Abstract
The state of neural oscillation is important for various brain functions. In the basolateral nucleus of amygdala (BA), the oscillation frequency is accelerated in retrieval of conditioned fear memory. The amygdala receives sensory inputs from associated cortex and thalamus. Therefore, we tried to apply the bimodal sensory stimulation at slow frequency (5 Hz, functional frequency in behavioral context) for the entrainment of the BA oscillation. Young adult rats (P24-30) were stimulated by LED illuminator and acoustic speaker at 1 or 5 Hz for 1 hour. Immediately after the stimulus was finished, BA slices were prepared and whole-cell recording was applied to projection neuron. The slow (0.5-2 Hz) rhythmic IPSCs obtained from the pyramidal neuron was accelerated at ∼4 Hz by synchronous opto-acoustic stimulation at 5 Hz. However, the frequency of the neuron at the later recording did not change in the same slice, suggesting that this induced entrainment is transient and reversible phenomenon. As a result, the power distribution was shifted from 0.1-2 to 2-6 Hz by synchronous bimodal 5 Hz stimulation. The regularity of the interval between IPSCs, quantified by rhythm index and the concentration of power around peak frequency in the power spectrum, was not changed by rhythmic sensory stimulation. These results suggest that synchronous bimodal sensory stimuli control the neuronal oscillation frequency by applying with rhythmicity.
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Abstract
The state of neural oscillation is important for various brain functions. In the basolateral nucleus of amygdala (BA), the oscillation frequency is accelerated in retrieval of conditioned fear memory. The amygdala receives sensory inputs from associated cortex and thalamus. Therefore, we tried to apply the bimodal sensory stimulation at slow frequency (5 Hz, functional frequency in behavioral context) for the entrainment of the BA oscillation. Young adult rats (P24-30) were stimulated by LED illuminator and acoustic speaker at 1 or 5 Hz for 1 hour. Immediately after the stimulus was finished, BA slices were prepared and whole-cell recording was applied to projection neuron. The slow (0.5-2 Hz) rhythmic IPSCs obtained from the pyramidal neuron was accelerated at ∼4 Hz by synchronous opto-acoustic stimulation at 5 Hz. However, the frequency of the neuron at the later recording did not change in the same slice, suggesting that this induced entrainment is transient and reversible phenomenon. As a result, the power distribution was shifted from 0.1-2 to 2-6 Hz by synchronous bimodal 5 Hz stimulation. The regularity of the interval between IPSCs, quantified by rhythm index and the concentration of power around peak frequency in the power spectrum, was not changed by rhythmic sensory stimulation. These results suggest that synchronous bimodal sensory stimuli control the neuronal oscillation frequency by applying with rhythmicity.
Competing Interest Statement
The authors have declared no competing interest.
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