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231225s2021 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2021.108713
|2 doi
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|a pubmed24n1075.xml
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|a DE-627
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|a eng
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|a Pimentel, Pollyana Maria de Oliveira
|e verfasserin
|4 aut
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|a Tityus serrulatus scorpion venom as a potential drug source for Chagas' disease
|b Trypanocidal and immunomodulatory activity
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|c 2021
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 24.06.2021
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|a Date Revised 24.06.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2021 Elsevier Inc. All rights reserved.
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|a Current chemical therapies for Chagas Disease (CD) lack ability to clear Trypanosoma cruzi (Tc) parasites and cause severe side effects, making search for new strategies extremely necessary. We evaluated the action of Tityus serrulatus venom (TsV) components during Tc infection. TsV treatment increased nitric oxide and pro-inflammatory cytokine production by Tc-infected macrophages (MØ), decreased intracellular parasite replication and trypomastigotes release, also triggering ERK1/2, JNK1/2 and p38 activation. Ts7 demonstrated the highest anti-Tc activity, inducing high levels of TNF and IL-6 in infected MØ. TsV/Ts7 presented synergistic effect on p38 activation when incubated with Tc antigen. KPP-treatment of MØ also decreased trypomastigotes releasing, partially due to p38 activation. TsV/Ts7-pre-incubation of Tc demonstrated a direct effect on parasite decreasing MØ-trypomastigotes releasing. In vivo KPP-treatment of Tc-infected mice resulted in decreased parasitemia. Summarizing, this study opens perspectives for new bioactive molecules as CD-therapeutic treatment, demonstrating the TsV/Ts7/KPP-trypanocidal and immunomodulatory activity during Tc infection
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Infectious disease
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|a Macrophage
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|a Mitogen-activated protein kinase (MAPK)
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|a Peptides
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|a Tityus serrulatus
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|a Trypanosoma cruzi
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|a Interleukin-6
|2 NLM
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|a Scorpion Venoms
|2 NLM
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|a Tumor Necrosis Factors
|2 NLM
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|a Nitric Oxide
|2 NLM
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|a 31C4KY9ESH
|2 NLM
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|a de Assis, Diego Rodney Rodrigues
|e verfasserin
|4 aut
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|a Gualdrón-Lopez, Melisa
|e verfasserin
|4 aut
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|a Barroso, Andréia
|e verfasserin
|4 aut
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|a Brant, Fátima
|e verfasserin
|4 aut
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|a Leite, Paulo Gaio
|e verfasserin
|4 aut
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|a de Lima Oliveira, Bruno Cabral
|e verfasserin
|4 aut
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|a Esper, Lisia
|e verfasserin
|4 aut
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|a McKinnie, Shaun M K
|e verfasserin
|4 aut
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|a Vederas, John C
|e verfasserin
|4 aut
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|a do Nascimento Cordeiro, Marta
|e verfasserin
|4 aut
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|a Dos Reis, Pablo Victor Mendes
|e verfasserin
|4 aut
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|a Teixeira, Mauro Martins
|e verfasserin
|4 aut
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|a de Castro Pimenta, Adriano Monteiro
|e verfasserin
|4 aut
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|a Borges, Márcia Helena
|e verfasserin
|4 aut
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|a de Lima, Maria Elena
|e verfasserin
|4 aut
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|a Machado, Fabiana Simão
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 226(2021) vom: 15. Mai, Seite 108713
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:226
|g year:2021
|g day:15
|g month:05
|g pages:108713
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|u http://dx.doi.org/10.1016/j.clim.2021.108713
|3 Volltext
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