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Route of dexamethasone administration influences parasite burden in Strongyloides hyperinfection model
Rodents infected with Strongyloides venezuelensis are experimental models applied to strongyloidiasis research. This study evaluated oral and subcutaneous dexamethasone (DEX) treatments to establish immunosuppression in an experimental model of Strongyloides hyperinfection. Rattus norvegicus Wistar...
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Published in: | Journal of parasitic diseases 2023-09, Vol.47 (3), p.520-526 |
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creator | Corrêa, Luisa Queiroz do Couto, Bruna Patrícia de Carvalho, Edson Fernando Goulart de Sousa, José Eduardo Neto da Silva Ribeiro, Vanessa Gonzaga, Henrique Tomaz Costa-Cruz, Julia Maria |
description | Rodents infected with
Strongyloides venezuelensis
are experimental models applied to strongyloidiasis research. This study evaluated oral and subcutaneous dexamethasone (DEX) treatments to establish immunosuppression in an experimental model of
Strongyloides
hyperinfection.
Rattus norvegicus
Wistar were divided: G I (−): untreated and uninfected animals, G II (+): untreated and infected, G III (o −) orally treated and uninfected, G IV (o +) orally treated and infected, G V (sc −) subcutaneously treated and uninfected, G VI (sc +) subcutaneously treated and infected. For oral administration, DEX was diluted in sterile water (5 µg/ml) and made available to the animals on intervals in experimental days − 5–0, 8–13 and 21–26. For subcutaneous administration, animals received daily injections of DEX disodium phosphate (2 mg/kg). Infection was established by the subcutaneous inoculation of 3000
S. venezuelensis
filarioid larvae. Groups were evaluated by egg per gram of feces and parasite females counts and IgG, IgG1 and IgG2a detection. GIV (o +) had egg peaks count on days 13 and 26 and maintained egg elimination until the last experimental day. Parasitic females recovery at day 30 was significantly higher in G IV (o +) when compared to G VI (sc +). Levels of IgG, IgG1 and IgG2a of all groups, except the positive control GII (+), were below the detection threshold. Pharmacological immunosuppression induced by oral administration of DEX produced high parasitic burden, and is a noninvasive method, useful to establish immunosuppression in strongyloidiasis hyperinfection model in rats. |
doi_str_mv | 10.1007/s12639-023-01595-6 |
format | article |
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Strongyloides venezuelensis
are experimental models applied to strongyloidiasis research. This study evaluated oral and subcutaneous dexamethasone (DEX) treatments to establish immunosuppression in an experimental model of
Strongyloides
hyperinfection.
Rattus norvegicus
Wistar were divided: G I (−): untreated and uninfected animals, G II (+): untreated and infected, G III (o −) orally treated and uninfected, G IV (o +) orally treated and infected, G V (sc −) subcutaneously treated and uninfected, G VI (sc +) subcutaneously treated and infected. For oral administration, DEX was diluted in sterile water (5 µg/ml) and made available to the animals on intervals in experimental days − 5–0, 8–13 and 21–26. For subcutaneous administration, animals received daily injections of DEX disodium phosphate (2 mg/kg). Infection was established by the subcutaneous inoculation of 3000
S. venezuelensis
filarioid larvae. Groups were evaluated by egg per gram of feces and parasite females counts and IgG, IgG1 and IgG2a detection. GIV (o +) had egg peaks count on days 13 and 26 and maintained egg elimination until the last experimental day. Parasitic females recovery at day 30 was significantly higher in G IV (o +) when compared to G VI (sc +). Levels of IgG, IgG1 and IgG2a of all groups, except the positive control GII (+), were below the detection threshold. Pharmacological immunosuppression induced by oral administration of DEX produced high parasitic burden, and is a noninvasive method, useful to establish immunosuppression in strongyloidiasis hyperinfection model in rats.</description><identifier>ISSN: 0971-7196</identifier><identifier>EISSN: 0975-0703</identifier><identifier>DOI: 10.1007/s12639-023-01595-6</identifier><identifier>PMID: 37520210</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Animal models ; detection limit ; Dexamethasone ; eggs ; feces ; Health Promotion and Disease Prevention ; Immunoglobulin G ; Immunosuppression ; Infectious Diseases ; Inoculation ; Medicine ; Medicine & Public Health ; Oral administration ; Original ; Original Article ; parasite load ; Parasites ; phosphates ; Rattus norvegicus ; Strongyloides ; Strongyloides venezuelensis ; Strongyloidiasis ; subcutaneous injection</subject><ispartof>Journal of parasitic diseases, 2023-09, Vol.47 (3), p.520-526</ispartof><rights>Indian Society for Parasitology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3306-caa8e027dde868435497e1a7ba8166c7ea3e91d41e9ce0d34334b513ec1c37c23</cites><orcidid>0000-0003-1786-5724</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382442/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382442/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37520210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Corrêa, Luisa Queiroz</creatorcontrib><creatorcontrib>do Couto, Bruna Patrícia</creatorcontrib><creatorcontrib>de Carvalho, Edson Fernando Goulart</creatorcontrib><creatorcontrib>de Sousa, José Eduardo Neto</creatorcontrib><creatorcontrib>da Silva Ribeiro, Vanessa</creatorcontrib><creatorcontrib>Gonzaga, Henrique Tomaz</creatorcontrib><creatorcontrib>Costa-Cruz, Julia Maria</creatorcontrib><title>Route of dexamethasone administration influences parasite burden in Strongyloides hyperinfection model</title><title>Journal of parasitic diseases</title><addtitle>J Parasit Dis</addtitle><addtitle>J Parasit Dis</addtitle><description>Rodents infected with
Strongyloides venezuelensis
are experimental models applied to strongyloidiasis research. This study evaluated oral and subcutaneous dexamethasone (DEX) treatments to establish immunosuppression in an experimental model of
Strongyloides
hyperinfection.
