Objectives: The effects of estrogens on immune system formation and function are well documented. Diethylstilbestrol (DES), a synthetic estrogen, has been linked to neoplasia and immune cell dysfunction in humans and animals exposed in-utero. In-vitro effects of DES exposure of murine embryonic stem (ES) cells on the early embryonic immune system development and the expression of cellular surface markers associated with common hemangioblastic and hematopoietic precursors of the endothelial, lymphoid & myeloid lineages were investigated. Hypothesis: Early ES cell expression of CD45 a marker common to lymphoid lineage hematopoietic stem cells and differentiation of lymphoid lineage precursors are affected by in-vitro exposure to DES. Methods: Murine ES cells were cultured using a variety of techniques: an OP9 co-culture system, and formation of embryoid bodies (EBs) in a liquid medium and hanging drop system. The OP9 co-culture system did not appear to give rise to well differentiated lymphoid lineage cells during 12 days of differentiation. The hanging drop EB culture system, previously shown to promote differentiation of endothelial and lymphoid precursor cells, was chosen for further studies of ES cell differentiation. ES cells were harvested at five time points: undifferentiated (day 0), and differentiated (days 3, 8, 12 and 16). Differentiating ES cells were treated with DES beginning on day 3. The synthetic estrogen, DES, was chosen as a treatment because of its similar potency to 17β estradiol and documented association with neoplasia in women exposed in-utero. Surface marker expression, measured by real-time RT-PCR amplification, was recorded using fluorogenic TaqMan(R) probes designed specifically for the surface proteins of interest: oct4, c-Kit, Flk1, ERα, ERβ, CD45, Flt1, & VE-cadherin. Analysis & Results: Changes in surface marker gene expression between day 0 and day 16 of differentiation were analyzed using the RT-PCR threshold counts (CT) and the comparative threshhold cycle method. The expression of each target mRNA was normalized internally to a housekeeping gene (18s rRNA) and calculated relative to day 0. ANOVA (Type 3 fixed-effects analysis, SAS) was performed using the unexponentiated ΔΔCT values. The effects of DES, time, and the interaction between DES and time were evaluated for days 8, 12 and 16. Additionally, the effects of DES on the expression of each marker were evaluated for day 16. Expression of estrogen receptor receptor α & β (ERα & β) in the EBs was established, and did not appear to be affected at any time by treatment with DES. ERα was expressed in significant levels on day 16, while ERβ was expressed in low levels throughout the period of differentiation. The expression of the cell surface marker, c-Kit was significantly (P<0.0001) altered by the presence of DES between the three time points sampled. The expression of the VEGF receptor, Flt1, and the adhesion molecule, VE-cadherin, markers of endothelial cells, were also significantly (P<0.026) altered by treatment with DES on day 16 of differentiation. Treatment with DES appeared to have no effect on the expression of CD45, a marker common to lymphoid precursor cells. Conclusions: These results indicate the presence of estrogen receptors in differentiating ES cells as early as day three in-vitro (ERβ) until day 16 (ERα). DES alters expression of common hemangioblastic and hematopoietic precursor, as well as endothelial lineage markers, but has no effect on expression of the marker of lymphoid lineage development before day 16. These effects coincided with the expression of ERα. The enduring effects of DES exposure in-utero may not be manifest in this ES model, or may occur at later stages of differentiation or in selected subpopulations of CD45+ cells. / Master of Science

No

Call number: LD2668 .T4 1961 C44

No description available.

