Spatiotemporal Dynamics of Lateral Na <sup>+</sup> Diffusion in Apical Dendrites of Mouse CA1 Pyramidal Neurons

Sodium ions (Na<sup>+</sup>) are major charge carriers mediating neuronal excitation and play a fundamental role in brain physiology. Glutamatergic synaptic activity is accompanied by large transient Na<sup>+</sup> increases, but the spatiotemporal dynamics of Na<sup>+</sup> signals and properties of Na<sup>+</sup> diffusion within dendrites are largely unknown. To address these questions, we employed multiphoton Na<sup>+</sup> imaging combined with whole-cell patch clamp in dendrites of CA1 pyramidal neurons in tissue slices from mice of both sexes. Fluorescence lifetime microscopy revealed a dendritic baseline Na<sup>+</sup> concentration of ∼10 mM. Using intensity-based line scan imaging, we found that local, glutamate-evoked Na<sup>+</sup> signals spread rapidly within dendrites, with peak amplitudes decreasing and latencies increasing with increasing distance from the site of stimulation. Spread of Na<sup>+</sup> along dendrites was independent of dendrite diameter, order, or overall spine density in the ranges measured. Our experiments also show that dendritic Na<sup>+</sup> readily invades spines and suggest that spine necks may represent a partial diffusion barrier. Experimental data were well reproduced by mathematical simulations assuming normal diffusion with a diffusion coefficient of <i>D</i> <sub>Na+</sub> = 600 µm<sup>2</sup>/s. Modeling moreover revealed that lateral diffusion is key for the clearance of local Na<sup>+</sup> increases at early time points, whereas when diffusional gradients are diminished, Na<sup>+</sup>/K<sup>+</sup>-ATPase becomes more relevant. Taken together, our study thus demonstrates that Na<sup>+</sup> influx causes rapid lateral diffusion of Na<sup>+</sup> within spiny dendrites. This results in an efficient redistribution and fast recovery from local Na<sup>+</sup> transients which is mainly governed by concentration differences.

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Journal
Journal of Neuroscience
Published
2025-09-16
DOI
https://doi.org/10.1523/jneurosci.0077-25.2025
Primary Topic
Neuroscience and Neuropharmacology Research
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article
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article

Spatiotemporal Dynamics of Lateral Na + Diffusion in Apical Dendrites of Mouse CA1 Pyramidal Neurons

Christine R. Rose, J. D. Meyer, Niklas J. Gerkau, Fidel Santamarı́a et al.
Journal of Neuroscience
Neuroscience and Neuropharmacology Research
article

Spatiotemporal Dynamics of Lateral Na + Diffusion in Apical Dendrites of Mouse CA1 Pyramidal Neurons

Christine R. Rose, J. D. Meyer, Niklas J. Gerkau, Fidel Santamarı́a, Sacha B. Nelson, Karl W. Kafitz, Ghanim Ullah
article en

Abstract

Sodium ions (Na<sup>+</sup>) are major charge carriers mediating neuronal excitation and play a fundamental role in brain physiology. Glutamatergic synaptic activity is accompanied by large transient Na<sup>+</sup> increases, but the spatiotemporal dynamics of Na<sup>+</sup> signals and properties of Na<sup>+</sup> diffusion within dendrites are largely unknown. To address these questions, we employed multiphoton Na<sup>+</sup> imaging combined with whole-cell patch clamp in dendrites of CA1 pyramidal neurons in tissue slices from mice of both sexes. Fluorescence lifetime microscopy revealed a dendritic baseline Na<sup>+</sup> concentration of ∼10 mM. Using intensity-based line scan imaging, we found that local, glutamate-evoked Na<sup>+</sup> signals spread rapidly within dendrites, with peak amplitudes decreasing and latencies increasing with increasing distance from the site of stimulation. Spread of Na<sup>+</sup> along dendrites was independent of dendrite diameter, order, or overall spine density in the ranges measured. Our experiments also show that dendritic Na<sup>+</sup> readily invades spines and suggest that spine necks may represent a partial diffusion barrier. Experimental data were well reproduced by mathematical simulations assuming normal diffusion with a diffusion coefficient of <i>D</i> <sub>Na+</sub> = 600 µm<sup>2</sup>/s. Modeling moreover revealed that lateral diffusion is key for the clearance of local Na<sup>+</sup> increases at early time points, whereas when diffusional gradients are diminished, Na<sup>+</sup>/K<sup>+</sup>-ATPase becomes more relevant. Taken together, our study thus demonstrates that Na<sup>+</sup> influx causes rapid lateral diffusion of Na<sup>+</sup> within spiny dendrites. This results in an efficient redistribution and fast recovery from local Na<sup>+</sup> transients which is mainly governed by concentration differences.

Journal of NeuroscienceVol. 45(44)
University of South Florida (US), Heinrich Heine University Düsseldorf (DE), The University of Texas at San Antonio (US)
Openalex Percentile: Top 73%
Neuroscience and Neuropharmacology Research
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