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1.
Toxicol Pathol ; 32(3): 338-44, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15204976

RESUMEN

The specificity of copromotion effects of caffeine with known goitrogenic factors on thyroid carcinogenesis was examined in rats pretreated with N-bis(2-hydroxypropyl)nitrosamine (DHPN). Male F344 rats were divided into 8 groups, each consisting of 10 animals, and received a single sc injection of 2,800 mg/kg DHPN. From one week after the DHPN initiation, they were given basal diet, iodine deficiency (ID) diet, 500 ppm phenobarbital (PB) solution or 1,000 ppm sulfadimethoxine (SDM) solution with or without 1,500 ppm caffeine feeding for 12 weeks. The caffeine, PB, SDM, and ID treatments significantly (p < 0.05 or 0.01) increased the relative thyroid weights, and the increases with PB or ID were further (p < 0.05 or 0.01) enhanced in combination with caffeine. SDM drastically promoted thyroid carcinogenesis in association with increased serum TSH levels regardless of the caffeine treatment. Thyroid follicular carcinomas and adenomas were more frequently observed in the additional caffeine groups than in the ID alone groups. The incidence and multiplicity of focal thyroid follicular hyperplasias in the ID-treated groups were significantly (p < 0.05 and 0.01) elevated in the case of combination with caffeine. Increases in serum TSH levels with PB or ID were also further enhanced in combination with caffeine. Serum thyroid hormone levels were significantly (p < 0.01) decreased by SDM but significantly (p < 0.05 or 0.01) increased by caffeine, PB or ID. Our results clearly indicate that dietary caffeine at a high dose of 1,500 ppm interacts with ID, but neither SDM nor PB, to promote rat thyroid carcinogenesis although the combined caffeine + PB treatment somewhat affected thyroid weights as well as thyroid hormone levels.


Asunto(s)
Cafeína/toxicidad , Carcinógenos/toxicidad , Estimulantes del Sistema Nervioso Central/toxicidad , Cocarcinogénesis , Neoplasias de la Tiroides/inducido químicamente , Animales , Antiinfecciosos/toxicidad , Modelos Animales de Enfermedad , Antagonistas de Aminoácidos Excitadores/toxicidad , Masculino , Nitrosaminas/toxicidad , Fenobarbital/toxicidad , Ratas , Ratas Endogámicas F344 , Sulfadimetoxina/toxicidad , Neoplasias de la Tiroides/patología , Tirotropina/sangre
2.
Jpn J Cancer Res ; 92(4): 390-5, 2001 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-11346460

RESUMEN

The specificity and dose dependence of the synergistic effects of soybean intake with iodine deficiency on the induction of thyroid proliferation were investigated in female F344 rats. In the first experiment, rats were divided into 6 groups, each consisting of 5 animals, and fed a basal diet containing 20% gluten, an iodine-deficient basal diet alone or an iodine-deficient diet containing 0.2%, 1.0%, 5.0% or 25% defatted soybean for 5 weeks. Soybean feeding synergistically induced thyroid hyperplasias with iodine deficiency only at the 25% dose. In the second experiment, rats were also divided into 6 groups, each consisting of 5 animals, and fed a basal diet, a diet containing 20% defatted soybean, 0.025% sulfadimethoxine (SDM), 20% defatted soybean + 0.025% SDM, 0.05% phenobarbital (PB) or 20% defatted soybean + 0.05% PB for 5 weeks. The SDM treatments significantly (P < 0.05 - 0.01) increased the thyroid weights, but this increase rate was less prominent in the SDM + soybean group than in the SDM alone group. The PB treatment was also associated with a tendency for increase in thyroid weight, but again this was smaller in the PB + soybean group than in the PB alone group. Although the SDM or PB treatments reduced the serum triiodothyronine and thyroxine levels and consequently increased the serum thyroid-stimulating hormone (TSH) levels, the soybean feeding did not affect or rather attenuated these changes. Our results clearly indicate that soybean feeding does not synergistically enhance the effects of SDM or PB on the rat thyroid. Thus it can be concluded that soybean intake specifically interacts with iodine deficiency in induction of thyroid proliferative lesions in rats, only at high doses.


Asunto(s)
Glycine max/toxicidad , Yodo/deficiencia , Fenobarbital/toxicidad , Sulfadimetoxina/toxicidad , Glándula Tiroides/efectos de los fármacos , Animales , División Celular/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Sinergismo Farmacológico , Femenino , Hiperplasia/inducido químicamente , Ratas , Ratas Endogámicas F344 , Glándula Tiroides/metabolismo , Glándula Tiroides/patología , Neoplasias de la Tiroides/inducido químicamente , Tirotropina/sangre , Tiroxina/sangre , Triyodotironina/sangre
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