Loading…
Curcumin as a Stabilizer of Macrophage Polarization during Plasmodium Infection
Malaria is a parasitic infection responsible for high morbidity and mortality rates worldwide. During the disease, phagocytosis of infected red blood cells by the macrophages induces the production of reactive oxygen (ROS) and nitrogen species (RNS), culminating in parasite death. Curcumin (CUR) is...
Saved in:
Published in: | Pharmaceutics 2023-10, Vol.15 (10), p.2505 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c431t-b72aa35e81ece0485ac790d779e488d338d4cfc19d5c80a5813046c58de32a223 |
container_end_page | |
container_issue | 10 |
container_start_page | 2505 |
container_title | Pharmaceutics |
container_volume | 15 |
creator | Cordeiro, Maria Clara C. Tomé, Fernanda D. Arruda, Felipe S. da Fonseca, Simone Gonçalves Nagib, Patrícia R. A. Celes, Mara R. N. |
description | Malaria is a parasitic infection responsible for high morbidity and mortality rates worldwide. During the disease, phagocytosis of infected red blood cells by the macrophages induces the production of reactive oxygen (ROS) and nitrogen species (RNS), culminating in parasite death. Curcumin (CUR) is a bioactive compound that has been demonstrated to reduce the production of pro-inflammatory cytokines and chemokines produced by macrophages but to reduce parasitemia in infected mice. Hence, the main purpose of this study is to investigate whether curcumin may interfere with macrophage function and polarization after Plasmodium berghei infection in vitro. In our findings, non-polarized macrophage (M0), classically activated (M1), and alternatively activated (M2) phenotypes showed significantly increased phagocytosis of infected red blood cells (iRBCs) when compared to phagocytosis of uninfected red blood cells (RBCs) 3 h after infection. After 24 h, M1 macrophages exposed to RBCs + CUR showed greater elimination capacity when compared to macrophages exposed to iRBCs + CUR, suggesting the interference of curcumin with the microbicidal activity. Additionally, curcumin increased the phagocytic activity of macrophages when used in non-inflammatory conditions (M0) and reduced the inducible nitric oxide synthase (iNOS) and arginase activities in all macrophage phenotypes infected (M0, M1, and M2), suggesting interference in arginine availability by curcumin and balance promotion in macrophage polarization in neutral phenotype (M0). These results support the view of curcumin treatment in malaria as an adjuvant, promoting a balance between pro- and anti-inflammatory responses for a better clinical outcome. |
doi_str_mv | 10.3390/pharmaceutics15102505 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_d337201c6f7541569d16d453dedd9000</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_d337201c6f7541569d16d453dedd9000</doaj_id><sourcerecordid>2883580562</sourcerecordid><originalsourceid>FETCH-LOGICAL-c431t-b72aa35e81ece0485ac790d779e488d338d4cfc19d5c80a5813046c58de32a223</originalsourceid><addsrcrecordid>eNptkk9r3DAQxUVpacI2H6Fg6KWXbSWNZUunUpb-WUhJoO1ZzErjjRbb2kpWofn0tbMhJKW6SMw8fvN4GsZeC_4OwPD3xxtMAzoqU3BZKMGl4uoZOxfGmHVtJDx_9D5jFzkf-HwAhAbzkp1Bq00jG3XOrjYluTKEscJcYfV9wl3owy2lKnbVN3QpzrP2VF3HHlO4xSnEsfIlhXFfXfeYh-hDGart2JFbeq_Yiw77TBf394r9_Pzpx-br-vLqy3bz8XLtahDTetdKRFCkBTnitVboWsN92xqqtfYA2teuc8J45TRHpQXwunFKewKJUsKKbU9cH_FgjykMmP7YiMHeFWLaW0xzOj3ZmdZKLlzTtaoWqjFeNL5W4Ml7s6SyYh9OrGPZDeQdjVPC_gn0aWcMN3Yff1vBmzn6O8Lbe0KKvwrlyQ4hO-p7HCmWbKXWoDRXzWL8zT_SQyxpnLNaVLI1mhuYVeqkmj8g50TdgxvB7bIC9r8rAH8BqnqmXw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2882798093</pqid></control><display><type>article</type><title>Curcumin as a Stabilizer of Macrophage Polarization during Plasmodium Infection</title><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Coronavirus Research Database</source><creator>Cordeiro, Maria Clara C. ; Tomé, Fernanda D. ; Arruda, Felipe S. ; da Fonseca, Simone Gonçalves ; Nagib, Patrícia R. A. ; Celes, Mara R. N.