Evaluation of acute toxicity of babassu mesocarp in mice

Detalhes bibliográficos
Autor(a) principal: Barroqueiro,Elizabeth S. B.
Data de Publicação: 2011
Outros Autores: Barroqueiro,Fernanda S. B., Pinheiro,Mayara T., Maciel,Márcia C. G., Barcellos,Priscila S., Silva,Lucilene A., Lopes,Adelson S., Nascimento,Flávia R. F., Guerra,Rosane N. M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Brasileira de Farmacognosia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2011000400022
Resumo: The safety of babassu mesocarp (Orbignya phalerata Mart., Arecaceae), which exhibited anti-inflammatory and antithrombotic activities, was evaluated by determining the potential acute toxicity in mice. A lyophilized ethanol extract of babassu mesocarp (BME) was administered to C3H/HePas mice (10/group) in a single dose of 1000, 3000 and 5000 mg/kg, by gavage. General behavior adverse effects and mortality were determined for up to fourteen days. Selected biochemical parameters including glucose, triacylglyceride, cholesterol, urea, alkaline phosphatase and creatinine were determined by colorimetric assay. The heart, liver, spleen, kidneys and brain were weighted and evaluated macro and microscopically. The median lethal dose (LD50) of BME was greater than 5000 mg/kg. No behavior or body weight alterations were detected after the treatment. The acute treatment with BME has no effect on macroscopic and microscopic aspect of examined organs. Instead, BME increased the alkaline phosphatase and reduced the urea concentration in all groups. A significant increase on triacylglyceride was detected in the group BME1000. In conclusion, the acute treatment with high doses of BME can affect some biochemical parameters with a long lasting effect, although any change was detected at tissue level or body and organ weight.
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spelling Evaluation of acute toxicity of babassu mesocarp in micebabassublood biochemistrymesocarporal acute toxicityOrbignya phalerataThe safety of babassu mesocarp (Orbignya phalerata Mart., Arecaceae), which exhibited anti-inflammatory and antithrombotic activities, was evaluated by determining the potential acute toxicity in mice. A lyophilized ethanol extract of babassu mesocarp (BME) was administered to C3H/HePas mice (10/group) in a single dose of 1000, 3000 and 5000 mg/kg, by gavage. General behavior adverse effects and mortality were determined for up to fourteen days. Selected biochemical parameters including glucose, triacylglyceride, cholesterol, urea, alkaline phosphatase and creatinine were determined by colorimetric assay. The heart, liver, spleen, kidneys and brain were weighted and evaluated macro and microscopically. The median lethal dose (LD50) of BME was greater than 5000 mg/kg. No behavior or body weight alterations were detected after the treatment. The acute treatment with BME has no effect on macroscopic and microscopic aspect of examined organs. Instead, BME increased the alkaline phosphatase and reduced the urea concentration in all groups. A significant increase on triacylglyceride was detected in the group BME1000. In conclusion, the acute treatment with high doses of BME can affect some biochemical parameters with a long lasting effect, although any change was detected at tissue level or body and organ weight.Sociedade Brasileira de Farmacognosia2011-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2011000400022Revista Brasileira de Farmacognosia v.21 n.4 2011reponame:Revista Brasileira de Farmacognosia (Online)instname:Sociedade Brasileira de Farmacognosia (SBFgnosia)instacron:SBFGNOSIA10.1590/S0102-695X2011005000121info:eu-repo/semantics/openAccessBarroqueiro,Elizabeth S. B.Barroqueiro,Fernanda S. B.Pinheiro,Mayara T.Maciel,Márcia C. G.Barcellos,Priscila S.Silva,Lucilene A.Lopes,Adelson S.Nascimento,Flávia R. F.Guerra,Rosane N. M.eng2011-08-15T00:00:00Zoai:scielo:S0102-695X2011000400022Revistahttp://www.sbfgnosia.org.br/revista/https://old.scielo.br/oai/scielo-oai.phprbgnosia@ltf.ufpb.br1981-528X0102-695Xopendoar:2011-08-15T00:00Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia)false
dc.title.none.fl_str_mv Evaluation of acute toxicity of babassu mesocarp in mice
title Evaluation of acute toxicity of babassu mesocarp in mice
spellingShingle Evaluation of acute toxicity of babassu mesocarp in mice
Barroqueiro,Elizabeth S. B.
