Adhesion Molecules in Lung Inflammation from Repeated Glyphosate Exposures

Int J Environ Res Public Health. 2023 Apr 12;20(8):5484. doi: 10.3390/ijerph20085484.

Abstract

Glyphosate is an active ingredient in herbicides. Exposure to glyphosate-based herbicides has been associated with respiratory dysfunctions in agricultural workers. The ability of inhaled glyphosate to induce lung inflammation is not well understood. Further, the role of adhesion molecules in glyphosate-induced lung inflammation has not been studied. We evaluated lung inflammatory responses from single and repeated glyphosate exposures. Male C57BL/6 mice were intranasally exposed to glyphosate (1 μg/40 μL) for 1 day or once daily for 5 days or 10 days. Lung tissue and bronchoalveolar lavage (BAL) fluid were collected and analyzed. Repeated exposure to glyphosate for 5 days and 10 days resulted in an increase in neutrophils in BAL fluid and higher eosinophil peroxidase levels in lungs, with leukocyte infiltration further confirmed through lung histology. Repetitive exposure to glyphosate increased IL-33 and Th2 cytokines IL-5 and IL-13. A single glyphosate treatment revealed expression for ICAM-1, VCAM-1, and vWF adhesion molecules in the perivascular region of lung sections; with repeated treatment (5 and 10 days), adhesion molecule expression was found in the perivascular, peribronchiolar, and alveolar regions of the lungs. Repetitive exposure to glyphosate induced cellular inflammation in which adhesion molecules may be important to the lung inflammatory process.

Keywords: adhesion markers; glyphosate; lung inflammation; repetitive exposure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid
  • Cell Adhesion Molecules
  • Glyphosate
  • Herbicides* / metabolism
  • Herbicides* / toxicity
  • Inflammation / metabolism
  • Intercellular Adhesion Molecule-1 / adverse effects
  • Intercellular Adhesion Molecule-1 / metabolism
  • Lung / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Pneumonia* / chemically induced
  • Pneumonia* / metabolism

Substances

  • Cell Adhesion Molecules
  • Intercellular Adhesion Molecule-1
  • Herbicides

Grants and funding

The research work was supported by a Discovery Grant from Natural Sciences and Engineering Research Council (NSERC) awarded to BS (NSERC: RGPIN-2014-04308). UP acknowledges the financial support from: the Integrated Graduate Training Program in Infectious Diseases, Food Safety and Public Policy (ITraP) funded by NSERC/CREATE, the University of Saskatchewan’s University Graduate Scholarship (UGS), the Respiratory Research Centre Graduate Student Award (RRCGSA) from the Respiratory Research Centre, the Founding Chairs Fellowship from CCHSA, and the University of Saskatchewan Health Sciences Graduate Scholarship (HSGS).