Rattus norvegicus
Wistar were divided: G I (−): untreated and uninfected animals, G II (+): untreated and infected, G III (o −) orally treated and uninfected, G IV (o +) orally treated and infected, G V (sc −) subcutaneously treated and uninfected, G VI (sc +) subcutaneously treated and infected. For oral administration, DEX was diluted in sterile water (5 µg/ml) and made available to the animals on intervals in experimental days − 5–0, 8–13 and 21–26. For subcutaneous administration, animals received daily injections of DEX disodium phosphate (2 mg/kg). Infection was established by the subcutaneous inoculation of 3000
S. venezuelensis
filarioid larvae. Groups were evaluated by egg per gram of feces and parasite females counts and IgG, IgG1 and IgG2a detection. GIV (o +) had egg peaks count on days 13 and 26 and maintained egg elimination until the last experimental day. Parasitic females recovery at day 30 was significantly higher in G IV (o +) when compared to G VI (sc +). Levels of IgG, IgG1 and IgG2a of all groups, except the positive control GII (+), were below the detection threshold. Pharmacological immunosuppression induced by oral administration of DEX produced high parasitic burden, and is a noninvasive method, useful to establish immunosuppression in strongyloidiasis hyperinfection model in rats.</description><subject>Animal models</subject><subject>detection limit</subject><subject>Dexamethasone</subject><subject>eggs</subject><subject>feces</subject><subject>Health Promotion and Disease Prevention</subject><subject>Immunoglobulin G</subject><subject>Immunosuppression</subject><subject>Infectious Diseases</subject><subject>Inoculation</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oral administration</subject><subject>Original</subject><subject>Original Article</subject><subject>parasite load</subject><subject>Parasites</subject><subject>phosphates</subject><subject>Rattus norvegicus</subject><subject>Strongyloides</subject><subject>Strongyloides venezuelensis</subject><subject>Strongyloidiasis</subject><subject>subcutaneous injection</subject><issn>0971-7196</issn><issn>0975-0703</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkUmP1DAQhSMEYoaBP8ABReLCJVDlNTkhNGKTRkJiOVtuu7rbo8Ru7ATR_x539zAsBzjZcn3vlate0zxGeI4A-kVBpvjQAeMdoBxkp-405zBo2YEGfvd4x07joM6aB6VcA8j63t9vzriWDBjCebP-mJaZ2rRuPX23E81bW1Kk1vopxFDmbOeQYhvielwoOirtzmZbQtWsluzpUGo_zTnFzX5MwVdgu99RrgJyR-mUPI0Pm3trOxZ6dHNeNF_evP58-a67-vD2_eWrq85xDqpz1vYETHtPveoFl2LQhFavbI9KOU2W04BeIA2OwHPBuVhJ5OTQce0Yv2hennx3y2oi7yjWCUazy2GyeW-SDebPSgxbs0nfDNbFMCEODs9uHHL6ulCZzRSKo3G0kdJSDEfJUaGQ4r8o64WAXivAij79C71OS451FQeKC6YQZKXYiXI5lZJpfftxBHOI3JwiNzVyc4zcqCp68vvIt5KfGVeAn4BSS3FD-Vfvf9j-ANBruQ8</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Corrêa, Luisa Queiroz</creator><creator>do Couto, Bruna Patrícia</creator><creator>de Carvalho, Edson Fernando Goulart</creator><creator>de Sousa, José Eduardo Neto</creator><creator>da Silva Ribeiro, Vanessa</creator><creator>Gonzaga, Henrique Tomaz</creator><creator>Costa-Cruz, Julia Maria</creator><general>Springer India</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1786-5724</orcidid></search><sort><creationdate>20230901</creationdate><title>Route of dexamethasone administration influences parasite burden in Strongyloides hyperinfection model</title><author>Corrêa, Luisa Queiroz ; do Couto, Bruna Patrícia ; de Carvalho, Edson Fernando Goulart ; de Sousa, José Eduardo Neto ; da Silva Ribeiro, Vanessa ; Gonzaga, Henrique Tomaz ; Costa-Cruz, Julia Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3306-caa8e027dde868435497e1a7ba8166c7ea3e91d41e9ce0d34334b513ec1c37c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal models</topic><topic>detection limit</topic><topic>Dexamethasone</topic><topic>eggs</topic><topic>feces</topic><topic>Health Promotion and Disease Prevention</topic><topic>Immunoglobulin G</topic><topic>Immunosuppression</topic><topic>Infectious Diseases</topic><topic>Inoculation</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oral