Le testicule des mammifères possède deux fonctions majeures : la production des spermatozoïdes et la synthèse des androgènes. Le maintien et la régulation de cette fonction sont sous le contrôle des facteurs endocrines et paracrines, mais sont aussi liés à l’homéostasie des lipides, notamment le cholestérol. Les récepteurs nucléaires des oxystérols (LXRs) sont des facteurs de transcription appartenant à la superfamille des récepteurs nucléaires. Les LXRs sont exprimés dans le tractus génital mâle et les testicules et leurs ligands y sont présents à des concentrations physiologiquement actives. Dans ces organes, ces récepteurs régulent l’homéostasie du cholestérol, un précurseur indispensable pour la synthèse des stéroïdes testiculaires. Ils contrôlent aussi les différentes étapes de la stéroïdogenèse en régulant les enzymes de la stéroïdogenèse. Enfin, leur rôle dans la balance prolifération/apoptose des cellules germinales est éminent. On assiste depuis les dernières décennies à une augmentation des anomalies de la différenciation de l’appareil génital mâle (hypospadias, cryptorchidisme) et du cancer du testicule, ainsi qu’à une diminution quantitative et qualitative de la production de spermatozoïdes. Il a été proposé que ces anomalies aient pour origine une perturbation du développement du testicule pendant la vie foetale. Des arguments écologiques, expérimentaux et cliniques laissent supposer que ces troubles résultent, au moins en partie, de l’augmentation du nombre et de la concentration des perturbateurs endocriniens dans l’environnement et dans la nourriture. Ainsi, les xénoestrogènes comme le diéthylstilbestrol (DES), agissent sur les récepteurs des oestrogènes en provoquant des effets néfastes sur la fonction de reproduction masculine. Le but de ce travail a été d’évaluer l’effet postnatal du DES sur la fonction de reproduction chez la souris mâle. Pour pouvoir comprendre l’intervention des LXRs, nous avons choisi d’étudier cet effet chez les souris KO pour les deux isoformes de ces récepteurs nucléaires (lxrαβ-/-). Ce modèle doit nous permettre d’identifier si les effets délétères du DES sur le testicule passent par lxrαβ et d’identifier plus précisément les mécanismes mis en jeu. Nous avons pu montrer que le DES provoque la perturbation de la stéroïdogenèse en diminuant les transcrits de la plupart des gènes stéroïdogéniques (StAR, Cyp11A1, Cyp17a1). Les analyses histologiques montrent que le DES altère la balance prolifération/apoptose quel que soit le génotype, indiquant la perturbation des spermatogonies pré- et post-méiotiques. Nous avons pu montrer également que l’effet du DES sur le phénotype lxrαβ-/- est plus accentué, suggérant un effet protecteur des LXRs in vivo contre l’effet délétère du diéthylstilbestrol. / The mammalian testis has two major functions, sperm production, and synthesis of androgens. The maintenance and regulation of those two functions are under the control of endocrine and paracrine factors, but are also related to lipid homeostasis, including cholesterol. The nuclear oxysterol receptors (LXRs) are transcription factors belonging to the superfamily of nuclear receptors. The LXRs are expressed in the male genital tract and testis, and their ligands are active at physiological concentrations. In these organs, these receptors regulate cholesterol homeostasis, a precursor essential for the synthesis of testicular steroids. They also control the different steps of steroidogenesis by regulating the enzymes of steroidogenesis. In the end, their role in the balance proliferation / apoptosis of germ cells is prominent. In recent decades, there has been an increase in abnormal differentiation of the male genital tract (hypospadias, cryptorchidism) and testicular cancer, as well as a decrease in quantity and quality of sperm production. It was proposed that these abnormalities originate from a disturbance of testicular development during fetal life. Environmental, experimental and clinical arguments suggest that these disorders result, at least in part, to the increased number and concentration of endocrine disruptors in the environment and in food. Thus, xenoestrogens such as diethylstilbestrol (DES) act on the estrogen receptors, causing adverse effects on male reproductive function. The aim of this study was to assess the effect of DES on postnatal reproductive function in male mice. To understand the involvement of nuclear oxysterol receptors, we chose to study this effect in LXRαβ-null mice (lxrαβ-/-). This model should allow us to determine whether the deleterious effects of DES on testis go through lxrαβ and to identify more precisely the mechanisms involved. We have shown that DES causes disruption of steroidogenesis by decreasing transcripts of most steroidogenic genes (StAR, CYP11A1 and Cyp17a1). The histological analysis showed that DES alters the proliferation / apoptosis ratio whatever the genotype, indicating the disruption of pre-and post-meiotic spermatogonia. We have also shown that the effect of DES on the phenotype lxrαβ-/- is more pronounced, suggesting a protective effect of LXRs in vivo against the deleterious effect of diethylstilbestrol.

