Local inflammatory reaction induced by Scolopendra viridicornis centipede venom in mice
Centipede envenomation is generally mild, and human victims usually manifest burning pain, erythema and edema. Despite the abundance and ubiquity of these animals, centipede venom has been poorly characterized in literature. For this reason, the aim of this work was to investigate local inflammatory...
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creator | Kimura, Louise Faggionato Prezotto-Neto, José Pedro Távora, Bianca de Carvalho Lins Fernandes Antoniazzi, Marta Maria Knysak, Irene Gióia Guizze, Samuel Paulo Santoro, Marcelo Larami Barbaro, Katia Cristina |
description | Centipede envenomation is generally mild, and human victims usually manifest burning pain, erythema and edema. Despite the abundance and ubiquity of these animals, centipede venom has been poorly characterized in literature. For this reason, the aim of this work was to investigate local inflammatory features induced by Scolopendra viridicornis centipede envenomation in mice, evaluating edema formation, leukocyte infiltration, production of inflammatory mediators, and also performing histological analysis. The highest edematogenic activity induced by the venom, determined by plethysmometry, was noticed 0.5 h after injection in mice footpad. At 24 h, edema was still detected in animals that received 15 and 60 μg of venom, and at 48 h, only in animals injected with 60 μg of venom. In relation to leukocyte count, S. viridicornis venom induced cell recruitment, mainly neutrophils and monocytes/macrophages, in all doses and time periods analyzed in comparison with PBS-injected mice. An increase in lymphocytes was detected especially between 1 and 24 h at 60 μg dose. Besides, eosinophil recruitment was observed mainly for 15 and 60 μg doses in early time periods. Edema formation and cell recruitment were also confirmed by histological analysis. Moreover, S. viridicornis venom stimulated the release of IL-6, MCP-1, KC, and IL-1β. Conversely, S. viridicornis venom did not induce the release of detectable levels of TNF-α. We demonstrated that the edematogenic activity induced by S. viridicornis venom was of rapid onset, and the venom stimulated secretion of pro-inflammatory mediators which contribute to the inflammatory reaction induced by S. viridicornis venom in an experimental model.
•Scolopendra viridicornis venom quickly promoted edema, which persisted for up to 48 h.•S. viridicornis venom causes an intense inflammatory influx and release of pro-inflammatory mediators.•Histological analysis of footpad injected with S. viridicornis venom showed edema, tissue damage, and a great cell influx. |
doi_str_mv | 10.1016/j.toxicon.2013.10.017 |
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•Scolopendra viridicornis venom quickly promoted edema, which persisted for up to 48 h.•S. viridicornis venom causes an intense inflammatory influx and release of pro-inflammatory mediators.•Histological analysis of footpad injected with S. viridicornis venom showed edema, tissue damage, and a great cell influx.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/j.toxicon.2013.10.017</identifier><identifier>PMID: 24140924</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Arthropod Venoms - toxicity ; Arthropods - chemistry ; Centipede venom ; Chemokine CCL2 - metabolism ; Counting ; Edema ; erythema ; Formations ; humans ; Inflammation - chemically induced ; Inflammatory mediators ; interleukin-1beta ; Interleukin-1beta - metabolism ; interleukin-6 ; Interleukin-6 - metabolism ; leukocyte count ; Leukocyte influx ; Leukocytes ; Local reaction ; Lymphocytes ; Lymphocytes - drug effects ; macrophages ; Mice ; monocytes ; neutrophils ; pain ; Recruitment ; Scolopendra ; secretion ; Secretions ; tumor necrosis factor-alpha ; Tumor Necrosis Factor-alpha - metabolism ; venoms</subject><ispartof>Toxicon (Oxford), 2013-12, Vol.76, p.239-246</ispartof><rights>2013 Elsevier Ltd</rights><rights>Copyright © 2013 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-f1073140da8b7eefea119762e54e9f283a443a0d30d0bf08084def7d40d181773</citedby><cites>FETCH-LOGICAL-c455t-f1073140da8b7eefea119762e54e9f283a443a0d30d0bf08084def7d40d181773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.toxicon.2013.10.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24140924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kimura, Louise Faggionato</creatorcontrib><creatorcontrib>Prezotto-Neto, José Pedro</creatorcontrib><creatorcontrib>Távora, Bianca de Carvalho Lins Fernandes</creatorcontrib><creatorcontrib>Antoniazzi, Marta Maria</creatorcontrib><creatorcontrib>Knysak, Irene</creatorcontrib><creatorcontrib>Gióia Guizze, Samuel Paulo</creatorcontrib><creatorcontrib>Santoro, Marcelo Larami</creatorcontrib><creatorcontrib>Barbaro, Katia Cristina</creatorcontrib><title>Local inflammatory reaction induced by Scolopendra viridicornis centipede venom in mice</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>Centipede envenomation is generally mild, and human victims usually manifest burning pain, erythema and edema. Despite the abundance and ubiquity of these animals, centipede venom has been poorly characterized in literature. For this reason, the aim of this work was to investigate local inflammatory features induced by Scolopendra viridicornis centipede envenomation in mice, evaluating edema formation, leukocyte infiltration, production of inflammatory mediators, and also performing histological analysis. The highest edematogenic activity induced by the venom, determined by plethysmometry, was noticed 0.5 h after injection in mice footpad. At 24 h, edema was still detected in animals that received 15 and 60 μg of venom, and at 48 h, only in animals injected with 60 μg of venom. In relation to leukocyte count, S. viridicornis venom induced cell recruitment, mainly neutrophils and monocytes/macrophages, in all doses and time periods analyzed in comparison with PBS-injected mice. An increase in lymphocytes was detected especially between 1 and 24 h at 60 μg dose. Besides, eosinophil recruitment was observed mainly for 15 and 60 μg doses in early time periods. Edema formation and cell recruitment were also confirmed by histological analysis. Moreover, S. viridicornis venom stimulated the release of IL-6, MCP-1, KC, and IL-1β. Conversely, S. viridicornis venom did not induce the release of detectable levels of TNF-α. We demonstrated that the edematogenic activity induced by S. viridicornis venom was of rapid onset, and the venom stimulated secretion of pro-inflammatory mediators which contribute to the inflammatory reaction induced by S. viridicornis venom in an experimental model.
