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1.
J Ethnopharmacol ; 252: 112551, 2020 Apr 24.
Artículo en Inglés | MEDLINE | ID: mdl-31923540

RESUMEN

ETHNOPHARMACOLOGICAL RELEVANCE: Bojungikki-tang is a traditional herbal medicine used to boost immunity and reduce fatigue. However, there is not enough scientific evidence about its toxicological safety profile to support its continued clinical application. AIM OF THE STUDY: The objective of this study was to investigate the subchronic toxicity profile of Bojungikki-tang water extract (BITW) in Sprague Dawley rats who were exposed to it in multiple doses and various concentrations. MATERIALS AND METHODS: BITW was administered to rats orally, once daily at doses of 0, 500, 1000, or 2000 mg/kg/day for 13 weeks. We checked toxicological parameters including general observations, organ/body weights, food consumption, ophthalmological signs, hematological and serum biochemical values, urinalysis values and histopathological findings. RESULTS: The 13 week repeated oral administration of BITW to rats at doses at doses levels of less than or equal to 2000 mg/kg/day caused no significant toxicological changes and only minor nonsignificant changes. CONCLUSIONS: Our findings indicate that administration of BITW for up to 13 weeks may be safe and nontoxic, with a no-observed-adverse-effect-level of >2000 mg/kg/day for both male and female rats.


Asunto(s)
Medicamentos Herbarios Chinos/toxicidad , Animales , Femenino , Masculino , Ratas Sprague-Dawley , Solventes/química , Pruebas de Toxicidad Subcrónica , Agua/química
2.
Regul Toxicol Pharmacol ; 62(3): 553-60, 2012 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-22154825

RESUMEN

Gumiganghwaltang is a traditional oriental herbal medicine that has been commonly used to treat colds and inflammatory diseases. Aqueous extract of Gumiganghwaltang (GMGHT) was administrated daily by oral gavage to male and female rats for 13 weeks. A dose of 2000 mg/kg/day was selected as a maximum, and doses of 1000 and 500 mg/kg/day were determined as medium and low doses, respectively. No treatment-related clinical signs or mortality were observed in the treatment group. We observed no clear treatment-related effects with regard to body weight, food consumption, ophthalmology, hematology, or urinalysis data. The serum biochemistry values for sodium and chloride in the treated male and female groups (1000 mg/kg/day) were lower than in those treated with the vehicle control. However, these changes lacked dose dependence, and no abnormalities were found in corresponding pathological findings. Our results indicated that the no-observed-adverse-effect-level (NOAEL) for GMGHT was determined to be a dietary dose of over 2000 mg/kg/day for both sexes under the present experimental conditions.


Asunto(s)
Extractos Vegetales/administración & dosificación , Extractos Vegetales/toxicidad , Preparaciones de Plantas/administración & dosificación , Preparaciones de Plantas/toxicidad , Administración Oral , Animales , Evaluación de Medicamentos , Femenino , Riñón/efectos de los fármacos , Riñón/patología , Hígado/efectos de los fármacos , Hígado/patología , Masculino , Tamaño de los Órganos/efectos de los fármacos , Extractos Vegetales/aislamiento & purificación , Preparaciones de Plantas/aislamiento & purificación , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Factores de Tiempo
3.
Drug Chem Toxicol ; 32(3): 191-203, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19538015

