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1.
Environ Sci Pollut Res Int ; 23(9): 8518-28, 2016 May.
Article in English | MEDLINE | ID: mdl-26791027

ABSTRACT

Estrogen-like endocrine disrupting compounds (EEDC) such as bisphenol A, nonylphenol, and phthalic acid esters are toxic compounds that may occur in both raw- and drinking water. The aim of this study was to combine chemical- and bioassay to evaluate the risk of EEDCs in the drinking water treatment plants (DWTPs). Fifty-six samples were collected from seven DWTPs located in northern-, central-, and southern Taiwan from 2011 to 2012 and subjected to chemical analyses and two bioassay methods for total estrogenic activity (E-Screen and T47D-KBluc assay). Among of the considered EEDCs, only dibutyl phthalate (DBP) and di (2-ethylhexyl) phthalate (DEHP) were detected in both drinking and raw water samples. DBP levels in drinking water ranged from

Subject(s)
Drinking Water/chemistry , Environmental Exposure/statistics & numerical data , Estrogens/analysis , Wastewater/chemistry , Water Pollutants, Chemical/analysis , Water Purification , Benzhydryl Compounds/analysis , Biological Assay , Dibutyl Phthalate/analysis , Endocrine Disruptors/analysis , Estradiol/analysis , Female , Humans , Male , Phenols/analysis , Phthalic Acids/analysis , Taiwan
2.
Int J Environ Res Public Health ; 11(5): 4886-904, 2014 May 06.
Article in English | MEDLINE | ID: mdl-24806195

ABSTRACT

Our goal was to determine dioxin levels in 800 soil samples collected from Taiwan. An in vitro DR-CALUX® assay was carried out with the help of an automated Soxhlet system and fast cleanup column. The mean dioxin level of 800 soil samples was 36.0 pg-bioanalytical equivalents (BEQs)/g dry weight (d.w.). Soil dioxin-BEQs were higher in northern Taiwan (61.8 pg-BEQ/g d.w.) than in central, southern, and eastern Taiwan (22.2, 24.9, and 7.80 pg-BEQ/g d.w., respectively). Analysis of multiple linear regression models identified four major predictors of dioxin-BEQs including soil sampling location (ß = 0.097, p < 0.001), land use (ß = 0.065, p < 0.001), soil brightness (ß = 0.170, p < 0.001), and soil moisture (ß = 0.051, p = 0.020), with adjusted R2 = 0.947 (p < 0.001) (n = 662). An univariate logistic regression analysis with the cut-off point of 33.4 pg-BEQ/g d.w. showed significant odds ratios (ORs) for soil sampling location (OR = 2.43, p < 0.001), land use (OR = 1.47, p < 0.001), and soil brightness (OR = 2.83, p = 0.009). In conclusion, four variables, including soil sampling location, land use, soil brightness, and soil moisture, may be related to soil-dioxin contamination. Soil samples collected in northern Taiwan, and especially in Bade City, soils near industrial areas, and soils with darker color may contain higher dioxin-BEQ levels.


Subject(s)
Dioxins/analysis , Environmental Monitoring/methods , Environmental Restoration and Remediation , Soil Pollutants/analysis , Soil/chemistry , Biological Assay , Gas Chromatography-Mass Spectrometry , Multivariate Analysis , Taiwan
3.
J Trop Med ; 2012: 969243, 2012.
Article in English | MEDLINE | ID: mdl-21941569

ABSTRACT

Trypanosoma cruzi, the etiologic Chagas' disease agent, induces changes in protein pattern of the human placenta syncytiotrophoblast. The glucose transporter protein-1 (GLUT1) is the primary isoform involved in transplacental glucose transport. We carried out in vitro assays to determine if T. cruzi infection would induce changes in placental GLUT1 protein expression under normal and high concentration of glucose. Using Western blot and immunohistological techniques, GLUT1 expression was determined in normal placental villi cultured under normal or high concentrations of glucose, with or without in vitro T. cruzi infection, for 24 and 48 hours. High glucose media or T. cruzi infection alone reduced GLUT1 expression. A yet more accentuated reduction was observed when infection and high glucose condition took place together. We inform, for the first time, that T. cruzi infection may induce reduction of GLUT1 expression under normal and high glucose concentrations, and this effect is synergic to high glucose concentrations.