babassu
blood biochemistry
mesocarp
oral acute toxicity
Orbignya phalerata
title_short Evaluation of acute toxicity of babassu mesocarp in mice
title_full Evaluation of acute toxicity of babassu mesocarp in mice
title_fullStr Evaluation of acute toxicity of babassu mesocarp in mice
title_full_unstemmed Evaluation of acute toxicity of babassu mesocarp in mice
title_sort Evaluation of acute toxicity of babassu mesocarp in mice
author Barroqueiro,Elizabeth S. B.
author_facet Barroqueiro,Elizabeth S. B.
Barroqueiro,Fernanda S. B.
Pinheiro,Mayara T.
Maciel,Márcia C. G.
Barcellos,Priscila S.
Silva,Lucilene A.
Lopes,Adelson S.
Nascimento,Flávia R. F.
Guerra,Rosane N. M.
author_role author
author2 Barroqueiro,Fernanda S. B.
Pinheiro,Mayara T.
Maciel,Márcia C. G.
Barcellos,Priscila S.
Silva,Lucilene A.
Lopes,Adelson S.
Nascimento,Flávia R. F.
Guerra,Rosane N. M.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Barroqueiro,Elizabeth S. B.
Barroqueiro,Fernanda S. B.
Pinheiro,Mayara T.
Maciel,Márcia C. G.
Barcellos,Priscila S.
Silva,Lucilene A.
Lopes,Adelson S.
Nascimento,Flávia R. F.
Guerra,Rosane N. M.
dc.subject.por.fl_str_mv babassu
blood biochemistry
mesocarp
oral acute toxicity
Orbignya phalerata
topic babassu
blood biochemistry
mesocarp
oral acute toxicity
Orbignya phalerata
description The safety of babassu mesocarp (Orbignya phalerata Mart., Arecaceae), which exhibited anti-inflammatory and antithrombotic activities, was evaluated by determining the potential acute toxicity in mice. A lyophilized ethanol extract of babassu mesocarp (BME) was administered to C3H/HePas mice (10/group) in a single dose of 1000, 3000 and 5000 mg/kg, by gavage. General behavior adverse effects and mortality were determined for up to fourteen days. Selected biochemical parameters including glucose, triacylglyceride, cholesterol, urea, alkaline phosphatase and creatinine were determined by colorimetric assay. The heart, liver, spleen, kidneys and brain were weighted and evaluated macro and microscopically. The median lethal dose (LD50) of BME was greater than 5000 mg/kg. No behavior or body weight alterations were detected after the treatment. The acute treatment with BME has no effect on macroscopic and microscopic aspect of examined organs. Instead, BME increased the alkaline phosphatase and reduced the urea concentration in all groups. A significant increase on triacylglyceride was detected in the group BME1000. In conclusion, the acute treatment with high doses of BME can affect some biochemical parameters with a long lasting effect, although any change was detected at tissue level or body and organ weight.
publishDate 2011
dc.date.none.fl_str_mv 2011-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2011000400022
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2011000400022
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0102-695X2011005000121
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Farmacognosia
publisher.none.fl_str_mv Sociedade Brasileira de Farmacognosia
dc.source.none.fl_str_mv Revista Brasileira de Farmacognosia v.21 n.4 2011
reponame:Revista Brasileira de Farmacognosia (Online)
instname:Sociedade Brasileira de Farmacognosia (SBFgnosia)
instacron:SBFGNOSIA
instname_str Sociedade Brasileira de Farmacognosia (SBFgnosia)
instacron_str SBFGNOSIA
institution SBFGNOSIA
reponame_str Revista Brasileira de Farmacognosia (Online)
collection Revista Brasileira de Farmacognosia (Online)
repository.name.fl_str_mv Revista Brasileira de Farmacognosia (Online) - Sociedade Brasileira de Farmacognosia (SBFgnosia)
repository.mail.fl_str_mv rbgnosia@ltf.ufpb.br
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