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Updated: Jan 29, 2026

A Pipeline to Investigate the Structures and Signaling Pathways of Sphingosine 1-Phosphate Receptors
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Neonicotinoids and the Androgen Receptor: Structural Dynamics and Potential Signaling Disruption.

Mohd Amin Beg1,2, Md Amjad Beg3, Ummer Rashid Zargar4

  • 1King Fahd Medical Research Center, King Abdulaziz University, Jeddah 21859, Saudi Arabia.

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|January 28, 2026
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Summary

Neonicotinoids bind to the androgen receptor (AR), potentially disrupting testosterone binding and male reproductive function. This insecticide exposure may impact male fertility by interfering with critical hormonal pathways.

Keywords:
androgen receptorendocrine disruptionmale reproductive problemsmolecular dynamics simulationneonicotinoids

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Area of Science:

  • Environmental Science
  • Toxicology
  • Molecular Biology

Background:

  • Neonicotinoids are widely used insecticides with potential public health risks.
  • Neonicotinoid exposure is linked to abnormal semen analysis in limited studies.
  • The mechanism of neonicotinoid disruption on male reproductive health is not fully understood.

Purpose of the Study:

  • To investigate the potential disruption of the androgen receptor (AR) by eight common neonicotinoids.
  • To elucidate the binding interactions and molecular dynamics of neonicotinoids with the AR.

Main Methods:

  • Molecular docking simulations were performed for eight neonicotinoids against the AR.
  • Molecular dynamics (MD) simulations were used to analyze the stability and behavior of AR-neonicotinoid complexes.
  • Binding energy, affinity, and structural dynamics were evaluated.

Main Results:

  • Most neonicotinoids showed strong binding affinity and stability with the AR.
  • Imidacloprid (IMI) formed a stable complex with the AR, confirmed by MD simulations.
  • Neonicotinoids bind to the same site as testosterone, suggesting interference with natural hormone signaling.

Conclusions:

  • Neonicotinoids can stably bind to the androgen receptor's ligand-binding domain.
  • This binding may competitively inhibit testosterone and disrupt male reproductive pathways.
  • Further research is needed to confirm the impact on male reproductive dysfunction.