4.
Lung Cancer ; 75(3): 285-92, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21920623

ABSTRACT

Women have a higher risk of lung adenocarcinoma than men, suggesting that estrogen pathway may be involved in the pathogenesis of this cancer. This study was designed to determine whether ERα expression, estrogen levels, and endocrine disruptor exposure would influence tumor growth of lung adenocarcinoma cells using a xenograft model in which human lung adenocarcinoma cells with and without transgenic ERα expression were transplanted into female nude mice. Results showed that estrogen promoted tumor growth of ERα(+) lung adenocarcinoma cells but inhibited that of ERα(-) lung adenocarcinoma cells. Endocrine disruptor benzo[a]pyrene stimulated ERα(-) tumor growth dose dependently. Either of ovariectomy and ERα expression abolished the tumor growth-promoting effect of benzo[a]pyrene. The high CYP1B1/CYP1A1 and low COMT/CYP1B1 expression ratios detected in ERα(+) tumors suggested an accumulation of 4-hydroxyestradiol metabolite under high body estrogen, whereas comparable CYP1A1 and CYP1B1 expression plus estrogen-inducible COMT expression might favor the formation of 2-methoxyestradiol in ERα(-) tumors. Inhibition of estrogen on ERα(-) tumor growth might be partly attributable to the anti-proliferative action of 2-methoxyestradiol. Benzo[a]pyrene increased expression of CYP1B1 over CYP1A1 and suppressed estrogen-induced COMT up-regulation in ERα(-) tumor cells, probably switching estrogen metabolism to 4-hydroxyestradiol formation and removing the inhibition of 2-methoxyestradiol on ERα(-) tumors. ERα inhibited AhR from up-regulating CYP1 in response to benzo[a]pyrene exposure, but it increased angiogenic VEGF-A expression with body estrogen levels. Estrogen might increase ERα(+) lung adenocarcinoma growth by up-regulating cancer-related ERα target gene expression.


Subject(s)
Adenocarcinoma/metabolism , Benzo(a)pyrene/toxicity , Estrogen Receptor alpha/metabolism , Estrogens/metabolism , Lung Neoplasms/metabolism , 2-Methoxyestradiol , Adenocarcinoma/chemically induced , Adenocarcinoma/pathology , Adenocarcinoma of Lung , Animals , Aryl Hydrocarbon Hydroxylases/genetics , Cell Line, Tumor , Cytochrome P-450 CYP1A1/genetics , Cytochrome P-450 CYP1B1 , Estradiol/analogs & derivatives , Estradiol/metabolism , Estrogen Receptor alpha/genetics , Estrogens, Catechol , Female , Gene Expression Regulation, Neoplastic , Humans , Lung Neoplasms/chemically induced , Lung Neoplasms/pathology , Mice , Mice, Nude , Ovariectomy , Up-Regulation/drug effects , Xenograft Model Antitumor Assays
5.
J Chem Inf Model ; 51(10): 2538-48, 2011 Oct 24.
Article in English | MEDLINE | ID: mdl-21939286

ABSTRACT

Alkaline phosphatases (APs) catalyze the hydrolysis and transphosphorylation of phosphate monoesters. Quantum mechanical, molecular dynamics, and molecular docking techniques were applied to computationally model the catalytic mechanism of human placental AP (PLAP). Kinetic and thermodynamic evaluations were performed for each reaction step. The functional significances of the more important residues within the active site were analyzed. The role of the metal ion at the metal binding site M3 was also examined. The calculated activation and reaction energy and free energy values obtained suggested the nucleophilic attack of the Ser92 alkoxide on the phosphorus atom of the substrate would be the rate-limiting step of the catalytic hydrolysis of alkyl phosphate monoesters by PLAP. The reactivities of the wild-type M3-Mg enzyme and the M3-Zn protein were compared, and the main difference observed was a change in the coordination number of the M3 metal for the M3-Zn enzyme. This modification in the active site structure lowered the free energy profile for the second chemical step of the catalytic mechanism (hydrolysis of the covalent phosphoserine intermediate). Consequently, a greater stabilization of the phosphoseryl moiety resulted in a small increment in the activation free energy of the phosphoserine hydrolysis reaction. These computational results suggest that the activation of APs by magnesium at the M3 site is caused by the preference of Mg(2+) for octahedral coordination, which structurally stabilizes the active site into a catalytically most active conformation. The present theoretical results are in good agreement with previously reported experimental studies.


