<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0120-548X</journal-id>
<journal-title><![CDATA[Acta Biológica Colombiana]]></journal-title>
<abbrev-journal-title><![CDATA[Acta biol.Colomb.]]></abbrev-journal-title>
<issn>0120-548X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional de Colombia, Facultad de Ciencias, Departamento de Biología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-548X2012000300003</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[BIOMARCADORES DE DAÑO GENÉTICO EN POBLACIONES HUMANAS EXPUESTAS A PLAGUICIDAS]]></article-title>
<article-title xml:lang="en"><![CDATA[Biomarkers of Genetic Damage in Human Populations Exposed to Pesticides]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[AIASSA]]></surname>
<given-names><![CDATA[DELIA]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[MAÑAS]]></surname>
<given-names><![CDATA[FERNANDO]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[BOSCH]]></surname>
<given-names><![CDATA[BEATRIZ]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[GENTILE]]></surname>
<given-names><![CDATA[NATALIA]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[BERNARDI]]></surname>
<given-names><![CDATA[NATALÍ]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[GORLA]]></surname>
<given-names><![CDATA[NORA]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad Nacional de Río Cuarto Facultad de Ciencias Exactas, Físico-Químicas y Naturales ]]></institution>
<addr-line><![CDATA[Río Cuarto ]]></addr-line>
<country>Argentina</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad Nacional de Río Cuarto Facultad de Agronomía y Veterinaria ]]></institution>
<addr-line><![CDATA[Río Cuarto ]]></addr-line>
<country>Argentina</country>
</aff>
<aff id="A03">
<institution><![CDATA[,CONICET  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Argentina</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2012</year>
</pub-date>
<volume>17</volume>
<numero>3</numero>
<fpage>485</fpage>
<lpage>510</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-548X2012000300003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-548X2012000300003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-548X2012000300003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[El efecto de los plaguicidas sobre la salud humana, animal y ambiental es preocupación de la comunidad científica desde hace mucho tiempo. Numerosos estudios reportan que los plaguicidas no son inofensivos y que su uso puede conducir a efectos biológicos dañinos a mediano y a largo plazo, en los grupos humanos y animales expuestos, en el presente o en los descendientes. La importancia en la detección precoz del daño genético radica en que permite tomar las medidas necesarias para disminuir o suprimir la exposición al agente deletéreo cuando aún éste es reversible, y de ese modo prevenir y disminuir el riesgo de desarrollar neoplasias y otras alteraciones patológicas. En este trabajo se revisan los principales conceptos en la temática, la utilidad de los estudios de genotoxicidad y se hace referencia a los trabajos realizados en los últimos veinticinco años sobre monitoreo genético de personas expuestas laboralmente a plaguicidas. Los ensayos de genotoxicidad, que incluyen aberraciones cromosómicas, micronúcleos, intercambio de cromátidas hermanas y cometa, deberían ser considerados como herramientas indispensables en la implementación de una vigilancia médica completa en personas potencialmente expuestas a diversos contaminantes ambientales y en especial aquellas que habitan en el mismo lugar con personas que ya han desarrollado algún tipo de neoplasia en edades tempranas, con el fin de prevenir la ocurrencia de tumores de origen ambiental y especialmente laboral.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[The effect of pesticides on human, animal and environmental health has been cause of concern in the scientific community for a long time. Numerous studies have reported that pesticides are not harmless and that their use can lead to harmful biological effects in the medium and long term, in exposed human and animals, and their offspring. The importance of early detection of genetic damage is that it allows us to take the necessary measures to reduce or eliminate the exposure to the deleterious agent when damage is still reversible, and thus to prevent and to diminish the risk of developing tumors or other alterations. In this paper we reviewed the main concepts in the field, the usefulness of genotoxicity studies and we compiled studies performed during the last twenty years on genetic monitoring of people occupationally exposed to pesticides. We think that genotoxicity tests, including that include chromosomal aberrations, micronucleous, sister chromatid exchanges and comet assays, should be considered as essential tools in the implementation of complete medical supervision for people exposed to potential environmental pollutants, particularly for those living in the same place as others who where others have already developed some type of malignancy. This action is particularly important at early stages to prevent the occurrence of tumors, especially from environmental origins.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[biomonitoreo]]></kwd>
<kwd lng="es"><![CDATA[biomarcadores]]></kwd>
