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Timing Mechanisms Underlying Gate Control by Feedforward Inhibition.


ABSTRACT: The gate control theory proposes that A? mechanoreceptor inputs to spinal pain transmission T neurons are gated via feedforward inhibition, but it remains unclear how monosynaptic excitation is gated by disynaptic inhibitory inputs that arrive later. Here we report that A?-evoked, non-NMDAR-dependent EPSPs in T neurons are subthreshold, allowing time for inhibitory inputs to prevent action potential firing that requires slow-onset NMDAR activation. Potassium channel activities-including IA, whose sizes are established constitutively by PreprodynorphinCre-derived inhibitory neurons-either completely filter away A? inputs or make them subthreshold, thereby creating a permissive condition to achieve gate control. Capsaicin-activated nociceptor inputs reduce IA and sensitize the T neurons, allowing A? inputs to cause firing before inhibitory inputs arrive. Thus, distinct kinetics of glutamate receptors and electric filtering by potassium channels solve the timing problem underlying the gating by feedforward inhibition, and their modulation offers a way to bypass the gate control.

SUBMITTER: Zhang Y 

PROVIDER: S-EPMC6309466 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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Timing Mechanisms Underlying Gate Control by Feedforward Inhibition.

Zhang Yan Y   Liu Shenbin S   Zhang Yu-Qiu YQ   Goulding Martyn M   Wang Yan-Qing YQ   Ma Qiufu Q  

Neuron 20180816 5


The gate control theory proposes that Aβ mechanoreceptor inputs to spinal pain transmission T neurons are gated via feedforward inhibition, but it remains unclear how monosynaptic excitation is gated by disynaptic inhibitory inputs that arrive later. Here we report that Aβ-evoked, non-NMDAR-dependent EPSPs in T neurons are subthreshold, allowing time for inhibitory inputs to prevent action potential firing that requires slow-onset NMDAR activation. Potassium channel activities-including I<sub>A<  ...[more]

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