Induction of secretory and tumoricidal activities in peritoneal macrophages activated by an acidic heteropolysaccharide (ARAGAL) from the gum of Anadenanthera colubrina (Angico branco)
The immunomodulatory and anti-tumoral effects of an acidic heteropolysaccharide containing mainly galactose and arabinose (ARAGAL), isolated from the gum of the leguminous tree Anadenanthera colubrina (Angico branco) native to Brazil, were studied. It has been demonstrated that activation of mice pe...
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Published in | Immunology letters Vol. 93; no. 2; pp. 189 - 197 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
15.05.2004
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Abstract | The immunomodulatory and anti-tumoral effects of an acidic heteropolysaccharide containing mainly galactose and arabinose (ARAGAL), isolated from the gum of the leguminous tree
Anadenanthera colubrina (Angico branco) native to Brazil, were studied. It has been demonstrated that activation of mice peritoneal macrophages both in vivo and in vitro, increases phagocytic ability and anion superoxide production. In order to obtain further insights on the biological effects of ARAGAL, the capacity of eliciting peritoneal macrophages and tumor necrosis factor-α (TNF-α) production, and anti-tumoral effect against Sarcoma 180 (S-180), are now evaluated. Cell eliciting activity was observed in ARAGAL-treated animals in a dose dependent manner. Treatment of animals with 50, 100 or 200
mg/kg of ARAGAL increased peritoneal exudate cell (PEC) numbers by ∼18, ∼44 and ∼88%, respectively. ARAGAL also increased 26-fold TNF-α production by peritoneal macrophages. Macrophages, treated in vitro for 18
h with ARAGAL, were able to kill Sarcoma 180 cells, as observed by their structures inside the macrophage cytoplasm. ARAGAL (100
mg/kg) showed anti-tumoral activity against S-180 in ascites or solid tumors, the tumoral inhibition being 63 and 38%, respectively. The results suggest a possible role as a BRM for ARAGAL. |
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AbstractList | The immunomodulatory and anti-tumoral effects of an acidic heteropolysaccharide containing mainly galactose and arabinose (ARAGAL), isolated from the gum of the leguminous tree Anadenanthera colubrina (Angico branco) native to Brazil, were studied. It has been demonstrated that activation of mice peritoneal macrophages both in vivo and in vitro, increases phagocytic ability and anion superoxide production. In order to obtain further insights on the biological effects of ARAGAL, the capacity of eliciting peritoneal macrophages and tumor necrosis factor- alpha (TNF- alpha ) production, and anti-tumoral effect against Sarcoma 180 (S-180), are now evaluated. Cell eliciting activity was observed in ARAGAL-treated animals in a dose dependent manner. Treatment of animals with 50, 100 or 200mg/kg of ARAGAL increased peritoneal exudate cell (PEC) numbers by similar to 18, similar to 44 and similar to 88%, respectively. ARAGAL also increased 26-fold TNF- alpha production by peritoneal macrophages. Macrophages, treated in vitro for 18h with ARAGAL, were able to kill Sarcoma 180 cells, as observed by their structures inside the macrophage cytoplasm. ARAGAL (100mg/kg) showed anti-tumoral activity against S-180 in ascites or solid tumors, the tumoral inhibition being 63 and 38%, respectively. The results suggest a possible role as a BRM for ARAGAL. The immunomodulatory and anti-tumoral effects of an acidic heteropolysaccharide containing mainly galactose and arabinose (ARAGAL), isolated from the gum of the leguminous tree Anadenanthera colubrina (Angico branco) native to Brazil, were studied. It has been demonstrated that activation of mice peritoneal macrophages both in vivo and in vitro, increases phagocytic ability and anion superoxide production. In order to obtain further insights on the biological effects of ARAGAL, the capacity of eliciting peritoneal macrophages and tumor necrosis factor-alpha (TNF-alpha) production, and anti-tumoral effect against Sarcoma 180 (S-180), are now evaluated. Cell eliciting activity was observed in ARAGAL-treated animals in a dose dependent manner. Treatment