<kwd lng="es"><![CDATA[cáncer]]></kwd>
<kwd lng="es"><![CDATA[plaguicidas]]></kwd>
<kwd lng="es"><![CDATA[salud]]></kwd>
<kwd lng="en"><![CDATA[Biomonitoring]]></kwd>
<kwd lng="en"><![CDATA[cancer biomarkers]]></kwd>
<kwd lng="en"><![CDATA[health]]></kwd>
<kwd lng="en"><![CDATA[pesticides]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="verdana" size="2">      <P align="center" ><font size="4">BIOMARCADORES DE DA&Ntilde;O GEN&Eacute;TICO EN POBLACIONES HUMANAS EXPUESTAS A PLAGUICIDAS</font></p>      <p align="center">Biomarkers of Genetic Damage in Human Populations Exposed to Pesticides</p>      <p>DELIA AIASSA<Sup>1</Sup>, Ph. D.; FERNANDO MA&Ntilde;AS<Sup>2</Sup>, Ph. D.; BEATRIZ BOSCH<Sup>1</Sup>, Lic.; NATALIA GENTILE<Sup>1</Sup>, Lic.; NATAL&Iacute; BERNARDI<Sup>1</Sup>, Prof.; NORA GORLA<Sup>2,3</Sup>, Ph. D.</p>             <p><Sup>1</Sup>GeMA. Facultad de Ciencias Exactas, F&iacute;sico-Qu&iacute;micas y Naturales, Universidad Nacional de R&iacute;o Cuarto. R&iacute;o Cuarto, Argentina.    <br>   <Sup>2</Sup>Facultad de Agronom&iacute;a y Veterinaria, Universidad Nacional de R&iacute;o Cuarto. R&iacute;o Cuarto, Argentina.    <br>     <Sup>3</Sup>CONICET. Argentina.</p>        <p>Correspondencia: Dra. Delia Aiassa. GeMA- Departamento de Ciencias Naturales, Facultad de Ciencias Exactas, F&iacute;sico-Qu&iacute;micas y Naturales, Universidad Nacional de R&iacute;o Cuarto.R&iacute;o Cuarto, Argentina. <a href="mailto:daiassa@exa.unrc.edu.ar">lblanco@neuro.ciren.cu</a></p>      <p>Presentado el 14 de agosto de 2012, aceptado el 16 de septiembre de 2012, correcciones el 16 de octubre de 2012.</p>  <hr size="1">      <p><b>RESUMEN</b></p>     ]]></body>
<body><![CDATA[<p>El efecto de los plaguicidas sobre la salud humana, animal y ambiental es preocupaci&oacute;n de la comunidad cient&iacute;fica desde hace mucho tiempo. Numerosos estudios reportan que los plaguicidas no son inofensivos y que su uso puede conducir a efectos biol&oacute;gicos da&ntilde;inos a mediano y a largo plazo, en los grupos humanos y animales expuestos, en el presente o en los descendientes. La importancia en la detecci&oacute;n precoz del da&ntilde;o gen&eacute;tico radica en que permite tomar las medidas necesarias para disminuir o suprimir la exposici&oacute;n al agente delet&eacute;reo cuando a&uacute;n &eacute;ste es reversible, y de ese modo prevenir y disminuir el riesgo de desarrollar neoplasias y otras alteraciones patol&oacute;gicas. En este trabajo se revisan los principales conceptos en la tem&aacute;tica, la utilidad de los estudios de genotoxicidad y se hace referencia a los trabajos realizados en los &uacute;ltimos veinticinco a&ntilde;os sobre monitoreo gen&eacute;tico de personas expuestas laboralmente a plaguicidas. Los ensayos de genotoxicidad, que incluyen aberraciones cromos&oacute;micas, micron&uacute;cleos, intercambio de crom&aacute;tidas hermanas y cometa, deber&iacute;an ser considerados como herramientas indispensables en la implementaci&oacute;n de una vigilancia m&eacute;dica completa en personas potencialmente expuestas a diversos contaminantes ambientales y en especial aquellas que habitan en el mismo lugar con personas que ya han desarrollado alg&uacute;n tipo de neoplasia en edades tempranas, con el fin de prevenir la ocurrencia de tumores de origen ambiental y especialmente laboral.</p>     <p>Palabras clave: biomonitoreo, biomarcadores, c&aacute;ncer, plaguicidas, salud.</p> <hr size="1">      <p><b>ABSTRACT</b></p>      <p>The effect of pesticides on human, animal and environmental health has been cause of concern in the scientific community for a long time. Numerous studies have reported that pesticides are not harmless and that their use can lead to harmful biological effects in the medium and long term, in exposed human and animals, and their offspring. The importance of early detection of genetic damage is that it allows us to take the necessary measures to reduce or eliminate the exposure to the deleterious agent when damage is still reversible, and thus to prevent and to diminish the risk of developing tumors or other  alterations.</p>     <p>In this paper we reviewed the main concepts in the field, the usefulness of genotoxicity studies and we compiled studies performed during the last twenty years on genetic monitoring of people occupationally exposed to pesticides. We think that genotoxicity tests, including that include chromosomal aberrations, micronucleous, sister chromatid exchanges and comet assays, should be considered as essential tools in the implementation of complete medical supervision for people exposed to potential environmental pollutants, particularly for those living in the same place as others who where others have already developed some type of malignancy. This action is particularly important at early stages to prevent the occurrence of tumors, especially from environmental origins.</p>     <p>Keywords: Biomonitoring, cancer biomarkers, health, pesticides.