•Scolopendra viridicornis venom quickly promoted edema, which persisted for up to 48 h.•S. viridicornis venom causes an intense inflammatory influx and release of pro-inflammatory mediators.•Histological analysis of footpad injected with S. viridicornis venom showed edema, tissue damage, and a great cell influx.</description><subject>Animals</subject><subject>Arthropod Venoms - toxicity</subject><subject>Arthropods - chemistry</subject><subject>Centipede venom</subject><subject>Chemokine CCL2 - metabolism</subject><subject>Counting</subject><subject>Edema</subject><subject>erythema</subject><subject>Formations</subject><subject>humans</subject><subject>Inflammation - chemically induced</subject><subject>Inflammatory mediators</subject><subject>interleukin-1beta</subject><subject>Interleukin-1beta - metabolism</subject><subject>interleukin-6</subject><subject>Interleukin-6 - metabolism</subject><subject>leukocyte count</subject><subject>Leukocyte influx</subject><subject>Leukocytes</subject><subject>Local reaction</subject><subject>Lymphocytes</subject><subject>Lymphocytes - drug effects</subject><subject>macrophages</subject><subject>Mice</subject><subject>monocytes</subject><subject>neutrophils</subject><subject>pain</subject><subject>Recruitment</subject><subject>Scolopendra</subject><subject>secretion</subject><subject>Secretions</subject><subject>tumor necrosis factor-alpha</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>venoms</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFuEzEQhq0KREPhEYA99rJhvPbuek8IVRQqReqhrThajj2uHO3awd5E5O07UQJXOFn69f0zo8-MfeCw5MC7z5vlnH4Hm-KyAS4oWwLvL9iCq36oBW_hFVsASF4D4ZfsbSkbABBq6N6wy0ZyCUMjF-znKlkzViH60UyTmVM-VBmNnUOKlLqdRVetD9WDTWPaYnTZVPuQg6PVOYZSWYxz2KLDao8xTdSppmDxHXvtzVjw_fm9Yk-33x5vftSr--93N19XtZVtO9eeQy_oFmfUukf0aDgf-q7BVuLgGyWMlMKAE-Bg7UGBkg5976jBFe97ccWuT3O3Of3aYZn1FIrFcTQR065o3nWDapVU_4VKcqmEILQ9oTanUjJ6vc1hMvmgOeijfr3RZ_36qP8Yk37qfTyv2K0ndH9bf3wT8OkEeJO0ec6h6KcHmtACDR2U5ER8ORFI1vYBsy42YKRvCBntrF0K_zjiBVU3omI</recordid><startdate>20131215</startdate><enddate>20131215</enddate><creator>Kimura, Louise Faggionato</creator><creator>Prezotto-Neto, José Pedro</creator><creator>Távora, Bianca de Carvalho Lins Fernandes</creator><creator>Antoniazzi, Marta Maria</creator><creator>Knysak, Irene</creator><creator>Gióia Guizze, Samuel Paulo</creator><creator>Santoro, Marcelo Larami</creator><creator>Barbaro, Katia Cristina</creator><general>Elsevier Ltd</general><scope>FBQ</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>7U7</scope><scope>C1K</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20131215</creationdate><title>Local inflammatory reaction induced by Scolopendra viridicornis centipede venom in mice</title><author>Kimura, Louise Faggionato ; Prezotto-Neto, José Pedro ; Távora, Bianca de Carvalho Lins Fernandes ; Antoniazzi, Marta Maria ; Knysak, Irene ; Gióia Guizze, Samuel Paulo ; Santoro, Marcelo Larami ; Barbaro, Katia Cristina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-f1073140da8b7eefea119762e54e9f283a443a0d30d0bf08084def7d40d181773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Arthropod Venoms - toxicity</topic><topic>Arthropods - chemistry</topic><topic>Centipede venom</topic><topic>Chemokine CCL2 - metabolism</topic><topic>Counting</topic><topic>Edema</topic><topic>erythema</topic><topic>Formations</topic><topic>humans</topic><topic>Inflammation - chemically induced</topic><topic>Inflammatory mediators</topic><topic>interleukin-1beta</topic><topic>Interleukin-1beta - metabolism</topic><topic>interleukin-6</topic><topic>Interleukin-6 - metabolism</topic><topic>leukocyte count</topic><topic>Leukocyte influx</topic><topic>Leukocytes</topic><topic>Local reaction</topic><topic>Lymphocytes</topic><topic>Lymphocytes - drug effects</topic><topic>macrophages</topic><topic>Mice</topic><topic>monocytes</topic><topic>neutrophils</topic><topic>pain</topic><topic>Recruitment</topic><topic>Scolopendra</topic><topic>secretion</topic><topic>Secretions</topic><topic>tumor necrosis