Dynamic isomerization of diethylstilbestrol (DES) makes it difficult to ascertain the active estrogen between its E and Z isomers. An indirect approach has been used in this project to identify the active estrogen. Methoxylated E- and Z-DES (13 and 14) and 9,10-diethylphenanthrene-3,6-diol (15), a closed ring analog of Z-DES, were synthesized and tested for their estrogenicity. The estrogenicity of 13 is higher than that of 14 and 15, which indicates that E-DES is more estrogenic than Z-DES. Dimethylstilbestrol (16), another analog of DES, was also synthesized and tested. Its estrogenicity is lower than that of DES. Non-estrogenic analogs of bisphenol-A were designed based on the observation that (15) is far less estrogenic than DES. Closed ring analogs of bisphenol-A, 3,6-dihydroxy-9,9-dimethylfluorene (34), 2,6-dihydroxy-9,9-dimethylfluorene (35), and 2,7-dhydroxy-9,9-dimethylfluorene (36) were synthesized and they were found to have little or no estrogenicity. An open ring analog of bisphenol-A, 2-(3-hydroxyphenyl)-2-(4-hydroxyphenyl)propane (33) was also synthesized and its estrogenicity is much lower than that of bisphenol-A. Polycarbonate of 36 was also synthesized and its glass transition temperature was measured using differential scanning calorimetry (DSC). Glass transition temperature of polycarbonate of 36 was found to be 199.92 oC, which is about 50o higher than that of bisphenol-A polycarbonate (150 oC). This indicates that polycarbonate of 36 forms a harder plastic than bisphenol-A polycarbonate. Compounds 2,8-dihydroxy-5,5-dioxo-dibenzothiophene (69) and 2,8-dihydroxydibenzothiophene (70) were also synthesized and were tested as non-estrogenic alternatives for bisphenol-S and bisphenol sulfide, respectively. Compound 69 and 70 were found to be less estrogenic than bisphenol-S and bisphenol sulfide respectively agreeing with our hypothesis. Iodane/quaternary ammonium halide in nitromethane was utilized to explore aromatic bromination, N-nitrosation-dealkylation, and benzoate ester formation from benzylamines. Koser's reagent was found to be a suitable iodane for aromatic bromination reaction, whereas for N-nitrosation-dealkylation, IBX gave the best yields. Further, for N-nitrosation-dealkylation reaction, the halides of quaternary ammonium salts play a crucial role. The effectiveness of halides follows F- > Cl- > Br- ~ I-. The lack of N-nitrosation-dealkylation and ester formation in the absence of nitromethane indicates that nitromethane is playing an essential role as well. Yields of benzoate ester from benzyl amines were low (~22%). Optimization experiments will be performed in the future. Plausible reaction mechanisms for these reactions were proposed. Aromatic bromination was thought to be induced either by iodane/halide adduct or by BrOH that was formed from iodane/halide adduct. Ester formation and N-nitrosation-dealkylation were believed to be induced either by alkyl nitrite or by nitrous acid, generated from the reaction of iodane/halide adduct with nitromethane.

Yes / The spermatogonial stem cells (SSCs) are the only germline stem cells in adults that are responsible for the transmission of genetic information from mammals to the next generation. SSCs play a very important role in the maintenance of progression of spermatogenesis and help provide an understanding of the reproductive biology of future gametes and a strategy for diagnosis and treatment of infertility and male reproductive toxicity. Androgens/oestrogens are very important for the suitable maintenance of male germ cells. There is also evidence confirming the damaging effects of oestrogen-like compounds on male reproductive health. We investigated the effects in vitro, of diethylstilbestrol (DES) on mouse spermatogonial stem cells separated using Staput unit-gravity velocity sedimentation, evaluating any DNA damage using the Comet assay and apoptotic cells in the TUNEL assay. Immunocytochemistry assays showed that the purity of isolated mouse spermatogonial cells was 90%, and the viability of these isolated cells was over 96%. Intracellular superoxide anion production (O2−) in SSCs was detected using p-Nitro Blue Tetrazolium (NBT) assay. The viability of cells after DES treatment was examined in the CCK8 (cell counting kit-8) cytotoxicity assay. The results showed that DES-induced DNA damage causes an increase in intracellular superoxide anions which are reduced by the flavonoid, quercetin. Investigating the molecular mechanisms and biology of SSCs provides a better understanding of spermatogonial stem cell regulation in the testis.