</p>  <hr size="1">       <p><b>INTRODUCCI&Oacute;N</b></p>      <p>Existen razones sumamente importantes para justificar la preocupaci&oacute;n por la exposici&oacute;n del hombre a los agentes genot&oacute;xicos. El uso del t&eacute;rmino genot&oacute;xico se refiere a aquellos agentes que tienen afinidad para interaccionar con el ADN, produciendo alteraciones estructurales o funcionales tanto en c&eacute;lulas germinales como som&aacute;ticas. El incremento de alteraciones en el material hereditario de las c&eacute;lulas germinales (&oacute;vulos, espermatozoides) y las c&eacute;lulas que las originan, puede provocar un aumento en la ocurrencia de enfermedades gen&eacute;ticas, monog&eacute;nicas, cromos&oacute;micas y multifactoriales, en generaciones futuras. Adem&aacute;s, existe una estrecha relaci&oacute;n entre las alteraciones del ADN de c&eacute;lulas som&aacute;ticas con el c&aacute;ncer y las enfermedades degenerativas cr&oacute;nicas (Stoneham <i>et al.</i>, 2000; Mortelmans <i>et al.</i>, 2004).</p>     <p>En modelos experimentales (roedores) se ha demostrado que aquellos agentes que causan alteraciones en las c&eacute;lulas som&aacute;ticas tambi&eacute;n causan cambios en sus gametos (Venitt y Phillips, 1995; Creus, 2001).</p>      <p>Existen suficientes evidencias experimentales y epidemiol&oacute;gicas que demuestran que el da&ntilde;o gen&eacute;tico produce mutaciones y que el proceso cancer&iacute;geno se inicia y se favorece por la presencia de mutaciones en los oncogenes, en genes supresores de tumores y en los que codifican para los sistemas de reparaci&oacute;n del ADN (Au <i>et al.</i>, 2001; Bonassi y Au, 2002). Los compuestos qu&iacute;micos empleados en la agricultura podr&iacute;an ser los responsables de la elevada incidencia de c&aacute;ncer de labio, est&oacute;mago, cerebro, pr&oacute;stata, tejido conectivo, linf&aacute;tico y hematopoy&eacute;tico en trabajadores agr&iacute;colas (Khuder <i>et al.</i>, 1998; van Maele-Fabry y Willems, 2003; van Maele-Fabry y Willems, 2004; Alavanja <i>et al.</i>, 2005; Boers <i>et al.</i>, 2005). En los pocos estudios reportados de exposici&oacute;n a agroqu&iacute;micos en mujeres, se ha encontrado relaci&oacute;n del c&aacute;ncer de ovario con el herbicida triazina, c&aacute;ncer de mama con insecticidas,  mieloma m&uacute;ltiple  y  linfoma no  Hodgkin  con varios  compuestos qu&iacute;micos (Alavanja <i>et al.</i>, 1999; Alavanja <i>et al.</i>, 2004; Kohen y Nyska 2002).</p>      ]]></body>
<body><![CDATA[<p>Datos experimentales revelan que varios componentes de los agroqu&iacute;micos, especialmente de los plaguicidas, producen genotoxicidad y provocan alteraciones en el material gen&eacute;tico, (Dearfield <i>et al.</i>, 1999; IARC, 2002; Ma&ntilde;as, 2006; Ma&ntilde;as, 2009a; Ma&ntilde;as, 2009b). Se ha demostrado que la concentraci&oacute;n de plaguicidas en el ambiente es mayor en comunidades agr&iacute;colas y cerca de los campos tratados (Whitmore <i>et al.</i>, 1994; Baker <i>et al.</i>, 1996; Woodrow <i>et al.</i>, 1997; Teske <i>et al.</i>, 2002; Weppner <i>et al.</i>, 2006). Tambi&eacute;n las mediciones en polvo en el interior de los hogares demuestran que las concentraciones de residuos de plaguicidas son mayores en las residencias cerca de los cultivos (Simcox <i>et al.</i>, 1995; Lu <i>et al.</i>, 2000; Fenske <i>et al.</i>, 2002; Curwin <i>et al.</i>, 2005; Obendorf <i>et al.</i>, 2006; Ward <i>et al.</i>, 2006).</p>      <p>En relaci&oacute;n a las poblaciones expuestas sin motivo laboral, los ni&ntilde;os constituyen un grupo que tiene caracter&iacute;sticas particulares de exposici&oacute;n y especial vulnerabilidad a los t&oacute;xicos ambientales, y que requieren una estrategia para la evaluaci&oacute;n del riesgo, que considere sus caracter&iacute;sticas particulares. Los pocos estudios que han evaluado la asociaci&oacute;n entre el uso de plaguicidas agr&iacute;colas cerca de las viviendas y la leucemia infantil evidencia una relaci&oacute;n etiol&oacute;gica (Reynolds <i>et al.</i>, 2002; Reynolds <i>et al.</i>, 2005a; Reynolds <i>et al.</i>, 2005b). Rull <i>et al.</i>, 2009, en California, examinaron si la proximidad residencial a las aplicaciones de plaguicidas en zonas agr&iacute;colas est&aacute; asociado con el desarrollo de leucemia linfobl&aacute;stica aguda, el subtipo m&aacute;s com&uacute;n de este c&aacute;ncer infantil. Los resultados de ese trabajo sugieren la identificaci&oacute;n de plaguicidas espec&iacute;ficos que pueden desempe&ntilde;ar un papel en la etiolog&iacute;a de la leucemia infantil.</p>     <p>El aumento en la prevalencia de c&aacute;ncer que se observa en ni&ntilde;os muy peque&ntilde;os hace pensar que la exposici&oacute;n paterna o materna a cancer&iacute;genos podr&iacute;a ser, en estos casos, el factor que desencadena el desarrollo de enfermedad neopl&aacute;sica (Fabia y Thuy, 1974; Holly <i>et al.</i>, 1992; Winn <i>et al.</i>, 1992; Sharpe <i>et al.</i>, 1995).</p>      <p>Por otro lado, estudios toxicol&oacute;gicos en animales proporcionan evidencias de que altas dosis de algunos plaguicidas pueden alterar la funci&oacute;n reproductiva y producir defectos al nacer, pero son pocos los estudios epidemiol&oacute;gicos realizados de exposici&oacute;n a plaguicidas y toxicidad reproductiva en humanos (Calvert <i>et al.</i>, 2007).</p>      <p>Se ha observado que la descendencia de los agricultores tiene un mayor riesgo de anomal&iacute;as cong&eacute;nitas. Mientras que las anomal&iacute;as cong&eacute;nitas en la primera mitad de la d&eacute;cada del 90 representaron alrededor del 20 % de las muertes fetales durante el primer a&ntilde;o de vida en algunos pa&iacute;ses, en otros, el porcentaje fue de casi el 40 % (Regidor <i>et al.