of animals with 50, 100 or 200 mg/kg of ARAGAL increased peritoneal exudate cell (PEC) numbers by approximately 18, approximately 44 and approximately 88%, respectively. ARAGAL also increased 26-fold TNF-alpha production by peritoneal macrophages. Macrophages, treated in vitro for 18 h with ARAGAL, were able to kill Sarcoma 180 cells, as observed by their structures inside the macrophage cytoplasm. ARAGAL (100 mg/kg) showed anti-tumoral activity against S-180 in ascites or solid tumors, the tumoral inhibition being 63 and 38%, respectively. The results suggest a possible role as a BRM for ARAGAL. The immunomodulatory and anti-tumoral effects of an acidic heteropolysaccharide containing mainly galactose and arabinose (ARAGAL), isolated from the gum of the leguminous tree Anadenanthera colubrina (Angico branco) native to Brazil, were studied. It has been demonstrated that activation of mice peritoneal macrophages both in vivo and in vitro, increases phagocytic ability and anion superoxide production. In order to obtain further insights on the biological effects of ARAGAL, the capacity of eliciting peritoneal macrophages and tumor necrosis factor-α (TNF-α) production, and anti-tumoral effect against Sarcoma 180 (S-180), are now evaluated. Cell eliciting activity was observed in ARAGAL-treated animals in a dose dependent manner. Treatment of animals with 50, 100 or 200 mg/kg of ARAGAL increased peritoneal exudate cell (PEC) numbers by ∼18, ∼44 and ∼88%, respectively. ARAGAL also increased 26-fold TNF-α production by peritoneal macrophages. Macrophages, treated in vitro for 18 h with ARAGAL, were able to kill Sarcoma 180 cells, as observed by their structures inside the macrophage cytoplasm. ARAGAL (100 mg/kg) showed anti-tumoral activity against S-180 in ascites or solid tumors, the tumoral inhibition being 63 and 38%, respectively. The results suggest a possible role as a BRM for ARAGAL. |
Author | Zampronio, Aleksander Roberto Oliveira, Maria Benigna M Gorin, Philip A.J Iacomini, Marcello Moretão, Mariana Piemonte |
Author_xml | – sequence: 1 givenname: Mariana Piemonte surname: Moretão fullname: Moretão, Mariana Piemonte organization: Departamento de Bioquı́mica e Biologia Molecular, Universidade Federal do Paraná, CP 19046, CEP 81531-990 Curitiba, Paraná, PR, Brazil – sequence: 2 givenname: Aleksander Roberto surname: Zampronio fullname: Zampronio, Aleksander Roberto organization: Departamento de Farmacologia, Universidade Federal do Paraná, Paraná, PR, Brazil – sequence: 3 givenname: Philip A.J surname: Gorin fullname: Gorin, Philip A.J organization: Departamento de Bioquı́mica e Biologia Molecular, Universidade Federal do Paraná, CP 19046, CEP 81531-990 Curitiba, Paraná, PR, Brazil – sequence: 4 givenname: Marcello surname: Iacomini fullname: Iacomini, Marcello organization: Departamento de Bioquı́mica e Biologia Molecular, Universidade Federal do Paraná, CP 19046, CEP 81531-990 Curitiba, Paraná, PR, Brazil – sequence: 5 givenname: Maria Benigna M surname: Oliveira fullname: Oliveira, Maria Benigna M email: mbmo@ufpr.br organization: Departamento de Bioquı́mica e Biologia Molecular, Universidade Federal do Paraná, CP 19046, CEP 81531-990 Curitiba, Paraná, PR, Brazil |
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SubjectTerms | Anadenanthera colubrina Animals Ascitic Fluid - drug effects Ascitic Fluid - pathology Brazil Carbohydrate Sequence Cell Count Cell Line, Tumor Coculture Techniques Cytotoxicity, Immunologic - physiology Drug Screening Assays, Antitumor Fabaceae - chemistry Galactans - pharmacology Injections, Intraperitoneal Macrophage Macrophage Activation - immunology Macrophage Activation - physiology Macrophages, Peritoneal - cytology Macrophages, Peritoneal - drug effects Macrophages, Peritoneal - physiology Male Mice Neoplasms - drug therapy Neoplasms - pathology Peritoneal Cavity - cytology Plant arabinogalactan Polysaccharides - pharmacology TNF-α Tumor Necrosis Factor-alpha - metabolism |
Title | Induction of secretory and tumoricidal activities in peritoneal macrophages activated by an acidic heteropolysaccharide (ARAGAL) from the gum of Anadenanthera colubrina (Angico branco) |
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