Effect of zinc supplementation on E-ADA activity, seric zinc, and cytokines levels of Trypanosoma evansi infected wistar rats

The aim of this study was to evaluate the effect of zinc supplementation on the ecto-adenosine deaminase activity (E-ADA), zinc seric levels and cytokines (TNF-α, IL-1, IL-6, and IL -10) on rats experimentally infected by Trypanosoma evansi. Four groups with 10 rats each were used as negative contro...

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Veröffentlicht in:Microbial pathogenesis 2014-09, Vol.74, p.15-19
Hauptverfasser: Bottari, Nathieli B., Baldissera, Matheus D., Oliveira, Camila B., Duarte, Thiago, Duarte, Marta M.M.F., Leal, Marta L.R., Thomé, Gustavo R., Zanini, Daniela, Schetinger, Maria Rosa C., Nunes, Matheus A.G., Dressler, Valderi L., Monteiro, Silvia G., Tonin, Alexandre A., Da Silva, Aleksandro S.
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container_end_page 19
container_issue
container_start_page 15
container_title Microbial pathogenesis
container_volume 74
creator Bottari, Nathieli B.
Baldissera, Matheus D.
Oliveira, Camila B.
Duarte, Thiago
Duarte, Marta M.M.F.
Leal, Marta L.R.
Thomé, Gustavo R.
Zanini, Daniela
Schetinger, Maria Rosa C.
Nunes, Matheus A.G.
Dressler, Valderi L.
Monteiro, Silvia G.
Tonin, Alexandre A.
Da Silva, Aleksandro S.
description The aim of this study was to evaluate the effect of zinc supplementation on the ecto-adenosine deaminase activity (E-ADA), zinc seric levels and cytokines (TNF-α, IL-1, IL-6, and IL -10) on rats experimentally infected by Trypanosoma evansi. Four groups with 10 rats each were used as negative controls (groups A and B), while the animals from the groups C and D were infected intraperitoneally with 0.1 mL of cryopreserved blood containing 1.4 × 104 of trypanosomes. Animals of groups B and D received two doses of Zinc (Zn) at 5 mg kg−1, subcutaneously, on the 2nd and 7th day post-infection (PI). Blood samples were collected on days 5 (n = 5) and 15 PI (n = 5). Zn supplementation was able to increase the rat's longevity and to reduce their parasitemia. It was observed that seric Zn levels were increased on infected animals under Zn supplementation. Animals that were infected and supplemented with Zn showed changes in E-ADA activity and in cytokine levels (P 
doi_str_mv 10.1016/j.micpath.2014.06.004
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Four groups with 10 rats each were used as negative controls (groups A and B), while the animals from the groups C and D were infected intraperitoneally with 0.1 mL of cryopreserved blood containing 1.4 × 104 of trypanosomes. Animals of groups B and D received two doses of Zinc (Zn) at 5 mg kg−1, subcutaneously, on the 2nd and 7th day post-infection (PI). Blood samples were collected on days 5 (n = 5) and 15 PI (n = 5). Zn supplementation was able to increase the rat's longevity and to reduce their parasitemia. It was observed that seric Zn levels were increased on infected animals under Zn supplementation. Animals that were infected and supplemented with Zn showed changes in E-ADA activity and in cytokine levels (P &lt; 0.05). Zn supplementation of healthy animals (Group B), increased the E-ADA activity, as well as reduced the concentration of cytokines. Infected animals from groups C and D showed increased levels of cytokines. Finally, we observed that Zn supplementation led to a modulation on cytokine's level in rats infected by T. evansi, as well as in E-ADA activity. •Trypanosoma evansi is a flagellated protozoan that causes disease in many domestic and wild animals.•Rats infected with trypanosomes and treated with zinc showed the improvement of the immune status and has prolonged life.•Zinc supplementation was able to increase the seric levels of zinc, a mineral that has been proved to be reduced in serum.