Subject(s)
Alkaline Phosphatase/chemistry , Alkaline Phosphatase/metabolism , Biocatalysis , Computer Simulation , Isoenzymes/chemistry , Isoenzymes/metabolism , Catalytic Domain , GPI-Linked Proteins/chemistry , GPI-Linked Proteins/metabolism , Humans , Kinetics , Magnesium/metabolism , Molecular Dynamics Simulation , Quantum Theory , Thermodynamics , Zinc/metabolism
6.
Chemosphere ; 82(7): 947-55, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21075419

ABSTRACT

Phthalate exposure was found to be associated with endocrine disruption, respiratory effects, reproductive and developmental toxicity. The intensive use of plastics may be increasing the exposure to phthalates in Taiwanese population, particularly for young children. We studied phthalate metabolites in pregnant women and their newborns in a prospective cohort from a medical center in Central Taiwan. One hundred maternal urine samples and 30 paired cord blood and milk samples were randomly selected from all of participants (430 pregnant women). Eleven phthalate metabolites (MEHP, 5OH-MEHP, 2cx-MEHP, 5cx-MEPP, 5oxo-MEHP, MiBP, MnBP, MBzP, OH-MiNP, oxo-MiNP, and cx-MiNP) representing the exposure to five commonly used phthalates (DEHP, di-isobutyl phthalate (DiBP), DnBP, BBP, DiNP) were measured in urine of pregnant women, cord serum and breast milk after delivery, and in urine of their children. Exposure was estimated with excretion factors and correlation among metabolites of the same parent compound. Thirty and 59 urinary samples from 2 and 5 years-old children were randomly selected from 185 children successfully followed. Total urinary phthalate metabolite concentration (geometric mean, µg L⁻¹) was found to be higher in 2-years-olds (398.6) and 5-years-olds (333.7) than pregnant women (205.2). Metabolites in urine are mainly from DEHP. The proportion of DiNP metabolites was higher in children urine (4.39 and 8.31%, ages 2 and 5) than in adults (0.83%) (p<0.01). Compared to urinary levels, phthalate metabolite levels are low in cord blood (37.45) and milk (14.90). DEHP metabolite levels in women's urine and their corresponding cord blood are significantly correlated. Compared to other populations in the world, DEHP derived metabolites in maternal urine were higher, while phthalate metabolite levels in milk and cord blood were similar. The level of phthalate metabolites in milk and cord blood were comparable to those found in other populations. Further studies of health effects related to DEHP and DiNP exposure are necessary for the children.


Subject(s)
Environmental Exposure/analysis , Environmental Pollutants/metabolism , Phthalic Acids/metabolism , Adult , Biomarkers/urine , Child , Child, Preschool , Creatinine/metabolism , Environmental Exposure/statistics & numerical data , Environmental Pollutants/blood , Environmental Pollutants/urine , Female , Fetal Blood/metabolism , Humans , Infant, Newborn , Male , Milk, Human/metabolism , Phthalic Acids/blood , Phthalic Acids/urine , Pregnancy , Taiwan , Young Adult
7.
Talanta ; 73(1): 76-80, 2007 Aug 15.
Article in English | MEDLINE | ID: mdl-19071852

ABSTRACT

A sensitive and robust high-performance liquid chromatography-electrospray ionization tandem mass spectrometry method to analyze 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and its five metabolites in one passage was developed and validated. The method achieved excellent reproducibility and accuracy. Linearity was observed for all six compounds (R(2)=0.999) with detection limits (S/N> or =3) ranging from 0.2 to 2.4 pg on column and 0.01-0.12 ng ml(-1) in samples injected. Average intra-day and inter-day variations (% R.S.D.) were 1.2 and 3.5%, respectively. A sample preparation method involving C8 and C18 solid phase extraction provided satisfactory recovery of the analytes in mouse urine. Each NNK metabolite was identified by its chromatographic retention time and specific fragmentation pattern. Since the carcinogenicity of NNK is related to its metabolism, the method described in this report should facilitate toxicological investigations into the carcinogenesis due to NNK exposure in the environment.

8.
Rev Soc Bras Med Trop ; 38 Suppl 2: 87-91, 2005.
Article in Spanish | MEDLINE | ID: mdl-16482823

ABSTRACT

Trypanosoma cruzi induces changes in the protein pattern of human placenta syncytiotrophoblast. Placental alkaline phosphatase (PLAP) is a glycoenzyme anchored to the membrane by a glycosyl-phosphatidylinositol molecule. PLAP activity and its presence was altered by the parasite in cultures of human placental villi and HEp2 cells with T.cruzi. The cells treated before the cultures with agents which affect PILAP or glycosyl-phosphatidylinositol (antibodies, PL-C, genistein, lithium) presented less parasitic invasion than the control ones. It was also observed a modification in the pattern of actine filaments of the host cells infected. We concluded that PLAP would participate in the process of T. cruzi invasion into placental syncitiotrophoblast cells, by a mechanism that involves hydrolysis of the glycosyl-phosphatidylinositol molecules, the activation of tyrosine kinase proteins, the increase of cytosolic calcium and the rearrangement of actine filaments of the host cells.


