Abstract

BackgroundTranscranial ultrasound stimulation can acutely modulate brain activity, but the lasting effects on neurons are unknown. ObjectiveTo assess the excitability profile of neurons in the hours following transient ultrasound stimulation. MethodsPrimary rat cortical neurons were stimulated with a 40 s, 200 kHz pulsed ultrasound stimulation or sham-stimulation. Intrinsic firing properties were investigated through whole-cell patch-clamp recording by evoking action potentials in response to somatic current injection. Recordings were taken at set timepoints following ultrasound stimulation: 0–2 h, 6–8 h, 12–14 h and 24–26 h. Transmission electron microscopy was used to assess synaptic ultrastructure at the same timepoints. ResultsIn the 0–2 h window, neurons stimulated with ultrasound displayed an increase in the mean frequency of evoked action potentials of 32% above control cell levels (p = 0.023). After 4–6 h this increase was measured as 44% (p = 0.0043). By 12–14 h this effect was eliminated and remained absent 24–26 h post-stimulation. These changes to action potential firing occurred in conjunction with statistically significant differences between control and ultrasound-stimulated neurons in action potential half-width, depolarisation rate, and repolarisation rate, that were similarly eliminated by 24 h following stimulation. These effects occurred in the absence of alterations to intrinsic membrane properties or synaptic ultrastructure. ConclusionWe report that stimulating neurons with 40 s of ultrasound enhances their excitability for up to 8 h in conjunction with modifications to action potential kinetics. This occurs in the absence of major ultrastructural change or modification of intrinsic membrane properties. These results can inform the application of transcranial ultrasound in experimental and therapeutic settings.

Highlights

  • Exogenous stimulation of the brain has been extensively used to define cognitive processes and map out neural circuitry [1]

  • In neurons stimulated with ultrasound, mean spike frequency was significantly increased by 32% above control cell levels (Fig. 1Aii; effect of ultrasound stimulation: F(1, 28) 1⁄4 5.77, p 1⁄4 0.023; effect of treatment  current interaction: F(7, 188) 1⁄4 1.95, p 1⁄4 0.064), indicating enhanced excitability induced by ultrasound stimulation

  • There remained a robust 44% increase in mean spike frequency in ultrasound-stimulated compared with sham-stimulated neurons (Fig. 1Bii; effect of ultrasound stimulation: F(1, 27) 1⁄4 9.74, p 1⁄4 0.004; effect of current: F(7, 174) 1⁄4 187.0, p < 0.0001; effect of treatment  current interaction: F(7, 174) 1⁄4 9.57, p < 0.0001)

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Summary

Introduction

Exogenous stimulation of the brain has been extensively used to define cognitive processes and map out neural circuitry [1]. By 12e14 h this effect was eliminated and remained absent 24 e26 h post-stimulation These changes to action potential firing occurred in conjunction with statistically significant differences between control and ultrasound-stimulated neurons in action potential halfwidth, depolarisation rate, and repolarisation rate, that were eliminated by 24 h following stimulation. These effects occurred in the absence of alterations to intrinsic membrane properties or synaptic ultrastructure. Conclusion: We report that stimulating neurons with 40 s of ultrasound enhances their excitability for up to 8 h in conjunction with modifications to action potential kinetics This occurs in the absence of major ultrastructural change or modification of intrinsic membrane properties. These results can inform the application of transcranial ultrasound in experimental and therapeutic settings

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