RESUMO
We investigated the estrogenic activity of various environmental pollutants (xenobiotics), in particular the xenoestrogen o,p-DDT, and compared their effects with those of endogenous estrogens, phytoestrogens, and mycoestrogens on estrogen receptor binding capacity, induction of estrogen end products, and activation of cell proliferation in estrogen-sensitive human breast cancer cells in monolayer culture. We also quantified the levels of phytoestrogens in extracts of some common foods, herbs, and spices and in human saliva following consumption of a high phytoestrogen food source (soy milk) to compare phytoestrogen abundance and bioavailability relative to the reported xenoestrogen burden in humans. Results show that natural endogenous estrogens, phytoestrogens, mycoestrogens, and xenoestrogens bind estrogen receptor (ER) in intact cells, but demonstrate marked differences in their ability to induce end products of estrogen action and to regulate cell proliferation. All of the different classes of estrogens stimulated cell proliferation at concentrations that half-saturated ER, but only some classes were able to induce estrogen-regulated end products. Genistein, a common phytoestrogen found in soy foods, differed from the xenoestrogen DDT in its effects on cell proliferation and ability to induce estrogen-regulated end products. Moreover, we found that many of the foods, herbs, and spices commonly consumed by humans contain significant amounts of phytoestrogens, and consumption of soy milk, a phytoestrogen-rich food, markedly increases the levels of phytoestrogens in saliva. In conclusion, our in vitro results predict that a diet high in phytoestrogens would significantly reduce the binding of weak xenoestrogens to ER in target tissues in vivo.
Assuntos
Neoplasias da Mama/etiologia , Congêneres do Estradiol/toxicidade , Estrogênios não Esteroides/toxicidade , Estrogênios/toxicidade , Isoflavonas , Neoplasias da Mama/metabolismo , Neoplasias da Mama/patologia , Divisão Celular/efeitos dos fármacos , DDT/metabolismo , DDT/toxicidade , Dieta , Saúde Ambiental , Poluentes Ambientais/metabolismo , Poluentes Ambientais/toxicidade , Congêneres do Estradiol/metabolismo , Estrogênios/metabolismo , Estrogênios não Esteroides/metabolismo , Estrogênios não Esteroides/farmacologia , Feminino , Análise de Alimentos , Humanos , Neoplasias Hormônio-Dependentes/etiologia , Neoplasias Hormônio-Dependentes/metabolismo , Neoplasias Hormônio-Dependentes/patologia , Fitoestrógenos , Preparações de Plantas , Receptores de Estrogênio/efeitos dos fármacos , Receptores de Estrogênio/metabolismo , Saliva/metabolismo , Células Tumorais CultivadasRESUMO
PURPOSE: The aim of study was to determine the rates of dental caries and assess the restorative needs of children under three years of age attending an urban university clinic from 1993-1997. METHODS: In this retrospective study, data were abstracted from patient records and included demographic information, caries experience, and restorative needs. RESULTS: Gender distribution of the sample included 55% males and 45% females. The study population was predominantly African-American (51%) and Hispanic (34%), with a mean age of 20 months. A majority of the population had dental benefits through Medicaid (92%). Nearly one-third of the study population and as many as 56% of the children between 24 and 36 months had dental caries. Among those off the bottle (50%), children with severe dental caries had been weaned off the bottle at a significantly older age compared to those without any caries (16.9 vs. 10 months, P = 0.000). CONCLUSIONS: This study provides further validity to the early oral health exam and early dental treatment, not only for preventive measures but also for restorative needs. The relatively high prevalence of early childhood caries could have been prevented by appropriate primary preventive strategies.
Assuntos
Cárie Dentária/epidemiologia , Distribuição por Idade , Análise de Variância , Pré-Escolar , Índice CPO , Clínicas Odontológicas , Feminino , Hospitais Universitários , Humanos , Lactente , Masculino , Estudos Retrospectivos , Inquéritos e Questionários , Texas/epidemiologia , População Urbana/estatística & dados numéricosRESUMO
In this study we report on the content and bioactivity of plant (phyto) estrogens and progestins in various foods, herbs, and spices, before and after human consumption. Over 150 herbs traditionally used by herbalists for treating a variety of health problems were extracted and tested for their relative capacity to compete with estradiol and progesterone binding to intracellular receptors for progesterone (PR) and estradiol (ER) in intact human breast cancer cells. The six highest ER-binding herbs that are commonly consumed were soy, licorice, red clover, thyme, tumeric, hops, and verbena. The six highest PR-binding herbs and spices commonly consumed were oregano, verbena, tumeric, thyme, red clover and damiana. Some of the herbs and spices found to contain high phytoestrogens and phytoprogestins were further tested for bioactivity based on their ability to regulate cell growth rate in ER (+) and ER (-) breast cancer cell lines and to induce or inhibit the synthesis of alkaline phosphatase, an end product of progesterone action, in PR (+) cells. In general, we found that ER-binding herbal extracts were agonists, much like estradiol, whereas PR-binding extracts, were neutral or antagonists. The bioavailability of phytoestrogens and phytoprogestins in vivo were studied by quantitating the ER-binding and PR-binding capacity of saliva following consumption of soy milk, exogenous progesterone, medroxyprogesterone acetate, or wild mexican yam products containing diosgenin. Soy milk caused a dramatic increase in saliva ER-binding components without a concomitant rise in estradiol. Consumption of PR-binding herbs increased the progestin activity of saliva, but there were marked differences in bioactivity. In summary, we have demonstrated that many of the commonly consumed foods, herbs, and spices contain phytoestrogens and phytoprogestins that act as agonists and antagonists in vivo.