•The treatment with zinc presented immunomodulatory effect, as this relates various physiological functions.•Administration of zinc showed different actions on E-ADA activity, reducing its on lymphocytes and increasing on serum.</description><identifier>ISSN: 0882-4010</identifier><identifier>EISSN: 1096-1208</identifier><identifier>DOI: 10.1016/j.micpath.2014.06.004</identifier><identifier>PMID: 24994023</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adenosine deaminase ; Adenosine Deaminase - blood ; Animals ; Cytokines - blood ; Disease Models, Animal ; Immune response ; Immunologic Factors - administration &amp; dosage ; Immunologic Factors - blood ; Longevity ; Parasite Load ; Parasitemia ; Rats, Wistar ; Serum - chemistry ; Survival Analysis ; Treatment ; Trypanosoma ; Trypanosoma - immunology ; Trypanosoma evansi ; Trypanosomiasis - immunology ; Trypanosomiasis - pathology ; Zinc - administration &amp; dosage ; Zinc - blood</subject><ispartof>Microbial pathogenesis, 2014-09, Vol.74, p.15-19</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. 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Four groups with 10 rats each were used as negative controls (groups A and B), while the animals from the groups C and D were infected intraperitoneally with 0.1 mL of cryopreserved blood containing 1.4 × 104 of trypanosomes. Animals of groups B and D received two doses of Zinc (Zn) at 5 mg kg−1, subcutaneously, on the 2nd and 7th day post-infection (PI). Blood samples were collected on days 5 (n = 5) and 15 PI (n = 5). Zn supplementation was able to increase the rat's longevity and to reduce their parasitemia. It was observed that seric Zn levels were increased on infected animals under Zn supplementation. Animals that were infected and supplemented with Zn showed changes in E-ADA activity and in cytokine levels (P &lt; 0.05). Zn supplementation of healthy animals (Group B), increased the E-ADA activity, as well as reduced the concentration of cytokines. Infected animals from groups C and D showed increased levels of cytokines. 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Baldissera, Matheus D. ; Oliveira, Camila B. ; Duarte, Thiago ; Duarte, Marta M.M.F. ; Leal, Marta L.R. ; Thomé, Gustavo R. ; Zanini, Daniela ; Schetinger, Maria Rosa C. ; Nunes, Matheus A.G. ; Dressler, Valderi L. ; Monteiro, Silvia G. ; Tonin, Alexandre A. ; Da Silva, Aleksandro S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-af838021ade1f701c2fa5cc15848f869194bf5802c26fadee91bbc4ae666f7c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenosine deaminase</topic><topic>Adenosine Deaminase - blood</topic><topic>Animals</topic><topic>Cytokines - blood</topic><topic>Disease Models, Animal</topic><topic>Immune response</topic><topic>Immunologic Factors - administration &amp; dosage</topic><topic>Immunologic Factors - blood</topic><topic>Longevity</topic><topic>Parasite Load</topic><topic>Parasitemia</topic><topic>Rats, Wistar</topic><topic>Serum - chemistry</topic><topic>Survival Analysis</topic><topic>Treatment</topic><topic>Trypanosoma</topic><topic>Trypanosoma - immunology</topic><topic>Trypanosoma evansi</topic><topic>Trypanosomiasis - immunology</topic><topic>Trypanosomiasis - pathology</topic><topic>Zinc - administration &amp; dosage</topic><topic>Zinc - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bottari, Nathieli B.</creatorcontrib><creatorcontrib>Baldissera, Matheus D.</creatorcontrib><creatorcontrib>Oliveira, Camila B.</creatorcontrib><creatorcontrib>Duarte, Thiago</creatorcontrib><creatorcontrib>Duarte, Marta M.M.F.</creatorcontrib><creatorcontrib>Leal, Marta L.R.</creatorcontrib><creatorcontrib>Thomé, Gustavo R.</creatorcontrib><creatorcontrib>Zanini, Daniela</creatorcontrib><creatorcontrib>Schetinger, Maria Rosa C.</creatorcontrib><creatorcontrib>Nunes, Matheus A.G.