</i>, 2004). Por todo lo antes expuesto, los estudios citados indican que los plaguicidas no son inofensivos y que su uso puede conducir a efectos da&ntilde;inos a mediano y a largo plazo, en los grupos humanos y animales expuestos, en el presente o en los descendientes. Las lesiones en el material gen&eacute;tico pueden aumentar el riesgo de padecer c&aacute;ncer, problemas reproductivos o que se desarrollen malformaciones en la descendencia. Por este motivo, es que el uso de biomarcadores es &uacute;til para detectar el da&ntilde;o gen&eacute;tico temprano donde ese nivel de da&ntilde;o es todav&iacute;a reversible (Bonassi y Au, 2002; Ram&iacute;rez y Cuenca, 2002; Castro <i>et al.</i>, 2004; Cuenca y Ram&iacute;rez, 2004).</p>      <p>PREVENIR Y DISMINUIR EL RIESGO DE DESARROLLAR TUMORES Y OTRAS ALTERACIONES </p>      <p>Medir la frecuencia de da&ntilde;o gen&eacute;tico en grupos humanos expuestos a agentes ambientales ha sido, en muchos pa&iacute;ses, una prioridad en estudios de salud p&uacute;blica por d&eacute;cadas, y el aumento del nivel de aberraciones cromos&oacute;micas (AC) es corrientemente interpretado como evidencia de exposici&oacute;n genot&oacute;xica y efecto biol&oacute;gico temprano sobre el ADN. Dentro de los factores capaces de influir en la integridad del material gen&eacute;tico se pueden mencionar el estilo de vida, exposici&oacute;n a rayos UV (debido al progresivo debilitamiento de la capa de ozono), los tratamientos m&eacute;dicos, algunos polimorfismos gen&eacute;ticos individuales, entre otros. Es importante, por todo ello, determinar qu&eacute; se conoce como un nivel "aceptable" de da&ntilde;o gen&eacute;tico en una poblaci&oacute;n concreta, realizar ensayos de genotoxicidad de manera rutinaria y estudiar aquellos individuos que, por su ocupaci&oacute;n laboral o estilo de vida, se encuentran m&aacute;s expuestos o con mayor riesgo de sufrir alteraciones capaces de modificar su estabilidad gen&eacute;tica (Fenech <i>et al.</i>, 1993).</p>     <p>Los estudios que pueden realizarse a partir de sangre de personas expuestas a genot&oacute;xicos y que permiten detectar efectos tempranos pueden agruparse en estudios citogen&eacute;ticos, moleculares y bioqu&iacute;micos. Los estudios citogen&eacute;ticos son 1) el ensayo de aberraciones cromos&oacute;micas (AC), 2) el ensayo de micron&uacute;cleos (MN), que tambi&eacute;n puede realizarse en c&eacute;lulas epiteliales obtenidas de las mucosas y 3) el ensayo de intercambio de crom&aacute;tidas hermanas (ICH).</p>     <p>El ensayo de aberraciones cromos&oacute;micas permite detectar alteraciones num&eacute;ricas (efecto aneug&eacute;nico) o estructurales (efecto clastog&eacute;nico) a nivel de los cromosomas. La importancia de este ensayo radica en que existen evidencias experimentales y epidemiol&oacute;gicas de que las aberraciones estructurales est&aacute;n involucradas en el proceso de carcinog&eacute;nesis y por lo tanto un incremento en el n&uacute;mero de aberraciones cromos&oacute;micas est&aacute; asociado con un aumento de riesgo de padecer c&aacute;ncer en el futuro (Hagmar <i>et al.</i>, 1994; Hagmar <i>et al.</i>, 1998; Bonassi <i>et al.</i>, 1995; Mitelman <i>et al.</i>, 1997; Albertini <i>et al.</i>, 2000).</p>     <p>El ensayo de micron&uacute;cleos detecta rupturas a nivel de los cromosomas y alteraciones a nivel del aparato mit&oacute;tico, por lo que permite tambi&eacute;n identificar compuestos con efectos aneug&eacute;nicos y clastog&eacute;nicos. Su ventaja radica en que el an&aacute;lisis es m&aacute;s sencillo y debido a que se analizan al menos mil c&eacute;lulas, es m&aacute;s robusto desde el punto de vista estad&iacute;stico.</p>     ]]></body>
<body><![CDATA[<p>Los resultados de un an&aacute;lisis prospectivo de una base de datos de 6700 sujetos de 20 laboratorios representando diez pa&iacute;ses diferentes han confirmado que una frecuencia elevada de micron&uacute;cleos es predictiva de un riesgo aumentado de c&aacute;ncer (Bonassi <i>et al.</i>, 2007). Otra t&eacute;cnica citogen&eacute;tica que puede ser empleada para evaluar alteraciones a nivel de los cromosomas es la de ICH. El intercambio entre crom&aacute;tides hermanas se produce justamente por el intercambio rec&iacute;proco de ADN entre dos crom&aacute;tides hermanas de un cromosoma duplicado. La frecuencia de intercambio en c&eacute;lulas eucariotas se ve incrementada por la exposici&oacute;n a agentes genot&oacute;xicos que inducen da&ntilde;o al ADN interfiriendo con la replicaci&oacute;n del mismo; y no por aquellos agentes que solo inducen rupturas en las cadenas del ADN (Albertini <i>et al.</i>, 2000). Sin embargo, los mecanismos de formaci&oacute;n no est&aacute;n completamente dilucidados y por lo tanto su significado biol&oacute;gico es a&uacute;n incierto (Albertini <i>et al.</i>, 2000).</p>      <p>En lo que respecta a estudios moleculares pueden citarse: 1) citogen&eacute;tica molecular para buscar inversiones, deleciones y translocaciones complejas no detectables en citogen&eacute;tica cl&aacute;sica, o para identificar el origen cromos&oacute;mico de los micron&uacute;cleos; 2) ensayo cometa en linfocitos.