The antineoplastic drug doxorubicin is widely used in the treatment of various types of cancers including breast, colon and lung cancer. However, doxorubicin has adverse effects on the heart and prolonged doxorubicin administration results in cardiomyopathy and congestive heart failure. In the present study we have established that treatment of rat cardiac myoblasts (H9c2 cells) for 24 hours with doxorubicin resulted in concentration and time dependent cell death as determined by proliferation assay. Almost 50-55% cell death was attained at 24 hours treatment of H9c2 cells with 5 μM doxorubicin. We have selected about 50% cell injury as an optimum doxorubicin-induced cell injury because once this threshold is reached, cells became irreversibly injured and are unable to respond to protective treatment. We have observed that another potent antineoplastic drug, cyclophosphamide, had no cardiotoxic effects even with exposure at 35 μM concentrations for a treatment time of up to 72 hours. Pretreatment of H9c2 cells for 24 hours with 100 nM 17β-estradiol protects about 30% cell death against subsequent treatment for 24 hours with 5 μM doxorubicin. Interestingly 500 nM quecertin and 20 μM resveratrol pretreatment provide about 30% and 40% protection, respectively, to the H9c2 cells against subsequent doxorubicin treatment. However, diethylstilbestrol (DES), bisphenol A, and estrone exhibit no protective effects. It is concluded that 17β-estradiol, resveratrol and quercetin considerably protect H9c2 cells against doxorubicin-induced cell death.

Reports of endocrine disrupting potential of common environmental chemicals and the effects on reproductive health are well documented in literature. It has been suggested that deteriorating male reproductive health could be due to in utero exposures to these chemicals. The effects mediated through endocrine disrupting chemicals (EDCs) are on the fetus and may therefore be trans-generational. Ultimately, these chemicals land up in aquatic systems and affect wildlife and humans. Humans are exposed to these chemicals through multiple routes including atmosphere, water, occupational, domestic and food consumption. South Africa (SA) is an important livestock producer with about 13.8 million cattle within the feedlot industry contributing up to 80% of the total beef production. Veterinary growth stimulants (VGS) are used by beef producers to enhance growth in cattle. In SA, the following five VGS have been approved for use in beef products under the Register Act 36 of 1947, estradiol, progesterone and testosterone (natural), α'-zearalanol and trenbolone (synthetic). These VGS and their metabolites are environmentally stable compounds. The excretions from the animals are not treated and land up in the local aquatic systems, indirectly posing a health risk. In SA no research has been done on VGS associated with feedlot activities. The aim of this study was to investigate the effects of a mixture of VGS, as possible EDCs on the reproductive health and thyroid function in male rats in utero, during lactation and life-time exposure. The (anti)estrogenic and (anti)androgenic activity in water from specific feedlots was determined by using a battery of screening bio-assays. Water samples were collected over a period of a year and assessed for EDC activity in the recombinant yeast screen (YES), the T47D-KBluc (estrogenic) and the MDA-Kb2 (androgenic) bioassays. The OECD (Organization for Economic Co-operation and Development) 415 protocol, (1983) for a one-generation reproduction toxicity study, was modified to accommodate one control and three experimental groups. The experimental groups were orally gavaged with mixtures of: zilpaterol, diethylstilbestrol (DES) and α-zearalanol (Group 2; estogenic); with β'-trenbolone and methyltestosterone (MT) (Group 3; androgenic); a combination of compounds (Group 4; estrogenic and androgenic) and the Control group received cottonseed oil only. The bio-assay results indicated that water samples analysed from selected feedlots contained compounds with estrogenic activity. The shorter anogenital distance (AGD) (Group 3), decreased seminal vesicle mass (Group 4), decreased prostate mass (Group 4), increased lumen diameter (Group 3 and 