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B-esterase determination and organophosphate insecticide inhibitory effects in JEG-3 trophoblasts.
Espinoza, Marlon; Rivero Osimani, Valeria; Sánchez, Victoria; Rosenbaum, Enrique; Guiñazú, Natalia.
Afiliación
  • Espinoza M; Departamento de Ciencias del Ambiente, Facultad de Ciencias del Ambiente y la Salud, Universidad Nacional del Comahue, Neuquén, Argentina.
  • Rivero Osimani V; Facultad de Medicina, Universidad Nacional del Comahue, Río Negro, Argentina.
  • Sánchez V; LIBIQUIMA, Facultad de Ingeniería, Universidad Nacional del Comahue, Neuquén, Argentina.
  • Rosenbaum E; LIBIQUIMA, Facultad de Ingeniería, Universidad Nacional del Comahue, Neuquén, Argentina.
  • Guiñazú N; Departamento de Ciencias del Ambiente, Facultad de Ciencias del Ambiente y la Salud, Universidad Nacional del Comahue, Neuquén, Argentina; LIBIQUIMA, Facultad de Ingeniería, Universidad Nacional del Comahue, Neuquén, Argentina. Electronic address: natanien@hotmail.com.
Toxicol In Vitro ; 32: 190-7, 2016 Apr.
Article en En | MEDLINE | ID: mdl-26790371
The placenta and trophoblasts express several B-esterases. This family includes acethylcholinesterase (AChE), carboxylesterase (CES) and butyrylcholinesterase (BChE), which are important targets of organophosphate insecticide (OP) toxicity. To better understand OP effects on trophoblasts, B-esterase basal activity and kinetic behavior were studied in JEG-3 choriocarcinoma cell cultures. Effects of the OP azinphos-methyl (Am) and chlorpyrifos (Cp) on cellular enzyme activity were also evaluated. JEG-3 cells showed measurable activity levels of AChE and CES, while BChE was undetected. Recorded Km for AChE and CES were 0.33 and 0.26 mM respectively. Native gel electrophoresis and RT-PCR analysis demonstrated CES1 and CES2 isoform expression. Cells exposed for 4 and 24 h to the OP Am or Cp, showed a differential CES and AChE inhibition profiles. Am inhibited CES and AChE at 4 h treatment while Cp showed the highest inhibition profile at 24 h. Interestingly, both insecticides differentially affected CES1 and CES2 activities. Results demonstrated that JEG-3 trophoblasts express AChE, CES1 and CES2. B-esterase enzymes were inhibited by in vitro OP exposure, indicating that JEG-3 cells metabolization capabilities include phase I enzymes, able to bioactivate OP. In addition, since CES enzymes are important for medicinal drug activation/deactivation, OP exposure may interfere with trophoblast CES metabolization, probably being relevant in a co-exposure scenario during pregnancy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Azinfosmetilo / Trofoblastos / Carboxilesterasa / Cloropirifos / Insecticidas Límite: Humans Idioma: En Revista: Toxicol In Vitro Asunto de la revista: TOXICOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Argentina

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Azinfosmetilo / Trofoblastos / Carboxilesterasa / Cloropirifos / Insecticidas Límite: Humans Idioma: En Revista: Toxicol In Vitro Asunto de la revista: TOXICOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Argentina
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