4.7 Article

Metabolomic and Transcript Analysis Revealed a Sex-Specific Effect of Glyphosate in Zebrafish Liver

Journal

Publisher

MDPI
DOI: 10.3390/ijms23052724

Keywords

Danio rerio; metabolomic; liver; glyphosate; Roundup(R); purine metabolism; oxidative stress

Funding

  1. Natural Sciences and Engineering Research Council of Canada [1254045]
  2. Fondi di Ateneo, Universita Politecnica delle Marche
  3. NSERC
  4. Alberta Graduate Excellence Scholarship (AGES)

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Glyphosate exposure had sex-specific effects in zebrafish, with females showing disrupted purine and pyrimidine metabolism, increased stress inflammatory response, and males exhibiting impaired lysine degradation and oxidative stress response. These findings provide evidence of the adverse effects of glyphosate on hepatic metabolism and stress response in zebrafish.
Glyphosate is a component of commonly used herbicides for controlling weeds in crops, gardens and municipal parks. There is increasing awareness that glyphosate-based herbicides, in addition to acting on plants, may also exert toxicity in wildlife and humans. In this study, male and female adult zebrafish were exposed to 700 mu g/L of glyphosate (GLY), for 28 days. We used the metabolomic approach and UHPLC-ESI-MS to analyze liver samples to investigate the adverse effects of glyphosate on hepatic metabolism. The impact of GLY was found to be sex-specific. In female, GLY exposure affected purine metabolism by decreasing the levels of AMP, GMP and inosinic acid, consequently increasing uric acid levels with respect to the control (CTRL). Exposure to GLY also caused a decrease of UMP levels in the pyrimidine metabolism pathway. In male, GLY exposure decreased the aminoadipic acid within the lysine degradation pathway. Transcript analysis of genes involved in stress response, oxidative stress and the immune system were also performed. Results demonstrated an increased stress response in both sexes, as suggested by higher nr3c1 expression. However, the hsp70.2 transcript level was increased in female but decreased in male. The results demonstrated reduced sod1, sod2, and gpx1a in male following exposure to GLY, indicating an impaired oxidative stress response. At the same time, an increase in the cat transcript level in female was observed. mRNA levels of the pro-inflammatory interleukins litaf and cxcl8b.1 were increased in female. Taken together, the results provide evidence of disrupted nucleotide hepatic metabolism, increased stress inflammatory response in female and disruption of oxidative stress response in male.

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