</p>      <p>El ensayo cometa es una t&eacute;cnica de electroforesis en microgeles de agarosa considerada de alta sensibilidad para detectar da&ntilde;o al ADN, a nivel de c&eacute;lulas individuales. Permite evidenciar rupturas de simple y doble cadena del ADN, sitios &aacute;lcali l&aacute;biles, y entrecruzamientos ADN/ADN o ADN prote&iacute;na asociados con sitios de reparaci&oacute;n por escisi&oacute;n incompleta en c&eacute;lulas individuales. Cuando el n&uacute;cleo es sometido a la electroforesis, los fragmentos rotos de ADN migran fuera del mismo, d&aacute;ndole la apariencia de cometa que dio lugar al nombre de la t&eacute;cnica (Rojas <i>et al.</i>, 1999).</p>     <p>En lo que respecta a estudios bioqu&iacute;micos, la Organizaci&oacute;n Mundial de la Salud (OMS, 1987), sugiere medir la actividad de la enzima colinesterasa en el plasma como indicador biol&oacute;gico de la exposici&oacute;n a algunos plaguicidas (organofosforados y/o carbamatos) porque la toxicidad de algunas de estas sustancias recae principalmente sobre el sistema nervioso, inhibiendo la acetil colinesterasa neuronal, produciendo un incremento de la acetilcolina en las sinapsis y desencadenando un s&iacute;ndrome colin&eacute;rgico agudo v&iacute;a una neurotransmisi&oacute;n continua, que puede llevar a la muerte si no existe una apropiada y r&aacute;pida intervenci&oacute;n (Kushik y Chandrabhan, 2003). Un estudio efectuado en Honduras (1982) en una comunidad vecina a una zona arrocera donde se efect&uacute;an pulverizaciones a&eacute;reas constantes durante todo el a&ntilde;o, se encontr&oacute; que el 9,1 % de una muestra de personas de dicha poblaci&oacute;n ten&iacute;a una disminuci&oacute;n del 25 % o m&aacute;s del nivel de colinesterasa en relaci&oacute;n a los valores de referencia, indicando claramente una alta exposici&oacute;n a insecticidas organofosforados y/o carbamatos.</p>      <p>Con las metodolog&iacute;as citogen&eacute;ticas, moleculares y bioqu&iacute;micas que existen actualmente, es posible detectar cambios o alteraciones que act&uacute;an como se&ntilde;al de alarma y que permiten tomar las medidas oportunas para minimizar el riesgo para la salud (Bonassi y Au, 2002). Los estudios de biomonitoreo en poblaciones agr&iacute;colas publicados desde la d&eacute;cada de los a&ntilde;os 70 han utilizado una amplia variedad de biomarcadores citogen&eacute;ticos en poblaciones de diferentes caracter&iacute;sticas que dificultan su comparaci&oacute;n. Asimismo es importante considerar que los estudios de exposici&oacute;n a plaguicidas y otros agentes genot&oacute;xicos deben tomar en cuenta la confiabilidad del da&ntilde;o en relaci&oacute;n a la exposici&oacute;n, la solidez de los estudios, la similitud de los grupos de referencia (controles no expuestos) y los protocolos usados para determinar la genotoxicidad.</p>     <p>En la <a href="img/revistas/abc/v17n3/v17n3a3t1.jpg" target="_blank">tabla 1</a> se muestran los biomarcadores de da&ntilde;o gen&eacute;tico estudiados en grupos humanos con exposici&oacute;n principalmente laboral a plaguicidas, indicando si existen diferencias significativas o no entre grupos humanos expuestos y no expuestos. Los trabajos fueron tomados aleatoriamente de internet incluyendo publicaciones de los &uacute;ltimos 25 a&ntilde;os. Estos cien trabajos reunidos han sido realizados en distintas partes del mundo, 21 investigaciones en Am&eacute;rica del Sur en los siguientes pa&iacute;ses: Argentina (6), Bolivia (2), Chile (3), Brasil (7), Colombia (2), Ecuador (1); 14 en Am&eacute;rica del Norte: M&eacute;xico (7), Estados Unidos (6), Columbia Brit&aacute;nica (1); cuatro (4) en Am&eacute;rica Central: Costa Rica (3), Cuba (1); 37 en Europa: Hungr&iacute;a (4), Rep&uacute;blica Checa (1), Rusia (2), Espa&ntilde;a (8), Grecia (5), Italia (8), Dinamarca (1), Portugal (1), ex-Yugoslavia (1), Finlandia (1), Croacia (3), Polonia (1), Pa&iacute;ses Europeos (1); dos en Ocean&iacute;a: Australia (2), dos en &Aacute;frica: Egipto (2); diez en Asia: Siria (1), Turqu&iacute;a (3), Pakist&aacute;n (1), Taiw&aacute;n (2), Israel (1), India (2).</p>      <p>En 73 trabajos se informa un incremento en la frecuencia de aberraciones cromos&oacute;micas, micron&uacute;cleos, da&ntilde;o al ADN (cuantificado por el ensayo cometa) y/o ICH en linfocitos de sangre perif&eacute;rica o c&eacute;lulas de la mucosa bucal de los individuos expuestos laboral o no laboral a plaguicidas.</p>     <p>Como puede observarse en la <a href="img/revistas/abc/v17n3/v17n3a3t1.jpg" target="_blank">tabla 1</a>, en la mayor&iacute;a (73 %) de los trabajos publicados, la evaluaci&oacute;n de da&ntilde;o gen&eacute;tico se realiza mediante la implementaci&oacute;n de un ensayo de genotoxicidad. Sin embargo, es conveniente utilizar al menos dos t&eacute;cnicas en los estudios de biomonitoreo porque existen diferencias entre las t&eacute;cnicas, en cuanto a la capacidad de cuantificar el da&ntilde;o gen&eacute;tico en estructuras o mol&eacute;culas con distintos niveles de organizaci&oacute;n y actividad biol&oacute;gica, y en la sensibilidad de cada una de ellas. Esto hace que el an&aacute;lisis de un conjunto de t&eacute;cnicas permitan obtener resultados concluyentes. De las t&eacute;cnicas empleadas en las investigaciones analizadas, la de mayor sensibilidad es el ensayo cometa, lo que explicar&iacute;a que con excepci&oacute;n de una sola publicaci&oacute;n, el resto de los reportes incluidos en la <a href="img/revistas/abc/v17n3/v17n3a3t1.jpg" target="_blank">tabla 1</a> para esta t&eacute;cnica, evidencien diferencias estad&iacute;sticamente significativas entre los grupos expuestos y de referencia.