Original scientific paper

https://doi.org/10.2478/aiht-2025-76-4007

Effects of N-alkyl quaternary quinuclidines on oxidative stress biomarkers in SH-SY5Y cells

Antonio Zandona ; Institute for Medical Research and Occupational Health, Division of Toxicology, Zagreb, Croatia
Lucija Marcelić orcid.org/0009-0006-5085-8525 ; Institute for Medical Research and Occupational Health, Division of Toxicology, Zagreb, Croatia
Suzana Žunec orcid.org/0000-0002-7710-8250 ; Institute for Medical Research and Occupational Health, Division of Toxicology, Zagreb, Croatia
Josip Madunić orcid.org/0000-0003-4724-9236 ; Institute for Medical Research and Occupational Health, Division of Toxicology, Zagreb, Croatia
Maja Katalinić orcid.org/0000-0001-7043-4291 ; Institute for Medical Research and Occupational Health, Division of Toxicology, Zagreb, Croatia *

* Corresponding author.

Abstract

Having a broad spectrum of biological and pharmacological activities, including anticholinergic, antihistaminic, antiparasitic, antioxidant, and antitumour, quinuclidine derivatives have piqued much interest in the field of drug discovery and biomedical research. This study investigates the oxidative stress effects of six N-alkyl quaternary quinuclidine derivatives, namely three oximes (QNOH-C12,14,16) and three alcohols (QOH-C12,14,16) in SH-SY5Y neuroblastoma cells to evaluate their safety profile as potential therapeutics. We treated SH-SY5Y cells with their lowest-observed-adverse-effect levels (LOAEL) for 4 h and measured reactive oxygen/nitrogen species (ROS/RNS), lipid peroxidation, glutathione (GSH), superoxide dismutase (SOD) activity, and DNA damage. Q(N)OHs significantly increased ROS and RNS levels, particularly the QNOHs, while lipid peroxidation remained unaffected, and GSH depletion was minimal. Cytosolic Cu/Zn-SOD activity increased significantly with longer alkyl chain substituents, while Mn-SOD activity decreased, indicating mitochondrial damage. DNA damage was not elevated. The observed effects of the tested quinuclidine derivatives appear to depend on their structural properties, as compounds containing hydroxyl groups and shorter alkyl chains had a lower impact. Furthermore, even non-cytotoxic doses of the tested compounds affected cell homeostasis, which underlines the importance of such testing early in the evaluation of new potential drugs.

Keywords

DNA damage; glutathione; mitochondrial dysfunction; oximes; reactive nitrogen species; reactive oxygen species; superoxide dismutase

Hrčak ID:

335404

URI

https://hrcak.srce.hr/335404

Publication date:

15.9.2025.

Article data in other languages: croatian

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