Nonmonotonic synaptic excitation and imbalanced inhibition underlying cortical intensity tuning
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作者:
Wu, Guangying K.
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机构:Univ So Calif, Zilkha Neurogenet Inst, Keck Sch Med, Los Angeles, CA 90033 USA
Wu, Guangying K.
Li, Pingyang
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机构:Univ So Calif, Zilkha Neurogenet Inst, Keck Sch Med, Los Angeles, CA 90033 USA
Li, Pingyang
Tao, Huizhong W.
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机构:Univ So Calif, Zilkha Neurogenet Inst, Keck Sch Med, Los Angeles, CA 90033 USA
Tao, Huizhong W.
Zhang, Li I.
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Univ So Calif, Zilkha Neurogenet Inst, Keck Sch Med, Los Angeles, CA 90033 USAUniv So Calif, Zilkha Neurogenet Inst, Keck Sch Med, Los Angeles, CA 90033 USA
Zhang, Li I.
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机构:
[1] Univ So Calif, Zilkha Neurogenet Inst, Keck Sch Med, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Physiol & Biophys, Keck Sch Med, Los Angeles, CA 90033 USA
[3] Univ So Calif, Dept Ophthalmol, Keck Sch Med, Los Angeles, CA 90033 USA
[4] Univ So Calif, Grad Program Neurosci, Los Angeles, CA 90033 USA
Intensity-tuned neurons, characterized by their nonmonotonic response-level function, may play important roles in the encoding of sound intensity-related information. The synaptic mechanisms underlying intensity tuning remain unclear. Here, in vivo whole-cell recordings in rat auditory cortex revealed that intensity-tuned neurons, mostly clustered in a posterior zone, receive imbalanced tone-evoked excitatory and inhibitory synaptic inputs. Excitatory inputs exhibit nonmonotonic intensity tuning, whereas with tone intensity increments, the temporally delayed inhibitory inputs increase monotonically in strength. In addition, this delay reduces with the increase of intensity, resulting in an enhanced suppression of excitation at high intensities and a significant sharpening of intensity tuning. In contrast, non-intensity-tuned neurons exhibit covaried excitatory and inhibitory inputs, and the relative time interval between them is stable with intensity increments, resulting in monotonic response-level function. Thus, cortical intensity tuning is primarily determined by excitatory inputs and shaped by cortical inhibition through a dynamic control of excitatory and inhibitory timing.