</creatorcontrib><creatorcontrib>Dressler, Valderi L.</creatorcontrib><creatorcontrib>Monteiro, Silvia G.</creatorcontrib><creatorcontrib>Tonin, Alexandre A.</creatorcontrib><creatorcontrib>Da Silva, Aleksandro S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Microbial pathogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bottari, Nathieli B.</au><au>Baldissera, Matheus D.</au><au>Oliveira, Camila B.</au><au>Duarte, Thiago</au><au>Duarte, Marta M.M.F.</au><au>Leal, Marta L.R.</au><au>Thomé, Gustavo R.</au><au>Zanini, Daniela</au><au>Schetinger, Maria Rosa C.</au><au>Nunes, Matheus A.G.</au><au>Dressler, Valderi L.</au><au>Monteiro, Silvia G.</au><au>Tonin, Alexandre A.</au><au>Da Silva, Aleksandro S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of zinc supplementation on E-ADA activity, seric zinc, and cytokines levels of Trypanosoma evansi infected wistar rats</atitle><jtitle>Microbial pathogenesis</jtitle><addtitle>Microb Pathog</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>74</volume><spage>15</spage><epage>19</epage><pages>15-19</pages><issn>0882-4010</issn><eissn>1096-1208</eissn><abstract>The aim of this study was to evaluate the effect of zinc supplementation on the ecto-adenosine deaminase activity (E-ADA), zinc seric levels and cytokines (TNF-α, IL-1, IL-6, and IL -10) on rats experimentally infected by Trypanosoma evansi. Four groups with 10 rats each were used as negative controls (groups A and B), while the animals from the groups C and D were infected intraperitoneally with 0.1 mL of cryopreserved blood containing 1.4 × 104 of trypanosomes. Animals of groups B and D received two doses of Zinc (Zn) at 5 mg kg−1, subcutaneously, on the 2nd and 7th day post-infection (PI). Blood samples were collected on days 5 (n = 5) and 15 PI (n = 5). Zn supplementation was able to increase the rat's longevity and to reduce their parasitemia. It was observed that seric Zn levels were increased on infected animals under Zn supplementation. Animals that were infected and supplemented with Zn showed changes in E-ADA activity and in cytokine levels (P &lt; 0.05). Zn supplementation of healthy animals (Group B), increased the E-ADA activity, as well as reduced the concentration of cytokines. Infected animals from groups C and D showed increased levels of cytokines. Finally, we observed that Zn supplementation led to a modulation on cytokine's level in rats infected by T. evansi, as well as in E-ADA activity. •Trypanosoma evansi is a flagellated protozoan that causes disease in many domestic and wild animals.•Rats infected with trypanosomes and treated with zinc showed the improvement of the immune status and has prolonged life.•Zinc supplementation was able to increase the seric levels of zinc, a mineral that has been proved to be reduced in serum.•The treatment with zinc presented immunomodulatory effect, as this relates various physiological functions.•Administration of zinc showed different actions on E-ADA activity, reducing its on lymphocytes and increasing on serum.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>24994023</pmid><doi>10.1016/j.micpath.2014.06.004</doi><tpages>5</tpages></addata></record>
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subjects Adenosine deaminase
Adenosine Deaminase - blood
Animals
Cytokines - blood
Disease Models, Animal
Immune response
Immunologic Factors - administration & dosage
Immunologic Factors - blood
Longevity
Parasite Load
Parasitemia
Rats, Wistar
Serum - chemistry
Survival Analysis
Treatment
Trypanosoma
Trypanosoma - immunology
Trypanosoma evansi
Trypanosomiasis - immunology
Trypanosomiasis - pathology
Zinc - administration & dosage
Zinc - blood
title Effect of zinc supplementation on E-ADA activity, seric zinc, and cytokines levels of Trypanosoma evansi infected wistar rats
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