Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats

Detalhes bibliográficos
Autor(a) principal: Dalmacio, Monica S. C.
Data de Publicação: 2012
Outros Autores: Campos, Sylvia M. N., Carvalho, Jorge J. J., Pereira, Mário J. S., Nascimento, Ana Lúcia, Paschoal, Patricia O. [UNESP], Sobrinho, Andrea P., Pedruzzi, Monique M. B., Garrido, Valeria, Moreno, Silvana R. F., Teixeira, Gerlinde A. P. B., Cardoso, Gilberto P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0102-695X2012005000093
http://hdl.handle.net/11449/211394
Resumo: Wistar rats (n=20) were divided in two groups: G1 received 2 mg/kg of GBE (Ginkgo biloba extract 761), whereas G2 received the same volume of a sodium chloride solution (0.9%), both for 10 days. After a 7-day interval, the treatment was repeated for 8 days. Urine volume and food and water intake were measured daily during this protocol. Histological assessments were performed. No significant difference (p>0.05) was observed in food and water intake of animals during treatment with GBE. Animals who received GBE had a smaller urine volume and increase of weight with a significance difference (p<0.05) during the first and second exposure period. No histological alteration was observed in tissues, except for the kidney of the experimental group, which revealed a higher concentration of red cells in the glomerulus with a strong staining for Vascular Endothelial Growth Factor (VEGF). The introduction of GBE (therapeutic dose) in health rats may promote alterations in the physiology of the kidney, but no sufficient to modify the glomerulus architecture, including at ultra structural level (electron microscopy).
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spelling Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar ratselectron microscopeGinkgo bilobakidneyVEGFWistar rats (n=20) were divided in two groups: G1 received 2 mg/kg of GBE (Ginkgo biloba extract 761), whereas G2 received the same volume of a sodium chloride solution (0.9%), both for 10 days. After a 7-day interval, the treatment was repeated for 8 days. Urine volume and food and water intake were measured daily during this protocol. Histological assessments were performed. No significant difference (p>0.05) was observed in food and water intake of animals during treatment with GBE. Animals who received GBE had a smaller urine volume and increase of weight with a significance difference (p<0.05) during the first and second exposure period. No histological alteration was observed in tissues, except for the kidney of the experimental group, which revealed a higher concentration of red cells in the glomerulus with a strong staining for Vascular Endothelial Growth Factor (VEGF). The introduction of GBE (therapeutic dose) in health rats may promote alterations in the physiology of the kidney, but no sufficient to modify the glomerulus architecture, including at ultra structural level (electron microscopy).Universidade Federal Fluminense, Hospital Universitário Antônio PedroUniversidade Estadual Paulista, Hospital da CriançaUniversidade do Estado do Rio de Janeiro, Departamento de Histologia e EmbriologiaUniversidade Estadual Paulista, Hospital da CriançaSociedade Brasileira de FarmacognosiaUniversidade Federal FluminenseUniversidade Estadual Paulista (Unesp)Universidade do Estado do Rio de JaneiroDalmacio, Monica S. C.Campos, Sylvia M. N.Carvalho, Jorge J. J.Pereira, Mário J. S.Nascimento, Ana LúciaPaschoal, Patricia O. [UNESP]Sobrinho, Andrea P.Pedruzzi, Monique M. B.Garrido, ValeriaMoreno, Silvana R. F.Teixeira, Gerlinde A. P. B.Cardoso, Gilberto P.2021-07-14T10:23:45Z2021-07-14T10:23:45Z2012-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1060-1069application/pdfhttp://dx.doi.org/10.1590/S0102-695X2012005000093Revista Brasileira de Farmacognosia. Curitiba, PR, Brazil: Sociedade Brasileira de Farmacognosia, v. 22, n. 5, p. 1060-1069, 2012.0102-695X1981-528Xhttp://hdl.handle.net/11449/21139410.1590/S0102-695X2012005000093S0102-695X2012000500018S0102-695X2012000500018.pdfSciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista Brasileira de Farmacognosiainfo:eu-repo/semantics/openAccess2023-10-16T06:09:28Zoai:repositorio.unesp.br:11449/211394Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-16T06:09:28Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
title Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
spellingShingle Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
Dalmacio, Monica S. C.
electron microscope
Ginkgo biloba
kidney
VEGF
title_short Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
title_full Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
title_fullStr Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
title_full_unstemmed Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
title_sort Therapeutic dose of Ginkgo biloba extract 761 may alter the urine excretion of Wistar rats
author Dalmacio, Monica S. C.
author_facet Dalmacio, Monica S. C.