Subject(s)
Alkaline Phosphatase/metabolism , Chagas Disease/enzymology , Placenta/enzymology , Trypanosoma cruzi/physiology , Alkaline Phosphatase/analysis , Analysis of Variance , Animals , Biomarkers , Cell Culture Techniques , Chagas Disease/immunology , Chagas Disease/parasitology , Chorionic Villi/enzymology , Chorionic Villi/parasitology , Female , Glycosylphosphatidylinositols/metabolism , Humans , Immunohistochemistry , Placenta/parasitology , Pregnancy , Trophoblasts/enzymology , Trophoblasts/parasitology
9.
Nucleic Acids Res ; 32(Database issue): D456-8, 2004 Jan 01.
Article in English | MEDLINE | ID: mdl-14681456

ABSTRACT

The Signal Transduction Classification Database (STCDB) is a database of information relative to the classification of signal transduction. It is based primarily on a proposed classification of signal transduction and it describes each type of characterized signal transduction for which a unique ST number has been provided. This document presents, in its first version, the classification of signal transduction in eukaryotic cells. Approved classifications are available for web browsing at http://www.techfak.uni-bielefeld.de/~ mchen/STCDB.


Subject(s)
Databases, Factual , Signal Transduction/physiology , Animals , Computational Biology , Eukaryotic Cells/metabolism , Information Storage and Retrieval , Internet , Software
10.
Rev. Fac. Cienc. Méd. (Córdoba) ; 55(1/2): 5-8, 1997. tab, graf
Article in English | LILACS | ID: lil-231895

ABSTRACT

The Kinetic properties of plasma placental alkaline phosphatase patients with Chagas' disease were studied. When Cl2 Mg was used as activator the same increase of activity (17-20 per cent) was found in the chagasic and non chagasic groups. The enzyme was not inhibited by F-ion in any of the groups. No significant differences were detected between the two groups (chagasic and non chagasic) when the enzyme was treated with inhibitors such as EDTA and L-phenylamine. However, when the CN- ion was used, the enzyme of the normal pregnant women followed a Michaelian curve, whereas in the chagasic group a sigmoideal plot was observed. Thus, the Hill coefficient was 1.1 for the normal group and over 1.5 for the chagasic.


Subject(s)
Adult , Female , Humans , Pregnancy , Alkaline Phosphatase/blood , Chagas Disease/enzymology , Edetic Acid , Placenta/enzymology , Pregnancy Complications, Parasitic/enzymology , Alkaline Phosphatase/drug effects , Alkaline Phosphatase/metabolism , Chagas Disease/blood , Edetic Acid , Enzyme Inhibitors/pharmacology , Enzyme Reactivators/pharmacology , Pregnancy Complications, Parasitic/blood , Pregnancy Trimester, Third
11.
Rev. Fac. Cienc. Méd. [Córdoba] ; 55(1/2): 5-8, 1997. tab, gra
Article in English | BINACIS | ID: bin-16374

ABSTRACT

The Kinetic properties of plasma placental alkaline phosphatase patients with Chagas disease were studied. When Cl2 Mg was used as activator the same increase of activity (17-20 per cent) was found in the chagasic and non chagasic groups. The enzyme was not inhibited by F-ion in any of the groups. No significant differences were detected between the two groups (chagasic and non chagasic) when the enzyme was treated with inhibitors such as EDTA and L-phenylamine. However, when the CN- ion was used, the enzyme of the normal pregnant women followed a Michaelian curve, whereas in the chagasic group a sigmoideal plot was observed. Thus, the Hill coefficient was 1.1 for the normal group and over 1.5 for the chagasic. (AU)


Subject(s)
Adult , Female , Humans , Pregnancy , Chagas Disease/enzymology , Alkaline Phosphatase/blood , Pregnancy Complications, Parasitic/enzymology , Placenta/enzymology , Edetic Acid , Pregnancy Trimester, Third , Pregnancy Complications, Parasitic/blood , Chagas Disease/blood , Edetic Acid , Enzyme Inhibitors/pharmacology , Enzyme Reactivators/pharmacology , Alkaline Phosphatase/metabolism , Alkaline Phosphatase/drug effects
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