</p>     <p>Si bien el ensayo cometa es evidentemente una t&eacute;cnica sumamente sensible, es conveniente que la evaluaci&oacute;n del material gen&eacute;tico incluya otras t&eacute;cnicas que permitan evaluar la integridad y el funcionamiento de estructuras m&aacute;s complejas, como los cromosomas para el caso del ensayo de aberraciones cromos&oacute;micas, e incluso el "aparato mit&oacute;tico" para el caso del ensayo de micron&uacute;cleos. Hay que resaltar el significado biol&oacute;gico que representa el da&ntilde;o cromos&oacute;mico, y las evidencias que soportan la tesitura de que un incremento de da&ntilde;o cromos&oacute;mico ser&iacute;a un elemento predictivo de mayor riesgo de padece c&aacute;ncer en el futuro. En este sentido, una gran cantidad de las investigaciones analizadas que eval&uacute;an da&ntilde;o gen&eacute;tico mediante el ensayo de aberraciones cromos&oacute;micas en poblaciones en contacto con plaguicidas, arrojan resultados que podr&iacute;an sugerir que las mismas tendr&iacute;an un riesgo incrementado de desarrollar procesos neopl&aacute;sicos. Esto podr&iacute;a relacionarse con numerosos reportes de carcinog&eacute;nesis vinculada a exposici&oacute;n a diversos plaguicidas en todo el mundo.</p>      <p>Seg&uacute;n se desprende del an&aacute;lisis de estas cien publicaciones, el 90 % de los trabajadores expuestos laboralmente a plaguicidas est&aacute;n en contacto con mezclas de compuestos, lo que dificulta establecer una correlaci&oacute;n entre tipo de plaguicida y tipo de da&ntilde;o observado. Esto conlleva a otro problema, la evaluaci&oacute;n de riesgo por mezclas de plaguicidas. La acci&oacute;n combinada de mezclas puede resultar en una no interacci&oacute;n o en interacci&oacute;n. Si la acci&oacute;n toxicol&oacute;gica de los componentes de la mezcla es diferente, la interacci&oacute;n puede resultar en una potenciaci&oacute;n, cuando el efecto combinado es mayor que un efecto aditivo y antag&oacute;nica cuando el efecto combinado es menor que el aditivo. Escasos estudios relacionados al problema de mezclas de plaguicidas han sido realizados.</p>     ]]></body>
<body><![CDATA[<p>En Argentina, el problema derivado del uso de plaguicidas tiene poca atenci&oacute;n en el sistema de salud. Esta situaci&oacute;n se relaciona con un subregistro de las intoxicaciones (Souza, 2007). Un alto porcentaje de la poblaci&oacute;n argentina se dedica a la agricultura y vive en sectores rurales donde se emplean grandes cantidades de sustancias para el control de plagas en actividades agr&iacute;colas. Igualmente se conoce que una alta proporci&oacute;n de la poblaci&oacute;n est&aacute; real y potencialmente expuesta a estos plaguicidas no solo por participar directamente en actividades laborales, sino tambi&eacute;n por las diversas pulverizaciones que se realizan y que llegan involuntariamente a las viviendas, provocando un aumento de las posibilidades de que se presenten efectos nocivos en la salud de estos pobladores. En relaci&oacute;n a los estudios de genotoxicidad, Larripa <i>et al., </i>(1983); Dulout <i>et al., </i>(1985); Dulout <i>et al., </i>(1987) y Dulout <i>et al., </i>(1992), analizan grupos expuestos a plaguicidas de la provincia de Buenos Aires, a trav&eacute;s de los ensayos de intercambio de crom&aacute;tidas hermanas y aberraciones cromos&oacute;micas. Simoniello <i>et al.</i>, (2010), en la provincia de Santa Fe, realizan estudios de poblaciones expuestas a diferentes mezclas de plaguicidas con el ensayo cometa. Para C&oacute;rdoba los primeros reportes de estudios gen&eacute;ticos en personas y animales expuestos a plaguicidas son los realizados por Ma&ntilde;as <i>et al.</i>, (2009a); Ma&ntilde;as <i>et al.</i>, (2009b); Ma&ntilde;as <i>et al.</i>, (2010); Aiassa <i>et al.</i>, (2010); Peralta <i>et al.</i>, (2011); Bosch <i>et al.</i>, (2011); Gentile <i>et al.</i>, (2012), utilizando los ensayos de AC, MN y cometa.</p>      <p><b>CONCLUSIONES</b></p>      <p>Los ensayos de genotoxicidad a corto plazo: aberraciones cromos&oacute;micas, micron&uacute;cleos, intercambio de crom&aacute;tidas hermanas y cometa, permiten de forma r&aacute;pida y vers&aacute;til la detecci&oacute;n de alteraciones en el material gen&eacute;tico durante el biomonitoreo de poblaciones humanas potencialmente afectadas por plaguicidas. Esto admite la evaluaci&oacute;n de da&ntilde;os en el material gen&eacute;tico en poblaciones expuestas a un agente t&oacute;xico y es una herramienta valiosa porque brinda informaci&oacute;n antes de que ocurran situaciones irreversibles.  Desde finales de la d&eacute;cada de los 80, los ensayos de genotoxicidad se utilizan en gran cantidad de estudios de biomonitoreo como marcadores de efecto en exposiciones medioambientales y ocupacionales, utilizando diferentes tipos celulares.