RESUMEN

Successful wound healing depends upon angiogenesis, and impaired angiogenesis is a hallmark of the chronic wounds encountered with diabetes and venous or arterial insufficiency. To intervene and improve wound closure, it is essential to investigate the effects of different natural remedies in wound healing. The chicken dorsum skin excisional wound assay was used to investigate the influence of different concentrations of aged garlic solution (AGS) on wound healing. Gross, histopathology, scanning electron microscopy (SEM) and computer-based three-dimensional (3D) image-probing techniques were utilized to determine the effects of AGS on wound closure, re-epithelialization, dermal matrix regeneration, and angiogenesis. Ninety chicks, aged 1 week and divided in 6 groups, were topically exposed to different concentrations of AGS for 6 days: control (group A), 1% (group B), 5% (group C), 10% (group D), 15% (group E), and skin lotion (group F). Different patterns, ranging from incomplete to almost complete wound closure, were observed among different groups with highly significant results (P < 0.001) in group E. Histological investigations revealed a positive augment in the re-epithelialization of all AGS exposed wounds. An increase in the number of new loosely packed collagen and maturation of collagen bundles was observed in all treated wounds at days 4 and 6 post-wounding, respectively. Similar results were achieved through SEM of treated wounds. Histological investigations revealed the profuse dose-dependent neovascularization among AGS-treated wounds. Abbott curve, angular spectrum, and different parameters of 3D surface roughness of wounds were also measured for the precise quantification of angiogenesis. A very highly significant (P < 0.001) increase in angiogenesis was observed among all treated groups. No significant change was observed among control and skin lotion-treated groups. These observations substantiate the beneficial use of AGS in the treatment of wounds. Additional studies are needed to study the specific wound-healing mechanisms of chemical, or group of chemicals, present in AGS.


Asunto(s)
Epidermis/efectos de los fármacos , Ajo/química , Extractos Vegetales/farmacología , Cicatrización de Heridas/efectos de los fármacos , Animales , Movimiento Celular/efectos de los fármacos , Movimiento Celular/fisiología , Pollos , Dermis/efectos de los fármacos , Dermis/ultraestructura , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Epidermis/lesiones , Epidermis/ultraestructura , Células Epiteliales/efectos de los fármacos , Células Epiteliales/patología , Células Epiteliales/fisiología , Matriz Extracelular/efectos de los fármacos , Matriz Extracelular/ultraestructura , Procesamiento de Imagen Asistido por Computador , Microscopía Electrónica de Rastreo , Neovascularización Fisiológica/efectos de los fármacos , Neovascularización Fisiológica/fisiología , Propiedades de Superficie/efectos de los fármacos , Factores de Tiempo , Cicatrización de Heridas/fisiología
4.
Genomics ; 87(4): 520-6, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16455232

RESUMEN

A novel autosomal recessive mutant was produced using N-ethyl-N-nitrosourea mutagenesis. The characteristics of the mutant mice included progressive irreversible hair loss within a month of birth, wrinkled skin, and long curved nails. Linkage analysis revealed that the causative gene is linked to D14Mit193 on chromosome 14. Sequence analysis of the complete cDNA of the candidate gene, hairless (Hr), identified a homozygous G-to-T transition at nucleotide 3572, leading to the substitution of glycine by tryptophan, designated Gly960Trp. This missense mutation occurs in the vicinity of repression domain 3 of the hairless protein (HR). This allele was named Hr(m1Enu). The relative amounts of Hr mRNA and HR protein determined by real-time PCR and Western blot analyses, respectively, were slightly elevated in the mutant mice. Quantitative real-time PCR analysis revealed the increased expression of Kc1 and Vdr in the mutant mice, whereas the expression of Nrs1 and Krtap16-6 was decreased. These results suggest that the Gly960Trp substitution in HR protein in Hr(m1Enu) mice may alter the function of HR as a transcriptional corepressor.


Asunto(s)
Alopecia/genética , Genes Recesivos , Mutación Missense , Factores de Transcripción/genética , Alelos , Secuencia de Aminoácidos , Animales , Western Blotting , Mapeo Cromosómico , Cromosomas de los Mamíferos , Secuencia Conservada , Cruzamientos Genéticos , Análisis Mutacional de ADN , ADN Complementario/genética , Etilnitrosourea/farmacología , Ligamiento Genético , Haplotipos , Homocigoto , Ratones , Ratones Endogámicos C57BL , Ratones Mutantes , Datos de Secuencia Molecular , Mutágenos/farmacología , Estructura Terciaria de Proteína , ARN Mensajero/análisis , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Análisis de Secuencia de ADN , Homología de Secuencia de Aminoácido , Triptófano/metabolismo , Dedos de Zinc
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