Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats

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Background:Euphorbia huachahana (Klotzch & Garcke) Boissier (Huachangana)(EhKGBh)has been used for over a century for medicinal purposes in the Peruvian population; however, itssafety and possible toxic effects of use have not been reported. The purpose of this study was todetermine the acute he...

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Autores: Villafuerte, Graciela, Ñañez, Daniel, Félix, Luis M., Moya-Salazar, Marcia M., Torres-Véliz, Ernesto R., Ramos, Antonio G., Contreras-Pulache, Hans
Formato: artículo
Fecha de Publicación:2022
Institución:Universidad Privada Norbert Wiener
Repositorio:UWIENER-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.uwiener.edu.pe:20.500.13053/6920
Enlace del recurso:https://hdl.handle.net/20.500.13053/6920
https://doi.org/10.3390/pr10071286
Nivel de acceso:acceso abierto
Materia:toxicity; kidney; liver; LD50; acute; in vivo studies
http://purl.org/pe-repo/ocde/ford#3.03.00
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dc.title.es_ES.fl_str_mv Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
title Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
spellingShingle Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
Villafuerte, Graciela
toxicity; kidney; liver; LD50; acute; in vivo studies
http://purl.org/pe-repo/ocde/ford#3.03.00
title_short Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
title_full Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
title_fullStr Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
title_full_unstemmed Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
title_sort Acute Hepatic and Renal Toxicity Assessment of Euphorbia huanchahana (Klotzsch & Garcke) Boissier (Huachangana) in Holtzman Rats
author Villafuerte, Graciela
author_facet Villafuerte, Graciela
Ñañez, Daniel
Félix, Luis M.
Moya-Salazar, Marcia M.
Torres-Véliz, Ernesto R.
Ramos, Antonio G.
Contreras-Pulache, Hans
author_role author
author2 Ñañez, Daniel
Félix, Luis M.
Moya-Salazar, Marcia M.
Torres-Véliz, Ernesto R.
Ramos, Antonio G.
Contreras-Pulache, Hans
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Villafuerte, Graciela
Ñañez, Daniel
Félix, Luis M.
Moya-Salazar, Marcia M.
Torres-Véliz, Ernesto R.
Ramos, Antonio G.
Contreras-Pulache, Hans
Moya-Salazar, Marcia M.
dc.subject.es_ES.fl_str_mv toxicity; kidney; liver; LD50; acute; in vivo studies
topic toxicity; kidney; liver; LD50; acute; in vivo studies
http://purl.org/pe-repo/ocde/ford#3.03.00
dc.subject.ocde.es_ES.fl_str_mv http://purl.org/pe-repo/ocde/ford#3.03.00
description Background:Euphorbia huachahana (Klotzch & Garcke) Boissier (Huachangana)(EhKGBh)has been used for over a century for medicinal purposes in the Peruvian population; however, itssafety and possible toxic effects of use have not been reported. The purpose of this study was todetermine the acute hepatic and renal toxicity of EhKGBh in Holtzman rats. Methods: Analyticaland experimental study. The population consisted of 52 rats of both sexes weighing between 300 and350 g divided into four groups: G1 and G2 EhKGBh groups (26 rats each) and two control groups(10 rats each). The experimental group was administered EhKGBh at a single dose of 2000 mg/kg P.O.to demonstrate toxicity during the 14-day follow-up. A daily assessment of alanine aminotransferase(ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total bilirubin (TBIL), andconjugated bilirubin (CBIL) was performed. Results: Evaluation of the liver tissue showed mildchanges in inflammation, predominantly vascular, with small clots. Kidney tissue did not showinflammatory or necrotic changes. However, we showed differences in the weight of the rats betweenboth groups (p< 0.004) and significant increases in TBIL (0.98–1.07 mg/dL), CBIL (0.43–0.45 mg/dL),AST (126.4–141.8 U/L), and ALP (254–298 U/L) but not ALT (39.7–41.1 U/L) (p< 0.05). Conclusion:The single dose of EhKGBh extract at 2000 mg/kg has no toxicity, and there is no change in tissuetoxicity during the 14-day follow-up.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2022-10-24T21:10:37Z
dc.date.available.none.fl_str_mv 2022-10-24T21:10:37Z
dc.date.issued.fl_str_mv 2022-06-30
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dc.identifier.doi.es_ES.fl_str_mv https://doi.org/10.3390/pr10071286
url https://hdl.handle.net/20.500.13053/6920
https://doi.org/10.3390/pr10071286
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language eng
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spelling Villafuerte, GracielaÑañez, DanielFélix, Luis M.Moya-Salazar, Marcia M.Torres-Véliz, Ernesto R.Ramos, Antonio G.Contreras-Pulache, HansMoya-Salazar, Marcia M.2022-10-24T21:10:37Z2022-10-24T21:10:37Z2022-06-30https://hdl.handle.net/20.500.13053/6920https://doi.org/10.3390/pr10071286Background:Euphorbia huachahana (Klotzch & Garcke) Boissier (Huachangana)(EhKGBh)has been used for over a century for medicinal purposes in the Peruvian population; however, itssafety and possible toxic effects of use have not been reported. The purpose of this study was todetermine the acute hepatic and renal toxicity of EhKGBh in Holtzman rats. Methods: Analyticaland experimental study. The population consisted of 52 rats of both sexes weighing between 300 and350 g divided into four groups: G1 and G2 EhKGBh groups (26 rats each) and two control groups(10 rats each). The experimental group was administered EhKGBh at a single dose of 2000 mg/kg P.O.to demonstrate toxicity during the 14-day follow-up. A daily assessment of alanine aminotransferase(ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total bilirubin (TBIL), andconjugated bilirubin (CBIL) was performed. Results: Evaluation of the liver tissue showed mildchanges in inflammation, predominantly vascular, with small clots. Kidney tissue did not showinflammatory or necrotic changes. However, we showed differences in the weight of the rats betweenboth groups (p< 0.004) and significant increases in TBIL (0.98–1.07 mg/dL), CBIL (0.43–0.45 mg/dL),AST (126.4–141.8 U/L), and ALP (254–298 U/L) but not ALT (39.7–41.1 U/L) (p< 0.05). 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