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1.
J Food Sci ; 74(2): T24-30, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19323775

RESUMEN

A 2-y carcinogenicity study of Aloe, Aloe arborescens Miller var. natalensis Berger, a food additive, was conducted for assessment of toxicity and carcinogenic potential in the diet at doses of 4% or 0.8% in groups of male and female Wistar Hannover rats. Both sexes receiving 4% showed diarrhea, with loss of body weight gain. The survival rate in the 4% female group was significantly increased compared with control females after 2 y. Hematological and biochemical examination showed increase of RBC, Hb, and Alb in the 4% males. The cause of these increases could conceivably have been dehydration through diarrhea. AST and Na were significantly decreased in the males receiving 4%, and Cl was significantly decreased in both 4% and 0.8% males. A/G was significantly increased in the 4% females, and Cl was significantly decreased (0.8%) in the female group. Histopathologically, both sexes receiving 4% showed severe sinus dilatation of ileocecal lymph nodes, and yellowish pigmentation of ileocecal lymph nodes and renal tubules. Adenomas or adenocarcinomas in the cecum, colon, and rectum were observed in 4% males but not in the 0.8% and control male groups. Similarly, in females, adenomas in the colon were also observed in the 4% but not 0.8% and control groups. In conclusion, Aloe, used as a food additive, exerted equivocal carcinogenic potential at 4% high-dose level on colon in the 2-y carcinogenicity study in rats. Aloe is not carcinogenic at nontoxic-dose levels and that carcinogenic potential in at 4% high-dose level on colon is probably due to irritation of the intestinal tract by diarrhea.


Asunto(s)
Aloe/toxicidad , Neoplasias del Colon/inducido químicamente , Extractos Vegetales/toxicidad , Animales , Neoplasias del Colon/mortalidad , Diarrea/inducido químicamente , Modelos Animales de Enfermedad , Emodina/análogos & derivados , Emodina/toxicidad , Femenino , Glucósidos/toxicidad , Masculino , Hojas de la Planta , Ratas , Ratas Wistar , Tasa de Supervivencia
2.
J Food Sci ; 73(7): C561-8, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18803703

RESUMEN

To clarify the effects of purple corn color, enzymatically modified isoquercitrin (EMIQ), and isoquercitrin (IQ), registered as natural food additives in Japan, on liver carcinogenesis in vivo, a medium-term bioassay was employed. A total of 100 male F344 rats were divided into 5 groups; groups 1 to 4 were given a single intraperitoneal injection of diethylnitrosamine (200 mg/kg b.w.) on day 1. From weeks 2 to 8, they were administered basal diet purple corn color, EMIQ, or IQ as containing test chemicals at doses of 1.0% (groups 1 and 5), 0.1% (group 2), 0.01% (group 3), or 0% (group 4) (experiments 1, 4, and 5). All rats were subjected to two-thirds partial hepatectomy at week 3 and were sacrificed at week 8. Purple corn color exerted no significant modifying effects on GST-P positive foci, preneoplastic foci, development in the liver. However, serum of rats treated with purple corn color provided evidence of antioxidant power significantly by potential antioxidant (PAO) test in vivo (experiment 2). And microarray analyses showed purple corn color to induce RNA expression such as P450 (cytochrome) oxidoreductase, phosphatidylinositol 3-kinase, and phospholipase A2 (experiment 3). Higher doses of EMIQ or IQ with strong antioxidant power in vivo by PAO test treated groups were correlated with smaller numbers of GST-P positive foci, with Spearman's rank correlation coefficients of P= 0.002 and P= 0.049, respectively (experiments 4 and 5). Therefore, the tested food additives may be effective as antioxidants in vivo and have chemopreventive potential against liver preneoplastic lesion development.


Asunto(s)
Anticarcinógenos/farmacología , Antioxidantes/farmacología , Flavonoides/farmacología , Aditivos Alimentarios/farmacología , Neoplasias Hepáticas Experimentales/prevención & control , Quercetina/análogos & derivados , Animales , Antocianinas/farmacología , Dietilnitrosamina/toxicidad , Expresión Génica , Glutatión Transferasa/metabolismo , Neoplasias Hepáticas Experimentales/genética , Masculino , Análisis de Secuencia por Matrices de Oligonucleótidos , Quercetina/farmacología , ARN/metabolismo , Ratas , Ratas Endogámicas F344
3.
J Food Sci ; 73(3): T26-32, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-18387132

RESUMEN

A medium-term multi-organ carcinogenesis bioassay in rats was conducted to assess any possible tumor promoting effects of madder color extracted from the root of madder. Male F344 rats were divided into 5 groups of 20 each. All rats of groups 1 to 4 were given DMD treatment, consisted of multicarcinogens, N-nitrosodiethylamine (DEN), N-methyl-N-nitrosourea (MNU), and N-bis (2-hydroxypropyl) nitrosamine (DHPN), for 4 wk, while group 5 served as untreated control without carcinogens. The animals were then administered a basal diet containing madder color at doses of 5.0% (group 1), 2.5% (group 2 with 0.75% additional dextrin), or 0 (groups 3 with 1.5% additional dextrin, 4 without dextrin and 5) for the following 28 wk (total 32 wk). The total amount of dextrin in groups 1 to 3 diets was adjusted to 1.5% by extra dextrin because madder color powder contained dextrin. Key organs were observed histopathologically and glutathione S-transferase placental form (GST-P) positive foci of the liver were quantified. In the liver, 5.0% and 2.5% treated groups showed statistically significant dose-related increases in both number and area of GST-P positive foci, number: 2.81 +/- 0.90 and 1.96 +/- 0.93 (groups 1 and 2), area: 0.99 +/- 2.49 and 0.37 +/- 0.77, as compared with control, number: 0.87 +/- 0.72, area: 0.06 +/- 0.06 (group 3). In the kidneys, incidences (and numbers) of adenoma treated with 5.0% and 2.5%, 47.4% (0.20 +/- 0.24), and 47.4% (0.13 +/- 0.15) (groups 1 and 2) were significantly increased compared to control, 0% (0) (group 3). In conclusion, madder color demonstrated significant tumor promoting effects in the liver and kidneys in the DMD model.


Asunto(s)
Pruebas de Carcinogenicidad , Carcinógenos/toxicidad , Neoplasias Renales/inducido químicamente , Neoplasias Hepáticas Experimentales/inducido químicamente , Extractos Vegetales/toxicidad , Rubia/toxicidad , Adenoma/inducido químicamente , Adenoma/patología , Animales , Bioensayo , Relación Dosis-Respuesta a Droga , Neoplasias Renales/patología , Neoplasias Hepáticas Experimentales/patología , Masculino , Neoplasias Experimentales/inducido químicamente , Neoplasias Experimentales/patología , Distribución Aleatoria , Ratas , Ratas Endogámicas F344
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