Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals
Descripción del Articulo
Objective: To determine liver and renal toxicity of Croton palanostigma latex oral swallowing, in therapeutic and larger doses. Materials and Methods: Sixty albino male rats were studied in two groups: one group swallowed for a short time during 7 days and another group swallowed ad libitum during 3...
| Autores: | , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2005 |
| Institución: | Universidad Nacional Mayor de San Marcos |
| Repositorio: | Revistas - Universidad Nacional Mayor de San Marcos |
| Lenguaje: | español |
| OAI Identifier: | oai:ojs.csi.unmsm:article/1359 |
| Enlace del recurso: | https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/1359 |
| Nivel de acceso: | acceso abierto |
| Materia: | Croton palanostigma plantas medicinales farmacognosia hígado toxicidad riñón investigación plants medicinal pharmacognosy liver toxicity kidney research |
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Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals Evaluación de la toxicidad hepática y renal aguda y subaguda del látex de Croton palanostigma (sangre de grado) en animales de experimentación |
| title |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals |
| spellingShingle |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals Sandoval, Miguel Croton palanostigma plantas medicinales farmacognosia hígado toxicidad riñón investigación Croton palanostigma plants medicinal pharmacognosy liver toxicity kidney research |
| title_short |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals |
| title_full |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals |
| title_fullStr |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals |
| title_full_unstemmed |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals |
| title_sort |
Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animals |
| dc.creator.none.fl_str_mv |
Sandoval, Miguel Ayala, Salomón Oré, María Valdivieso, Lázaro Loli, Rudi Ricra, Vides Huaman, Oscar |
| author |
Sandoval, Miguel |
| author_facet |
Sandoval, Miguel Ayala, Salomón Oré, María Valdivieso, Lázaro Loli, Rudi Ricra, Vides Huaman, Oscar |
| author_role |
author |
| author2 |
Ayala, Salomón Oré, María Valdivieso, Lázaro Loli, Rudi Ricra, Vides Huaman, Oscar |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Croton palanostigma plantas medicinales farmacognosia hígado toxicidad riñón investigación Croton palanostigma plants medicinal pharmacognosy liver toxicity kidney research |
| topic |
Croton palanostigma plantas medicinales farmacognosia hígado toxicidad riñón investigación Croton palanostigma plants medicinal pharmacognosy liver toxicity kidney research |
| description |
Objective: To determine liver and renal toxicity of Croton palanostigma latex oral swallowing, in therapeutic and larger doses. Materials and Methods: Sixty albino male rats were studied in two groups: one group swallowed for a short time during 7 days and another group swallowed ad libitum during 30 days. In each group there were 3 subgroups: (A) 1/1000 diluted latex (therapeutic dose), (B) 1/100 diluted latex, (C) water (control group). The animal weight and the water or diluted latex consumption were measured. Then, the rats were given ether anesthesia, their blood was obtained by cardiac puncture and centrifuged at 5000 rpm during 5 minutes to obtain plasma. Alkaline phosphatase and transferase glutamyl gamma activity were measured; urea, creatinine, total protein, albumin and globulin levels were studied by espectrophotometry. Results: The average latex consumption in the first group were: in A, 0,14 mL/kg-1/day-1/rat-1; in B, 1,34 mL/kg-1/day-1/ rat-1; and, in C, water. There was no significative difference in the daily latex consumption between the 7 and 30-day trated groups. Both the alkaline phosphatase and transferase glutamyl gamma activities, the blood metabolites and both animal liver/weight ratio and animal renal/weight ratio did not present any significative difference (p>0,05) from the control group. Conclusions: In experimental conditions, the short time and long time sangre de grado oral swallowing, in both therapeutic dose and larger concentrations, did not produce any biochemical, liver or renal alteration in the animals. |
| publishDate |
2005 |
| dc.date.none.fl_str_mv |
2005-06-13 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/1359 10.15381/anales.v66i2.1359 |
| url |
https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/1359 |
| identifier_str_mv |
10.15381/anales.v66i2.1359 |
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spa |
| language |
spa |
| dc.relation.none.fl_str_mv |
https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/1359/1154 |
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https://creativecommons.org/licenses/by-nc-sa/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by-nc-sa/4.0 |
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openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
Universidad Nacional Mayor de San Marcos, Facultad de Medicina Humana |
| publisher.none.fl_str_mv |
Universidad Nacional Mayor de San Marcos, Facultad de Medicina Humana |
| dc.source.none.fl_str_mv |
