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Latex proteins downregulate inflammation and restores blood-coagulation homeostasis in acute Salmonella infection
Sousa, Brandon Ferraz; Silva, Ayrles Fernanda Brandão da; Lima-Filho, José Vitor; Agostinho, Anderson Gomes; Oliveira, Denise Nunes; de Alencar, Nylane Maria Nunes; de Freitas, Cleverson Diniz Teixeira; Ramos, Márcio Viana.
  • Sousa, Brandon Ferraz; Universidade Federal do Ceará. Departamento de Bioquímica e Biologia Molecular. Fortaleza. BR
  • Silva, Ayrles Fernanda Brandão da; Universidade Federal do Ceará. Departamento de Bioquímica e Biologia Molecular. Fortaleza. BR
  • Lima-Filho, José Vitor; Universidade Federal Rural de Pernambuco. Departamento de Biologia. Recife. BR
  • Agostinho, Anderson Gomes; Universidade Federal do Ceará. Departamento de Bioquímica e Biologia Molecular. Fortaleza. BR
  • Oliveira, Denise Nunes; Universidade de Fortaleza. Departamento de Patologia. Fortaleza. BR
  • de Alencar, Nylane Maria Nunes; Universidade Federal do Ceará. Departamento de Fisiologia e Farmacologia. Fortaleza. BR
  • de Freitas, Cleverson Diniz Teixeira; Universidade Federal do Ceará. Departamento de Bioquímica e Biologia Molecular. Fortaleza. BR
  • Ramos, Márcio Viana; Universidade Federal do Ceará. Departamento de Bioquímica e Biologia Molecular. Fortaleza. BR
Mem. Inst. Oswaldo Cruz ; 115: e200458, 2020. graf
Article in English | LILACS, SES-SP | ID: biblio-1135229
ABSTRACT
BACKGROUND Calotropis procera latex protein fraction (LP) was previously shown to protect animals from septic shock. Further investigations showed that LP modulate nitric oxide and cytokines levels. OBJECTIVES To evaluate whether the protective effects of LP, against lethal bacterial infection, is observed in its subfractions (LPPII and LPPIII). METHODS Subfractions (5 and 10 mg/kg) were tested by i.p. administration, 24 h before challenging with lethal injection (i.p.) of Salmonella Typhimurium. LPPIII (5 mg/kg) which showed higher survival rate was assayed to evaluate bacterial clearance, histopathology, leukocyte recruitment, plasma coagulation time, cytokines and NO levels. FINDINGS LPPIII protected 70% of animals of death. The animals given LPPIII exhibited reduced bacterial load in blood and peritoneal fluid after 24 h compared to the control. LPPIII promoted macrophage infiltration in spleen and liver. LPPIII restored the coagulation time of infected animals, increased IL-10 and reduced NO in blood. MAIN CONCLUSIONS LPPIII recruited macrophages to the target organs of bacterial infection. This addressed inflammatory stimulus seems to reduce bacterial colonisation in spleen and liver, down regulate bacterial spread and contribute to avoid septic shock.
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Full text: Available Index: LILACS (Americas) Main subject: Plant Proteins / Salmonella Infections / Plant Extracts / Calotropis / Homeostasis / Inflammation / Latex / Anti-Bacterial Agents Type of study: Evaluation studies Limits: Animals Language: English Journal: Mem. Inst. Oswaldo Cruz Year: 2020 Type: Article Institution/Affiliation country: Universidade Federal Rural de Pernambuco/BR / Universidade Federal do Ceará/BR / Universidade de Fortaleza/BR

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Full text: Available Index: LILACS (Americas) Main subject: Plant Proteins / Salmonella Infections / Plant Extracts / Calotropis / Homeostasis / Inflammation / Latex / Anti-Bacterial Agents Type of study: Evaluation studies Limits: Animals Language: English Journal: Mem. Inst. Oswaldo Cruz Year: 2020 Type: Article Institution/Affiliation country: Universidade Federal Rural de Pernambuco/BR / Universidade Federal do Ceará/BR / Universidade de Fortaleza/BR