4), lowered sperm concentration (Group 3), and increased T4 (Group 2 and 3) differed significantly from the control. The body weight of the males in Group 2 in the F2 generation was significantly lower than the control. The F2 females in Group 2, 3 and 4 were also significantly lower than the control. The reduced AGD, decreased seminal vesicle and increased T4 (thyroxine) might be the result of an estrogenic effect. The reduced sperm concentration might be the result of in utero and lactation exposure to these VGS. The bio-assays confirmed estrogenic activity in the feedlot water sources. The reproductive toxicology study findings confirm the hypothesis that VGS can act as EDCs and could therefore be responsible for negative reproductive effects and thyroid function. More research is needed to investigate the effects of VGS mixtures at different concentrations on male reproductive health, thyroid function and their offspring. AFRIKAANS : Goed gedokumenteerde literatuur dui aan dat chemikalieë wat algemeen in die omgewing gevind word, die potensiaal het om die manlike voortplantingstelsel aan te tas. Dit word gespekuleer dat in utero blootstelling verantwoordelik kan wees vir hierdie agteruitgang. Die fetus en daarop- volgende geslagte se gesondheid kan ook beÏnvloed word deur chemikalieë. Hierdie chemikalieë het die potensiaal om die watersisteme te bereik en gevolglik dier en menslike gesondheid te beÏnvloed. Blootstelling kan plaasvind deur verskeie roetes wat die atmosfeer, water, werksomstandighede, huishoudelike produkte en gekontamineerde voedsel insluit. Suid-Afrika (SA) is 'n belangrike produsent van vleisprodukte met omtrent 13.8 miljoen beeste wat bydra tot 80% van die vleisproduksie. Veterinêre-groei-stimulante (VGS) word gebruik om die vleisproduksie te verbeter. Vyf groei stimulante naamlik estradiol, progesteroon, testosteroon (natuurlike), α-zearalanol en trenboloon (sinteties) is goedgekeur onder die Wet 36 van 1947, vir groei produksie van beeste. Hierdie VGS en hul metaboliete is stabiel in die natuur. Die fekale en urinere uitskeidingsprodukte van die diere word nie behandel nie en eindig op in ons waterstelsels. Geen navorsing is nog in SA gedoen om die potensiële bydraes wat voerkrale tot die besoedeling van water lewer, te bestudeer nie. Die doel van die studie was om die gesamentlike effekte van mengsels VGS as moontlike endokrien-ontwrigtende chemicalieë (EOC) op die manlike voortplantingstelsel en tiroïdhormone van mannetjiesrotte na in utero-, gedurende laktasie- en na 'n leeftyd-blootstelling te bepaal. Die (anti)estrogeniese en (anti)androgeniese aktiwiteit in water vanaf spesifieke voerkrale is met behulp van 'n reeks biologiese seltoetse bepaal. Watermonsters is geanaliseer met die gisseltoets (YES)(estrogenies), die T47D-KBluc (estrogenies) en die MDA-Kb2 (androgenies). Die OECD 415 protokol (1983) vir een generasie reproduktiewe toksologie toets was aangepas om een kontrole en drie eksperimentele groepe te huisves. Die eksperimentele groepe rotte is oraal gedoseer met 'n mengsel van zilpaterol, dietielstilbestrol (DES) en α-zearalanol (Groep 2); β-trenboloon en metieltestosteroon (Groep 3); 'n kombinasie van al bogenoemde (Groep 4); en 'n kontrole groep wat katoensaad olie VGS ontvang het nie. Estrogeniese aktiwiteit en sitotoksisiteit was teenwoordig in die water vanaf die voerkrale. Die verkorte anogenitale afstand (AGD) (Groep 3), kleiner seminale vesikel (SV) massa (Groep 4), kleiner prostaat massa (Groep 4), groter lumen deursneë (Groep 3 en 4), laer spermtelling (Groep 3), verhoogde T4 (Groep 2 en 3), het almal statisties-betekenisvol van die kontrole groep verskil. In die F2 generasie het die liggaamsmassas van die mannetjies in Groep 2 en liggaamsmassas van die wyfies in Groepe 2, 3 , 4, almal statisties-betekenisvol laer as die kontrole Groep. Die verkorte AGD, kleiner SV en verhoogde T4 kan moonlik wees as gevolg van 'n estrogeniese effek en die verlaagde sperm konsentrasie weens 'n in utero en laktasie blootstelling. Die biologiese seltoetse het die teenwoordigheid van estrogeniese aktiwiteit in voerkrale se water bevestig. Die gevolge van die blootstelling van EOC mengsels op voortplantings-parameters bevestig die moontlikheid van EOC effek geassosieer met VGS. Verdere navorsing is nodig om die dosisresponsverhoudings van verskillende VGS te ondersoek. Copyright / Dissertation (MSc)--University of Pretoria, 2011. / School of Health Systems and Public Health (SHSPH) / Unrestricted