</p>     <p>El da&ntilde;o en el material gen&eacute;tico puede ocurrir debido a la exposici&oacute;n a agentes cancer&iacute;genos, defectos en la mitosis o en la reparaci&oacute;n del ADN. Si el da&ntilde;o se produce en la l&iacute;nea som&aacute;tica puede derivar en c&aacute;ncer, contribuir al envejecimiento prematuro, producir enfermedades vasculares, entre otras. Si el da&ntilde;o se induce en c&eacute;lulas germinales puede tener efectos sobre la fertilidad de las personas expuestas a estos agentes, como as&iacute; tambi&eacute;n sobre su descendencia. Las t&eacute;cnicas citadas pueden ser aplicadas tanto en c&eacute;lulas sangu&iacute;neas como en c&eacute;lulas epiteliales del tracto respiratorio, urinario, reproductor y digestivo, siendo esta &uacute;ltima alternativa menos invasiva que los m&eacute;todos tradicionales en sangre perif&eacute;rica.</p>     <p>Estos m&eacute;todos son cada vez m&aacute;s utilizados en estudios epidemiol&oacute;gicos moleculares para investigar el impacto de la nutrici&oacute;n, el estilo de vida, la exposici&oacute;n a agentes genot&oacute;xicos y las diferencias de susceptibilidades individuales frente a dicha exposici&oacute;n.</p>     <p>Debido justamente a que los resultados de los ensayos de genotoxicidad pueden variar por factores tales como la alimentaci&oacute;n (por ejemplo, mayor o menor consumo de antioxidantes en la dieta), estilo de vida (por ejemplo, consumo de tabaco, alcohol, etc.) y la exposici&oacute;n a otros agentes potencialmente genot&oacute;xicos (por ejemplo radiaci&oacute;n solar, rayos X, algunos medicamentos, etc.), entre otros, es que resulta imprescindible identificar en las poblaciones estudiadas estos "factores de confusi&oacute;n" a los fines de evitar posibles interferencias con los resultados obtenidos.</p>     <p>Como se dijo previamente, en las publicaciones analizadas hay una gran variabilidad en cuanto a los datos relacionados a los posibles factores de confusi&oacute;n, por lo que no es posible obtener conclusiones en este sentido.</p>     <p>La evaluaci&oacute;n de los niveles de da&ntilde;o gen&eacute;tico en poblaciones expuestas a plaguicidas, deber&iacute;a acompa&ntilde;arse en todos los casos de un cuestionario individual que permita identificar si el participante est&aacute; o no expuesto a plaguicidas, de qu&eacute; modo, con qu&eacute; frecuencia, y si es posible identificar a cu&aacute;les y detallar la cantidad de a&ntilde;os totales de exposici&oacute;n. Tambi&eacute;n es necesario recopilar informaci&oacute;n relacionada al estado de salud del participante y sus familiares directos, incluyendo datos sobre la presencia de estados patol&oacute;gicos previos o actuales, relacionados o no a la exposici&oacute;n a plaguicidas. En este sentido, es necesario resaltar que no solo la presencia de determinadas enfermedades puede afectar los resultados de los ensayos de genotoxicidad, sino que el consumo de los medicamentos vinculados a la misma tambi&eacute;n puede restarle confiabilidad a los resultados obtenidos.</p>     <p>Cuando se trabaja con poblaciones expuestas en forma laboral existen variables que deben ser incluidas en el an&aacute;lisis, dentro de las cu&aacute;les resulta de particular importancia la utilizaci&oacute;n del equipo de protecci&oacute;n personal correspondiente. Por este motivo, en el cuestionario deber&iacute;a tambi&eacute;n indagarse sobre el uso de guantes, m&aacute;scaras, botas y otros elementos que tiendan a disminuir la exposici&oacute;n laboral a plaguicidas y que determinen una elevada variabilidad de exposici&oacute;n en la poblaci&oacute;n estudiada. En la mayor&iacute;a de los art&iacute;culos analizados no se precisa los elementos de protecci&oacute;n personal utilizados durante las pulverizaciones o el manejo de los plaguicidas en general. Sin embargo, existen publicaciones en las que se evidencian diferencias estad&iacute;sticamente significativas en cuanto a los niveles de da&ntilde;o gen&eacute;tico entre las personas que utilizan medidas de protecci&oacute;n y las que no las emplean.</p>     <p>La importancia en la detecci&oacute;n precoz del da&ntilde;o gen&eacute;tico radica en que permite tomar las medidas necesarias para disminuir o suprimir la exposici&oacute;n al agente delet&eacute;reo cuando a&uacute;n &eacute;ste es reversible, disminuyendo por tanto el riesgo de desarrollar enfermedades. Por ese motivo, los ensayos de genotoxicidad deber&iacute;an ser considerados como herramientas indispensables en la implementaci&oacute;n de una completa vigilancia m&eacute;dica en personas potencialmente expuestas a diversos contaminantes ambientales y en especial aquellas que habitan en el mismo lugar con personas que ya han desarrollado alg&uacute;n tipo de neoplasia en edades tempranas con el fin de prevenir la ocurrencia de tumores de origen ambiental y especialmente laboral. Por otro lado, la aplicaci&oacute;n de estos ensayos es &uacute;til para detectar posibles efectos a largo plazo de sustancias que se introducen al mercado sin conocer con exactitud su capacidad de afectar la salud humana y ambiental.</p>     ]]></body>
