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Aminomethylphosphonic acid (AMPA), a glyphosate metabolite, decreases plasma cholinesterase activity in rats
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  • Bruno Antonio Marichal-Cancino,
  • Jesús Chávez-Reyes,
  • Fernando Saráchaga-Terrazas,
  • Oliver Alejandro Colis-Arenas,
  • Carlos Humberto López-Lariz,
  • C. M. Villalon
Bruno Antonio Marichal-Cancino
Universidad Autonoma de Aguascalientes Centro de Ciencias Basicas

Corresponding Author:[email protected]

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Jesús Chávez-Reyes
Universidad Autonoma de Aguascalientes Centro de Ciencias Basicas
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Fernando Saráchaga-Terrazas
Universidad Autonoma de Aguascalientes Centro de Ciencias de la Salud
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Oliver Alejandro Colis-Arenas
Universidad Autonoma de Aguascalientes Centro de Ciencias de la Salud
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Carlos Humberto López-Lariz
Universidad Autonoma de Aguascalientes Centro de Ciencias Basicas
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C. M. Villalon
Centro de Investigacion y de Estudios Avanzados del Instituto Politecnico Nacional
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Abstract

Glyphosate, a widely used herbicide, is linked to a plethora of deleterious effects in both clinical and preclinical studies. Nevertheless, the effects of its main metabolite, aminomethylphosphonic acid (AMPA), whose half-life in soil is even longer than that of glyphosate, have been little explored. On this basis, as a first approach, in this work we report that intraperitoneal (i.p.) administration of AMPA or glyphosate (at 10, 56, and 100 mg/kg) decreased, to a similar extent, plasma cholinesterase (ChE) activity in acutely exposed rats. Moreover, we designed an experimental protocol to analyze and compare the effects of AMPA and glyphosate on human plasma ChE activity; this protocol consisted of adding these compounds to human plasma to subsequently test the effects of this plasma on the contraction to acetylcholine (ACh) in the frog rectus abdominis muscle (an indirect estimate of ChE activity). Accordingly, this muscular contraction to ACh was evaluated before and after pre‑incubation of ACh with: (i) plasma alone; (ii) plasma with AMPA; and (iii) plasma with glyphosate. Our results indicate that AMPA, like glyphosate, decreased ChE activity in the plasma of rats (when given i.p.) and humans (when added in vitro), suggesting that both xenobiotics may exert similar toxicological effects.