</creator><creatorcontrib>Cordeiro, Maria Clara C. ; Tomé, Fernanda D. ; Arruda, Felipe S. ; da Fonseca, Simone Gonçalves ; Nagib, Patrícia R. A. ; Celes, Mara R. N.</creatorcontrib><description>Malaria is a parasitic infection responsible for high morbidity and mortality rates worldwide. During the disease, phagocytosis of infected red blood cells by the macrophages induces the production of reactive oxygen (ROS) and nitrogen species (RNS), culminating in parasite death. Curcumin (CUR) is a bioactive compound that has been demonstrated to reduce the production of pro-inflammatory cytokines and chemokines produced by macrophages but to reduce parasitemia in infected mice. Hence, the main purpose of this study is to investigate whether curcumin may interfere with macrophage function and polarization after Plasmodium berghei infection in vitro. In our findings, non-polarized macrophage (M0), classically activated (M1), and alternatively activated (M2) phenotypes showed significantly increased phagocytosis of infected red blood cells (iRBCs) when compared to phagocytosis of uninfected red blood cells (RBCs) 3 h after infection. After 24 h, M1 macrophages exposed to RBCs + CUR showed greater elimination capacity when compared to macrophages exposed to iRBCs + CUR, suggesting the interference of curcumin with the microbicidal activity. Additionally, curcumin increased the phagocytic activity of macrophages when used in non-inflammatory conditions (M0) and reduced the inducible nitric oxide synthase (iNOS) and arginase activities in all macrophage phenotypes infected (M0, M1, and M2), suggesting interference in arginine availability by curcumin and balance promotion in macrophage polarization in neutral phenotype (M0). These results support the view of curcumin treatment in malaria as an adjuvant, promoting a balance between pro- and anti-inflammatory responses for a better clinical outcome.</description><identifier>ISSN: 1999-4923</identifier><identifier>EISSN: 1999-4923</identifier><identifier>DOI: 10.3390/pharmaceutics15102505</identifier><identifier>PMID: 37896265</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antigens ; arginase ; Blood ; curcumin ; Cytokines ; Enzymes ; FDA approval ; Genotype & phenotype ; Infections ; iNOS ; Malaria ; Pathogens ; phagocytosis ; RAW 264.7 cells ; Yeast</subject><ispartof>Pharmaceutics, 2023-10, Vol.15 (10), p.2505</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c431t-b72aa35e81ece0485ac790d779e488d338d4cfc19d5c80a5813046c58de32a223</cites><orcidid>0000-0002-1331-0441 ; 0000-0002-4733-007X ; 0000-0003-4700-9646 ; 0000-0002-5126-6306 ; 0000-0002-6775-390X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2882798093/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2882798093?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids></links><search><creatorcontrib>Cordeiro, Maria Clara C.</creatorcontrib><creatorcontrib>Tomé, Fernanda D.</creatorcontrib><creatorcontrib>Arruda, Felipe S.</creatorcontrib><creatorcontrib>da Fonseca, Simone Gonçalves</creatorcontrib><creatorcontrib>Nagib, Patrícia R. A.</creatorcontrib><creatorcontrib>Celes, Mara R. N.</creatorcontrib><title>Curcumin as a Stabilizer of Macrophage Polarization during Plasmodium Infection</title><title>Pharmaceutics</title><description>Malaria is a parasitic infection responsible for high morbidity and mortality rates worldwide. During the disease, phagocytosis of infected red blood cells by the macrophages induces the production of reactive oxygen (ROS) and nitrogen species (RNS), culminating in parasite death. Curcumin (CUR) is a bioactive compound that has been demonstrated to reduce the production of pro-inflammatory cytokines and chemokines produced by macrophages but to reduce parasitemia in infected mice. Hence, the main purpose of this study is to investigate whether curcumin may interfere with macrophage function and polarization after Plasmodium berghei infection in vitro. In our findings, non-polarized macrophage (M0), classically activated (M1), and alternatively activated (M2) phenotypes showed significantly increased phagocytosis of infected red blood cells (iRBCs) when compared to phagocytosis of uninfected red blood cells (RBCs) 3 h after infection. After 24 h, M1 macrophages exposed to RBCs + CUR showed greater elimination capacity when compared to macrophages exposed to iRBCs + CUR, suggesting the interference of curcumin with the microbicidal activity. Additionally, curcumin increased the phagocytic activity of macrophages when used in non-inflammatory conditions (M0) and reduced the inducible nitric oxide synthase (iNOS) and arginase activities in all macrophage phenotypes infected (M0, M1, and M2), suggesting interference in arginine availability by curcumin and balance promotion in macrophage polarization in neutral phenotype (M0). These results support the view of curcumin treatment in malaria as an adjuvant, promoting a balance between pro- and anti-inflammatory responses for a better clinical outcome.</description><subject>Antigens</subject><subject>arginase</subject><subject>Blood</subject><subject>curcumin</subject><subject>Cytokines</subject><subject>Enzymes</subject><subject>FDA approval</subject><subject>Genotype & phenotype</subject><subject>Infections</subject><subject>iNOS</subject><subject>Malaria</subject><subject>Pathogens</subject><subject>phagocytosis</subject><subject>RAW 264.7 cells</subject><subject>Yeast</subject><issn>1999-4923</issn><issn>1999-4923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk9r3DAQxUVpacI2H6Fg6KWXbSWNZUunUpb-WUhJoO1ZzErjjRbb2kpWofn0tbMhJKW6SMw8fvN4GsZeC_4OwPD3xxtMAzoqU3BZKMGl4uoZOxfGmHVtJDx_9D5jFzkf-HwAhAbzkp1Bq00jG3XOrjYluTKEscJcYfV9wl3owy2lKnbVN3QpzrP2VF3HHlO4xSnEsfIlhXFfXfeYh-hDGart2JFbeq_Yiw77TBf394r9_Pzpx-br-vLqy3bz8XLtahDTetdKRFCkBTnitVboWsN92xqqtfYA2teuc8J45TRHpQXwunFKewKJUsKKbU9cH_FgjykMmP7YiMHeFWLaW0xzOj3ZmdZKLlzTtaoWqjFeNL5W4Ml7s6SyYh9OrGPZDeQdjVPC_gn0aWcMN3Yff1vBmzn6O8Lbe0KKvwrlyQ4hO-p7HCmWbKXWoDRXzWL8zT_SQyxpnLNaVLI1mhuYVeqkmj8g50TdgxvB7bIC9r8rAH8BqnqmXw</recordid><startdate>20231021</startdate><enddate>20231021</enddate><creator>Cordeiro, Maria Clara C.</creator><creator>Tomé, Fernanda D.</creator><creator>Arruda, Felipe S.</creator><creator>da Fonseca, Simone Gonçalves</creator><creator>Nagib, Patrícia R. A.</creator><creator>Celes, Mara R. N.</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1331-0441</orcidid><orcidid>https://orcid.org/0000-0002-4733-007X</orcidid><orcidid>https://orcid.org/0000-0003-4700-9646</orcidid><orcidid>https://orcid.org/0000-0002-5126-6306</orcidid><orcidid>https://orcid.org/0000-0002-6775-390X</orcidid></search><sort><creationdate>20231021</creationdate><title>Curcumin as a Stabilizer of Macrophage Polarization during Plasmodium Infection</title><author>Cordeiro, Maria Clara C. ; Tomé, Fernanda D. ; Arruda, Felipe S. ; da Fonseca, Simone Gonçalves ; Nagib, Patrícia R. A. ; Celes, Mara R. N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-b72aa35e81ece0485ac790d779e488d338d4cfc19d5c80a5813046c58de32a223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigens</topic><topic>arginase</topic><topic>Blood</topic><topic>curcumin</topic><topic>Cytokines</topic><topic>Enzymes</topic><topic>FDA approval</topic><topic>Genotype & phenotype</topic><topic>Infections</topic><topic>iNOS</topic><topic>Malaria</topic><topic>Pathogens</topic><topic>phagocytosis</topic><topic>RAW 264.7 cells</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cordeiro, Maria Clara C.</creatorcontrib><creatorcontrib>Tomé, Fernanda D.</creatorcontrib><creatorcontrib>Arruda, Felipe S.</creatorcontrib><creatorcontrib>da Fonseca, Simone Gonçalves</creatorcontrib><creatorcontrib>Nagib, Patrícia R. A.</creatorcontrib><creatorcontrib>Celes, Mara R. N.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</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>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content 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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cordeiro, Maria Clara C.