<body><![CDATA[<p><b>AGRADECIMIENTOS</b></p>     <p>Este trabajo se realiz&oacute; en el marco de proyectos de investigaci&oacute;n subsidiados por la Secretar&iacute;a de Ciencia y T&eacute;cnica de la Universidad Nacional de R&iacute;o Cuarto y el Consejo Nacional de Investigaciones Cient&iacute;ficas y Tecnol&oacute;gicas (CONICET).</p>     <p><b>BIBLIOGRAF&Iacute;A</b></p>      <!-- ref --><p>AIASSA D, MA&Ntilde;AS F, BOSCH B, PERALTA L, GENTILE N, BEVILACQUA S, <i>et al. </i>Los plaguicidas. Su relaci&oacute;n con la salud humana y ambiental en la Provincia de C&oacute;rdoba. Exp M&eacute;d. 2010;28(1):39-44.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000056&pid=S0120-548X201200030000300001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>ALAVANJA MC, SANDLER DP, MCDONNELL C, LYNCH C, PENNYBACKER M, ZAHM S, <i>et al. </i>Characteristics of pesticide use in a pesticide applicator cohort: the agricultural health study. Environ Res. 1999;80(Suppl 1):172-179.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000058&pid=S0120-548X201200030000300002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>ALAVANJA MC, HOPPIN JA, KAMEL F. Health effects of chronic pesticide exposure: cancer and neurotoxicity. Annu Rev Public Health. 2004;25:155-197&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000060&pid=S0120-548X201200030000300003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p>ALAVANJA MC, SANDLER DP, LYNCH CF, KNOTT C, LUBIN JH, TARONE R. Cancer incidence in the agricultural health study. Scand J Work Environ Health. 2005;31(Sl1):39-45.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000061&pid=S0120-548X201200030000300004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     ]]></body>
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<body><![CDATA[<!-- ref --><p>BOLOGNESI C, CARRASQUILLA G, VOLPI S, SOLOMON KR, MARSHALL EJ. Biomonitoring of genotoxic risk in agricultural workers from five colombian regions: association to occupational exposure to glyphosate. J Toxicol Environ Health A. 2009;72(15-16):986-997.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000083&pid=S0120-548X201200030000300015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>BOLOGNESI C, LANDINI E, PERRONE E, ROGGIERI P. Cytogenetic biomonitoring of a floriculturist population in Italy: micronucleus analysis by fluorescence in situ hybridization (FISH) with an all-chromosome centromeric probe. Mutat Res. 2004;557(2):109-117.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000085&pid=S0120-548X201200030000300016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>BOLOGNESI C, PARRINI M, MERLO F, BONASSI S. Frequency of micronuclei in lymphocytes from a group of floriculturists exposed to pesticides. J Toxicol Environ Health.   1993;40(2-3):405-411.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000087&pid=S0120-548X201200030000300017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>BOLOGNESI C, PERRONE E, LANDINI E. Micronucleus monitoring of a floriculturist population from western Liguria, Italy. Mutag. 2002;17(5):391-397.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000089&pid=S0120-548X201200030000300018&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>BONASSI C, ABBONDANDOLO A, CAMURRI L, DAL PRA L, DE FERRARI M, DEGRASSI F. Are chromosome aberrations in circulating lymphocytes predictive of a future cancer onset in humans preliminary results of an Italian cohort study. Cancer Genet Cytogenet. 1995;79(2):133-135.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000091&pid=S0120-548X201200030000300019&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      ]]></body>
<body><![CDATA[<!-- ref --><p>BONASSI S, AU WW. Biomarkers in molecular epidemiology studies for health risk prediction. Mutat Res. 2002;511(1):73-86.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000093&pid=S0120-548X201200030000300020&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>BONASSI S, ZNAOR A, CEPPI M, LANDO C, CHANG WP, HOLLAND N, <i>et al. </i>An increased micronucleus frequency in peripheral blood lymphocytes predicts the risk of cancer in humans. Carcinog. 2007;28(3):625-631.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000095&pid=S0120-548X201200030000300021&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>    <!-- ref --><p>BORTOLI GM, AZEVEDO MB, SILVA LB. Cytogenetic biomonitoring of Brazilian workers exposed to pesticides: micronucleus analysis in buccal epithelial cells of soybean growers. Mutat Res. 2009;675(1-2):1-4.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000097&pid=S0120-548X201200030000300022&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>BOSCH B, MA&Ntilde;AS F, GORLA N, AIASSA D. Micronucleus test in post metamorphic <i>Odontophrynus cordobae </i>and <i>Rhinella arenarum </i>(Amphibia:Anura) for environmental monitoring. J Toxicol Environ Health Sci. 2011;3(6):154-163.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000099&pid=S0120-548X201200030000300023&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>      <!-- ref --><p>BREGA SM, VASSILIEFF I, ALMEIDA A, MERCADANTE A, BISSACOT D, CURY PR, <i>et al. </i>Clinical, cytogenetic and toxicological studies in rural workers exposed to pesticides in Botucatu, Sao Paulo, Brazil. Cad Saude Pub. 1998;14(3):109-115.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000101&pid=S0120-548X201200030000300024&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     ]]></body>
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