factor-alpha</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>venoms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimura, Louise Faggionato</creatorcontrib><creatorcontrib>Prezotto-Neto, José Pedro</creatorcontrib><creatorcontrib>Távora, Bianca de Carvalho Lins Fernandes</creatorcontrib><creatorcontrib>Antoniazzi, Marta Maria</creatorcontrib><creatorcontrib>Knysak, Irene</creatorcontrib><creatorcontrib>Gióia Guizze, Samuel Paulo</creatorcontrib><creatorcontrib>Santoro, Marcelo Larami</creatorcontrib><creatorcontrib>Barbaro, Katia Cristina</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimura, Louise Faggionato</au><au>Prezotto-Neto, José Pedro</au><au>Távora, Bianca de Carvalho Lins Fernandes</au><au>Antoniazzi, Marta Maria</au><au>Knysak, Irene</au><au>Gióia Guizze, Samuel Paulo</au><au>Santoro, Marcelo Larami</au><au>Barbaro, Katia Cristina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Local inflammatory reaction induced by Scolopendra viridicornis centipede venom in mice</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2013-12-15</date><risdate>2013</risdate><volume>76</volume><spage>239</spage><epage>246</epage><pages>239-246</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><abstract>Centipede envenomation is generally mild, and human victims usually manifest burning pain, erythema and edema. Despite the abundance and ubiquity of these animals, centipede venom has been poorly characterized in literature. For this reason, the aim of this work was to investigate local inflammatory features induced by Scolopendra viridicornis centipede envenomation in mice, evaluating edema formation, leukocyte infiltration, production of inflammatory mediators, and also performing histological analysis. The highest edematogenic activity induced by the venom, determined by plethysmometry, was noticed 0.5 h after injection in mice footpad. At 24 h, edema was still detected in animals that received 15 and 60 μg of venom, and at 48 h, only in animals injected with 60 μg of venom. In relation to leukocyte count, S. viridicornis venom induced cell recruitment, mainly neutrophils and monocytes/macrophages, in all doses and time periods analyzed in comparison with PBS-injected mice. An increase in lymphocytes was detected especially between 1 and 24 h at 60 μg dose. Besides, eosinophil recruitment was observed mainly for 15 and 60 μg doses in early time periods. Edema formation and cell recruitment were also confirmed by histological analysis. Moreover, S. viridicornis venom stimulated the release of IL-6, MCP-1, KC, and IL-1β. Conversely, S. viridicornis venom did not induce the release of detectable levels of TNF-α. We demonstrated that the edematogenic activity induced by S. viridicornis venom was of rapid onset, and the venom stimulated secretion of pro-inflammatory mediators which contribute to the inflammatory reaction induced by S. viridicornis venom in an experimental model.
•Scolopendra viridicornis venom quickly promoted edema, which persisted for up to 48 h.•S. viridicornis venom causes an intense inflammatory influx and release of pro-inflammatory mediators.•Histological analysis of footpad injected with S. viridicornis venom showed edema, tissue damage, and a great cell influx.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>24140924</pmid><doi>10.1016/j.toxicon.2013.10.017</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Arthropod Venoms - toxicity Arthropods - chemistry Centipede venom Chemokine CCL2 - metabolism Counting Edema erythema Formations humans Inflammation - chemically induced Inflammatory mediators interleukin-1beta Interleukin-1beta - metabolism interleukin-6 Interleukin-6 - metabolism leukocyte count Leukocyte influx Leukocytes Local reaction Lymphocytes Lymphocytes - drug effects macrophages Mice monocytes neutrophils pain Recruitment Scolopendra secretion Secretions tumor necrosis factor-alpha Tumor Necrosis Factor-alpha - metabolism venoms |
title | Local inflammatory reaction induced by Scolopendra viridicornis centipede venom in mice |
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