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2.
Cancer Lett ; 204(1): 15-21, 2004 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-14744530

RESUMEN

Disinfection of drinking water has been one of the greatest public health successes. Numerous halogenated disinfection by-products (DBPs) occur and chronic ingestion has been associated with an increased risk for colorectal cancer in human populations. Because the intestinal microbiota can bioactivate xenobiotics, studies have been performed to examine the effects of individual DBPs on intestinal microbial metabolism. No studies have been conducted on a defined mixture of DBPs to determine if there is an enhancement of response to a mixture. Ten-week-old male Long-Evans rats were treated in their drinking water for 17 weeks with 0.4 g/l potassium bromate, 1.8 g/l chloroform, 0.7 g/l bromodichloromethane (BDCM), 0.07 g/l 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX), or a mixture of the four chemicals or distilled water. Cecal nitroreductase (NR), azoreductase (AR), dechlorinase (DC), beta-glucuronidase (GLR), beta-galactosidase (GAL), and beta-glucosidase (GLU) were assayed. No change in GLU or GLR activity was detected after treatment. BDCM treatment reduced DC and GAL activities and elevated NR and AR activity. GAL, AR, and NR activities were significantly different after treatment with bromate, chloroform, BDCM, and MX, but not the mixture. DC activity after chloroform-, MX-, or BDCM-treatment was significantly below control levels. The present study shows that changes in intestinal microbial metabolism do occur after treatment with individual and a mixture of DBPs but the changes were not additive in the mixture group.


Asunto(s)
Bacterias/efectos de los fármacos , Bacterias/metabolismo , Ciego/microbiología , Mutágenos/toxicidad , Contaminantes Químicos del Agua/toxicidad , Animales , Peso Corporal/efectos de los fármacos , Bromatos/toxicidad , Cloroformo/toxicidad , Combinación de Medicamentos , Furanos/toxicidad , Glucuronidasa/metabolismo , Heterocigoto , Masculino , NADH NADPH Oxidorreductasas/metabolismo , Nitrorreductasas/metabolismo , Ratas , Ratas Long-Evans , Proteínas Represoras/genética , Proteínas Represoras/fisiología , Trihalometanos/toxicidad , Proteína 2 del Complejo de la Esclerosis Tuberosa , Proteínas Supresoras de Tumor , beta-Galactosidasa/metabolismo , beta-Glucosidasa/metabolismo
3.
Toxicol Sci ; 60(2): 232-41, 2001 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-11248134

RESUMEN

Haloacetic acids are by-products of drinking water disinfection. Several compounds in this class are genotoxic and have been identified as rodent hepatocarcinogens. Enzymes produced by the normal intestinal bacteria can transform some promutagens and procarcinogens to their biologically active forms. The present study was designed to investigate the influence of the cecal microbiota on the mutagenicity of haloacetic acids, and to look at changes in the microbiota populations and enzyme activities associated with exposure to haloacetic acids. PYG medium containing 1 mg/ml of monochloroacetic (MCA), monobromoacetic (MBA), dichloroacetic (DCA), dibromoacetic (DBA), trichloroacetic (TCA), tribromoacetic (TBA), or bromochloroacetic (BCA) acid was inoculated with rat cecal homogenate and incubated anaerobically at 37 degrees C. Growth curves were performed with enumeration of the microflora populations on selective media. Mutagenicity in a Salmonella microsuspension bioassay was determined after incubation for various lengths of time, with or without the cecal microbiota. At 15 h of incubation, enzyme assays determined the activities for beta-glucuronidase, beta-galactosidase, beta-glucosidase, azoreductase, nitroreductase, dechlorinase, and dehydrochlorinase. The haloacetic acids, with the exception of BCA, were toxic to the cecal microbiota, and especially to the enterococci. DBA, TBA, and BCA were mutagenic in the microsuspension assay, but the presence of the intestinal flora did not significantly alter the mutagenicity. BCA increased the activities of several enzymes, and therefore has the potential to affect the biotransformation of co-exposed compounds.


Asunto(s)
Acetatos , Bacteroides/efectos de los fármacos , Ciego/microbiología , Acetatos/metabolismo , Acetatos/toxicidad , Animales , Bacteroides/enzimología , Bacteroides/crecimiento & desarrollo , ADN Bacteriano/efectos de los fármacos , Desinfección , Técnicas In Vitro , Masculino , Microsomas Hepáticos/efectos de los fármacos , Microsomas Hepáticos/metabolismo , Pruebas de Mutagenicidad , Mutágenos/metabolismo , Mutágenos/toxicidad , Ratas , Salmonella typhimurium/efectos de los fármacos , Salmonella typhimurium/genética , Contaminantes Químicos del Agua/metabolismo , Contaminantes Químicos del Agua/toxicidad
4.
J Sch Health ; 65(10): 411-5, 1995 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-8789705

RESUMEN

This evaluation addressed long-term implementation of the Teenage Health Teaching Modules (THTM) by trained teachers in Indiana. Structured random sample telephone interviews and cross-sectional written surveys determined the extent to which teachers implemented THTM and factors related to its implementation. Although most schools and teachers continued to use THTM, many teachers failed to maintain implementation fidelity. Barriers to THTM implementation included insufficient time for health instruction, reassignment of THTM teachers to other instructional areas, and the need for revised middle school modules. ANOVA and Mann-Whitney U tests revealed more favorable THTM perceptions and implementation practices among teachers without implementation difficulties and among teachers who intended to attend a reconvening workshop. Evaluation of the long-term implementation of THTM revealed the impact of environmental barriers on the use of innovative health education curricula by trained teachers.


Asunto(s)
Curriculum , Difusión de Innovaciones , Educación en Salud/métodos , Servicios de Salud Escolar , Enseñanza/métodos , Adolescente , Análisis de Varianza , Actitud , Estudios Transversales , Femenino , Humanos , Indiana , Capacitación en Servicio , Masculino , Evaluación de Programas y Proyectos de Salud
5.
Br Med J ; 2(6136): 573, 1978 Aug 19.
Artículo en Inglés | MEDLINE | ID: mdl-698596
6.
Ment Health (Lond) ; 25(3): 47, 1966.
Artículo en Inglés | MEDLINE | ID: mdl-28908388
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