ScholarWorks@중앙대학교

초록

Xylene is an aromatic hydrocarbon widely used as a solvent and emitted from numerous commercial products in industrial or indoor settings. Epidemiological studies of occupational exposure indicate that xylene primarily targets the central nervous system, producing neurobehavioral impairments and other neurological disorders. Both environmental and occupational exposure to volatile organic compounds, therefore, raise concerns about neurodevelopmental risk; however, the specific neurotoxicity of xylene in developing neurons remains poorly characterized. Here, we investigated the effects of xylene (2 or 5 mM) on developing mouse hippocampal neurons, with a focus on Ca2+ homeostasis, presynaptic function, and electrophysiological activity. We assessed Ca2+ homeostasis with selective inhibitors of voltage-gated Ca2+ channels and organelle-specific Ca2+ indicators. Presynaptic activity was evaluated in transgenic mouse pups expressing a genetically encoded pH sensor within the synaptic vesicle lumen. Xylene suppressed cytosolic Ca2+ transients by inhibiting P/Q-type Ca2+ channels, thereby reducing Ca2+ uptake into the endoplasmic reticulum. It also decreased Ca2+ influx at both presynaptic and postsynaptic sites, impairing synaptic vesicle exocytosis and endocytosis. Electrophysiological and morphological analyses further showed reduced spontaneous firing and hindered synaptic maturation. Collectively, these findings provide mechanistic insight into the neurotoxic actions of xylene and underscore its potential hazard to brain development and function.

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