4.4 Article

Exposure to glyphosate during pregnancy induces neurobehavioral alterations and downregulation of Wnt5a-CaMKII pathway

期刊

REPRODUCTIVE TOXICOLOGY
卷 96, 期 -, 页码 390-398

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.reprotox.2020.08.006

关键词

Glyphosate; Neurotoxicity; Gestational exposure; Wnt pathway; CaMKII

资金

  1. Agencia Nacional de Promocion Cientifica y Tecnologica [PICT 2014-1326]
  2. Consejo Nacional de Investigaciones Cientificas y Tecnicas [PIP 0947]
  3. Universidad Nacional de Rosario [UNR BIO 382]

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Glyphosate-based formulations are the most popular herbicide used around the world. These herbicides are widely applied in agriculture to control weeds on genetically modified crops. Although there is much evidence showing that glyphosate-based herbicides induce toxic effect on reproductive and hepatic systems, and also cause oxidative damage on cells, studies from recent years revealed that the nervous system may represent a key target for their toxicity. In the present work, we evaluated the effect of glyphosate (without adjuvants) in neonate rats after gestational exposure. Particularly, we examined whether glyphosate during gestation affected the nervous system function at early development. Pregnant Wistar rats were treated with 24 or 35 mg/kg of pure glyphosate every 48 h and neurobehavioral studies were performed. Our results indicated that gestational exposure to glyphosate induced changes in reflexes development, motor activity and cognitive function, in a dose-dependent manner. To go further, we evaluated whether prenatal exposure to glyphosate affected the Ca+2-mediated Wnt non-canonical signaling pathway. Results indicated that embryos exposed to glyphosate showed an inhibition of Wnt5a-CaMKII signaling pathway, an essential cascade controlling the formation and integration of neural circuits. Taken together, these findings suggest that gestational exposure to glyphosate leads to a downregulation of Wnt/Ca+2 pathway that could induce a developmental neurotoxicity evidenced by deficits at behavioral and cognitive levels in rat pups.

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