Effect of antioxidant supplements on lipid peroxidation levels in primary cortical neuron cultures.

Abstract Oxidative stress, specifically lipid peroxidation, is a major driving force in neurodegenerative processes. However, the exact role of lipid peroxidation remains elusive as reliable real-time detection and quantification of lipid peroxyl radicals proves to be challenging in vitro and in vivo. Motivated by this methodological limitation, we have optimized conditions for real-time imaging and quantification of lipid peroxyl radical generation in primary neuron cultures using the lipophilic fluorogenic antioxidant H 4 BPMHC (8-((6-hydroxy-2,5,7,8-tetramethylchroman-2-yl)-methyl)-1,5-di(3-chloropropyl)-pyrromethene fluoroborate), an α-tocopherol analog probe. By subjecting neurons to different antioxidant conditions in the presence and absence of lipid peroxidation inducing stressors (Haber-Weiss reagents), we maximized H 4 BPMHC sensitivity and confirmed its potential to temporally resolve subtle and marked differences in lipid peroxidation levels in real-time. Herein we report imaging and quantification of homeostatic and induced lipid peroxidation in primary neuron cultures, supporting the use of this probe for investigating healthy and diseased states. Overall these results provide the necessary foundation and impetus towards using H 4 BPMHC for elucidating and mapping lipid peroxyl radical contributions to ROS-associated pathological processes in neurons. Graphical abstract fx1 Highlights • Lipid peroxyl radicals were imaged and quantified real-time in primary neurons. • Antioxidant load impacted the rate of lipid peroxyl radical formation. • H 4 BPMHC has potential to detect subtle changes in lipid peroxyl radical levels. [ABSTRACT FROM AUTHOR]