4.7 Article

Functional alterations by a subgroup of neonicotinoid pesticides in human dopaminergic neurons

Journal

ARCHIVES OF TOXICOLOGY
Volume 95, Issue 6, Pages 2081-2107

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00204-021-03031-1

Keywords

Live-cell calcium imaging; Neurotoxicity; Nicotine; Desensitization; Molecular docking

Categories

Funding

  1. BMBF
  2. InViTe PhD program from the Baden-Wuerttemberg Ministry for Science, Research and Art (MWK Baden-Wurttemberg)
  3. EFSA
  4. DK-EPA [MST-667-00205]
  5. Swedish Research Council [VR-2018-03269]
  6. University of Konstanz
  7. Stockholm University
  8. European Union's ERASMUS+ programme
  9. Horizon 2020 research and innovation programme [681002, 825759]
  10. State Ministry of Baden-Wuerttemberg for Economic Affairs, Labour and Housing Construction
  11. Swedish Research Council [2018-03269] Funding Source: Swedish Research Council

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The study demonstrates that several neonicotinoid pesticides can trigger human neuronal signaling at low micromolar concentrations, raising concerns about their potential impact on nervous system development.
Neonicotinoid pesticides, originally developed to target the insect nervous system, have been reported to interact with human receptors and to activate rodent neurons. Therefore, we evaluated in how far these compounds may trigger signaling in human neurons, and thus, affect the human adult or developing nervous system. We used SH-SY5Y neuroblastoma cells as established model of nicotinic acetylcholine receptor (nAChR) signaling. In parallel, we profiled dopaminergic neurons, generated from LUHMES neuronal precursor cells, as novel system to study nAChR activation in human post-mitotic neurons. Changes of the free intracellular Ca2+ concentration ([Ca2+](i)) were used as readout, and key findings were confirmed by patch clamp recordings. Nicotine triggered typical neuronal signaling responses that were blocked by antagonists, such as tubocurarine and mecamylamine. Pharmacological approaches suggested a functional expression of alpha 7 and non-alpha 7 nAChRs on LUHMES cells. In this novel test system, the neonicotinoids acetamiprid, imidacloprid, clothianidin and thiacloprid, but not thiamethoxam and dinotefuran, triggered [Ca2+](i) signaling at 10-100 mu M. Strong synergy of the active neonicotinoids (at low micromolar concentrations) with the alpha 7 nAChR-positive allosteric modulator PNU-120596 was observed in LUHMES and SH-SY5Y cells, and specific antagonists fully inhibited such signaling. To provide a third line of evidence for neonicotinoid signaling via nAChR, we studied cross-desensitization: pretreatment of LUHMES and SH-SY5Y cells with active neonicotinoids (at 1-10 mu M) blunted the signaling response of nicotine. The pesticides (at 3-30 mu M) also blunted the response to the non-alpha 7 agonist ABT 594 in LUHMES cells. These data show that human neuronal cells are functionally affected by low micromolar concentrations of several neonicotinoids. An effect of such signals on nervous system development is a toxicological concern.

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