activity. Trichilia lactone D5 had potential antiproliferative activity against RAW 264.7 cancer cells. The limonoids had low cytotoxicity towards Vero cells lines. This study provided further examples of the importance of limonoids compounds as potential AChE inhibitors and anti-inflammatory agents targeting the inhibition of NO production.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26463660</pmid><doi>10.1186/s40659-015-0049-0</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-3568-6711</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0717-6287 |
ispartof | Biological research, 2015-10, Vol.48 (1), p.57-57, Article 57 |
issn | 0717-6287 0716-9760 0717-6287 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_5497d1a39ba741dd8da2456eb105eab4 |
source | SpringerLink Contemporary; Publicly Available Content (ProQuest); SciELO |
subjects | Acetylcholinesterase Animals Anti-Inflammatory Agents - pharmacology BIOLOGY Cell Proliferation - drug effects Cercopithecus aethiops Cholinesterase Inhibitors - pharmacology Cytotoxicity Inhibitory Concentration 50 Lactones - analysis Lactones - pharmacology Lethal Dose 50 Limonins - analysis Limonins - isolation & purification Limonins - pharmacology Limonoids Lipopolysaccharides Macrophages - drug effects Meliaceae Meliaceae - chemistry Mice Nitric oxide Nitric Oxide - analysis Nitric Oxide - antagonists & inhibitors Properties RAW 264.7 Cells Toxicity Trichilia welwitschii Vero Cells |
title | Cytotoxicity, nitric oxide and acetylcholinesterase inhibitory activity of three limonoids isolated from Trichilia welwitschii (Meliaceae) |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T23%3A40%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cytotoxicity,%20nitric%20oxide%20and%20acetylcholinesterase%20inhibitory%20activity%20of%20three%20limonoids%20isolated%20from%20Trichilia%20welwitschii%20(Meliaceae)&rft.jtitle=Biological%20research&rft.au=Dzoyem,%20Jean%20P&rft.date=2015-10-13&rft.volume=48&rft.issue=1&rft.spage=57&rft.epage=57&rft.pages=57-57&rft.artnum=57&rft.issn=0717-6287&rft.eissn=0717-6287&rft_id=info:doi/10.1186/s40659-015-0049-0&rft_dat=%3Cgale_doaj_%3EA541684919%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c671t-6412ac09e1ed414b0750494942821dc289ca9565b6ff5a55628b546cd8405a603%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1722423017&rft_id=info:pmid/26463660&rft_galeid=A541684919&rft_scielo_id=S0716_97602015000100057&rfr_iscdi=true |