administration</topic><topic>Original</topic><topic>Original Article</topic><topic>parasite load</topic><topic>Parasites</topic><topic>phosphates</topic><topic>Rattus norvegicus</topic><topic>Strongyloides</topic><topic>Strongyloides venezuelensis</topic><topic>Strongyloidiasis</topic><topic>subcutaneous injection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Corrêa, Luisa Queiroz</creatorcontrib><creatorcontrib>do Couto, Bruna Patrícia</creatorcontrib><creatorcontrib>de Carvalho, Edson Fernando Goulart</creatorcontrib><creatorcontrib>de Sousa, José Eduardo Neto</creatorcontrib><creatorcontrib>da Silva Ribeiro, Vanessa</creatorcontrib><creatorcontrib>Gonzaga, Henrique Tomaz</creatorcontrib><creatorcontrib>Costa-Cruz, Julia Maria</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of parasitic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Corrêa, Luisa Queiroz</au><au>do Couto, Bruna Patrícia</au><au>de Carvalho, Edson Fernando Goulart</au><au>de Sousa, José Eduardo Neto</au><au>da Silva Ribeiro, Vanessa</au><au>Gonzaga, Henrique Tomaz</au><au>Costa-Cruz, Julia Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Route of dexamethasone administration influences parasite burden in Strongyloides hyperinfection model</atitle><jtitle>Journal of parasitic diseases</jtitle><stitle>J Parasit Dis</stitle><addtitle>J Parasit Dis</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>47</volume><issue>3</issue><spage>520</spage><epage>526</epage><pages>520-526</pages><issn>0971-7196</issn><eissn>0975-0703</eissn><abstract>Rodents infected with
Strongyloides venezuelensis
are experimental models applied to strongyloidiasis research. This study evaluated oral and subcutaneous dexamethasone (DEX) treatments to establish immunosuppression in an experimental model of
Strongyloides
hyperinfection.
Rattus norvegicus
Wistar were divided: G I (−): untreated and uninfected animals, G II (+): untreated and infected, G III (o −) orally treated and uninfected, G IV (o +) orally treated and infected, G V (sc −) subcutaneously treated and uninfected, G VI (sc +) subcutaneously treated and infected. For oral administration, DEX was diluted in sterile water (5 µg/ml) and made available to the animals on intervals in experimental days − 5–0, 8–13 and 21–26. For subcutaneous administration, animals received daily injections of DEX disodium phosphate (2 mg/kg). Infection was established by the subcutaneous inoculation of 3000
S. venezuelensis
filarioid larvae. Groups were evaluated by egg per gram of feces and parasite females counts and IgG, IgG1 and IgG2a detection. GIV (o +) had egg peaks count on days 13 and 26 and maintained egg elimination until the last experimental day. Parasitic females recovery at day 30 was significantly higher in G IV (o +) when compared to G VI (sc +). Levels of IgG, IgG1 and IgG2a of all groups, except the positive control GII (+), were below the detection threshold. Pharmacological immunosuppression induced by oral administration of DEX produced high parasitic burden, and is a noninvasive method, useful to establish immunosuppression in strongyloidiasis hyperinfection model in rats.</abstract><cop>New Delhi</cop><pub>Springer India</pub><pmid>37520210</pmid><doi>10.1007/s12639-023-01595-6</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-1786-5724</orcidid></addata></record> |
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subjects | Animal models detection limit Dexamethasone eggs feces Health Promotion and Disease Prevention Immunoglobulin G Immunosuppression Infectious Diseases Inoculation Medicine Medicine & Public Health Oral administration Original Original Article parasite load Parasites phosphates Rattus norvegicus Strongyloides Strongyloides venezuelensis Strongyloidiasis subcutaneous injection |
title | Route of dexamethasone administration influences parasite burden in Strongyloides hyperinfection model |
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