</au><au>Tomé, Fernanda D.</au><au>Arruda, Felipe S.</au><au>da Fonseca, Simone Gonçalves</au><au>Nagib, Patrícia R. A.</au><au>Celes, Mara R. N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Curcumin as a Stabilizer of Macrophage Polarization during Plasmodium Infection</atitle><jtitle>Pharmaceutics</jtitle><date>2023-10-21</date><risdate>2023</risdate><volume>15</volume><issue>10</issue><spage>2505</spage><pages>2505-</pages><issn>1999-4923</issn><eissn>1999-4923</eissn><abstract>Malaria is a parasitic infection responsible for high morbidity and mortality rates worldwide. During the disease, phagocytosis of infected red blood cells by the macrophages induces the production of reactive oxygen (ROS) and nitrogen species (RNS), culminating in parasite death. Curcumin (CUR) is a bioactive compound that has been demonstrated to reduce the production of pro-inflammatory cytokines and chemokines produced by macrophages but to reduce parasitemia in infected mice. Hence, the main purpose of this study is to investigate whether curcumin may interfere with macrophage function and polarization after Plasmodium berghei infection in vitro. In our findings, non-polarized macrophage (M0), classically activated (M1), and alternatively activated (M2) phenotypes showed significantly increased phagocytosis of infected red blood cells (iRBCs) when compared to phagocytosis of uninfected red blood cells (RBCs) 3 h after infection. After 24 h, M1 macrophages exposed to RBCs + CUR showed greater elimination capacity when compared to macrophages exposed to iRBCs + CUR, suggesting the interference of curcumin with the microbicidal activity. Additionally, curcumin increased the phagocytic activity of macrophages when used in non-inflammatory conditions (M0) and reduced the inducible nitric oxide synthase (iNOS) and arginase activities in all macrophage phenotypes infected (M0, M1, and M2), suggesting interference in arginine availability by curcumin and balance promotion in macrophage polarization in neutral phenotype (M0). These results support the view of curcumin treatment in malaria as an adjuvant, promoting a balance between pro- and anti-inflammatory responses for a better clinical outcome.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>37896265</pmid><doi>10.3390/pharmaceutics15102505</doi><orcidid>https://orcid.org/0000-0002-1331-0441</orcidid><orcidid>https://orcid.org/0000-0002-4733-007X</orcidid><orcidid>https://orcid.org/0000-0003-4700-9646</orcidid><orcidid>https://orcid.org/0000-0002-5126-6306</orcidid><orcidid>https://orcid.org/0000-0002-6775-390X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1999-4923 |
ispartof | Pharmaceutics, 2023-10, Vol.15 (10), p.2505 |
issn | 1999-4923 1999-4923 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_d337201c6f7541569d16d453dedd9000 |
source | Publicly Available Content Database; PubMed Central; Coronavirus Research Database |
subjects | Antigens arginase Blood curcumin Cytokines Enzymes FDA approval Genotype & phenotype Infections iNOS Malaria Pathogens phagocytosis RAW 264.7 cells Yeast |
title | Curcumin as a Stabilizer of Macrophage Polarization during Plasmodium Infection |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T17%3A28%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Curcumin%20as%20a%20Stabilizer%20of%20Macrophage%20Polarization%20during%20Plasmodium%20Infection&rft.jtitle=Pharmaceutics&rft.au=Cordeiro,%20Maria%20Clara%20C.&rft.date=2023-10-21&rft.volume=15&rft.issue=10&rft.spage=2505&rft.pages=2505-&rft.issn=1999-4923&rft.eissn=1999-4923&rft_id=info:doi/10.3390/pharmaceutics15102505&rft_dat=%3Cproquest_doaj_%3E2883580562%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c431t-b72aa35e81ece0485ac790d779e488d338d4cfc19d5c80a5813046c58de32a223%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2882798093&rft_id=info:pmid/37896265&rfr_iscdi=true |