Evaluation of acute toxicity of babassu mesocarp in mice
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , |
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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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 |
_version_ |
1752122466101100544 |