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1.
Physiol Int ; 103(3): 334-343, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28229641

RESUMO

It has been reported that some of the food additives may cause sensitization, inflammation of tissues, and potentially risk factors in the development of several chronic diseases. Thus, we hypothesized that expressions of common inflammatory molecules - known to be involved in the development of various inflammatory conditions and cancers - are affected by these food additives. We investigated the effects of commonly used food preservatives and artificial food colorants based on the expressions of NFκB, GADD45α, and MAPK8 (JNK1) from the tissues of liver. RNA was isolated based on Trizol protocol and the activation levels were compared between the treated and the control groups. Tartrazine alone could elicit effects on the expressions of NFκB (p = 0.013) and MAPK8 (p = 0.022). Azorubine also resulted in apoptosis according to MAPK8 expression (p = 0.009). Preservatives were anti-apoptotic in high dose. Sodium benzoate (from low to high doses) dose-dependently silenced MAPK8 expression (p = 0.004 to p = 0.002). Addition of the two preservatives together elicited significantly greater expression of MAPK8 at half-fold dose (p = 0.002) and at fivefold dose (p = 0.008). This study suggests that some of the food preservatives and colorants can contribute to the activation of inflammatory pathways.


Assuntos
Proteínas de Ciclo Celular/genética , Aditivos Alimentares/farmacologia , Expressão Gênica/efeitos dos fármacos , Proteína Quinase 8 Ativada por Mitógeno/genética , NF-kappa B/genética , Proteínas Nucleares/genética , Animais , Proteínas de Ciclo Celular/metabolismo , Feminino , Corantes de Alimentos/farmacologia , Conservantes de Alimentos/farmacologia , Masculino , Camundongos , Proteína Quinase 8 Ativada por Mitógeno/metabolismo , NF-kappa B/metabolismo , Naftalenossulfonatos/farmacologia , Proteínas Nucleares/metabolismo , Benzoato de Sódio/farmacologia , Ácido Sórbico/farmacologia , Tartrazina/farmacologia
2.
Phytother Res ; 23(10): 1399-403, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19274701

RESUMO

Asian ginseng (Panax ginseng C. A. Meyer) has been used in Chinese medicine for two thousand years. The root of ginseng contains several saponins (ginsenosides) which are biologically active compounds. Individual ginsenosides suppress tumor cell growth, induce cell differentiation, regulate apoptosis and inhibit metastasis formation. The aim of this study was to evaluate its chemo-preventive effects in an animal test model, through its regulatory effects on apoptosis and the cell cycle.The expression of genes (Bcl-2, Bcl-x and Cyclin D1) which affect apoptosis were examined, in different organs of animals which had consumed a ginseng-containing diet in the presence of a known carcinogen (DMBA). The pattern of gene expression was determined by Q-RT-PCR. The increase of antiapoptotic gene expression after carcinogenic exposure was suppressed by consumption of ginseng which promoted apoptosis.The population is exposed to numerous physical and chemical insults in the modern environment and these include compounds which are known carcinogens. Research has shown that it is possible to interfere with the multi-step process of carcinogenesis through the use of compounds with chemo-preventive effects, such as the inhibition of the activation of antiapoptotic genes.These results support the efficacy of ginseng-containing diets and dietary supplements in the prevention of cancerous diseases.


Assuntos
Antineoplásicos Fitogênicos/uso terapêutico , Apoptose/efeitos dos fármacos , Neoplasias/prevenção & controle , Panax , Fitoterapia , Preparações de Plantas/uso terapêutico , 9,10-Dimetil-1,2-benzantraceno , Animais , Antineoplásicos Fitogênicos/farmacologia , Carcinógenos , Ciclina D1/genética , Ciclina D1/metabolismo , Modelos Animais de Doenças , Feminino , Expressão Gênica , Camundongos , Camundongos Endogâmicos AKR , Neoplasias/induzido quimicamente , Neoplasias/genética , Preparações de Plantas/farmacologia , Raízes de Plantas , Pós , Proteínas Proto-Oncogênicas c-bcl-2/genética , Proteínas Proto-Oncogênicas c-bcl-2/metabolismo , Proteína bcl-X/genética , Proteína bcl-X/metabolismo
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