Anales de la Facultad de Medicina; Vol. 66 No. 2 (2005); 119-126 Anales de la Facultad de Medicina; Vol. 66 Núm. 2 (2005); 119-126 1609-9419 1025-5583 reponame:Revistas - Universidad Nacional Mayor de San Marcos instname:Universidad Nacional Mayor de San Marcos instacron:UNMSM |
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Universidad Nacional Mayor de San Marcos |
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UNMSM |
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UNMSM |
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Revistas - Universidad Nacional Mayor de San Marcos |
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Revistas - Universidad Nacional Mayor de San Marcos |
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1795238242967093248 |
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Determination of both acute and sub acute liver and renal toxicity of Croton palanostigma (sangre de grado) latex in experimental animalsEvaluación de la toxicidad hepática y renal aguda y subaguda del látex de Croton palanostigma (sangre de grado) en animales de experimentaciónSandoval, MiguelAyala, SalomónOré, MaríaValdivieso, LázaroLoli, RudiRicra, VidesHuaman, OscarCroton palanostigmaplantas medicinalesfarmacognosiahígadotoxicidadriñóninvestigaciónCroton palanostigmaplantsmedicinalpharmacognosylivertoxicitykidneyresearchObjective: To determine liver and renal toxicity of Croton palanostigma latex oral swallowing, in therapeutic and larger doses. Materials and Methods: Sixty albino male rats were studied in two groups: one group swallowed for a short time during 7 days and another group swallowed ad libitum during 30 days. In each group there were 3 subgroups: (A) 1/1000 diluted latex (therapeutic dose), (B) 1/100 diluted latex, (C) water (control group). The animal weight and the water or diluted latex consumption were measured. Then, the rats were given ether anesthesia, their blood was obtained by cardiac puncture and centrifuged at 5000 rpm during 5 minutes to obtain plasma. Alkaline phosphatase and transferase glutamyl gamma activity were measured; urea, creatinine, total protein, albumin and globulin levels were studied by espectrophotometry. Results: The average latex consumption in the first group were: in A, 0,14 mL/kg-1/day-1/rat-1; in B, 1,34 mL/kg-1/day-1/ rat-1; and, in C, water. There was no significative difference in the daily latex consumption between the 7 and 30-day trated groups. Both the alkaline phosphatase and transferase glutamyl gamma activities, the blood metabolites and both animal liver/weight ratio and animal renal/weight ratio did not present any significative difference (p>0,05) from the control group. Conclusions: In experimental conditions, the short time and long time sangre de grado oral swallowing, in both therapeutic dose and larger concentrations, did not produce any biochemical, liver or renal alteration in the animals.Objetivo: Determinar la toxicidad hepática y renal de la administración oral del látex de Croton palanostigma, en dosis terapéutica y de mayor concentración. Materiales y Métodos: Se evaluó 60 ratas albinas, machos, en dos grupos: con administración oral aguda por 7 dìas y otro con administración oral subaguda por 30 días ad libitum. En cada grupo se tuvo tres subgrupos: (A) Látex diluido 1/1000 (dosis terapéutica), (B) Látex diluido 1/100, (C) Agua (grupo control). Medimos el peso del animal y consumo del bebedero. Después, bajo anestesia con éter, se obtuvo sangre por punción cardiaca y se centrifugó a 5000 rpm por 5 minutos para obtener plasma sanguíneo. Se determinó actividad de gamma glutamil transferasa y fosfatasa alcalina, se evaluó niveles de urea, creatinina, proteínas totales, albúmina y globulinas por espectrofotocolorimétría. Resultados: El consumo promedio del látex en el primer grupo fue: en A, 0,14 mL.kg-1/día-1/rata-1; en B, 1,34 mL/kg-1/día-1/rata-1; y, en C, agua. En el segundo grupo, fue: en A, 0,13 mL/kg-1/día-1/rata-1; en B, 1,21 mL/kg-1/día-1/rata-1; y, en C, agua. No hubo diferencia significativa en el consumo del látex diario entre los grupos tratados a 7 y 30 días. Las actividades de gamma glutamil transferasa y fosfatasa alcalina, así como los metabolitos sanguíneos y ratios hígado/peso animal y riñones/peso animal, de los grupos experimentales vs. grupo control, no presentaron diferencias significativas (p>0,05). Conclusiones: En condiciones experimentales, la administración oral de sangre de grado, aguda y subaguda, en dosis terapéuticas y de mayor concentración, no produce alteraciones bioquímicas hepáticas ni renales en animales de experimentación.Universidad Nacional Mayor de San Marcos, Facultad de Medicina Humana2005-06-13info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/135910.15381/anales.v66i2.1359Anales de la Facultad de Medicina; Vol. 66 No. 2 (2005); 119-126Anales de la Facultad de Medicina; Vol. 66 Núm. 2 (2005); 119-1261609-94191025-5583reponame:Revistas - Universidad Nacional Mayor de San Marcosinstname:Universidad Nacional Mayor de San Marcosinstacron:UNMSMspahttps://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/1359/1154Derechos de autor 2005 Miguel Sandoval, Salomón Ayala, María Oré, Lázaro Valdivieso, Rudi Loli, Vides Ricra, Oscar Huamanhttps://creativecommons.org/licenses/by-nc-sa/4.0info:eu-repo/semantics/openAccessoai:ojs.csi.unmsm:article/13592020-04-14T20:57:53Z |
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13.924177 |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).