This paper describes the development of an electrochemical sensor glassy carbon modified with gold nanoparticles and a film of multiâwalled carbon nanotube and cobalt phthalocyanine (CoPc-fMWCNTs/AuNp/GCE) for the determination of diethylstilbestrol hormone (DES) in water samples and meat, using a square wave technique voltammetry. (SWV). The electrolyte used was Britton-Robinson buffer (BR) 0.04 mol L-1 pH 10.0. Initially it was studied the electrode configuration to be used for the development work, after the optimization of solution pH, study scan speed to evaluate the charge transfer kinetics in the redox process of the DES, the optimized parameters for SWV, the analytical curve, and finally, applying the methodology developed. The optimized parameters for SWV were f = 5 sâ1, a = 50 mV and &#916;Es=1 mV. The CoPc-fMWCNTs/AuNp/GCE was ready to be used for the application since all conditions were optimized. Analytical curves were obtained in the concentration ranged from 7.9365 à 10&#8722;7 â 5.6604 à 10&#8722;6 mol Lâ1 (R = 0.9996) and there were obtained limits of detection (LOD) and quantification (LOQ) of 1.9910 x 10â7 mol Lâ1and 6.6367 x 10â7 mol Lâ1, respectively, being comparable to those reported in the literature. The repeatability and reproducibility of the proposed procedure were evaluated. The relative standard deviation (RSD) were 4.33% and 3.49%, respectively, indicating the precision of the assay. The recovery percentage was 98.56% for the water sample and 94.05% for beef sample (RSD of 0.40 and 1.55% respectively). The modified electrode has developed sensitivity, reproducibility and repeatability appropriate and consistent LOD and LOQ values with those reported in the literature. Moreover, the results obtained by the use of CoPc-fMWCNTs/AuNp/GCE proved very efficient as the detection and DES recovery, being thus a promising device in the detection and quantification of DES in water samples and food. / O presente trabalho descreve o desenvolvimento de um sensor eletroquÃmico de carbono vÃtreo modificado com nanopartÃculas de ouro, nanotubos de carbono de paredes mÃltiplas funcionalizados e ftalocianina de cobalto (CV/NpAu/NTCPMf-FcCo) para a determinaÃÃo do hormÃnio dietilestilbestrol (DES) em amostras de Ãgua e carne, utilizando a tÃcnica de voltametria de onda quadrada (VOQ). O eletrÃlito empregado foi tampÃo BrittonâRobinson (BR) 0,04 mol Lâ1 pH 10,0. Inicialmente estudou-se a configuraÃÃo do eletrodo a ser utilizado para o desenvolvimento do trabalho, depois a otimizaÃÃo do pH do meio, estudo da velocidade de varredura para avaliar a cinÃtica de transferÃncia de carga no processo redox do DES, otimizaÃÃo dos parÃmetros da VOQ, construÃÃo da curva analÃtica e por fim, a aplicaÃÃo da metodologia desenvolvida. Os parÃmetros otimizados para a VOQ foram: f = 5 sâ1, a = 50 mV e &#916;Es = 1 mV. De posse de todas as condiÃÃes otimizadas para aplicaÃÃo do CV/NpAu/NTCPMf-FcCo, curvas analÃticas foram obtidas no intervalo de concentraÃÃo de 7,9365 à 10&#8722;7 â 5,6604 à 10&#8722;6 mol Lâ1 (R = 0,9996) e os limites de detecÃÃo (LD) e de quantificaÃÃo (LQ) calculados foram 1,9910 x 10â7 mol Lâ1 e 6,6367 x 10â7 mol Lâ1, respectivamente, sendo comparÃveis aos citados na literatura. A repetibilidade e a reprodutibilidade do procedimento proposto foram avaliadas. Os valores de desvio padrÃo relativo (DPR) obtidos foram 4,33% e 3,49%, respectivamente, evidenciando a precisÃo da metodologia. O percentual de recuperaÃÃo foi de 98,56% para amostra de Ãgua e 94,05% para amostra de carne bovina (DPR de 0,40 e 1,55% respectivamente). O eletrodo modificado desenvolvido apresentou sensibilidade, reprodutibilidade e repetibilidade adequados, bem como valores de LD e LQ concordantes com os relatados na literatura. Os resultados obtidos pelo emprego do CV/NpAu/NTCPMf-FcCo se mostraram muito eficientes quanto à detecÃÃo e recuperaÃÃo de DES, mostrando-se, desse modo, um dispositivo promissor na detecÃÃo e na quantificaÃÃo de DES em amostras de Ãgua e alimentos.