Cytoprotective effect of alpha-2-macroglobulin against pesticide-induced generation of ROS in neuronal SH-SY5Y cells

Authors

  • Swati Dixit Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India
  • Haseeb Ahsan Department of Biochemistry, Faculty of Dentistry, Jamia Millia Islamia, New Delhi 110025, India
  • Fahim Halim Khan Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India

DOI:

https://doi.org/10.15419/bmrat.v10i2.792

Abstract

Introduction: Many clinical studies have demonstrated that continuous exposure to pesticides, especially organophosphates and pyrethroids, causes toxicities such as carcinogenicity and neurotoxicity that lead to disorders such as diabetes, lung cancer, and neurodegenerative diseases. The mechanism underlying pesticide-induced neurotoxicity involves the production of ROS, which causes neuronal injury through oxidative stress.

Methods: In the present study, the neuronal SHSY5Y cell line was used to investigate the effect of the pesticides chlorpyrifos (organophosphate), aldicarb (carbamate), and deltamethrin (pyrethroid) on ROS-mediated toxicity and the protective effect of alpha-2-macroglobulin (a2M), a protease inhibitor and beta-amyloid plaque scavenger in the human brain. For cell viability and cytotoxicity, the MTT assay was performed. To monitor ROS production, assays such as DCFHDA, H2O2, and MDA were performed, along with assays of the activity of antioxidant enzymes such as superoxide dismutase and glutathione peroxidase.

Results: The experimental findings suggest a cytoprotective role for a2M in ROS-mediated toxicity that causes neuronal injury in humans.

Conclusion: Hence, a2M could be possibly used as a protective agent against oxidative neurotoxicity caused by pesticides.

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Published

2023-02-28

Issue

Section

Original Research

How to Cite

Cytoprotective effect of alpha-2-macroglobulin against pesticide-induced generation of ROS in neuronal SH-SY5Y cells. (2023). Biomedical Research and Therapy, 10(2), 5537-5544. https://doi.org/10.15419/bmrat.v10i2.792