Campos, Sylvia M. N.
Carvalho, Jorge J. J.
Pereira, Mário J. S.
Nascimento, Ana Lúcia
Paschoal, Patricia O. [UNESP]
Sobrinho, Andrea P.
Pedruzzi, Monique M. B.
Garrido, Valeria
Moreno, Silvana R. F.
Teixeira, Gerlinde A. P. B.
Cardoso, Gilberto P.
author_role author
author2 Campos, Sylvia M. N.
Carvalho, Jorge J. J.
Pereira, Mário J. S.
Nascimento, Ana Lúcia
Paschoal, Patricia O. [UNESP]
Sobrinho, Andrea P.
Pedruzzi, Monique M. B.
Garrido, Valeria
Moreno, Silvana R. F.
Teixeira, Gerlinde A. P. B.
Cardoso, Gilberto P.
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal Fluminense
Universidade Estadual Paulista (Unesp)
Universidade do Estado do Rio de Janeiro
dc.contributor.author.fl_str_mv Dalmacio, Monica S. C.
Campos, Sylvia M. N.
Carvalho, Jorge J. J.
Pereira, Mário J. S.
Nascimento, Ana Lúcia
Paschoal, Patricia O. [UNESP]
Sobrinho, Andrea P.
Pedruzzi, Monique M. B.
Garrido, Valeria
Moreno, Silvana R. F.
Teixeira, Gerlinde A. P. B.
Cardoso, Gilberto P.
dc.subject.por.fl_str_mv electron microscope
Ginkgo biloba
kidney
VEGF
topic electron microscope
Ginkgo biloba
kidney
VEGF
description Wistar rats (n=20) were divided in two groups: G1 received 2 mg/kg of GBE (Ginkgo biloba extract 761), whereas G2 received the same volume of a sodium chloride solution (0.9%), both for 10 days. After a 7-day interval, the treatment was repeated for 8 days. Urine volume and food and water intake were measured daily during this protocol. Histological assessments were performed. No significant difference (p>0.05) was observed in food and water intake of animals during treatment with GBE. Animals who received GBE had a smaller urine volume and increase of weight with a significance difference (p<0.05) during the first and second exposure period. No histological alteration was observed in tissues, except for the kidney of the experimental group, which revealed a higher concentration of red cells in the glomerulus with a strong staining for Vascular Endothelial Growth Factor (VEGF). The introduction of GBE (therapeutic dose) in health rats may promote alterations in the physiology of the kidney, but no sufficient to modify the glomerulus architecture, including at ultra structural level (electron microscopy).
publishDate 2012
dc.date.none.fl_str_mv 2012-10
2021-07-14T10:23:45Z
2021-07-14T10:23:45Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0102-695X2012005000093
Revista Brasileira de Farmacognosia. Curitiba, PR, Brazil: Sociedade Brasileira de Farmacognosia, v. 22, n. 5, p. 1060-1069, 2012.
0102-695X
1981-528X
http://hdl.handle.net/11449/211394
10.1590/S0102-695X2012005000093
S0102-695X2012000500018
S0102-695X2012000500018.pdf
url http://dx.doi.org/10.1590/S0102-695X2012005000093
http://hdl.handle.net/11449/211394
identifier_str_mv Revista Brasileira de Farmacognosia. Curitiba, PR, Brazil: Sociedade Brasileira de Farmacognosia, v. 22, n. 5, p. 1060-1069, 2012.
0102-695X
1981-528X
10.1590/S0102-695X2012005000093
S0102-695X2012000500018
S0102-695X2012000500018.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista Brasileira de Farmacognosia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1060-1069
application/pdf
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 SciELO
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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